U.S. patent application number 17/722513 was filed with the patent office on 2022-08-18 for cd73 inhibitors.
The applicant listed for this patent is ORIC Pharmaceuticals, Inc.. Invention is credited to Xiaohui DU, John EKSTEROWICZ, Valeria R. FANTIN, Erica L. JACKSON, Jared MOORE, Daqing SUN, Qiuping YE, Tatiana ZAVOROTINSKAYA.
Application Number | 20220259253 17/722513 |
Document ID | / |
Family ID | 1000006269406 |
Filed Date | 2022-08-18 |
United States Patent
Application |
20220259253 |
Kind Code |
A1 |
DU; Xiaohui ; et
al. |
August 18, 2022 |
CD73 INHIBITORS
Abstract
Described herein are CD73 inhibitors and pharmaceutical
compositions comprising said compounds. The subject compounds and
compositions are useful for the treatment of cancer, infections,
and neurodegenerative diseases.
Inventors: |
DU; Xiaohui; (Belmont,
CA) ; EKSTEROWICZ; John; (Burlingame, CA) ;
FANTIN; Valeria R.; (Burlingame, CA) ; JACKSON; Erica
L.; (Burlingame, CA) ; SUN; Daqing; (Foster
City, CA) ; YE; Qiuping; (Foster City, CA) ;
MOORE; Jared; (San Rafael, CA) ; ZAVOROTINSKAYA;
Tatiana; (Moraga, CA) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
ORIC Pharmaceuticals, Inc. |
South San Francisco |
CA |
US |
|
|
Family ID: |
1000006269406 |
Appl. No.: |
17/722513 |
Filed: |
April 18, 2022 |
Related U.S. Patent Documents
|
|
|
|
|
|
Application
Number |
Filing Date |
Patent Number |
|
|
16760380 |
Apr 29, 2020 |
|
|
|
PCT/US2018/059004 |
Nov 2, 2018 |
|
|
|
17722513 |
|
|
|
|
62664841 |
Apr 30, 2018 |
|
|
|
62581574 |
Nov 3, 2017 |
|
|
|
Current U.S.
Class: |
1/1 |
Current CPC
Class: |
A61K 31/7064 20130101;
A61P 35/00 20180101; A61K 45/06 20130101; C07H 19/056 20130101;
A61K 31/706 20130101; C07H 19/23 20130101 |
International
Class: |
C07H 19/23 20060101
C07H019/23; A61P 35/00 20060101 A61P035/00; A61K 31/706 20060101
A61K031/706; C07H 19/056 20060101 C07H019/056; A61K 31/7064
20060101 A61K031/7064 |
Claims
1. A compound of Formula (IIa), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof: ##STR00340## wherein; A is
--O-- or --CH.sub.2--; Q.sup.1 is CW and Q.sup.2 is N; or Q.sup.1
is N and Q.sup.2 is N; W is hydrogen, halogen, --CN, --OH,
--OR.sup.a, --SH, --SR.sup.a, --S(.dbd.O)R.sup.a, --NO.sub.2,
--NR.sup.cR.sup.d, --S(.dbd.O).sub.2R.sup.a,
--NHS(.dbd.O).sub.2R.sup.a, --S(.dbd.O).sub.2NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --OC(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--OC(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
--OC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(.dbd.O)NR.sup.cR.sup.d,
--NR.sup.bC(.dbd.O)R.sup.a, --NR.sup.bC(.dbd.O)OR.sup.b,
C.sub.1-C.sub.6alkyl, C.sub.1-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30; Z is
--NR.sup.1R.sup.2, --OR.sup.60, --SR.sup.61, or
--CR.sup.62R.sup.63R.sup.64; R.sup.1 and R.sup.2 are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl),
C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--S(.dbd.O).sub.2R.sup.15a, --S(.dbd.O).sub.2NR.sup.16aR.sup.17a,
or --C(.dbd.).sub.2R.sup.15a, wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30a; or
R.sup.1 and R.sup.2 are taken together with the nitrogen atom to
which they are attached to form a heterocycloalkyl optionally
substituted with one, two, or three R.sup.30b; R.sup.60 is
hydrogen, --C(.dbd.O)R.sup.15e, --C(.dbd.O)OR.sup.16e,
--C(.dbd.O)NR.sup.16eR.sup.17e, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.30m; R.sup.61 is hydrogen,
--C(.dbd.O)R.sup.15f, --C(.dbd.O)OR.sup.16f,
--C(.dbd.O)NR.sup.16fR.sup.17f, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.30n; R.sup.62, R.sup.63, and R.sup.64 are each
independently hydrogen, halogen, --CN, --OH, --OR.sup.15g, --SH,
--SR.sup.15g, --S(.dbd.O)R.sup.15g, --NO.sub.2,
--NR.sup.16gR.sup.17g, --S(.dbd.O).sub.2R.sup.15g,
--NHS(.dbd.O).sub.2R.sup.15g, --S(.dbd.O).sub.2NR.sup.16gR.sup.17g,
--C(.dbd.O)R.sup.15g, --OC(.dbd.O)R.sup.15g, --C(.dbd.O)OR.sup.16g,
--OC(.dbd.O)OR.sup.16g, --C(.dbd.O)NR.sup.16gR.sup.17g,
--OC(.dbd.O)NR.sup.16gR.sup.17g,
--NR.sup.16gC(.dbd.O)NR.sup.16gR.sup.17g,
--NR.sup.16gC(.dbd.O)R.sup.15g, --NR.sup.16gC(O)OR.sup.16g,
C.sub.1-C.sub.6alkyl, C.sub.2-C.sub.6alkenyl, C.sub.2-C.sub.6
alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30o; R.sup.3
is halogen, --CN, --OH, --OR.sup.15b, --SR.sup.18b,
--NR.sup.18bR.sup.17b, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30c; R.sup.4 and R.sup.7 are each independently
hydrogen, halogen, --OH, --OR.sup.15c,
--NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.13c, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.30d; R.sup.5 and R.sup.6 are each independently hydrogen,
halogen, --OH, --OR.sup.15d, --NR.sup.16cS(.dbd.O).sub.2R.sup.15d,
--NR.sup.16dC(.dbd.O)R.sup.15d, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.30e; X.sup.1 is a bond; Y.sup.1 is --S(.dbd.O).sub.2--;
Y.sup.2 is --(CR.sup.45R.sup.46).sub.v2--; R.sup.45 and R.sup.46
are each independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; v2 is 1-3; R.sup.15a, R.sup.15b, R.sup.15c, R.sup.15d,
R.sup.15e, R.sup.15f, R.sup.15g are each independently
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.30g; R.sup.16a, R.sup.16b, R.sup.16c,
R.sup.16d, R.sup.16e, R.sup.16f, R.sup.16g, R.sup.17a, R.sup.17b,
R.sup.17e, R.sup.17f, and R.sup.17g are each independently
hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, cycloalkyl, or heterocycloalkyl; wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, and heterocycloalkyl is
independently optionally substituted with one, two, or three
R.sup.30h; or R.sup.16a and R.sup.17a or R.sup.16b and R.sup.17b or
R.sup.16e and R.sup.17c or R.sup.16f and R.sup.17f or R.sup.16g and
R.sup.17g are taken together with the nitrogen atom to which they
are attached to form a heterocycloalkyl optionally substituted with
one, two, or three halogen, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl; R.sup.18b is C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl,
aryl, and heteroaryl is independently optionally substituted with
one, two, or three R.sup.30h; R.sup.21 and R.sup.22 are each
independently hydrogen, C.sub.1-C.sub.20alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--(CR.sup.23R.sup.24).sub.wC(.dbd.O)OR.sup.25,
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)R.sup.26,
--(CR.sup.23R.sup.24).sub.wSC(.dbd.O)R.sup.26, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30k; or
R.sup.21 and R.sup.22 are taken together with the atoms to which
they are attached to form a heterocycloalkyl optionally substituted
with one, two, or three R.sup.30l; each R.sup.23 and R.sup.24 are
independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; each R.sup.25 is independently hydrogen,
C.sub.1-C.sub.6alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, or C.sub.1-C.sub.6 heteroalkyl; each R.sup.26 is
independently C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, or C.sub.1-C.sub.6 heteroalkyl; each w is
independently 1-4; each R.sup.30, R.sup.30a, R.sup.30b, R.sup.30c,
R.sup.30d, R.sup.30e, R.sup.30g, R.sup.30h, R.sup.30i, R.sup.30j,
R.sup.30k, R.sup.30l, R.sup.30m, R.sup.30n, and R.sup.30o are
independently halogen, --CN, --OH, --OR.sup.a, --SH, --SR.sup.a,
--S(.dbd.O)R.sup.a, --NO.sub.2, --NR.sup.cR.sup.d,
--S(.dbd.O).sub.2R.sup.a, --NHS(.dbd.O).sub.2R.sup.a,
--S(.dbd.O).sub.2NR.sup.cR.sup.d, --C(.dbd.O)R.sup.a,
--OC(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b, --OC(O)OR.sup.b,
--C(O)NR.sup.cR.sup.d, --OC(O)NR.sup.cR.sup.d,
--NR.sup.bC(O)NR.sup.cR.sup.d, --NR.sup.bC(.dbd.O)R.sup.a,
--NR.sup.bC(.dbd.O)OR.sup.b, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.31; each R.sup.31 is independently halogen, --CN,
--OH, --OR.sup.a, --SH, --SR.sup.a, --S(.dbd.O)R.sup.a, --NO.sub.2,
--NR.sup.cR.sup.d, --S(.dbd.O).sub.2R.sup.a,
--NHS(.dbd.O).sub.2R.sup.a, --S(.dbd.O).sub.2NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --OC(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--OC(O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
--OC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(O)NR.sup.cR.sup.d,
--NR.sup.bC(.dbd.O)R.sup.a, --NR.sup.bC(.dbd.O)OR.sup.b,
C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 haloalkyl, C.sub.1-C.sub.6
hydroxyalkyl, C.sub.1-C.sub.6 heteroalkyl, or cycloalkyl optionally
substituted with one, two, or three halogen, C.sub.1-C.sub.6 alkyl,
or C.sub.1-C.sub.6 haloalkyl; each R.sup.a is independently
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, C.sub.1-C.sub.6 heteroalkyl, cycloalkyl, heterocycloalkyl,
aryl, or heteroaryl; wherein the alkyl, alkenyl, alkynyl,
heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
halogen, --OH, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
each R.sup.b is independently hydrogen, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, C.sub.1-C.sub.6
heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl;
wherein the alkyl, alkenyl, alkynyl, heteroalkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three halogen, --OH, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6 haloalkyl; and R.sup.c and R.sup.d are
each independently hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, C.sub.1-C.sub.6 heteroalkyl,
cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; wherein the
alkyl, alkenyl, alkyl, heteroalkyl, cycloalkyl, heterocycloalkyl,
aryl, and heteroaryl is independently optionally substituted with
one, two, or three halogen, --OH, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl; or R.sup.c and R.sup.d are taken
together with the nitrogen atom to which they are attached to form
a heterocycloalkyl optionally substituted with one, two, or three
halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl.
2. The compound of claim 1, pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, wherein; R.sup.45 and R.sup.46
are each independently hydrogen, halogen, or C.sub.1-C.sub.6 alkyl;
and v2 is 1 or 2.
3. The compound of claim 1 or 2, pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, wherein; R.sup.45 and R.sup.46
are each hydrogen; and v2 is 1.
4. The compound of any one of claims 1-3, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; Q.sup.1
is CW; and Q.sup.2 is N.
5. The compound of any one of claims 1-3 pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; Q.sup.1
is N; and Q.sup.2 is N.
6. The compound of any one of claims 1-4, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; W is
hydrogen, halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
C.sub.1-C.sub.6alkyl, cycloalkyl, or heterocycloalkyl; wherein each
alkyl, cycloalkyl, and heterocycloalkyl, is independently
optionally substituted with one, two, or three R.sup.30.
7. The compound of any one of claims 1-4 or 6, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; W is
hydrogen, halogen, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
C.sub.1-C.sub.4 alkyl, or C.sub.1-C.sub.6 haloalkyl.
8. The compound of any one of claims 1-4 or 6 or 7,
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
wherein; W is hydrogen.
9. The compound of any one of claims 1-8, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; A is
--O--.
10. The compound of any one of claims 1-8, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; A is
--CH.sub.2--.
11. The compound of any one of claims 1-10, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.5
and R.sup.6 are each independently hydrogen, halogen,
C.sub.1-C.sub.6 alkyl, or cycloalkyl; wherein each alkyl and
cycloalkyl is independently optionally substituted with one, two,
or three R.sup.30e.
12. The compound of any one of claims 1-11, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; each
R.sup.30e is independently halogen or C.sub.1-C.sub.6 alkyl.
13. The compound of any one of claims 1-12, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.5
and R.sup.6 are each hydrogen.
14. The compound of any one of claims 1-13, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.4
and R.sup.7 are each independently hydrogen, halogen, --OH,
--OR.sup.15c, --NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.15c, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30d.
15. The compound of any one of claims 1-14, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; each
R.sup.30d is independently halogen or C.sub.1-C.sub.6 alkyl.
16. The compound of any one of claims 1-15, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.4
and R.sup.7 are each independently hydrogen, halogen, --OH,
--OR.sup.15c, --NR.sup.16cS(.dbd.O).sub.2R.sup.15c, or
--NR.sup.16cC(.dbd.O)R.sup.15c.
17. The compound of any one of claims 1-16, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein;
R.sup.15c and R.sup.15d are each independently C.sub.1-C.sub.6
alkyl or C.sub.1-C.sub.6 haloalkyl; and R.sup.16c and R.sup.16d are
each independently hydrogen, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl.
18. The compound of any one of claims 1-17, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein;
R.sup.15c and R.sup.15d are each independently C.sub.1-C.sub.6
alkyl; and R.sup.16c and R.sup.16d are each independently hydrogen
or C.sub.1-C.sub.6 alkyl.
19. The compound of any one of claims 1-18, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.4
and R.sup.7 are each independently hydrogen, halogen, or --OH.
20. The compound of any one of claims 1-19, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.4
and R.sup.7 are each independently halogen or --OH.
21. The compound of any one of claims 1-20, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.4
and R.sup.7 are each --OH.
22. The compound of any one of claims 1-21, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; Z is
--NR.sup.1R.sup.2.
23. The compound of any of claims 1-22, pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, wherein; R.sup.1 is
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl),
C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--S(.dbd.O).sub.2R.sup.15a, --S(.dbd.O).sub.2NR.sup.16aR.sup.17a,
or --C(.dbd.O).sub.2R.sup.15a; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.30a.
24. The compound of any of claims 1-23, pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, wherein; R.sup.15a is
C.sub.1-C.sub.6 alkyl, aryl, or C.sub.1-C.sub.6 alkyl(aryl);
wherein each alkyl and aryl is optionally substituted with one,
two, or three halogen; and R.sup.15a and R.sup.17a are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, aryl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl is
optionally substituted with one, two, or three halogen; and
25. The compound of any of claims 1-24, pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, wherein; R.sup.1 is
C.sub.1-C.sub.6 alkyl; and R.sup.16a and R.sup.17a are each
independently hydrogen or C.sub.1-C.sub.6 alkyl.
26. The compound of any one of claims 1-25, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.1
is C.sub.1-C.sub.6 alkyl, cycloalkyl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30a.
27. The compound of any one of claims 1-26, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.1
is C.sub.1-C.sub.6 alkyl, cycloalkyl, or C.sub.1-C.sub.6
alkyl(aryl); wherein each alkyl, cycloalkyl, and aryl is
independently optionally substituted with one, two, or three
R.sup.30a.
28. The compound of any one of claims 1-27, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.1
is cycloalkyl or C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl,
cycloalkyl, and aryl is independently optionally substituted with
one, two, or three R.sup.30a.
29. The compound of any one of claims 1-28, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; each
R.sup.30a is independently halogen, --CN, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl; wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optimally substituted with one,
two, or three R.sup.31.
30. The compound of any one of claims 1-29, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; each
R.sup.31 is independently halogen or C.sub.1-C.sub.6 alkyl.
31. The compound of any one of claims 1-30, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; each
R.sup.30a is independently halogen, --CN, --OH, --OR.sup.a,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl.
32. The compound of any one of claims 1-31, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; each
R.sup.30a is independently halogen.
33. The compound of any one of claims 1-32, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.2
is hydrogen or C.sub.1-C.sub.6 alkyl.
34. The compound of any one of claims 1-25, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.1
and R.sup.2 are taken together with the nitrogen atom to which they
are attached to form a heterocycloalkyl optionally substituted with
one, two, or three R.sup.31b.
35. The compound of any one of claims 1-25 or 34, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.1
and R.sup.2 are taken together with the nitrogen atom to which they
are attached to form a piperidine or a pyrrolidine optionally
substituted with one, two, or three R.sup.30b.
36. The compound of any one of claims 1-25 or 34 or 35,
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
wherein; each R.sup.30b is independently aryl optionally
substituted with one, two, or three R.sup.31; and each R.sup.31 is
independently halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl.
37. The compound of any one of claims 1-25 or 34-36,
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
wherein; R.sup.30b is aryl.
38. The compound of any one of claims 1-37, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.3
is halogen, --CN, --SR.sup.18b, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30c.
39. The compound of any one of claims 1-38, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.3
is halogen, --CN, --SR.sup.18b, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 alkyl(cycloalkyl); wherein each alkyl, and
cycloalkyl is independently optionally substituted with one, two,
or three R.sup.30c.
40. The compound of any one of claims 1-39, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein;
R.sup.18b is cycloalkyl or C.sub.1-C.sub.6 alkyl(cycloalkyl).
41. The compound of any one of claims 1-40, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; each
R.sup.30c is independently halogen or C.sub.1-C.sub.6 alkyl.
42. The compound of any one of claims 1-38, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.3
is halogen.
43. The compound of any one of claims 1-42, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein;
R.sup.21 and R.sup.22 are each independently hydrogen, aryl, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25.
44. The compound of any one of claims 1-43, pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein;
R.sup.21 and R.sup.22 are each hydrogen.
45. The compound of claim 1, pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, selected from: ##STR00341##
##STR00342##
46. A compound of Formula (III), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof: ##STR00343## wherein;
Q.sup.3 and Q.sup.4 are independently N or CW.sup.1; provided that
at least one of Q.sup.3 or Q.sup.4 is N; W.sup.1 is hydrogen,
halogen, --CN, --OH, --OR.sup.a, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl; A is --O-- or --CH.sub.2--; Z is
--NR.sup.1R.sup.2, --OR.sup.60, --SR.sup.61, or
--CR.sup.62R.sup.63R.sup.64; R.sup.1 and R.sup.2 are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl),
C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--S(.dbd.O).sub.2R.sup.15a, --S(.dbd.O).sub.2NR.sup.16aR.sup.17a,
or --C(.dbd.O).sub.2R.sup.15a; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.30a; or R.sup.1 and R.sup.2 are taken together with the
nitrogen atom to which they are attached to form a heterocycloalkyl
optionally substituted with one, two, or three R.sup.30b; R.sup.60
is hydrogen, --C(.dbd.O)R.sup.15e, --C(.dbd.O)OR.sup.16e,
--C(.dbd.O)NR.sup.16eR.sup.17e, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.30m; R.sup.61 is hydrogen,
--C(.dbd.O)R.sup.15f, --C(.dbd.O)OR.sup.16f,
--C(.dbd.O)NR.sup.16fR.sup.17f, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.30n; R.sup.62, R.sup.63, and R.sup.64 are each
independently hydrogen, halogen, --CN, --OH, --OR.sup.15g, --SH,
--SR.sup.15g, --S(.dbd.O)R.sup.15g, --NO.sub.2,
--NR.sup.16gR.sup.17g, --S(.dbd.O).sub.2R.sup.15g,
--NHS(.dbd.O).sub.2R.sup.15g, --S(.dbd.O).sub.2NR.sup.16gR.sup.17g,
--C(.dbd.O)R.sup.15g, --OC(.dbd.O)R.sup.15g, --C(.dbd.O)OR.sup.16g,
--OC(.dbd.O)OR.sup.16g, --C(.dbd.O)NR.sup.16gR.sup.17g,
--OC(.dbd.O)NR.sup.16gR.sup.17g,
--NR.sup.16gC(.dbd.O)NR.sup.16gR.sup.17g,
--NR.sup.16gC(.dbd.O)R.sup.15g, --NR.sup.16gC(.dbd.O)OR.sup.16g,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6alkenyl, C.sub.2-C.sub.6
alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30o; R.sup.3
is halogen, --CN, --OH, --OR.sup.15b, --SR.sup.18b,
--NR.sup.16bR.sup.17b, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30c; R.sup.4 and R.sup.7 are each independently
hydrogen, halogen, --OH, --OR.sup.15c,
--NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.15c, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.30d; R.sup.5 and R.sup.6 are each independently hydrogen,
halogen, --OH, --OR.sup.15d, --NR.sup.16dS(.dbd.O).sub.2R.sup.15d,
--NR.sup.16dC(.dbd.O)R.sup.15d, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.30e; R.sup.8 is hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; R.sup.9 and R.sup.10 are each independently hydrogen,
halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
X.sup.1 is bond, --C(.dbd.O)--, --S(.dbd.O).sub.2--, --O--, or
--CR.sup.40R.sup.41--; Y.sup.1 is --C(.dbd.O)--,
--(CR.sup.42R.sup.43).sub.v1--, --S(.dbd.O).sub.2--, --NR.sup.44--,
--S--, or --O--; Y.sup.1 is --(CR.sup.45R.sup.46).sub.v2--,
--NR.sup.47-- or --O--; R.sup.40, R.sup.41, R.sup.42, R.sup.43,
R.sup.45, and R.sup.46 are each independently hydrogen, halogen,
--OH, --OR.sup.a, --NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, or
heterocycloalkyl; wherein each alkyl, alkenyl, alkynyl, cycloalkyl,
and heterocycloalkyl is independently optionally substituted with
one, two, or three R.sup.30f; R.sup.44 and R.sup.47 are each
independently hydrogen, --S(.dbd.O)R.sup.a, --S(.dbd.O)--R.sup.a,
--S(.dbd.O).sub.2NR.sup.cR.sup.d, --C(.dbd.O)R.sup.a,
--C(.dbd.O)OR.sup.b, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, or heterocycloalkyl;
wherein each alkyl, alkenyl, alkynyl, cycloalkyl, and
heterocycloalkyl is independently optionally substituted with one,
two, or three R.sup.30f; v1 and v2 are each independently 1-3;
R.sup.15a, R.sup.15b, R.sup.15c, R.sup.15d, R.sup.15e, R.sup.15f,
R.sup.15g are each independently C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.30g; R.sup.16a, R.sup.16b, R.sup.16c, R.sup.16d, R.sup.16e,
R.sup.16f, R.sup.16gA, R.sup.17a, R.sup.17b, R.sup.17e, R.sup.17f,
and R.sup.17g are each independently hydrogen, C.sub.1-C.sub.6
alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl,
cycloalkyl, or heterocycloalkyl; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, and heterocycloalkyl is independently
optionally substituted with one, two, or three R.sup.30h; or
R.sup.16a and R.sup.17a or R.sup.16b and R.sup.17b or R.sup.16e and
R.sup.17e or R.sup.16f and R.sup.17f or R.sup.16g and R.sup.17g are
taken together with the nitrogen atom to which they are attached to
form a heterocycloalkyl optionally substituted with one, two, or
three halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
R.sup.18b is C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30i; R.sup.21 and R.sup.22 are each independently
hydrogen, C.sub.1-C.sub.20alkyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl),
C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--(CR.sup.23R.sup.24).sub.wC(.dbd.O)OR.sup.25,
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)R.sup.26,
--(CR.sup.23R.sup.24).sub.wSC(.dbd.O)R.sup.26, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30k; or
R.sup.21 and R.sup.22 are taken together with the atoms to which
they are attached to form a heterocycloalkyl optionally substituted
with one, two, or three R.sup.30l; each R.sup.23 and R.sup.14 are
independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; each R.sup.25 is independently hydrogen,
C.sub.1-C.sub.6alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, or C.sub.1-C.sub.6 heteroalkyl; each R.sup.26 is
independently C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, or C.sub.1-C.sub.6 heteroalkyl; each w is
independently 1-4; each R.sup.30a, R.sup.30b, R.sup.30c, R.sup.30d,
R.sup.30e, R.sub.30f, R.sup.30g, R.sup.30h, R.sup.30i, R.sup.30j,
R.sup.30k, R.sup.30l, R.sup.30m, R.sup.30n, R.sup.30o, and
R.sup.30p are independently halogen, --CN, --OH, --OR.sup.a, --SH,
--SR.sup.a, --S(.dbd.O)R.sup.a, --NO.sub.2, --NR.sup.cR.sup.d,
--S(.dbd.O).sub.2R.sup.a, --NHS(.dbd.O).sub.2R.sup.a,
--S(.dbd.O).sub.3NR.sup.cR.sup.d, --C(.dbd.O)R.sup.a,
--OC(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b, --OC(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, --OC(.dbd.O)NR.sup.cR.sup.d,
--NR.sup.bC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(.dbd.O)R.sup.a,
--NR.sup.bC(.dbd.O)OR.sup.b, C.sub.1-C.sub.6alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.31; each R.sup.31 is independently halogen, --CN,
--OH, --OR.sup.a, --SH, --SR.sup.a, --S(.dbd.O)R.sup.a, --NO.sub.2,
--NR.sup.cR.sup.d, --S(.dbd.O).sub.2R.sup.a,
--NHS(.dbd.O).sub.2R.sup.a, --S(.dbd.O).sub.2NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --OC(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--OC(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
--OC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(.dbd.O)NR.sup.cR.sup.d,
--NR.sup.bC(O)R.sup.a, --NR.sup.bC(O)OR.sup.b, C.sub.1-C.sub.6
alkyl, C.sub.1-C.sub.6haloalkyl, C.sub.1-C.sub.6 hydroxyalkyl,
C.sub.1-C.sub.6 heteroalkyl, or cycloalkyl optimally substituted
with one, two, or three halogen, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.4 haloalkyl; each R.sup.a is independently
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, C.sub.1-C.sub.6 heteroalkyl, cycloalkyl, heterocycloalkyl,
aryl, or heteroaryl; wherein the alkyl, alkenyl, alkynyl,
heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optimally substituted with one, two, or three
halogen, --OH, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
each R.sup.b is independently hydrogen, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, C.sub.1-C.sub.6
heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl;
wherein the alkyl, alkenyl, alkynyl, heteroalkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three halogen, --OH, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6 haloalkyl; and R.sup.c and R.sup.d are
each independently hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, C.sub.1-C.sub.6 heteroalkyl,
cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; wherein the
alkyl, alkenyl, alkynyl, heteroalkyl, cycloalkyl, heterocycloalkyl,
aryl, and heteroaryl is independently optionally substituted with
one, two, or three halogen, --OH, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl; or R.sup.c and R.sup.d are taken
together with the nitrogen atom to which they are attached to form
a heterocycloalkyl optionally substituted with one, two, or three
halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl.
47. The compound of claim 46, or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, wherein: ##STR00344##
48. The compound of claim 46 or 47, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein:
##STR00345##
49. The compound of any one of claims 46-48, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein:
##STR00346##
50. The compound of any one of claims 46-48, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein:
##STR00347##
51. The compound of any one of claims 46-50, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; Q.sup.3
is N and Q.sup.4 is CW.sup.1.
52. The compound of any one of claims 46-50, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; Q.sup.4
is N and Q.sup.3 is CW.sup.1.
53. The compound of any one of claims 46-50, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; Q.sup.3
is N and Q.sup.4 is N.
54. The compound of any one of claims 46-53, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; W.sup.1
is hydrogen, halogen, or C.sub.1-C.sub.6 alkyl.
55. The compound of any one of claims 46-54, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.8
is hydrogen or C.sub.1-C.sub.6 alkyl.
56. The compound of any one of claims 46-55, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.8
is hydrogen.
57. The compound of any one of claims 46-56, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.9
and R.sup.10 are each independently hydrogen or C.sub.1-C.sub.6
alkyl.
58. The compound of any one of claims 46-57, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.9
and R.sup.10 are each hydrogen.
59. The compound of any one of claims 46-58, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein;
R.sup.40 and R.sup.41 are each independently hydrogen, halogen,
--OH, --OR.sup.a, --NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl.
60. The compound of any one of claims 46-59, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein;
R.sup.40 and R.sup.41 are each independently hydrogen, halogen,
--OH, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl.
61. The compound of any one of claims 46-60, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein;
R.sup.40 and R.sup.41 are each hydrogen.
62. The compound of any one of claims 46-61, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein;
R.sup.42 and R.sup.43 are each independently hydrogen, halogen,
--OH, --OR.sup.a, or C.sub.1-C.sub.6 alkyl.
63. The compound of any one of claims 46-62, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein;
R.sup.42 and R.sup.43 are each hydrogen.
64. The compound of any one of claims 46-63, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein;
R.sup.44 is hydrogen, --S(.dbd.O)R.sup.a, --C(.dbd.O)R.sup.a,
C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 haloalkcyl, or
C.sub.1-C.sub.6 alkyl(aryl).
65. The compound of any one of claims 46-64, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein;
R.sup.44 is hydrogen or C.sub.1-C.sub.6 alkyl.
66. The compound of any one of claims 46-65, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein;
R.sup.45 and R.sup.46 are each independently hydrogen, halogen,
--OH, --OR.sup.a, --NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl,
cycloalkyl, or heterocycloalkyl; wherein each alkyl, cycloalkyl,
and heterocycloalkyl is independently optionally substituted with
one, two, or three R.sup.30p.
67. The compound of any one of claims 46-66, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein;
R.sup.45 and R.sup.46 are each independently hydrogen, halogen,
C.sub.1-C.sub.6 alkyl, or cycloalkyl; wherein each alkyl and
cycloalkyl is independently optionally substituted with one, two,
or three R.sup.30p.
68. The compound of any one of claims 46-67, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein;
R.sup.45 and R.sup.46 are each independently hydrogen, halogen,
C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 hydroxyalkyl,
C.sub.1-C.sub.6 haloalkyl, C.sub.1-C.sub.6 alkyl(cycloalkyl),
C.sub.1-C.sub.6 alkyl(aryl), or cycloalkyl.
69. The compound of any one of claims 46-68, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein;
R.sup.45 and R.sup.46 are each independently hydrogen or
C.sub.1-C.sub.6 alkyl.
70. The compound of any one of claims 46-69, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein;
R.sup.45 and R.sup.46 are each hydrogen.
71. The compound of any one of claims 46-67, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein;
R.sup.45 is halogen, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
C.sub.1-C.sub.6 alkyl, cycloalkyl, or heterocycloalkyl; wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, and heterocycloalkyl is
independently optionally substituted with one, two, or three
R.sup.30p; and R.sup.46 is hydrogen or C.sub.1-C.sub.6 alkyl.
72. The compound of any one of claims 46-67 or 71, or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
wherein; R.sup.45 is halogen, C.sub.1-C.sub.6 alkyl, or cycloalkyl;
wherein each alkyl and cycloalkyl is independently optionally
substituted with one, two, or three R.sup.30p; and R.sup.46 is
hydrogen or C.sub.1-C.sub.6 alkyl.
73. The compound of any one of claims 46-67 or 71 or 72, or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
wherein; R.sup.45 is halogen, C.sub.1-C.sub.6 alkyl,
C.sub.1-C.sub.6 hydroxyalkyl, C.sub.1-C.sub.6 haloalkyl,
C.sub.1-C.sub.6 alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(aryl), or
cycloalkyl; and R.sup.46 is hydrogen or C.sub.1-C.sub.6 alkyl.
74. The compound of any one of claims 46-67 or 71-73, or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
wherein; R.sup.45 is C.sub.1-C.sub.6 alkyl; and R.sup.46 is
hydrogen or C.sub.1-C.sub.6 alkyl.
75. The compound of any one of claims 46-74, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; A is
--O--.
76. The compound of any one of claims 46-74, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; A is
--CH.sub.2--.
77. The compound of any one of claims 46-76, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.5
and R.sup.6 are each independently hydrogen, halogen,
C.sub.1-C.sub.6 alkyl, or cycloalkyl; wherein each alkyl and
cycloalkyl is independently optionally substituted with one, two,
or three R.sup.30e.
78. The compound of any one of claims 46-77, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; each
R.sup.30c is independently halogen or C.sub.1-C.sub.6 alkyl.
79. The compound of any one of claims 46-78, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.5
and R.sup.6 are each hydrogen.
80. The compound of any one of claims 46-79, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.4
and R.sup.7 are each independently hydrogen, halogen, --OH,
--OR.sup.15c, --NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.15c, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30d.
81. The compound of any one of claims 46-80, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; each
R.sup.30d is independently halogen or C.sub.1-C.sub.6 alkyl.
82. The compound of any one of claims 46-80, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.4
and R.sup.7 are each independently hydrogen, halogen, --OH,
--OR.sup.15c, --NR.sup.16cS(.dbd.O).sub.2R.sup.15e, or
--NR.sup.16cC(.dbd.O)R.sup.15e.
83. The compound of any one of claims 46-82, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein;
R.sup.15c and R.sup.15d are each independently C.sub.1-C.sub.6
alkyl or C.sub.1-C.sub.6 haloalkyl; and R.sup.16c and R.sup.16d are
each independently hydrogen, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl.
84. The compound of any one of claims 46-83, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein;
R.sup.15c and R.sup.15d are each independently C.sub.1-C.sub.6
alkyl; and R.sup.16c and R.sup.16d are each independently hydrogen
or C.sub.1-C.sub.6 alkyl.
85. The compound of any one of claims 46-84, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.4
and R.sup.7 are each independently hydrogen, halogen, or --OH.
86. The compound of any one of claims 46-85, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.4
and R.sup.7 are each independently halogen or --OH.
87. The compound of any one of claims 46-86, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.4
and R.sup.7 are each --OH.
88. The compound of any one of claims 46-87, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; Z is
--NR.sup.1R.sup.2.
89. The compound of any one of claims 46-88, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.1
is C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30a.
90. The compound of any one of claims 46-89, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.1
is C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30a.
91. The compound of any one of claims 46-90, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.1
is C.sub.1-C.sub.6 alkyl, cycloalkyl, or C.sub.1-C.sub.6
alkyl(aryl); wherein each alkyl, cycloalkyl, and aryl is
independently optionally substituted with one, two, or three
R.sup.30a.
92. The compound of any one of claims 46-91, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.1
is cycloalkyl or C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl,
cycloalkyl, and aryl is independently optionally substituted with
one, two, or three R.sup.30a.
93. The compound of any one of claims 46-92, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; each
R.sup.30a is independently halogen, --CN, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl; wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.31.
94. The compound of any one of claims 46-93, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; each
R.sup.30a is independently halogen, --CN, --OH, --OR.sup.a,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl.
95. The compound of any one of claims 46-94, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; each
R.sup.30a is independently halogen.
96. The compound of any one of claims 46-95, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.2
is hydrogen or C.sub.1-C.sub.6 alkyl.
97. The compound of any one of claims 46-88, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.1
and R.sup.2 are taken together with the nitrogen atom to which they
are attached to form a heterocycloalkyl optionally substituted with
one, two, or three R.sup.30b.
98. The compound of any one of claims 46-88 or 97, or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
wherein; R.sup.1 and R.sup.2 are taken together with the nitrogen
atom to which they are attached to form an azetidine, a piperidine,
a morpholine, or a pyrrolidine optionally substituted with one,
two, or three R.sup.30b.
99. The compound of any one of claims 46-98, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.3
is halogen, --CN, --OR.sup.15b, --SR.sup.18b,
--NR.sup.16bR.sup.17b, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30c.
100. The compound of any one of claims 46-99, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, wherein; R.sup.3
is halogen, --CN, --OR.sup.15b, --NR.sup.16bR.sup.17b,
C.sub.1-C.sub.6 alkyl, cycloalkyl, or heterocycloalkyl; wherein
each alkyl, cycloalkyl, and heterocycloalkyl is independently
optionally substituted with one, two, or three R.sup.30c.
101. The compound of any one of claims 46-100, or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
wherein; R.sup.15b is C.sub.1-C.sub.6 alkyl.
102. The compound of any one of claims 46-101, or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
wherein; R.sup.16b and R.sup.17b are independently hydrogen or is
C.sub.1-C.sub.6 alkyl.
103. The compound of any one of claims 46-102, or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
wherein; each R.sup.30c is independently halogen or C.sub.1-C.sub.6
alkyl.
104. The compound of any one of claims 46-103, or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
wherein; R.sup.3 is halogen.
105. The compound of any one of claims 46-104, or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
wherein; R.sup.21 and R.sup.22 are each independently hydrogen,
aryl, or --(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25.
106. The compound of any one of claims 46-105, or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
wherein; R.sup.21 and R.sup.22 are each hydrogen.
107. The compound of any one of claims 46-106, or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
wherein; R.sup.21 and R.sup.22 are taken together with the atoms to
which they are attached to form a heterocycloalkyl optionally
substituted with one, two, or three R.sup.30l.
108. The compound of any one of claims 46-107, or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
wherein; R.sup.30l is C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optimally substituted with one, two, or three R.sup.31.
109. The compound of any one of claims 46-108, or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
wherein; R.sup.30l is aryl optionally substituted with one, two, or
three R.sup.31.
110. The compound of any one of claims 46-109, or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
wherein; each R.sup.31 is independently halogen or C.sub.1-C.sub.6
alkyl.
111. The compound of claim 46, pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, selected from: ##STR00348##
##STR00349##
112. A pharmaceutical composition comprising a compound of any one
of claims 1-111, or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, and a pharmaceutically acceptable
excipient.
113. A method of inhibiting CD73 comprising contacting CD73 with a
compound of any one of claims 1-111, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof.
114. A method of treating cancer in a subject, comprising
administering to the subject a compound of any one of claims 1-111,
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof.
115. A method of treating cancer in a subject, comprising
administering to the subject a pharmaceutical composition of claim
112.
116. The method of either of claim 114 or 115, wherein the cancer
is lung cancer, melanoma, breast cancer, ovarian cancer, colorectal
cancer, gastric cancer, gallbladder cancer, prostate cancer, renal
cancer, or a lymphoma.
117. The method of any one of claims 113-116, further comprising
administering a second therapeutic agent.
118. The method of claim 117, wherein the second therapeutic agent
is a chemotherapeutic agent or an immunotherapy agent.
119. A method of treating an infection in a subject, comprising
administering to the subject a compound of any one of claims 1-111,
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof.
120. A method of treating an infection in a subject, comprising
administering to the subject a pharmaceutical composition of claim
112.
121. The method of either of claim 119 or 120, wherein the
infection is a viral infection.
122. The method of either of claim 119 or 120, wherein the
infection is a parasitic infection.
123. A method of treating a neurodegenerative disease in a subject,
comprising administering to the subject a compound of any one of
claims 1-111, or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof.
124. A method of treating a neurodegenerative disease in a subject,
comprising administering to the subject a pharmaceutical
composition of claim 112.
125. The method of either of claim 123 or 124, wherein the
neurodegenerative disease is Alzheimer's disease, Parkinson's
disease, Huntington's disease, schizophrenia, or autism.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application is a continuation of U.S. application Ser.
No. 16/760,380, filed Apr. 29, 2020, which is a .sctn. 371 U.S.
National Stage Entry of International Application No.
PCT/US2018/059004, filed Nov. 2, 2018, which claims the benefit of
U.S. Provisional Application No. 62/581,574, filed Nov. 3, 2017,
and U.S. Provisional Application No. 62/664,841, filed Apr. 30,
2018, which are all hereby incorporated by reference in their
entirety.
BACKGROUND
[0002] A need exists in the art for an effective treatment of
cancer, infections, and neurodegenerative diseases.
BRIEF SUMMARY OF THE INVENTION
[0003] Provided herein are compounds of Formulas (I), (II), (IIa),
(IIb), (III), and (IV) or pharmaceutically acceptable salts,
solvates, or stereoisomers thereof, and pharmaceutical compositions
comprising said compounds. The subject compounds and compositions
are useful as CD73 inhibitors. Furthermore, the subject compounds
and compositions are useful for the treatment of cancers,
infections, and neurodegenerative diseases.
[0004] Provided herein are compounds having the structure of
Formula (Ita), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof:
##STR00001##
[0005] wherein; [0006] A is --O-- or --CH.sub.2--; [0007] Q.sup.1
is CW and Q.sup.2 is N; or [0008] Q.sup.1 is N and Q.sup.2 is N;
[0009] W is hydrogen, halogen, --CN, --OH, --OR.sup.a, --SH,
--SR.sup.a, --S(.dbd.O)R.sup.a, --NO.sub.2, --NR.sup.cR.sup.d,
--S(O).sub.2R.sup.8, --NHS(.dbd.O).sub.2R.sup.a,
--S(.dbd.O).sub.2NR.sup.cR.sup.d, --C(.dbd.O)R.sup.a,
--OC(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, --OC(.dbd.O)NR.sup.cR.sup.d,
--NR.sup.bC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(.dbd.O)R.sup.a,
--NR.sup.bC(C.sub.1-C.sub.6alkyl, C.sub.1-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30; [0010] Z is --NR.sup.1R.sup.2, --OR.sup.60,
--SR.sup.61, or --CR.sup.62R.sup.63R.sup.64; [0011] R.sup.1 and
R.sup.2 are each independently hydrogen, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--S(O).sub.2R.sup.15a, --S(.dbd.O).sub.2NR.sup.16aR.sup.17a, or
--C(.dbd.O).sub.2R.sup.15a; wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30a; [0012] or
R.sup.1 and R.sup.2 are taken together with the nitrogen atom to
which they are attached to form a heterocycloalkyl optionally
substituted with one, two, or three R.sup.30b; [0013] R.sup.60 is
hydrogen, --C(.dbd.O)R.sup.15e, --C(.dbd.O)OR.sup.16e,
--C(.dbd.O)NR.sup.16eR.sup.17e, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.30m; [0014] R.sup.61 is hydrogen,
--C(.dbd.O)R.sup.15f, --C(.dbd.O)OR.sup.16f,
--C(O)NR.sup.16fR.sup.17f, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl),
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30n; [0015] R.sup.62, R.sup.63, and R.sup.64 are
each independently hydrogen, halogen, --CN, --OH, --OR.sup.15g,
--SH, --SR.sup.15g, --S(.dbd.O)R.sup.15g, --NO.sub.2,
--NR.sup.16gR.sup.17g, --S(.dbd.O)+R.sup.15g,
--NHS(.dbd.O).sub.2R.sup.15g, --S(.dbd.O).sub.2NR.sup.16gR.sup.17g,
--C(.dbd.O)R.sup.15g, --OC(.dbd.O)R.sup.15g, --C(.dbd.O)OR.sup.16g,
--OC(.dbd.O)OR.sup.16R, --C(.dbd.O)NR.sup.16gR.sup.17g,
--OC(.dbd.O)NR.sup.16gR.sup.17g,
--NR.sup.16gC(.dbd.O)NR.sup.16gR.sup.17g,
--NR.sup.16gC(.dbd.O)R.sup.15g, --NR.sup.16gC(.dbd.O)OR.sup.16g,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30o; [0016]
R.sup.3 is halogen, --CN, --OH, --OR.sup.15b, --SR.sup.18b,
--NR.sup.16bR.sup.17b, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30c; [0017] R.sup.4 and R.sup.7 are each
independently hydrogen, halogen, --OH, --OR.sup.15c,
--NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.15c, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.30d; [0018] R.sup.5 and R.sup.6 are each independently
hydrogen, halogen, --OH, --OR.sup.15d,
--NR.sup.16cS(.dbd.O).sub.2R.sup.15d,
--NR.sup.16dC(.dbd.O)R.sup.15d, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.30e; [0019] X.sup.1 is a bond; [0020] Y.sup.1 is
--S(.dbd.O).sub.2--; [0021] Y.sup.2 is
--(CR.sup.45R.sup.46).sub.v2--; [0022] R.sup.45 and R.sup.46 are
each independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; [0023] v2 is 1-3; [0024] R.sup.15a, R.sup.15b,
R.sup.15c, R.sup.15d, R.sup.15e, R.sup.15f, R.sup.15g are each
independently C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl, aryl, or
heteroaryl; wherein each alkyl, alkenyl, alkynyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30g; [0025] R.sup.16a,
R.sup.16b, R.sup.16c, R.sup.16d, R.sup.16e, R.sup.16f, R.sup.16g,
R.sup.17a, R.sup.17b, R.sup.17c, R.sup.17f, and R.sup.17g are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, or heterocycloalkyl;
wherein each alkyl, alkenyl, alkynyl, cycloalkyl, and
heterocycloalkyl is independently optionally substituted with one,
two, or three R.sup.30h; [0026] or R.sup.16a and R.sup.17a or
R.sup.16b and R.sup.17b or R.sup.16e and R.sup.17e or R.sup.16f and
R.sup.17f or R.sup.16g and R.sup.17g are taken together with the
nitrogen atom to which they are attached to form a heterocycloalkyl
optionally substituted with one, two, or three halogen,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl; [0027]
R.sup.18b is C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.4 alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30i; [0028] R.sup.21 and R.sup.22 are each
independently hydrogen, C.sub.1-C.sub.20alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--(CR.sup.23R.sup.24).sub.wC(.dbd.O)OR.sup.23,
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)R.sup.26,
--(CR.sup.23R.sup.24).sub.wSC(.dbd.O)R.sup.26, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.2S; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30k; [0029] or
R.sup.21 and R.sup.22 are taken together with the atoms to which
they are attached to form a heterocycloalkyl optionally substituted
with one, two, or three R.sup.30l; [0030] each R.sup.23 and
R.sup.24 are independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; [0031] each R.sup.25 is independently hydrogen,
C.sub.1-C.sub.6alkyl, C.sub.2-6 alkenyl, C.sub.2-C.sub.6 alkynyl,
or C.sub.1-C.sub.6 heteroalkyl; [0032] each R.sup.26 is
independently C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0033]
each w is independently 1-4; [0034] each R.sup.30, R.sup.30a,
R.sup.30b, R.sup.30c, R.sup.30d, R.sup.30e, R.sup.30g, R.sup.30h,
R.sup.30i, R.sup.30j, R.sup.30k, R.sup.30l, R.sup.30m, R.sup.30n,
and R.sup.30o are independently halogen, --CN, --OH, --OR.sup.a,
--SH, --SR.sup.a, --S(O)R.sup.a, --NO.sub.2, --NR.sup.cR.sup.d,
--S(.dbd.O).sub.2R.sup.a, --NHS(.dbd.O).sub.2R.sup.a,
--S(.dbd.O).sub.2NR.sup.cR.sup.d, --C(.dbd.O)R.sup.a,
--OC(.dbd.O)RR, --C(.dbd.O)OR.sup.b, --OC(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, --OC(.dbd.O)NR.sup.cR.sup.d,
--NR.sup.bC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(.dbd.O)R.sup.a,
--NR.sup.bC(.dbd.O) R.sup.b, C.sub.1-C.sub.6alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.31; [0035] each R.sup.31 is independently halogen,
--CN, --OH, --OR.sup.a, --SH, --SR.sup.a, --S(.dbd.O)R.sup.a,
--NO.sub.2, --NR.sup.cR.sup.d, --S(.dbd.O).sub.2R.sup.a,
--NHS(.dbd.O).sub.2R.sup.a, --S(.dbd.O).sub.2NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --OC(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--OC(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
--OC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(.dbd.O)NR.sup.cR.sup.d,
--NR.sup.bC(.dbd.O)R.sup.a, --NR.sup.bC(.dbd.O)OR.sup.b,
C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 haloalkyl, C.sub.1-C.sub.6
hydroxyalkyl, C.sub.1-C.sub.6 heteroalkyl, or cycloalkyl optionally
substituted with one, two, or three halogen, C.sub.1-C.sub.6 alkyl,
or C.sub.1-C.sub.6 haloalkyl; [0036] each R.sup.a is independently
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, C.sub.1-C.sub.6 heteroalkyl, cycloalkyl, heterocycloalkyl,
aryl, or heteroaryl; wherein the alkyl, alkenyl, alkynyl,
heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optimally substituted with one, two, or three
halogen, --OH, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[0037] each R.sup.b is independently hydrogen, C.sub.1-C.sub.6
alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl,
C.sub.1-C.sub.6 heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, or
heteroaryl; wherein the alkyl, alkenyl, alkynyl, heteroalkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three halogen, --OH,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl; and [0038]
R.sup.c and R.sup.d are each independently hydrogen,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, C.sub.1-C.sub.6 heteroalkyl, cycloalkyl, heterocycloalkyl,
aryl, or heteroaryl; wherein the alkyl, alkenyl, alkynyl,
heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
halogen, --OH, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[0039] or R.sup.c and R.sup.d are taken together with the nitrogen
atom to which they are attached to form a heterocycloalkyl
optionally substituted with one, two, or three halogen,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl.
[0040] Also provided herein are compounds having the structure of
Formula (III), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof:
##STR00002##
wherein; [0041] Q.sup.3 and Q.sup.4 are independently N or
CW.sup.1; provided that at least one of Q.sup.3 or Q.sup.4 is N;
[0042] W.sup.1 is hydrogen, halogen, --CN, --OH, --OR.sup.a,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl; [0043] A is
--O-- or --CH.sub.2--:
[0044] Z is --NR.sup.1R.sup.2, --OR.sup.60, --SR.sup.61, or
--CR.sup.62R.sup.63R.sup.64; [0045] R.sup.1 and R.sup.2 are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl),
C.sub.1-C.sub.6 alkyl(heterocycloalkyl), --S(O).sub.2R.sup.15a,
--S(.dbd.O).sub.2NR.sup.16aR.sup.17a, or
--C(.dbd.O).sub.2R.sup.15a; wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30a; [0046] or
R.sup.1 and R.sup.2 are taken together with the nitrogen atom to
which they are attached to form a heterocycloalkyl optionally
substituted with one, two, or three R.sup.30b; [0047] R.sup.60 is
hydrogen, --C(.dbd.O)R.sup.15e, --C(.dbd.O)OR.sup.16e,
--C(.dbd.O)NR.sup.16eR.sup.17e, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.30m; [0048] R.sup.61 is hydrogen,
--C(.dbd.O)R.sup.15f, --C(.dbd.O)OR.sup.16f,
--C(O)NR.sup.16fR.sup.17f, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl),
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30n; [0049] R.sup.62, R.sup.63, and R.sup.64 are
each independently hydrogen, halogen, --CN, --OH, --OR.sup.15g,
--SH, --SR.sup.15g, --S(.dbd.O)R.sup.15g, --NO.sub.2,
--NR.sup.16gR.sup.17g, --S(.dbd.O)+R.sup.15g,
--NHS(.dbd.O).sub.2R.sup.15g, --S(O).sub.2NR.sup.16gR.sup.17g,
--C(.dbd.O)R.sup.15g, --OC(.dbd.O)R.sup.15g, --C(.dbd.O)OR.sup.16g,
--OC(.dbd.O)OR.sup.16g, --C(.dbd.O)NR.sup.16gR.sup.17g,
--OC(.dbd.O)NR.sup.16gR.sup.17g,
--NR.sup.16gC(.dbd.O)NR.sup.16gR.sup.17g,
--NR.sup.16gC(.dbd.O)R.sup.16g, --NR.sup.16gC(.dbd.O)OR.sup.16g,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6alkenyl, C.sub.2-C.sub.6
alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30o; [0050]
R.sup.3 is halogen, --CN, --OH, --OR.sup.15b, --SR.sup.18b,
--NR.sup.16bR.sup.17b, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30c; [0051] R.sup.4 and R.sup.7 are each
independently hydrogen, halogen, --OH, --OR.sup.15c,
--NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.15c, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.30d; [0052] R.sup.5 and R.sup.6 are each independently
hydrogen, halogen, --OH, --OR.sup.15d,
--NR.sup.16dS(.dbd.O).sub.2R.sup.15d,
--NR.sup.16dC(.dbd.O)R.sup.15d, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.30e; [0053] R.sup.8 is hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; [0054] R.sup.9 and R.sup.10 are each independently
hydrogen, halogen, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6haloalkyl; [0055] X.sup.1 is bond, --C(.dbd.O)--,
--S(.dbd.O).sub.2--, --O--, or --CR.sup.40R.sup.41--; [0056]
Y.sup.1 is --C(.dbd.O)--, --(CR.sup.42R.sup.43).sub.v1--,
--S(.dbd.O).sub.2--, --NR.sup.44--, --S--, or --O--; [0057] Y.sup.2
is --(CR.sup.45R.sup.46).sub.v2--, --NR.sup.47--, or --O--; [0058]
R.sup.40, R.sup.41, R.sup.42, R.sup.43, R.sup.45, and R.sup.46 are
each independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, cycloalkyl, or heterocycloalkyl; wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, and heterocycloalkyl is
independently optionally substituted with one, two, or three
R.sup.30p; [0059] R.sup.44 and R.sup.47 are each independently
hydrogen, --S(.dbd.O)R.sup.a, --S(.dbd.O).sub.2R.sup.a,
--S(.dbd.O).sub.2NR.sup.cR.sup.d, --C(.dbd.O)R.sup.a,
--C(.dbd.O)OR.sup.b, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, or heterocycloalkyl;
wherein each alkyl, alkenyl, alkynyl, cycloalkyl, and
heterocycloalkyl is independently optionally substituted with one,
two, or three R.sup.30f; [0060] v1 and v2 are each independently
1-3; [0061] R.sup.15a, R.sup.15b, R.sup.15c, R.sup.15d, R.sup.15e,
R.sup.15f, R.sup.15g are each independently C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.30g; [0062] R.sup.16a, R.sup.16b, R.sup.16c, R.sup.16d,
R.sup.16e, R.sup.16f, R.sup.16g, R.sup.17a, R.sup.17b, R.sup.17e,
R.sup.17g, and R.sup.17g are each independently hydrogen,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, cycloalkyl, or heterocycloalkyl; wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, and heterocycloalkyl is independently
optionally substituted with one, two, or three R.sup.30h; [0063] or
R.sup.16a and R.sup.17a or R.sup.16b and R.sup.17b or R.sup.16e and
R.sup.17e or R.sup.16f and R.sup.17f or R.sup.16g and R.sup.17g are
taken together with the nitrogen atom to which they are attached to
form a heterocycloalkyl optionally substituted with one, two, or
three halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6haloalkyl;
[0064] R.sup.18b is C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30i; [0065] R.sup.21 and R.sup.22 are each
independently hydrogen, C.sub.1-C.sub.20alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--(CR.sup.23R.sup.24).sub.wC(O)OR.sup.25,
--(CR.sup.23R.sup.24).sub.wOC(O)R.sup.26,
--(CR.sup.13R.sup.24).sub.wSC(.dbd.O)R.sup.25, or
--(CR.sup.13R.sup.24).sub.wOC(.dbd.O)OR.sup.25; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30k; [0066] or
R.sup.21 and R.sup.22 are taken together with the atoms to which
they are attached to form a heterocycloalkyl optionally substituted
with one, two, or three R.sup.30l; [0067] each R.sup.23 and
R.sup.24 are independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; [0068] each R.sup.25 is independently hydrogen,
C.sub.1-C.sub.6alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0069] each R.sup.26 is
independently C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0070]
each w is independently 1-4; [0071] each R.sup.30a, R.sup.30b,
R.sup.30c, R.sup.30d, R.sup.30e, R.sup.30f, R.sup.30g, R.sup.30h,
R.sup.30i, R.sup.30j, R.sup.30k, R.sup.30l, R.sup.30m, R.sup.30n,
R.sup.30o, and R.sup.30p are independently halogen, --CN, --OH,
--OR.sup.a, --SH, --SR.sup.a, --S(.dbd.O).sub.2R.sup.a, --NO.sub.2,
--NR.sup.cR.sup.d, --S(.dbd.O).sub.2R.sup.a,
--NHS(.dbd.O).sub.2R.sup.a, --S(.dbd.O).sub.2NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --OC(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--OC(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
--OC(O)NR.sup.cR.sup.d, --NR.sup.bC(.dbd.O)NR.sup.cR.sup.d,
--NR.sup.bC(.dbd.O)R.sup.a, --NR.sup.bC(.dbd.O)OR.sup.b,
C.sub.1-C.sub.6alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.31; [0072]
each R.sup.31 is independently halogen, --CN, --OH, --OR.sup.a,
--SH. --SR.sup.a, --S(.dbd.O)R.sup.a, --NO.sub.2,
--NR.sup.cR.sup.d, --S(.dbd.O).sub.2R.sup.a,
--NHS(.dbd.O).sub.2R.sup.a, --S(.dbd.O)NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --OC(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--OC(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
--OC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(O)NR.sup.cR.sup.d,
--NR.sup.bC(.dbd.O)R.sup.a, --NR.sup.bC(.dbd.O)OR.sup.b,
C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 haloalkyl, C.sub.1-C.sub.6
hydroxyalkyl, C.sub.1-C.sub.6 heteroalkyl, or cycloalkyl optionally
substituted with one, two, or three halogen, C.sub.1-C.sub.6 alkyl,
or C.sub.1-C.sub.6 haloalkyl; [0073] each R.sup.a is independently
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, C.sub.1-C.sub.6 heteroalkyl, cycloalkyl, heterocycloalkyl,
aryl, or heteroaryl; wherein the alkyl, alkenyl, alkynyl,
heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
halogen, --OH, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[0074] each R.sup.b is independently hydrogen, C.sub.1-C.sub.6
alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl,
C.sub.1-C.sub.6 heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, or
heteroaryl; wherein the alkyl, alkenyl, alkynyl, heteroalkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three halogen, --OH,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl; and [0075]
R.sup.c and R.sup.d are each independently hydrogen,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, C.sub.1-C.sub.6 heteroalkyl, cycloalkyl, heterocycloalkyl,
aryl, or heteroaryl; wherein the alkyl, alkenyl, alkynyl,
heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
halogen, --OH, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[0076] or R.sup.c and R.sup.d are taken together with the nitrogen
atom to which they are attached to form a heterocycloalkyl
optionally substituted with one, two, or three halogen,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl.
[0077] Also disclosed herein are pharmaceutical compositions
comprising a compound disclosed herein, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, and a
pharmaceutically acceptable excipient.
[0078] Also disclosed herein are methods of inhibiting CD73
comprising contacting CD73 with a compound disclosed herein, or a
pharmaceutically acceptable salt, solvate, or stereoisomer
thereof.
[0079] Also disclosed herein are methods of treating cancer in a
subject, comprising administering to the subject a compound
disclosed herein, or a pharmaceutically acceptable salt, solvate,
or stereoisomer thereof or administering to the subject a
pharmaceutical composition comprising a compound disclosed herein,
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, and a pharmaceutically acceptable excipient.
[0080] Also disclosed herein are methods of treating an infection
in a subject, comprising administering to the subject a compound
disclosed herein, or a pharmaceutically acceptable salt, solvate,
or stereoisomer thereof or administering to the subject a
pharmaceutical composition comprising a compound disclosed herein,
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, and a pharmaceutically acceptable excipient.
[0081] Also disclosed herein are methods of treating a
neurodegenerative disease in a subject, comprising administering to
the subject a compound disclosed herein, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof or administering
to the subject a pharmaceutical composition comprising a compound
disclosed herein, or a pharmaceutically acceptable salt, solvate,
or stereoisomer thereof, and a pharmaceutically acceptable
excipient.
INCORPORATION BY REFERENCE
[0082] All publications, patents, and patent applications mentioned
in this specification are herein incorporated by reference for the
specific purposes identified herein.
DETAILED DESCRIPTION OF THE INVENTION
[0083] CD73 is a glycosylphosphatidylinositol (GPI) anchored cell
surface protein that catalyzes the hydrolysis of AMP to adenosine,
and works in concert with CD39, which converts ATP into AMP. The
resulting adenosine functions as a signaling molecule that
activates the P1 receptors expressed on the cell surface in many
different tissues. Four G protein-coupled P1 or adenosine receptors
have been cloned and designated as A1, A2A, A2B, and A3. Adenosine
impacts a wide range of physiological processes including neural
function, vascular perfusion, and immune responses. In doing so,
this metabolite regulates CNS, cardiovascular, and immune system
functions, to name a few.
[0084] Increasing evidence suggests that interactions between tumor
cells and their microenvironment are essential for tumorigenesis.
The purinergic signaling pathway in which CD73 plays a critical
role, has emerged as an important player in cancer progression. It
has become clear in recent years that adenosine is one of the most
important immunosuppressive regulatory molecules in the tumor
microenvironment, and contributes to immune escape and tumor
progression.
[0085] CD73 is a key protein molecule in cancer development. CD73
has been found to be overexpressed in many cancer cell lines and
tumor types including, for example, breast cancer, colorectal
cancer, ovarian cancer, gastric cancer, gallbladder cancer, and
cancers associated with poor prognosis.
[0086] The expression of CD73 in tumors is regulated by a variety
of mechanisms. CD73 expression is negatively regulated by estrogen
receptor (ER) in breast cancer. Thus. CD73 is highly expressed in
ER negative breast cancer patients. The hypoxia-inducible
factor-1.alpha. (HIF-1.alpha.) has also been shown to regulate CD73
transcription. Additionally, inflammatory factors such as
IFN-.gamma. affect CD73 levels. CD73 expression is also
epigenetically regulated by CpG island methylation in cell lines
and clinical tumor samples.
[0087] In addition to being a prognostic biomarker in cancer
patients, overexpression of CD73 has also been found to be
functionally linked to therapy resistance. Elevated levels of CD73
were initially linked to resistance to a variety of
chemotherapeutic agents including vincristine and doxorubicin.
[0088] CD73 has also been shown to be involved in immunotherapy
resistance. This ectonucleotidase participates in the process of
tumor immune escape by inhibiting the activation, clonal expansion,
and homing of tumor-specific T cells (in particular, T helper and
cytotoxic T cells): impairing tumor cell killing by cytolytic
effector T lymphocytes; driving, via pericellular generation of
adenosine, the suppressive capabilities of Treg and Th 17 cells;
enhancing the conversion of type 1 macrophages into tumor-promoting
type 2 macrophages; and promoting the accumulation of MDSCs.
[0089] Small molecular inhibitors and monoclonal antibodies
targeting CD73 have shown anti-tumor activity in a variety of
immune-competent but not in immune-deficient mouse tumor models.
Overall, these studies suggest that anti-CD73 therapy activity is
dependent on its ability to elicit immune responses in vivo.
[0090] Antibodies which block PD-1, PD-L1, and CTLA-4 have shown
impressive objective response in cancer patients. Recent data
demonstrates that anti-CD73 mAb significantly enhances the activity
of both anti-CTLA-4 and anti-PD-1 mAbs in several mouse tumor
models. In addition to checkpoint blockade, CD73-mediated
production of adenosine could contribute to resistance to
additional immunotherapy modalities including CAR-T cells and
cancer vaccines.
[0091] Interfering with CD73 activity represents a strategy to
re-sensitize tumors to therapy. Based on the link between CD73 and
therapy resistance, combining anti-CD73 treatment with chemotherapy
or immunotherapy is an effective approach to enhance their activity
in cancer patients with high CD73 levels. In some instances, CD73
expression serves as a biomarker to identify patients that could
benefit from anti-CD73 combination therapy.
[0092] In some instances, the CD39/CD73 couple turns ATP-driven
pro-inflammatory cell activity toward an adenosine-mediated
anti-inflammatory state. A number of studies have shown changes in
the activity of the CD39/CD73 axis during infections induced by a
variety of microorganisms. An increase in CD73 expression has also
been observed in the brain of mice infected with Toxoplasma gondii,
which promotes the parasite life cycle through the production of
adenosine. Thus, the pharmacological blockade of CD73 is a
promising therapeutic approach to treat human toxoplasmosis.
[0093] Enhanced expression and activity of CD39 and CD73 have been
observed in endothelial cells infected with cytomegalovirus (CMV).
The increase in local adenosine production, associated with the
upregulation of ecto-nucleotidases, generates an immunosuppressive
and antithrombotic microenvironment, which facilitates viral entry
into target cells.
[0094] In some instances, inhibitors of CD73, by driving a decrease
on adenosine production, have applications as antiviral agents. The
elevated expression/activity of CD39 and CD73 on lymphocytes of
individuals infected with human immunodeficiency virus (HIV)
indicates a role for ecto-nucleotidases in the immune dysfunction
associated with this disease. In fact, an increased proportion of
Tregs expressing CD39, as well as a positive correlation between
CD39 expression on Tregs and disease progression has been observed
in different cohorts of HIV-infected patients. It has also been
shown that HIV-positive patients had a higher number of CD39+ Treg,
and that their Teff exhibited an increased sensitivity in vitro to
the suppressive effect of adenosine, which was related to the
elevated expression of immunosuppressive A2A receptors.
[0095] In the central nervous system, adenosine plays a critical
role in controlling a multitude of neural functions. Through the
activation of P1 receptors, adenosine is involved in diverse
physiological and pathological processes such as regulation of
sleep, general arousal state and activity, local neuronal
excitability, and coupling of the cerebral blood flow to the energy
demand. In some instances, manipulation of adenosine production via
CD73 inhibitors is useful for treating neurodegenerative diseases
such as Alzheimer's disease, Parkinson's disease and Huntington's
disease, and psychiatric disorders such as schizophrenia and
autism.
Definitions
[0096] As used herein and in the appended claims, the singular
forms "a," "and," and "the" include plural referents unless the
context clearly dictates otherwise. Thus, for example, reference to
"an agent" includes a plurality of such agents, and reference to
"the cell" includes reference to one or more cells (or to a
plurality of cells) and equivalents thereof known to those skilled
in the art, and so forth. When ranges are used herein for physical
properties, such as molecular weight, or chemical properties, such
as chemical formulae, all combinations and subcombinations of
ranges and specific embodiments therein are intended to be
included. The term "about" when referring to a number or a
numerical range means that the number or numerical range referred
to is an approximation within experimental variability (or within
statistical experimental error), and thus the number or numerical
range, in some instances, will vary between 1% and 15% of the
stated number or numerical range. The term "comprising" (and
related terms such as "comprise" or "comprises" or "having" or
"including") is not intended to exclude that in other certain
embodiments, for example, an embodiment of any composition of
matter, composition, method, or process, or the like, described
herein, "consist of" or "consist essentially of" the described
features.
[0097] As used in the specification and appended claims, unless
specified to the contrary, the following terms have the meaning
indicated below.
[0098] "Alkyl" refers to an optionally substituted straight-chain,
or optionally substituted branched-chain saturated hydrocarbon
monoradical having from one to about ten carbon atoms, or from one
to six carbon atoms, wherein a sp3-hybridized carbon of the alkyl
residue is attached to the rest of the molecule by a single bond.
Examples include, but are not limited to, methyl, ethyl, n-propyl,
isopropyl, 2-methyl-1-propyl, 2-methyl-2-propyl, 2-methyl-1-butyl,
3-methyl-1-butyl, 2-methyl-3-butyl, 2,2-dimethyl-1-propyl,
2-methyl-1-pentyl, 3-methyl-1-pentyl, 4-methyl-1-pentyl,
2-methyl-2-pentyl, 3-methyl-2-pentyl, 4-methyl-2-pentyl,
2,2-dimethyl-1-butyl, 3,3-dimethyl-1-butyl, 2-ethyl-1-butyl,
n-butyl, isobutyl, sec-butyl, t-butyl, n-pentyl, isopentyl,
neopentyl, tert-amyl and hexyl, and longer alkyl groups, such as
heptyl, octyl, and the like. Whenever it appears herein, a
numerical range such as "C.sub.1-C.sub.6 alkyl" means that the
alkyl group consists of 1 carbon atom, 2 carbon atoms, 3 carbon
atoms, 4 carbon atoms, 5 carbon atoms or 6 carbon atoms, although
the present definition also covers the occurrence of the term
"alkyl" where no numerical range is designated. In some
embodiments, the alkyl is a C.sub.1-C.sub.10alkyl, a
C.sub.1-C.sub.9 alkyl, a C.sub.1-C.sub.8 alkyl, a C.sub.1-C.sub.7
alkyl, a C.sub.1-C.sub.6 alkyl, a C.sub.1-C.sub.5alkyl, a
C.sub.1-C.sub.4 alkyl, a C.sub.1-C.sub.3 alkyl, a C.sub.1-C.sub.2
alkyl, or a C.sub.1 alkyl. Unless stated otherwise specifically in
the specification, an alkyl group is optionally substituted for
example, with oxo, halogen, amino, nitrile, nitro, hydroxyl,
haloalkyl, alkoxy, aryl, cycloalkyl, heterocycloalkyl, heteroaryl,
and the like. In some embodiments, the alkyl is optionally
substituted with oxo, halogen, --CN, --CF.sub.3, --OH, --OMe,
--NH.sub.2, or --NO.sub.2. In some embodiments, the alkyl is
optionally substituted with oxo, halogen, --CN, --CF.sub.3, --OH,
or --OMe. In some embodiments, the alkyl is optionally substituted
with halogen.
[0099] "Alkenyl" refers to an optionally substituted
straight-chain, or optionally substituted branched-chain
hydrocarbon monoradical having one or more carbon-carbon
double-bonds and having from two to about ten carbon atoms, more
preferably two to about six carbon atoms, wherein an sp2-hybridized
carbon of the alkenyl residue is attached to the rest of the
molecule by a single bond. The group may be in either the cis or
trans conformation about the double bond(s), and should be
understood to include both isomers. Examples include, but are not
limited to ethenyl (--CH.dbd.CH.sub.2), 1-propenyl
(--CH.sub.2CH.dbd.CH.sub.2), isopropenyl
[--C(CH.sub.3).dbd.CH.sub.2], butenyl, 1,3-butadienyl and the like.
Whenever it appears herein, a numerical range such as
"C.sub.2-C.sub.6 alkenyl" means that the alkenyl group may consist
of 2 carbon atoms. 3 carbon atoms. 4 carbon atoms, 5 carbon atoms
or 6 carbon atoms, although the present definition also covers the
occurrence of the term "alkenyl" where no numerical range is
designated. In some embodiments, the alkenyl is a C.sub.2-C.sub.10
alkenyl, a C.sub.2-C.sub.9 alkenyl, a C.sub.2-C.sub.8 alkenyl, a
C.sub.2-C.sub.7 alkenyl, a C.sub.2-C.sub.6 alkenyl, a
C.sub.2-C.sub.5 alkenyl, a C.sub.2-C.sub.4 alkenyl, a
C.sub.2-C.sub.3 alkenyl, or a C.sub.2 alkenyl. Unless stated
otherwise specifically in the specification, an alkenyl group is
optionally substituted for example, with oxo, halogen, amino,
nitrile, nitro, hydroxyl, haloalkyl, alkoxy, aryl, cycloalkyl,
heterocycloalkyl, heteroaryl, and the like. In some embodiments, an
alkenyl is optionally substituted with oxo, halogen, --CN,
--CF.sub.3, --OH, --OMe, --NH.sub.2, or --NO.sub.2. In some
embodiments, an alkenyl is optionally substituted with oxo,
halogen, --CN, --CF.sub.3, --OH, or --OMe. In some embodiments, the
alkenyl is optionally substituted with halogen.
[0100] "Alkynyl" refers to an optionally substituted straight-chain
or optionally substituted branched-chain hydrocarbon monoradical
having one or more carbon-carbon triple-bonds and having from two
to about ten carbon atoms, more preferably from two to about six
carbon atoms. Examples include, but are not limited to ethynyl,
2-propynyl, 2-butynyl, 1,3-butadiynyl and the like. Whenever it
appears herein, a numerical range such as "C.sub.2-C.sub.6 alkynyl"
means that the alkynyl group may consist of 2 carbon atoms, 3
carbon atoms, 4 carbon atoms, 5 carbon atoms or 6 carbon atoms,
although the present definition also covers the occurrence of the
term "alkynyl" where no numerical range is designated. In some
embodiments, the alkynyl is a C.sub.2-C.sub.10 alkynyl, a
C.sub.2-C.sub.9 alkynyl, a C.sub.2-C.sub.8 alkynyl, a
C.sub.2-C.sub.7 alkynyl, a C.sub.2-C.sub.6 alkynyl, a
C.sub.2-C.sub.5 alkynyl, a C.sub.2-C.sub.4 alkynyl, a
C.sub.2-C.sub.3 alkynyl, or a C.sub.2 alkynyl. Unless stated
otherwise specifically in the specification, an alkynyl group is
optionally substituted for example, with oxo, halogen, amino,
nitrile, nitro, hydroxyl, haloalkyl, alkoxy, aryl, cycloalkyl,
heterocycloalkyl, heteroaryl, and the like. In some embodiments, an
alkynyl is optionally substituted with oxo, halogen, --CN,
--CF.sub.3, --OH, --OMe, --NH.sub.2, or NO.sub.2. In some
embodiments, an alkynyl is optionally substituted with oxo,
halogen, --CN, --CF.sub.3, --OH, or --OMe. In some embodiments, the
alkynyl is optionally substituted with halogen.
[0101] "Alkylene" refers to a straight or branched divalent
hydrocarbon chain. Unless stated otherwise specifically in the
specification, an alkylene group may be optionally substituted for
example, with oxo, halogen, amino, nitrile, nitro, hydroxyl,
haloalkyl, alkoxy, aryl, cycloalkyl, heterocycloalkyl, heteroaryl,
and the like. In some embodiments, an alkylene is optionally
substituted with oxo, halogen, --CN, --CF.sub.3, --OH, --OMe,
--NH.sub.2, or --NO.sub.2. In some embodiments, an alkylene is
optionally substituted with oxo, halogen, --CN, --CF.sub.3, --OH,
or --OMe. In some embodiments, the alkylene is optionally
substituted with halogen.
[0102] "Alkoxy" refers to a radical of the formula --OR, where IL
is an alkyl radical as defined. Unless stated otherwise
specifically in the specification, an alkoxy group may be
optionally substituted for example, with oxo, halogen, amino,
nitrile, nitro, hydroxyl, haloalkyl, alkoxy, aryl, cycloalkyl,
heterocycloalkyl, heteroaryl, and the like. In some embodiments, an
alkoxy is optionally substituted with oxo, halogen, --CN,
--CF.sub.3, --OH, --OMe, --NH.sub.2, or --NO.sub.2. In some
embodiments, an alkoxy is optionally substituted with oxo, halogen,
--CN, --CF.sub.3, --OH, or --OMe. In some embodiments, the alkoxy
is optionally substituted with halogen.
[0103] "Aryl" refers to a radical derived from a hydrocarbon ring
system comprising hydrogen, 6 to 30 carbon atoms and at least one
aromatic ring. The aryl radical may be a monocyclic, bicyclic,
tricyclic or tetracyclic ring system, which may include fused (when
fused with a cycloalkyl or heterocycloalkyl ring, the aryl is
bonded through an aromatic ring atom) or bridged ring systems. In
some embodiments, the aryl is a 6- to 10-membered aryl. In some
embodiments, the aryl is a 6-membered aryl. Aryl radicals include,
but are not limited to, aryl radicals derived from the hydrocarbon
ring systems of anthrylene, naphthylene, phenanthrylene,
anthracene, azulene, benzene, chrysene, fluoranthene, fluorene,
as-indacene, s-indacene, indane, indene, naphthalene, phenalene,
phenanthrene, pleiadene, pyrene, and triphenylene. In some
embodiments, the aryl is phenyl. Unless stated otherwise
specifically in the specification, an aryl may be optionally
substituted for example, with halogen, amino, nitrile, nitro,
hydroxyl, alkyl, alkenyl, alkynyl, haloalkyl, alkoxy, aryl,
cycloalkyl, heterocycloalkyl, heteroaryl, and the like. In some
embodiments, an aryl is optionally substituted with halogen,
methyl, ethyl, --CN, --CF.sub.3, --OH, --OMe, --NH.sub.2, or
--NO.sub.2. In some embodiments, an aryl is optionally substituted
with halogen, methyl, ethyl, --CN, --CF.sub.3, --OH, or --OMe. In
some embodiments, the aryl is optionally substituted with
halogen.
[0104] "Cycloalkyl" refers to a stable, partially or fully
saturated, monocyclic or polycyclic carbocyclic ring, which may
include fused (when fused with an aryl or a heteroaryl ring, the
cycloalkyl is bonded through a non-aromatic ring atom) or bridged
ring systems. Representative cycloalkyls include, but are not
limited to, cycloalkyls having from three to fifteen carbon atoms
(C.sub.3-C.sub.15 cycloalkyl), from three to ten carbon atoms
(C.sub.3-C.sub.10 cycloalkyl), from three to eight carbon atoms
(C.sub.3-C.sub.8 cycloalkyl), from three to six carbon atoms
(C.sub.3-C.sub.6 cycloalkyl), from three to five carbon atoms
(C.sub.3-C.sub.5 cycloalkyl), or three to four carbon atoms
(C.sub.3-C.sub.4 cycloalkyl). In some embodiments, the cycloalkyl
is a 3- to 6-membered cycloalkyl. In some embodiments, the
cycloalkyl is a 5- to 6-membered cycloalkyl. Monocyclic cycloalkyls
include, for example, cyclopropyl, cyclobutyl, cyclopentyl,
cyclohexyl, cycloheptyl, and cyclooctyl. Polycyclic cycloalkyls or
carbocycles include, for example, adamantyl, norbomyl, decalinyl,
bicyclo[3.3.6]octane, bicyclo[4.3.0]nonane, cis-decalin,
trans-decalin, bicyclo[2.1.1]hexane, bicyclo[2.2.1]heptane,
bicyclo[2.2.2]octane, bicyclo[3.2.2]nonane, and
bicyclo[3.3.2]decane, and 7,7-dimethyl-bicyclo[2.2.1]heptanyl.
Partially saturated cycloalkyls include, for example cyclopentenyl,
cyclohexenyl, cycloheptenyl, and cyclooctenyl. Unless stated
otherwise specifically in the specification, a cycloalkyl is
optionally substituted for example, with oxo, halogen, amino,
nitrile, nitro, hydroxyl, alkyl, alkenyl, alkynyl, haloalkyl,
alkoxy, aryl, cycloalkyl, heterocycloalkyl, heteroaryl, and the
like. In some embodiments, a cycloalkyl is optionally substituted
with oxo, halogen, methyl, ethyl, --CN, --CF.sub.3, --OH, --OMe,
--NH.sub.2, or --NO.sub.2. In some embodiments, a cycloalkyl is
optionally substituted with oxo, halogen, methyl, ethyl, --CN,
--CF.sub.3, --OH, or --OMe. In some embodiments, the cycloalkyl is
optionally substituted with halogen.
[0105] "Halo" or "halogen" refers to bromo, chloro, fluoro or iodo.
In some embodiments, halogen is fluoro or chloro. In some
embodiments, halogen is fluoro.
[0106] "Haloalkyl" refers to an alkyl radical, as defined above,
that is substituted by one or more halo radicals, as defined above,
e.g., trifluoromethyl, di fluoromethyl, fluoromethyl,
trichloromethyl, 2,2,2-trifluoroethyl, 1,2-difluoroethyl,
3-bromo-2-fluoroamyl, 1,2-dibromoethyl, and the like.
[0107] "Heterocycloalkyl" refers to a stable 3- to 24-membered
partially or fully saturated ring radical comprising 2 to 23 carbon
atoms and from one to 8 heteroatoms selected from the group
consisting of nitrogen, oxygen, phosphorous and sulfur. Unless
stated otherwise specifically in the specification, the
heterocycloalkyl radical may be a monocyclic, bicyclic, tricyclic
or tetracyclic ring system, which may include fused (when fused
with an aryl or a heteroaryl ring, the heterocycloalkyl is bonded
through a non-aromatic ring atom) or bridged ring systems; and the
nitrogen, carbon or sulfur atoms in the heterocycloalkyl radical
may be optionally oxidized; the nitrogen atom may be optionally
quaternized. In some embodiments, the heterocycloalkyl is a 3- to
6-membered heterocycloalkyl. In some embodiments, the
heterocycloalkyl is a 5- to 6-membered heterocycloalkyl. Examples
of such heterocycloalkyl radicals include, but are not limited to,
aziridinyl, azetidinyl, dioxolanyl, thienyl[1,3]dithianyl,
decahydroisoquinolyl, imidazolinyl, imidazolidinyl,
isothiazolidinyl, isoxazolidinyl, morpholinyl, octahydroindolyl,
octahydroisoinddyl, 2-oxopiperazinyl, 2-oxopiperidinyl,
2-oxopyrrolidinyl, oxazolidinyl, piperidinyl, piperazinyl,
4-piperidonyl, pyrrolidinyl, pyrazolidinyl, quinuclidinyl,
thiazolidinyl, tetrahydrofuryl, trithianyl, tetrahydropyranyl,
thiomorpholinyl, thiamorpholinyl, 1-oxo-thiomorpholinyl,
1,1-dioxo-thiomorpholinyl, 1,3-dihydroisobenzofuran-1-yl,
3-oxo-1,3-dihydroisobenzofuran-1-yl, methyl-2-oxo-1,3-dioxol-4 yl,
and 2-oxo-1,3-dioxol-4-yl. The term heterocycloalkyl also includes
all ring forms of the carbohydrates, including but not limited to
the monosaccharides, the disaccharides and the oligosaccharides.
Unless otherwise noted, heterocycloalkyls have from 2 to 10 carbons
in the ring. It is understood that when referring to the number of
carbon atoms in a heterocycloalkyl, the number of carbon atoms in
the heterocycloalkyl is not the same as the total number of atoms
(including the heteroatoms) that make up the heterocycloalkyl (i.e.
skeletal atoms of the heterocycloalkyl ring). Unless stated
otherwise specifically in the specification, a heterocycloalkyl is
optionally substituted for example, with oxo, halogen, amino,
nitrile, nitro, hydroxyl, alkyl, alkenyl, alkynyl, haloalkyl,
alkoxy, aryl, cycloalkyl, heterocycloalkyl, heteroaryl, and the
like. In some embodiments, a heterocycloalkyl is optionally
substituted with oxo, halogen, methyl, ethyl, --CN, --CF.sub.3,
--OH, --OMe, --NH.sub.2, or --NO.sub.2. In some embodiments, a
heterocycloalkyl is optionally substituted with oxo, halogen,
methyl, ethyl, --CN, --CF.sub.3, --OH, or --OMe. In some
embodiments, the heterocycloalkyl is optionally substituted with
halogen.
[0108] "Heteroalkyl" refers to an alkyl group in which one or more
skeletal atoms of the alkyl are selected from an atom other than
carbon, e.g., oxygen, nitrogen (e.g., --NH--, --N(alkyl)-), sulfur,
or combinations thereof. A heteroalkyl is attached to the rest of
the molecule at a carbon atom of the heteroalkyl. In one aspect, a
heteroalkyl is a C.sub.1-C.sub.6 heteroalkyl wherein the
heteroalkyl is comprised of 1 to 6 carbon atoms and one or more
atoms other than carbon, e.g., oxygen, nitrogen (e.g. --NH--,
--N(alkyl)-), sulfur, or combinations thereof wherein the
heteroalkyl is attached to the rest of the molecule at a carbon
atom of the heteroalkyl. Unless stated otherwise specifically in
the specification, a heteroalkyl is optionally substituted for
example, with oxo, halogen, amino, nitrile, nitro, hydroxyl, alkyl,
alkenyl, alkynyl, haloalkyl, alkoxy, aryl, cycloalkyl,
heterocycloalkyl, heteroaryl, and the like. In some embodiments, a
heteroalkyl is optionally substituted with oxo, halogen, methyl,
ethyl, --CN, --CF.sub.3, --OH, --OMe, --NH.sub.2, or --NO.sub.2. In
some embodiments, a heteroalkyl is optionally substituted with oxo,
halogen, methyl, ethyl, --CN, --CF.sub.3, --OH, or --OMe. In some
embodiments, the heteroalkyl is optionally substituted with
halogen.
[0109] "Heteroaryl" refers to a 5- to 14-membered ring system
radical comprising hydrogen atoms, one to thirteen carbon atoms,
one to six heteroatoms selected from the group consisting of
nitrogen, oxygen, phosphorous and sulfur, and at least one aromatic
ring. The heteroaryl radical may be a monocyclic, bicyclic,
tricyclic or tetracyclic ring system, which may include fused (when
fused with a cycloalkyl or heterocycloalkyl ring, the heteroaryl is
bonded through an aromatic ring atom) or bridged ring systems; and
the nitrogen, carbon or sulfur atoms in the heteroaryl radical may
be optionally oxidized: the nitrogen atom may be optionally
quaternized. In some embodiments, the heteroaryl is a 5- to
10-membered heteroaryl. In some embodiments, the heteroaryl is a 5-
to 6-membered heteroaryl. Examples include, but are not limited to,
azepinyl, acridinyl, benzimidazolyl, benzothiazolyl, benzoindolyl,
benzodioxolyl, benzofuranyl, benzooxazolyl, benzothiazolyl,
benzothiadiazolyl, benzo[b][1,4]dioxepinyl, 1,4-benzodioxanyl,
benzonaphthofuranyl, benzoxazolyl, benzodioxolyl, benzodioxinyl,
benzopyranyl, benzopyranonyl, benzofuranyl, benzofuranonyl,
benzothienyl (benzothiophenyl), benzotriazolyl,
benzo[4,6]imidazo[1,2-a]pyridinyl, carbazolyl, cinnolinyl,
dibenzofuranyl, dibenzothiophenyl, furanyl, furanonyl,
isothiazolyl, imidazolyl, indazolyl, indolyl, indazolyl,
isoindolyl, indolinyl, isoindolinyl, isoquinolyl, indolizinyl,
isoxazolyl, naphthyridinyl, oxadiazolyl, 2-oxoazepinyl, oxazolyl,
oxiranyl, 1-oxidopyridinyl, 1-oxidopyrimidinyl, 1-oxidopyrazinyl,
1-oxidopyridazinyl, 1-phenyl-1H-pyrrolyl, phenazinyl,
phenothiazinyl, phenoxazinyl, phthalazinyl, pteridinyl, purinyl,
pyrrolyl, pyrazolyl, pyridinyl, pyrazinyl, pyrimidinyl,
pyridazinyl, quinazolinyl, quinoxalinyl, quindinyl, quinuclidinyl,
isoquinolinyl, tetrahydroquinolinyl, thiazolyl, thiadiazolyl,
triazolyl, tetrazolyl, triazinyl, and thiophenyl (i.e., thienyl).
Unless stated otherwise specifically in the specification, a
heteroaryl is optionally substituted for example, with halogen,
amino, nitrite, nitro, hydroxyl, alkyl, alkenyl, alkynyl,
haloalkyl, alkoxy, aryl, cycloalkyl, heterocycloalkyl, heteroaryl,
and the like. In some embodiments, a heteroaryl is optionally
substituted with halogen, methyl, ethyl, --CN, --CF.sub.3, --OH,
--OMe, --NH.sub.2, or --NO.sub.2. In some embodiments, a heteroaryl
is optionally substituted with halogen, methyl, ethyl, --CN,
--CF.sub.3, --OH, or --OMe. In some embodiments, the heteroaryl is
optionally substituted with halogen.
[0110] "Hydroxyalkyl" refers to an alkyl radical, as defined above,
that is substituted by one or more --OH e.g., hydroxymethyl,
hydroxyethyl, hydroxypropyl, hydroxybutyl, hydroxypentyl,
dihydroxymethyl, dihydroxyethyl, dihydroxypropyl, dihydroxybutyl,
dihydroxypentyl, and the like.
[0111] The term "optional" or "optionally" means that the
subsequently described event or circumstance may or may not occur,
and that the description includes instances where said event or
circumstance occurs and instances in which it does not. For
example, "optionally substituted alkyl" means either "alkyl" or
"substituted alkyl" as defined above. Further, an optionally
substituted group may be un-substituted (e.g., --CH.sub.2CH.sub.3),
fully substituted (e.g., --CF.sub.2CF.sub.3), mono-substituted
(e.g., --CH.sub.2CH.sub.2F) or substituted at a level anywhere
in-between fully substituted and mono-substituted (e.g.,
--CH.sub.2CHF.sub.2, --CH.sub.2CF.sub.3, --CF.sub.2CH.sub.3,
--CFHCHF.sub.2, etc.). It will be understood by those skilled in
the art with respect to any group containing one or more
substituents that such groups are not intended to introduce any
substitution or substitution patterns (e.g., substituted alkyl
includes optionally substituted cycloalkyl groups, which in turn
are defined as including optionally substituted alkyl groups,
potentially ad infinitum) that are sterically impractical and/or
synthetically non-feasible. Thus, any substituents described should
generally be understood as having a maximum molecular weight of
about 1,010 daltons, and more typically, up to about 500
daltons.
[0112] The terms "inhibit," "block," "suppress," and grammatical
variants thereof are used interchangeably herein and refer to any
statistically significant decrease in biological activity,
including full blocking of the activity. In some embodiments,
"inhibition" refers to a decrease of about 10%, about 20%, about
30%, about 40%, about 50%, about 60%, about 70%, about 80%, about
90% or about 100% in biological activity. Accordingly, when the
terms "inhibition" or "suppression" are applied to describe, e.g.,
an effect on the enzymatic activity of CD73, the term refers to the
ability of a compound disclosed herein to statistically
significantly decrease the 5'-nucleotidase activity of CD73
(catabolizing the hydrolysis of adenosine monophosphate, AMP, to
adenosine), relative to the CD73-mediated 5'-nucleotidase activity
in an untreated (control) cell. In some instances, the cell which
expresses CD73 is a naturally occurring cell or cell line (e.g., a
cancer cell) or is recombinantly produced by introducing a nucleic
acid encoding CD73 into a host cell. In some aspects, compounds
disclosed herein statistically significantly decrease the
5'-nucleotidase activity of a soluble form of CD73 in a biological
fluid. In one aspect, the compound disclosed herein inhibit
CD73-mediated 5'-nucleotidase activity by at least 10%, at least
15%, at least 20%, at least 25%, at least 30%, at least 35%, at
least 40%, at least 45%, at least 50%, at least 55%, at least 60%,
at least 65%, at least 70%, at least 75%, at least 80%, at least
85%, at least 90%, at least 95%, or about 100%, as determined, for
example, by the methods described in the Examples and/or methods
known in the art.
[0113] As used herein, "treatment" or "treating," or "palliating"
or "ameliorating" are used interchangeably. These terms refer to an
approach for obtaining beneficial or desired results including but
not limited to therapeutic benefit and/or a prophylactic benefit.
By "therapeutic benefit" is meant eradication or amelioration of
the underlying disorder being treated. Also, a therapeutic benefit
is achieved with the eradication or amelioration of one or more of
the physiological symptoms associated with the underlying disorder
such that an improvement is observed in the patient,
notwithstanding that the patient is still afflicted with the
underlying disorder. For prophylactic benefit, the compositions
are, in some embodiments, administered to a patient at risk of
developing a particular disease, or to a patient reporting one or
more of the physiological symptoms of a disease, even though a
diagnosis of this disease has not been made.
Compounds
[0114] Described herein are compounds that are CD73 inhibitors.
These compounds, and compositions comprising these compounds, are
useful for the treatment of cancer, infections, and
neurodegenerative diseases.
[0115] In some embodiments provided herein is a compound having the
structure of Formula (I), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof:
##STR00003##
wherein; [0116] A is --O-- or --CH.sub.2--; [0117] Q.sup.1 and
Q.sup.2 are independently N or CW; [0118] each W is independently
hydrogen, halogen, --CN, --OH, --OR.sup.a, --SH, --SR.sup.a,
--S(.dbd.O)R.sup.a, --NO.sub.2, --NR.sup.cR.sup.d,
--S(.dbd.O).sub.2R.sup.a, --NHS(.dbd.O).sub.2R.sup.a,
--S(O).sub.2NR.sup.cR.sup.d, --C(.dbd.O)R.sup.a,
--OC(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b, --OC(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, --OC(.dbd.O)NR.sup.cR.sup.d,
--NR.sup.bC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(.dbd.O)R.sup.a,
--NR.sup.bC(.dbd.O)OR.sup.b, alkyl, alkenyl, alkynyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, alkyl(aryl), alkyl(heteroaryl),
alkyl(cycloalkyl), or alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30; [0119] Z is --NR.sup.1R.sup.2, --OR.sup.60,
--SR.sup.61, or --CR.sup.62R.sup.63R.sup.64; [0120] R.sup.1 and
R.sup.2 are each independently hydrogen, alkyl, alkenyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkyl(aryl),
alkyl(heteroaryl), alkyl(cycloalkyl), alkyl(heterocycloalkyl),
--S(O).sub.2R.sup.15a, --S(.dbd.O).sub.2NR.sup.16aR.sup.17a or
--C(.dbd.O).sub.2R.sup.15a; wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30a; [0121] or
R.sup.1 and R.sup.2 are taken together with the nitrogen atom to
which they are attached to form a heterocycloalkyl optionally
substituted with one, two, or three R.sup.30b; [0122] R.sup.60 is
hydrogen, --C(.dbd.O)R.sup.15e, --C(.dbd.O)OR.sup.16e,
--C(.dbd.O)NR.sup.16eR.sup.17e, alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkyl(aryl),
alkyl(heteroaryl), alkyl(cycloalkyl), alkyl(heterocycloalkyl);
wherein each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl,
aryl, and heteroaryl is independently optionally substituted with
one, two, or three R.sup.30m; [0123] R.sup.61 is hydrogen,
--C(.dbd.O)R.sup.15f, --C(.dbd.O)OR.sup.16f,
--C(.dbd.O)NR.sup.16fR.sup.17f, alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkyl(aryl),
alkyl(heteroaryl), alkyl(cycloalkyl), alkyl(heterocycloalkyl);
wherein each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl,
aryl, and heteroaryl is independently optionally substituted with
one, two, or three R.sup.30n; [0124] R.sup.62, R.sup.63, and
R.sup.64 are each independently hydrogen, halogen, --CN, --OH,
--OR.sup.15g, --SH, --SR.sup.15g, --S(O)R.sup.15g, --NO.sub.2,
--NR.sup.16gR.sup.17g, --S(.dbd.O).sub.2R.sup.15g,
--NHS(.dbd.O).sub.2R.sup.15g, --S(.dbd.O).sub.2NR.sup.16gR.sup.17g,
--C(.dbd.O)R.sup.15g, --OC(O)R.sup.15g, --C(.dbd.O)OR.sup.16g,
--OC(.dbd.O)OR.sup.16g, --C(.dbd.O)NR.sup.16gR.sup.17g,
--OC(.dbd.O)NR.sup.16gR.sup.17g,
--NR.sup.16gC(.dbd.O)NR.sup.16gR.sup.17g,
--NR.sup.16gC(.dbd.O)R.sup.15g, --NR.sup.16gC(.dbd.O)OR.sup.16g,
alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, alkyl(aryl), alkyl(heteroaryl), alkyl(cycloalkyl), or
alkyl(heterocycloalkyl); wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optimally substituted with one, two, or three R.sup.30o; [0125]
R.sup.3 is halogen, --CN, --OH, --OR.sup.15b, --SR.sup.18b,
--NR.sup.16bR.sup.17b, alkyl, alkenyl, alkynyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, alkyl(aryl), alkyl(heteroaryl),
alkyl(cycloalkyl), or alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30c; [0126] R.sup.4 and R.sup.7 are each
independently hydrogen, halogen, --OH, --OR.sup.15c,
--NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.15c, alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; wherein each
alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30d;
[0127] R.sup.5 and R.sup.6 are each independently hydrogen,
halogen, --OH, --OR.sup.15d, --NR.sup.16dS(.dbd.O).sub.2R.sup.15d,
--NR.sup.16dC(.dbd.O)R.sup.15d, alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; wherein each
alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30e; [0128] R.sup.8 is hydrogen, halogen, --OH,
--OR.sup.a, --NR.sup.cR.sup.d, alkyl, or haloalkyl; [0129] R.sup.9
and R.sup.10 are each independently hydrogen, halogen, alkyl, or
haloalkyl; [0130] X is --O-- or --NR.sup.11--; [0131] Y is
--(CR.sup.13R.sup.14).sub.v-- or --NR.sup.12--; [0132] R.sup.11 and
R.sup.12 are each independently hydrogen, --S(O)R.sup.a,
--S(O).sub.2R.sup.a, --S(.dbd.O).sub.2NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b, alkyl, alkenyl, alkynyl,
cycloalkyl, or heterocycloalkyl; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, and heterocycloalkyl is independently
optionally substituted with one, two, or three R.sup.30f; [0133]
R.sup.13 and R.sup.14 are each independently hydrogen, halogen,
--OH, --OR.sup.a, --NR.sup.cR.sup.d, alkyl, or haloalkyl; [0134] v
is 1-3; [0135] R.sup.15a, R.sup.15b, R.sup.15c, R.sup.15d,
R.sup.15e, R.sup.15f, R.sup.15g are each independently alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, or
heteroaryl; wherein each alkyl, alkenyl, alkynyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30g; [0136] R.sup.16a,
R.sup.16b, R.sup.16c, R.sup.16d, R.sup.16e, R.sup.16f, R.sup.16g,
R.sup.17a, R.sup.17b, R.sup.17c, R.sup.17d, R.sup.17e, R.sup.17f,
and R.sup.17g are each independently hydrogen, alkyl, alkenyl,
alkynyl, cycloalkyl, or heterocycloalkyl; wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, and heterocycloalkyl is independently
optionally substituted with one, two, or three R.sup.30b; [0137] or
R.sup.16a and R.sup.17a or R.sup.16b and R.sup.17b or R.sup.16e and
R.sup.17e or R.sup.16f and R.sup.17f or R.sup.16g and R.sup.17g are
taken together with the nitrogen atom to which they are attached to
form a heterocycloalkyl optionally substituted with one, two, or
three halogen, alkyl, or haloalkyl; [0138] R.sup.18b is alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
alkyl(aryl), alkyl(heteroaryl), alkyl(cycloalkyl), or
alkyl(heterocycloalkyl); wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30i; [0139]
R.sup.20 is hydrogen, alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, alkyl(aryl), alkyl(heteroaryl), alkyl(cycloalkyl),
alkyl(heterocycloalkyl), --(CR.sup.23R.sup.24).sub.wC(O)OR.sup.25,
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)R.sup.26,
--(CR.sup.23R.sup.24).sub.wSC(.dbd.O)R.sup.26, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30k; [0140]
R.sup.21 and R.sup.22 are each independently hydrogen, alkyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkyl(aryl),
alkyl(heteroaryl), alkyl(cycloalkyl), alkyl(heterocycloalkyl),
--(CR.sup.23R.sup.24).sub.wC(.dbd.O)OR.sup.25,
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)R.sup.26,
--(CR.sup.23R.sup.24).sub.wSC(.dbd.O)R.sup.26, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30k; [0141] or
R.sup.21 and R.sup.22 are taken together with the atoms to which
they are attached to form a heterocycloalkyl optionally substituted
with one, two, or three R.sup.30l; [0142] each R.sup.23 and
R.sup.24 are independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, alkyl, or haloalkyl; [0143] each R.sup.25 is
independently hydrogen, alkyl, alkenyl, alkynyl, or heteroalkyl;
[0144] each R.sup.26 is independently alkyl, alkenyl, alkynyl, or
heteroalkyl; [0145] each w is independently 1-4; [0146] each
R.sup.30, R.sup.30a, R.sup.30b, R.sup.30c, R.sup.30d, R.sup.30e,
R.sup.30f, R.sup.30g, R.sup.30h, R.sup.30i, R.sup.30j, R.sup.30k,
R.sup.30l, R.sup.30m, R.sup.30n, and R.sup.30o is independently
halogen, --CN, --OH, --OR.sup.a, --SH, --SR.sup.a, --S(O)R.sup.a,
--NO.sub.2, --NR.sup.cR.sup.d, --S(.dbd.O).sub.2R.sup.a,
--NHS(.dbd.O).sub.2R.sup.a, --S(O).sub.2NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --OC(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--OC(.dbd.O)OR.sup.b, --C(O)NR.sup.cR.sup.d,
--OC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(.dbd.O)NR.sup.cR.sup.d,
--NR.sup.bC(.dbd.O)R.sup.a, --NR.sup.bC(O)OR.sup.b, alkyl, alkenyl,
alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
alkyl(aryl), alkyl(heteroaryl), alkyl(cycloalkyl), or
alkyl(heterocycloalkyl); wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.31; [0147]
each R.sup.31 is independently halogen, --CN, --OH, --OR.sup.a,
--SH, --SR.sup.a, --S(.dbd.O)R.sup.a, --NO.sub.2,
--NR.sup.cR.sup.d, --S(.dbd.O).sub.2R.sup.a,
--NHS(.dbd.O).sub.2R.sup.a, --S(.dbd.O).sub.2NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --OC(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--OC(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
--OC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(.dbd.O)NR.sup.cR.sup.d,
--NR.sup.bC(.dbd.O)R.sup.a, --NR.sup.bC(.dbd.O)OR.sup.b, alkyl,
haloalkyl, hydroxyalkyl, heteroalkyl, or cycloalkyl optionally
substituted with one, two, or three halogen, alkyl, or haloalkyl;
each R.sup.a is independently alkyl, alkenyl, alkynyl, heteroalkyl,
cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; wherein the
alkyl, alkenyl, alkynyl, heteroalkyl, cycloalkyl, heterocycloalkyl,
aryl, and heteroaryl is independently optionally substituted with
one, two, or three halogen, --OH, alkyl, or haloalkyl; [0148] each
R.sup.b is independently hydrogen, alkyl, alkenyl, alkynyl,
heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl;
wherein the alkyl, alkenyl, alkynyl, heteroalkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three halogen, --OH, alkyl, or
haloalkyl; and [0149] R.sup.c and R.sup.d are each independently
hydrogen, alkyl, alkenyl, alkynyl, heteroalkyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein the alkyl, alkenyl,
alkynyl, heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three halogen, --OH, alkyl, or haloalkyl; [0150] or R.sup.c and
R.sup.d are taken together with the nitrogen atom to which they are
attached to form a heterocycloalkyl optionally substituted with
one, two, or three halogen, alkyl, or haloalkyl.
[0151] In some embodiments provided herein is a compound having the
structure of Formula (I), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof wherein; [0152] A is --O-- or
--CH.sub.2--; [0153] Q.sup.1 and Q.sup.2 are independently N or CW;
[0154] each W is independently hydrogen, halogen, --CN, --OH,
--OR.sup.a, --SH, --SR.sup.a, --S(.dbd.O)R.sup.a, --NO.sub.2,
--NR.sup.cR.sup.d, --S(.dbd.O).sub.2R.sup.a,
--NHS(.dbd.O).sub.2R.sup.a, --S(.dbd.O).sub.2NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --OC(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--OC(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
--OC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(.dbd.O)NR.sup.cR.sup.d,
--NR.sup.bC(.dbd.O)R.sup.a, --NR.sup.bC(O)OR.sup.b, C.sub.1-C.sub.6
alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6
alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl,
aryl, and heteroaryl is independently optionally substituted with
one, two, or three R.sup.30; [0155] Z is --NR.sup.1R.sup.2,
--OR.sup.60, --SR.sup.61, or --CR.sup.62R.sup.63R.sup.64; [0156]
R.sup.1 and R.sup.2 are each independently hydrogen,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), C.sub.1-C.sub.6
alkyl(heterocycloalkyl), --S(.dbd.O).sub.2R.sup.15a,
--S(.dbd.O).sub.2NR.sup.16aR.sup.17a, or --C(O)R.sup.15a; wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.30a; [0157] or R.sup.1 and R.sup.2 are taken
together with the nitrogen atom to which they are attached to form
a heterocycloalkyl optionally substituted with one, two, or three
R.sup.30b; [0158] R.sup.60 is hydrogen, --C(.dbd.O)R.sup.15e,
--C(.dbd.O)OR.sup.16e, --C(.dbd.O)NR.sup.16eR.sup.17e,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30m; [0159]
R.sup.61 is hydrogen, --C(.dbd.O)R.sup.15f, --C(.dbd.O)OR.sup.16f,
--C(.dbd.O)NR.sup.16fR.sup.17f, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.30n; [0160] R.sup.62, R.sup.63, and R.sup.64
are each independently hydrogen, halogen, --CN, --OH, --OR.sup.15g,
--SH, --SR.sup.15g, --S(.dbd.O)R.sup.15g, --NO.sub.2,
--NR.sup.16gR.sup.17g, --S(.dbd.O).sub.2R.sup.15g,
--NHS(.dbd.O).sub.2R.sup.15g, --S(.dbd.O).sub.2NR.sup.16gR.sup.17g,
--C(.dbd.O)R.sup.15g, --OC(O)R.sup.15g, --C(.dbd.O)OR.sup.16g,
--OC(.dbd.O)OR.sup.16g, --C(.dbd.O)NR.sup.16gR.sup.17g,
--OC(.dbd.O)NR.sup.16gR.sup.17g,
--NR.sup.16gC(.dbd.O)NR.sup.16gR.sup.17g,
--NR.sup.16gC(.dbd.O)R.sup.15g, --NR.sup.16gC(.dbd.O)OR.sup.16g,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6alkenyl,
C.sub.2-C.sub.6alkynyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30o; [0161] R.sup.3 is halogen, --CN, --OH,
--OR.sup.15b, --SR.sup.18b, --NR.sup.16bR.sup.17b, C.sub.1-C.sub.6
alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6
alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl,
aryl, and heteroaryl is independently optionally substituted with
one, two, or three R.sup.30c; [0162] R.sup.4 and R.sup.7 are each
independently hydrogen, halogen, --OH, --OR.sup.15c,
--NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.15c, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.30d; [0163] R.sup.5 and R.sup.6 are each independently
hydrogen, halogen, --OH, --OR.sup.15d,
--NR.sup.16dS(.dbd.O).sub.2R.sup.15d,
--NR.sup.16dC(.dbd.O)R.sup.15d, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.30e; [0164] R.sup.8 is hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; [0165] R.sup.9 and R.sup.10 are each independently
hydrogen, halogen, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6haloalkyl; [0166] X is --O-- or --NR.sup.11--;
[0167] Y is --(CR.sup.13R.sup.14).sub.v-- or --NR.sup.12--; [0168]
R.sup.11 and R.sup.12 are each independently hydrogen,
--S(O)R.sup.a, --S(.dbd.O).sub.2R.sup.a,
--S(.dbd.O).sub.2NR.sup.cR.sup.d, --C(O)R.sup.a,
--C(.dbd.O)OR.sup.b, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, or heterocycloalkyl;
wherein each alkyl, alkenyl, alkynyl, cycloalkyl, and
heterocycloalkyl is independently optionally substituted with one,
two, or three R.sup.30f; [0169] R.sup.13 and R.sup.14 are each
independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; [0170] v is 1-3; [0171] R.sup.15a, R.sup.15b, R.sup.15c,
R.sup.15d, R.sup.15e, R.sup.15f, and R.sup.15g are each
independently C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl, aryl, or
heteroaryl; wherein each alkyl, alkenyl, alkynyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30g; [0172] R.sup.16a,
R.sup.16b, R.sup.16c, R.sup.16d, R.sup.16e, R.sup.16f, R.sup.16g,
R.sup.17a, R.sup.17b, R.sup.17c, R.sup.17d, R.sup.17e, R.sup.17f,
and R.sup.17g are each independently hydrogen, C.sub.1-C.sub.6
alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl,
cycloalkyl, or heterocycloalkyl; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, and heterocycloalkyl is independently
optionally substituted with one, two, or three R.sup.30h; [0173] or
R.sup.16a and R.sup.17a or R.sup.16b and R.sup.17b or R.sup.16e and
R.sup.17e or R.sup.16f and R.sup.17f or R.sup.16g and R.sup.17g are
taken together with the nitrogen atom to which they are attached to
form a heterocycloalkyl optionally substituted with one, two, or
three halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[0174] R.sup.18b is C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30i; [0175] R.sup.20 is hydrogen, C.sub.1-C.sub.20
alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), C.sub.1-C.sub.6
alkyl(heterocycloalkyl),
--(CR.sup.23R.sup.24).sub.wC(.dbd.O)OR.sup.25,
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)R.sup.26,
--(CR.sup.23R.sup.24).sub.wSC(.dbd.O)R.sup.26, or
--(CR.sup.23R.sup.24).sub.wOC(O)OR; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30j; [0176] R.sup.21 and
R.sup.22 are each independently hydrogen, C.sub.1-C.sub.20 alkyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6
alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--(CR.sup.23R.sup.24).sub.wC(.dbd.O)OR.sup.25,
--(CR.sup.23R.sup.24).sub.wOC(O)R.sup.26,
--(CR.sup.23R.sup.24).sub.wSC(.dbd.O)R.sup.26, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)R.sup.25; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30k; [0177] or
R.sup.21 and R.sup.22 are taken together with the atoms to which
they are attached to form a heterocycloalkyl optionally substituted
with one, two, or three R.sup.30l; [0178] each R.sup.23 and
R.sup.24 are independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; [0179] each R.sup.25 is independently hydrogen,
C.sub.1-C.sub.6alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0180] each R.sup.26 is
independently C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0181]
each w is independently 1-4; [0182] each R.sup.30, R.sup.30a,
R.sup.30b, R.sup.30c, R.sup.30d, R.sup.30e, R.sup.30f, R.sup.30g,
R.sup.30h, R.sup.30i, R.sup.30j, R.sup.30k, R.sup.30l, R.sup.30m,
R.sup.30n and R.sup.30o is independently halogen, --CN, --OH,
--OR.sup.a, --SH, --SR.sup.a, --S(.dbd.O)R.sup.a, --NO.sub.2,
--NR.sup.cR.sup.d, --S(.dbd.O).sub.2R.sup.a,
--NHS(.dbd.O).sub.2R.sup.a, --S(O).sub.2NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --OC(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--OC(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
--OC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(O)NR.sup.cR.sup.d,
--NR.sup.bC(.dbd.O)R.sup.a, --NR.sup.bC(.dbd.O)OR.sup.b, C.sub.1-6
alkyl, C.sub.2-C.sub.6alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl,
aryl, and heteroaryl is independently optionally substituted with
one, two, or three R.sup.31; [0183] each R.sup.31 is independently
halogen, --CN, --OH, --OR.sup.a, --SH, --SR.sup.a,
--S(.dbd.O)R.sup.a, --NO.sub.2, --NR.sup.cR.sup.d,
--S(.dbd.O).sub.2R.sup.a, --NHS(.dbd.O).sub.2R.sup.a,
--S(O).sub.2NR.sup.cR.sup.d, --C(.dbd.O)R.sup.a,
--OC(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b, --OC(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, --OC(.dbd.O)NR.sup.cR.sup.d,
--NR.sup.bC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(.dbd.O)R.sup.a,
--NR.sup.bC(.dbd.O)OR.sup.b, C.sub.1-C.sub.6 alkyl,
C.sub.1-C.sub.6haloalkyl, C.sub.1-C.sub.6 hydroxyalkyl,
C.sub.1-C.sub.6 heteroalkyl, or cycloalkyl optimally substituted
with one, two, or three halogen, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl; [0184] each R.sup.a is independently
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, C.sub.1-C.sub.6 heteroalkyl, cycloalkyl, heterocycloalkyl,
aryl, or heteroaryl; wherein the alkyl, alkenyl, alkyl,
heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optimally substituted with one, two, or three
halogen, --OH, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[0185] each R.sup.b is independently hydrogen, C.sub.1-C.sub.6
alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl,
C.sub.1-C.sub.6 heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, or
heteroaryl; wherein the alkyl, alkenyl, alkynyl, heteroalkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three halogen, --OH,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl; and [0186]
R.sup.c and R.sup.d are each independently hydrogen,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, C.sub.1-C.sub.6 heteroalkyl, cycloalkyl, heterocycloalkyl,
aryl, or heteroaryl; wherein the alkyl, alkenyl, alkynyl,
heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
halogen, --OH, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[0187] or R.sup.c and R.sup.d are taken together with the nitrogen
atom to which they are attached to form a heterocycloalkyl
optionally substituted with one, two, or three halogen,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl.
[0188] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
when X is --O--, Y is not --CH.sub.2--, --CCl.sub.2--,
--CF.sub.2--, or --C(CH.sub.3).sub.2--. In some embodiments of a
compound of Formula (I), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, X is --NR.sup.11--. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, X is
--NR.sup.11-- and R.sup.11 is hydrogen or alkyl. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, v is 2 or 3. In
some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
Y is --NR.sup.12--.
[0189] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof:
[0190] A is --O-- or --CH.sub.2--; [0191] Q.sup.1 and Q.sup.2 are
independently N or CW; [0192] each W is independently hydrogen,
halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30; [0193] Z
is --NR.sup.1R.sup.2; [0194] R.sup.1 and R.sup.2 are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30a; [0195] or R.sup.1 and R.sup.2 are taken
together with the nitrogen atom to which they are attached to form
a heterocycloalkyl optionally substituted with one, two, or three
R.sup.30b; [0196] R.sup.3 is halogen, --CN, --SR.sup.18b,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30c; [0197] R.sup.4 and
R.sup.7 are each independently hydrogen, halogen, --OH,
--OR.sup.15c, --NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.15c, C.sub.1-C.sub.6 alkyl, or
cycloalkyl; wherein each alkyl, and cycloalkyl is independently
optionally substituted with one, two, or three R.sup.30d; [0198]
R.sup.5 and R.sup.6 are each independently hydrogen, halogen,
C.sub.1-C.sub.6 alkyl, or cycloalkyl; wherein each alkyl, and
cycloalkyl is independently optionally substituted with one, two,
or three R.sup.30e; [0199] R.sup.8 is hydrogen, halogen, --OH,
--NH.sub.2, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[0200] R.sup.9 and R.sup.10 are each independently hydrogen,
halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6haloalkyl; [0201]
X is --O-- or --NR.sup.11--; [0202] Y is
--(CR.sup.13R.sup.14).sub.v-- or --NR.sup.12--; [0203] R.sup.11 and
R.sup.12 are each independently hydrogen, --S(O)R.sup.a,
--S(.dbd.O).sub.2R.sup.a. --S(.dbd.O).sub.2NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b, C.sub.1-C.sub.6 alkyl,
cycloalkyl, or heterocycloalkyl; wherein each alkyl, cycloalkyl,
and heterocycloalkyl is independently optionally substituted with
one, two, or three R.sup.30f; [0204] R.sup.13 and R.sup.14 are each
independently hydrogen, halogen, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6haloalkyl; [0205] v is 1-3; [0206] R.sup.15c is
C.sub.1-C.sub.6 alkyl, cycloalkyl, or heterocycloalkyl; wherein
each alkyl, cycloalkyl, and heterocycloalkyl is independently
optionally substituted with one, two, or three R.sup.30g; [0207]
R.sup.16c is hydrogen or C.sub.1-C.sub.6 alkyl optionally
substituted with one, two, or three R.sup.30h; [0208] R.sup.18b is
C.sub.1-C.sub.6 alkyl, cycloalkyl, C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, and heterocycloalkyl is
independently optionally substituted with one, two, or three
R.sup.30i; [0209] R.sup.20 is hydrogen, C.sub.1-C.sub.20 alkyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6
alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--(CR.sup.23R.sup.24).sub.wC(.dbd.O)OR.sup.25,
--(CR.sup.23R.sup.24).sub.wCO(.dbd.O)R.sup.26,
--(CR.sup.23R.sup.24).sub.wSC(.dbd.O)R.sup.26, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30j; [0210]
R.sup.21 and R.sup.22 are each independently hydrogen,
C.sub.1-C.sub.20 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6alkyl(cycloalkyl),
C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--(CR.sup.23R.sup.24).sub.wC(.dbd.O)OR.sup.25,
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)R.sup.26,
--(CR.sup.23R.sup.24).sub.wSC(.dbd.O)R.sup.26, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30k; [0211] or
R.sup.21 and R.sup.22 are taken together with the atoms to which
they are attached to form a heterocycloalkyl optionally substituted
with one, two, or three R.sup.30l; [0212] each R.sup.23 and
R.sup.24 are independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; [0213] each R.sup.25 is independently hydrogen,
C.sub.1-C.sub.6alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0214] each R.sup.26 is
independently C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0215]
each w is independently 1-4; [0216] each R.sup.30, R.sup.30a,
R.sup.30b, R.sup.30c, R.sup.30d, R.sup.30e, R.sup.30f, R.sup.30g,
R.sup.30h, R.sup.30i, R.sup.30j, R.sup.30k, and R.sup.30l is
independently halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --C(O)OR.sup.b, --C(O)NR.sup.cR.sup.d,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl, or
heteroaryl; wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.31; [0217] each R.sup.31 is independently
halogen, --OH, --OR.sup.a, or --NR.sup.cR.sup.d; [0218] each
R.sup.a is independently C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6
haloalkyl, C.sub.1-C.sub.6 hydroxyalkyl, or C.sub.1-C.sub.6
heteroalkyl; [0219] each R.sup.b is independently hydrogen,
C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 haloalkyl, C.sub.1-C.sub.6
hydroxyalkyl, or C.sub.1-C.sub.6 heteroalkyl; and [0220] R.sup.c
and R.sup.d are each independently hydrogen, C.sub.1-C.sub.6 alkyl,
C.sub.1-C.sub.6 haloalkyl, C.sub.1-C.sub.6 hydroxyalkyl, or
C.sub.1-C.sub.6 heteroalkyl; [0221] or R.sup.c and R.sup.d are
taken together with the nitrogen atom to which they are attached to
form a heterocycloalkyl optionally substituted with one, two, or
three halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[0222] provided that, when X is --O--, Y is not --CH.sub.2--,
--CCl.sub.2--, --CF.sub.2--, or --C(CH.sub.3).sub.2--.
[0223] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof;
[0224] A is --O-- or --CH.sub.2--; [0225] Q.sup.1 and Q.sup.2 are
independently N or CW; [0226] each W is hydrogen; [0227] Z is
--NR.sup.1R.sup.2; [0228] R.sup.1 and R.sup.2 are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, cycloalkyl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl, cycloalkyl, and
aryl is independently optionally substituted with one, two, or
three R.sup.30a; [0229] or R.sup.1 and R.sup.2 are taken together
with the nitrogen atom to which they are attached to form a
heterocycloalkyl optionally substituted with one, two, or three
R.sup.30b; [0230] R.sup.3 is halogen; [0231] R.sup.4 and R.sup.7
are each independently hydrogen, halogen, --OH, or --OR.sup.15c;
[0232] R.sup.5 and R.sup.6 are each hydrogen; [0233] R.sup.8 is
hydrogen; [0234] R.sup.9 and R.sup.10 are each hydrogen; [0235] X
is --O-- or --NR.sup.11--; [0236] Y is
--(CR.sup.13R.sup.14).sub.v-- or --NR.sup.12--; [0237] R.sup.11 and
R.sup.12 are each independently hydrogen or C.sub.1-C.sub.6 alkyl;
[0238] R.sup.13 and R.sup.14 are each independently hydrogen,
halogen, or C.sub.1-C.sub.6 alkyl; [0239] v is 1 or 2; [0240]
R.sup.15c is C.sub.1-C.sub.6 alkyl; [0241] R.sup.20 is hydrogen,
C.sub.1-C.sub.20alkyl, --(CR.sup.23R.sup.24).sub.wOC(O)OR.sup.25,
or aryl optionally substituted with one, two, or three R.sup.30j;
[0242] R.sup.21 and R.sup.22 are each hydrogen, C.sub.1-C.sub.20
alkyl, --(CR.sup.23R.sup.24).sub.nOC(.dbd.O)OR.sup.25, or aryl
optionally substituted with one, two, or three R.sup.30l; [0243] or
R.sup.21 and R.sup.22 are taken together with the atoms to which
they are attached to form a heterocycloalkyl optionally substituted
with one, two, or three R.sup.30l; [0244] each R.sup.23 and
R.sup.24 are independently hydrogen; [0245] each R.sup.25 is
independently hydrogen or C.sub.1-C.sub.6 alkyl; [0246] each w is
independently 1 or 2; [0247] each R.sup.30a, R.sup.30b, R.sup.30j,
R.sup.30k, and R.sup.30l is independently halogen, --OH,
--OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, or
C.sub.1-C.sub.6 alkyl optionally substituted with one, two, or
three R.sup.31; [0248] each R.sup.31 is independently halogen,
--OH, --OR.sup.a, or --NR.sup.cR.sup.d; [0249] each R.sup.a is
independently C.sub.1-C.sub.6 alkyl; [0250] each R.sup.b is
independently hydrogen or C.sub.1-C.sub.6 alkyl; and [0251] R.sup.c
and R.sup.d are each independently hydrogen or C.sub.1-C.sub.6
alkyl; [0252] or R.sup.c and R.sup.d are taken together with the
nitrogen atom to which they are attached to form a heterocycloalkyl
optionally substituted with one, two, or three halogen or
C.sub.1-C.sub.6 alkyl; [0253] provided that, when X is --O--, Y is
not --CH.sub.2--, --CCl.sub.2--, --CF.sub.2--, or
--C(CH.sub.3).sub.2--.
[0254] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof;
[0255] A is --O-- or --CH.sub.2--; [0256] Q.sup.1 and Q.sup.2 are
independently N or CW; [0257] each W is independently hydrogen,
halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optimally substituted with one, two, or three R.sup.30; [0258] Z is
--NR.sup.1R.sup.2; [0259] R.sup.1 and R.sup.2 are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30a; [0260] or R.sup.1 and R.sup.2 are taken
together with the nitrogen atom to which they are attached to form
a heterocycloalkyl optionally substituted with one, two, or three
R.sup.30b; [0261] R.sup.3 is halogen, --CN, --SR.sup.18b,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30c; [0262] R.sup.4 and
R.sup.7 are each independently hydrogen, halogen, --OH,
--OR.sup.15c, --NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.15c, C.sub.1-C.sub.6 alkyl, or
cycloalkyl; wherein each alkyl, and cycloalkyl is independently
optionally substituted with one, two, or three R.sup.30d; [0263]
R.sup.5 and R.sup.6 are each independently hydrogen, halogen,
C.sub.1-C.sub.6 alkyl, or cycloalkyl; wherein each alkyl, and
cycloalkyl is independently optionally substituted with one, two,
or three R.sup.30c; [0264] R.sup.8 is hydrogen, halogen, --OH,
--NH.sub.2, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[0265] R.sup.9 and R.sup.10 are each independently hydrogen,
halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[0266] X is --NR.sup.11--; [0267] Y is
--(CR.sup.13R.sup.14).sub.v-- or --NR.sup.12--; [0268] R.sup.11 and
R.sup.12 are each independently hydrogen, --S(.dbd.O)R.sup.a,
--S(.dbd.O).sub.2R.sup.a, --S(.dbd.O).sub.2NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b, C.sub.1-C.sub.6 alkyl,
cycloalkyl, or heterocycloalkyl; wherein each alkyl, cycloalkyl,
and heterocycloalkyl is independently optionally substituted with
one, two, or three R.sup.30f; [0269] R.sup.13 and R.sup.14 are each
independently hydrogen, halogen, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6haloalkyl; [0270] v is 1-3; [0271] R.sup.15c is
C.sub.1-C.sub.6 alkyl, cycloalkyl, or heterocycloalkyl; wherein
each alkyl, cycloalkyl, and heterocycloalkyl is independently
optionally substituted with one, two, or three R.sup.30g; [0272]
R.sup.16c is hydrogen or C.sub.1-C.sub.6 alkyl optionally
substituted with one, two, or three R.sup.30f; [0273] R.sup.18b is
C.sub.1-C.sub.6 alkyl, cycloalkyl, C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, and heterocycloalkyl is
independently optionally substituted with one, two, or three
R.sup.30j; [0274] R.sup.20 is hydrogen, C.sub.1-C.sub.20 alkyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6
alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--(CR.sup.23R.sup.24).sub.wC(.dbd.O)OR.sup.25,
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)R.sup.26,
--(CR.sup.23R.sup.24).sub.wSC(.dbd.O)R.sup.26, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.13; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30j; [0275]
R.sup.21 and R.sup.22 are each independently hydrogen,
C.sub.1-C.sub.20 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl),
C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--(CR.sup.23R.sup.24).sub.wC(O)OR.sup.25,
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)R.sup.26,
--(CR.sup.23R.sup.24).sub.wSC(.dbd.O)R.sup.26, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.23; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30k; [0276] or
R.sup.21 and R.sup.22 are taken together with the atoms to which
they are attached to form a heterocycloalkyl optionally substituted
with one, two, or three R.sup.30l; [0277] each R.sup.23 and
R.sup.24 are independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; [0278] each R.sup.25 is independently hydrogen,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0279] each R.sup.26 is
independently C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0280]
each w is independently 1-4; [0281] each R.sup.30, R.sup.30a,
R.sup.30b, R.sup.30c, R.sup.30d, R.sup.30e, R.sup.30f, R.sup.30g
and R.sup.30h, R.sup.30i, R.sup.30j, R.sup.30k, and R.sup.30l is
independently halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.31; [0282]
each R.sup.31 is independently halogen, --OH, --OR.sup.a, or
--NR.sup.cR.sup.d; [0283] each R.sup.a is independently
C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 haloalkyl, C.sub.1-C.sub.6
hydroxyalkyl, or C.sub.1-C.sub.6 heteroalkyl; [0284] each R.sup.b
is independently hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6
haloalkyl, C.sub.1-C.sub.6 hydroxyalkyl, or C.sub.1-C.sub.4
heteroalkyl; and [0285] R.sup.c and R.sup.d are each independently
hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 haloalkyl,
C.sub.1-C.sub.6 hydroxyalkyl, or C.sub.1-C.sub.6 heteroalkyl;
[0286] or R.sup.c and R.sup.d are taken together with the nitrogen
atom to which they are attached to form a heterocycloalkyl
optionally substituted with one, two, or three halogen,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl.
[0287] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof;
[0288] A is --O-- or --CH.sub.2--; [0289] Q.sup.1 and Q.sup.2 are
independently N or CW; [0290] each W is hydrogen; [0291] Z is
--NR.sup.1R.sup.2; [0292] R.sup.1 and R.sup.2 are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, cycloalkyl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl, cycloalkyl, and
aryl is independently optionally substituted with one, two, or
three R.sup.30a; [0293] or R.sup.1 and R.sup.2 are taken together
with the nitrogen atom to which they are attached to form a
heterocycloalkyl optionally substituted with one, two, or three
R.sup.30b; [0294] R.sup.3 is halogen; [0295] R.sup.4 and R.sup.7
are each independently hydrogen, halogen, --OH, or --OR.sup.15c;
[0296] R.sup.5 and R.sup.6 are each hydrogen; [0297] R.sup.8 is
hydrogen; [0298] R.sup.9 and R.sup.10 are each hydrogen; [0299] X
is --NR.sup.11--; [0300] Y is --(CR.sup.13R.sup.14).sub.v-- or
--NR.sup.12--; [0301] R.sup.11 and R.sup.12 are each independently
hydrogen or C.sub.1-C.sub.6 alkyl; [0302] R.sup.13 and R.sup.14 are
each independently hydrogen, halogen, or C.sub.1-C.sub.6 alkyl;
[0303] v is 1 or 2; [0304] R.sup.15c is C.sub.1-C.sub.6 alkyl;
[0305] R.sup.20 is hydrogen, C.sub.1-C.sub.20 alkyl,
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25, or aryl optionally
substituted with one, two, or three R.sup.30j; [0306] R.sup.21 and
R.sup.22 are each hydrogen, C.sub.1-C.sub.20 alkyl,
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25, or aryl optionally
substituted with one, two, or three R.sup.30k; [0307] or R.sup.21
and R.sup.22 are taken together with the atoms to which they are
attached to form a heterocycloalkyl optionally substituted with
one, two, or three R.sup.30k; [0308] each R.sup.23 and R.sup.24 are
independently hydrogen; [0309] each R.sup.25 is independently
hydrogen or C.sub.1-C.sub.6 alkyl; [0310] each w is independently 1
or 2; [0311] each R.sup.30a, R.sup.30b, R.sup.30j, R.sup.30k, and
R.sup.30l is independently halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, or C.sub.1-C.sub.6 alkyl
optionally substituted with one, two, or three R.sup.31; [0312]
each R.sup.31 is independently halogen, --OH, --OR.sup.a, or
--NR.sup.cR.sup.d; [0313] each R.sup.a is independently
C.sub.1-C.sub.6 alkyl; [0314] each R.sup.b is independently
hydrogen or C.sub.1-C.sub.6 alkyl; and [0315] R.sup.c and R.sup.d
are each independently hydrogen or C.sub.1-C.sub.6 alkyl; [0316] or
R.sup.c and R.sup.d are taken together with the nitrogen atom to
which they are attached to form a heterocycloalkyl optionally
substituted with one, two, or three halogen or C.sub.1-C.sub.6
alkyl.
[0317] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof;
[0318] A is --O-- or --CH.sub.2--; [0319] Q.sup.1 and Q.sup.2 are
independently N or CW; [0320] each W is independently hydrogen,
halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30; [0321] Z
is --NR.sup.1R.sup.2; [0322] R.sup.1 and R.sup.2 are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl. C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, my, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30a; [0323] or R.sup.1 and R.sup.2 are taken
together with the nitrogen atom to which they are attached to form
a heterocycloalkyl optionally substituted with one, two, or three
R.sup.30b; [0324] R.sup.3 is halogen, --CN, --SR.sup.18b,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30c; [0325] R.sup.4 and
R.sup.7 are each independently hydrogen, halogen, --OH,
--OR.sup.13c, --NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(O)R.sup.15c, C.sub.1-C.sub.6 alkyl, or cycloalkyl;
wherein each alkyl, and cycloalkyl is independently optionally
substituted with one, two, or three R.sup.30d; [0326] R.sup.5 and
R.sup.6 are each independently hydrogen, halogen, C.sub.1-C.sub.6
alkyl, or cycloalkyl; wherein each alkyl, and cycloalkyl is
independently optionally substituted with one, two, or three
R.sup.30e; [0327] R.sup.8 is hydrogen, halogen, --OH, --NH.sub.2,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl; [0328] R.sup.9
and R.sup.10 are each independently hydrogen, halogen,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl; [0329] X is
--O-- or --NR.sup.11--; [0330] Y is --(CR.sup.13R.sup.14), or
--NR.sup.12--; [0331] R.sup.11 and R.sup.12 are each independently
hydrogen, --S(O)R.sup.a, --S(.dbd.O).sub.2R.sup.a,
--S(.dbd.O).sub.2NR.sup.cR.sup.d, --C(.dbd.O)R.sup.a,
--C(.dbd.O)OR.sup.b, C.sub.1-C.sub.6 alkyl, cycloalkyl, or
heterocycloalkyl; wherein each alkyl, cycloalkyl, and
heterocycloalkyl is independently optionally substituted with one,
two, or three R.sup.30f; [0332] R.sup.13 and R.sup.14 are each
independently hydrogen, halogen, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6haloalkyl; [0333] v is 2 or 3; [0334] R.sup.15c is
C.sub.1-C.sub.6 alkyl, cycloalkyl, or heterocycloalkyl; wherein
each alkyl, cycloalkyl, and heterocycloalkyl is independently
optionally substituted with one, two, or three R.sup.30g; [0335]
R.sup.16c is hydrogen or C.sub.1-C.sub.6 alkyl optionally
substituted with one, two, or three R.sup.30h; [0336] R.sup.18b is
C.sub.1-C.sub.6 alkyl, cycloalkyl, C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, and heterocycloalkyl is
independently optionally substituted with one, two, or three
R.sup.30i; [0337] R.sup.20 is hydrogen, C.sub.1-C.sub.20 alkyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6
alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--(CR.sup.23R.sup.24).sub.wC(.dbd.O)OR.sup.25,
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)R.sup.26,
--(CR.sup.23R.sup.24).sub.wSC(.dbd.O)R.sup.26, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30j; [0338]
R.sup.21 and R.sup.22 are each independently hydrogen,
C.sub.1-C.sub.20alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl),
C.sub.1-C.sub.6 alkyl(heterocycloalkyl), --(CR.sup.23R.sup.24)
C(.dbd.O)OR.sup.25, --(CR.sup.13R.sup.24).sub.wOC(.dbd.O)R.sup.26,
--(CR.sup.23R.sup.24).sub.wSC(.dbd.O)R.sup.26, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30k; [0339] or
R.sup.21 and R.sup.22 are taken together with the atoms to which
they are attached to form a heterocycloalkyl optionally substituted
with one, two, or three R.sup.30l; [0340] each R.sup.23 and
R.sup.24 are independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; [0341] each R.sup.25 is independently hydrogen,
C.sub.1-C.sub.6alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0342] each R.sup.26 is
independently C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0343]
each w is independently 1-4; [0344] each R.sup.30, R.sup.30a,
R.sup.30b, R.sup.30c, R.sup.30d, R.sup.30e, R.sup.30f, R.sup.30g
and R.sup.30h, R.sup.30i, R.sup.30j, R.sup.30k, and R.sup.30l is
independently halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(O)R.sup.a, --C(.dbd.O)OR.sup.b, --C(O)NR.sup.cR.sup.d,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl, or
heteroaryl; wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.31; [0345] each R.sup.31 is independently
halogen, --OH, --OR.sup.a, or --NR.sup.cR.sup.d; [0346] each
R.sup.a is independently C.sub.1-C.sub.6 alkyl,
C.sub.1-C.sub.6haloalkyl, C.sub.1-C.sub.6 hydroxyalkyl, or
C.sub.1-C.sub.6 heteroalkyl; [0347] each R.sup.b is independently
hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 haloalkyl,
C.sub.1-C.sub.6 hydroxyalkyl, or C.sub.1-C.sub.6 heteroalkyl; and
[0348] R.sup.c and R.sup.d are each independently hydrogen,
C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 haloalkyl, C.sub.1-C.sub.6
hydroxyalkyl, or C.sub.1-C.sub.6 heteroalkyl; [0349] or R.sup.c and
R.sup.d are taken together with the nitrogen atom to which they are
attached to form a heterocycloalkyl optionally substituted with
one, two, or three halogen, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl.
[0350] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof;
[0351] A is --O-- or --CH.sub.2--; [0352] Q.sup.1 and Q.sup.2 are
independently N or CW; [0353] each W is hydrogen; [0354] Z is
--NR.sup.1R.sup.2 [0355] R.sup.1 and R.sup.2 are each independently
hydrogen, C.sub.1-C.sub.6 alkyl, cycloalkyl, or C.sub.1-C.sub.6
alkyl(aryl); wherein each alkyl, cycloalkyl, and aryl is
independently optionally substituted with one, two, or three
R.sup.30a; [0356] or R.sup.1 and R.sup.2 are taken together with
the nitrogen atom to which they are attached to form a
heterocycloalkyl optionally substituted with one, two, or three
R.sup.30b; [0357] R.sup.3 is halogen; [0358] R.sup.4 and R.sup.7
are each independently hydrogen, halogen, --OH, or --OR.sup.15c;
[0359] R.sup.5 and R.sup.6 are each hydrogen; [0360] R.sup.8 is
hydrogen; [0361] R.sup.9 and R.sup.10 are each hydrogen; [0362] X
is --O-- or --NR.sup.11--; [0363] Y is
--(CR.sup.13R.sup.14).sub.v-- or --NR.sup.12--; [0364] R.sup.11 and
R.sup.12 are each independently hydrogen or C.sub.1-C.sub.6
alkyl;
[0365] R.sup.13 and R.sup.14 are each independently hydrogen,
halogen, or C.sub.1-C.sub.6 alkyl; [0366] v is 2; [0367] R.sup.15c
is C.sub.1-C.sub.6 alkyl; [0368] R.sup.20 is hydrogen,
C.sub.1-C.sub.20 alkyl,
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25, or aryl optionally
substituted with one, two, or three R.sup.30j; [0369] R.sup.21 and
R.sup.22 are each hydrogen, C.sub.1-C.sub.20 alkyl,
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25, or aryl optionally
substituted with one, two, or three R.sup.30k; [0370] or R.sup.21
and R.sup.22 are taken together with the atoms to which they are
attached to form a heterocycloalkyl optionally substituted with
one, two, or three R.sup.30l; [0371] each R.sup.23 and R.sup.24 are
independently hydrogen; [0372] each R.sup.25 is independently
hydrogen or C.sub.1-C.sub.6 alkyl; [0373] each w is independently 1
or 2; [0374] each R.sup.30a, R.sup.30b, R.sup.30j, R.sup.30k, and
R.sup.30l is independently halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, or C.sub.1-C.sub.6 alkyl
optionally substituted with one, two, or three R.sup.31; [0375]
each R.sup.31 is independently halogen, --OH, --OR.sup.a, or
--NR.sup.cR.sup.d; [0376] each R.sup.a is independently
C.sub.1-C.sub.6 alkyl; [0377] each R.sup.b is independently
hydrogen or C.sub.1-C.sub.6 alkyl; and [0378] R.sup.c and R.sup.d
are each independently hydrogen or C.sub.1-C.sub.6 alkyl; [0379] or
R.sup.c and R.sup.d are taken together with the nitrogen atom to
which they are attached to form a heterocycloalkyl optionally
substituted with one, two, or three halogen or C.sub.1-C.sub.6
alkyl.
[0380] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof;
[0381] A is --O-- or --CH.sub.2--; [0382] Q.sup.1 and Q.sup.2 are
independently N or CW; [0383] each W is independently hydrogen,
halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30; [0384] Z
is --NR.sup.1R.sup.2; [0385] R.sup.1 and R.sup.2 are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30a; [0386] or R.sup.1 and R.sup.2 are taken
together with the nitrogen atom to which they are attached to form
a heterocycloalkyl optionally substituted with one, two, or three
R.sup.30b; [0387] R.sup.3 is halogen, --CN, --SR.sup.18b,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30c; [0388] R.sup.4 and
R.sup.7 are each independently hydrogen, halogen, --OH,
--OR.sup.15c, --NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(O)R.sup.13c, C.sub.1-C.sub.6 alkyl, or cycloalkyl;
wherein each alkyl, and cycloalkyl is independently optionally
substituted with one, two, or three R.sup.30d; [0389] R.sup.5 and
R.sup.6 are each independently hydrogen, halogen, C.sub.1-C.sub.6
alkyl, or cycloalkyl; wherein each alkyl, and cycloalkyl is
independently optionally substituted with one, two, or three
R.sup.30e; [0390] R.sup.8 is hydrogen, halogen, --OH, --NH.sub.2,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl; [0391] R.sup.9
and R.sup.10 are each independently hydrogen, halogen,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl; [0392] X is
--O-- or --NR.sup.11--; [0393] Y is --NR.sup.12--; [0394] R.sup.11
and R.sup.12 are each independently hydrogen, --S(.dbd.O)R.sup.a,
--S(.dbd.O).sub.2R.sup.a, --S(.dbd.O).sub.2NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b, C.sub.1-C.sub.6 alkyl,
cycloalkyl, or heterocycloalkyl; wherein each alkyl, cycloalkyl,
and heterocycloalkyl is independently optionally substituted with
one, two, or three R.sup.30f; [0395] R.sup.15c is C.sub.1-C.sub.6
alkyl, cycloalkyl, or heterocycloalkyl; wherein each alkyl,
cycloalkyl, and heterocycloalkyl is independently optionally
substituted with one, two, or three R.sup.30f; [0396] R.sup.16c is
hydrogen or C.sub.1-C.sub.6 alkyl optionally substituted with one,
two, or three R.sup.30b; [0397] R.sup.18b is C.sub.1-C.sub.6 alkyl,
cycloalkyl, C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, cycloalkyl, and
heterocycloalkyl is independently optionally substituted with one,
two, or three R.sup.30i; [0398] R.sup.20 is hydrogen,
C.sub.1-C.sub.20 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl),
C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--(CR.sup.23R.sup.24).sub.wC(.dbd.O)OR.sup.25,
--(CR.sup.23R.sup.24).sub.wOC(O)R.sup.26,
--(CR.sup.23R.sup.24).sub.wSC(.dbd.O)R.sup.26, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30j; [0399]
R.sup.21 and R.sup.22 are each independently hydrogen,
C.sub.1-C.sub.20alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl),
C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--(CR.sup.23R.sup.24).sub.wC(.dbd.O)OR.sup.25,
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)R.sup.26,
--(CR.sup.23R.sup.24).sub.wSC(.dbd.O)R.sup.26, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30k; [0400] or
R.sup.21 and R.sup.22 are taken together with the atoms to which
they are attached to form a heterocycloalkyl optionally substituted
with one, two, or three R.sup.30l; [0401] each R.sup.23 and
R.sup.24 are independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; [0402] each R.sup.25 is independently hydrogen,
C.sub.1-C.sub.6alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0403] each R.sup.26 is
independently C.sub.1-C.sub.6 alkyl, C.sub.2--Co alkenyl,
C.sub.2-C.sub.6 alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0404]
each w is independently 1-4; [0405] each R.sup.30, R.sup.30a,
R.sup.30b, R.sup.30c, R.sup.30d, R.sup.30e, R.sup.30f, R.sup.30g
and R.sup.30h, R.sup.30i, R.sup.30j, R.sup.30k, and R.sup.30l is
independently halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.31; [0406]
each R.sup.31 is independently halogen, --OH, --OR.sup.a, or
--NR.sup.cR.sup.d; [0407] each R.sup.a is independently
C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 haloalkyl, C.sub.1-C.sub.6
hydroxyalkyl, or C.sub.1-C.sub.6 heteroalkyl; [0408] each R.sup.b
is independently hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6
haloalkyl, C.sub.1-C.sub.6 hydroxyalkyl, or C.sub.1-C.sub.6
heteroalkyl; and [0409] R.sup.c and R.sup.d are each independently
hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 haloalkyl,
C.sub.1-C.sub.6 hydroxyalkyl, or C.sub.1-C.sub.6 heteroalkyl;
[0410] or R.sup.c and R.sup.d are taken together with the nitrogen
atom to which they are attached to form a heterocycloalkyl
optionally substituted with one, two, or three halogen,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl.
[0411] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof;
[0412] A is --O-- or --CH.sub.2--; [0413] Q.sup.1 and Q.sup.2 are
independently N or CW; [0414] each W is hydrogen; [0415] Z is
--NR.sup.1R.sup.2; [0416] R.sup.1 and R.sup.2 are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, cycloalkyl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl, cycloalkyl, and
aryl is independently optionally substituted with one, two, or
three R.sup.30a; [0417] or R.sup.1 and R.sup.2 are taken together
with the nitrogen atom to which they are attached to form a
heterocycloalkyl optionally substituted with one, two, or three
R.sup.30b; [0418] R.sup.3 is halogen; [0419] R.sup.4 and R.sup.7
are each independently hydrogen, halogen, --OH, or --OR.sup.15c;
[0420] R.sup.5 and R.sup.6 are each hydrogen; [0421] R.sup.8 is
hydrogen; [0422] R.sup.9 and R.sup.10 are each hydrogen; [0423] X
is --O-- or --NR.sup.11--; [0424] Y is --NR.sup.12--; [0425]
R.sup.11 and R.sup.12 are each independently hydrogen or
C.sub.1-C.sub.6 alkyl; [0426] R.sup.15c is C.sub.1-C.sub.6 alkyl;
[0427] R.sup.20 is hydrogen, C.sub.1-C.sub.20 alkyl,
--(CR.sup.23R.sup.24).sub.wOC(O)OR.sup.25, or aryl optionally
substituted with one, two, or three R.sup.30j; [0428] R.sup.21 and
R.sup.22 are each hydrogen, C.sub.1-C.sub.20 alkyl,
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.23, or aryl optionally
substituted with one, two, or three R.sup.30k; [0429] or R.sup.21
and R.sup.22 are taken together with the atoms to which they are
attached to form a heterocycloalkyl optionally substituted with
one, two, or three R.sup.30l; [0430] each R.sup.23 and R.sup.24 are
independently hydrogen; [0431] each R.sup.25 is independently
hydrogen or C.sub.1-C.sub.6 alkyl; [0432] each w is independently 1
or 2; [0433] each R.sup.30a, R.sup.30b, R.sup.30j, R.sup.30k, and
R.sup.30l is independently halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, or C.sub.1-C.sub.6 alkyl
optionally substituted with one, two, or three R.sup.31; [0434]
each R.sup.31 is independently halogen, --OH, --OR.sup.a, or
--NR.sup.cR.sup.d; [0435] each R.sup.a is independently
C.sub.1-C.sub.6 alkyl; [0436] each R.sup.b is independently
hydrogen or C.sub.1-C.sub.6 alkyl; and [0437] R.sup.c and R.sup.d
are each independently hydrogen or C.sub.1-C.sub.6 alkyl; [0438] or
R.sup.c and R.sup.d are taken together with the nitrogen atom to
which they are attached to form a heterocycloalkyl optionally
substituted with one, two, or three halogen or C.sub.1-C.sub.6
alkyl. For any and all of the embodiments of Formula (I),
substituents are selected from among a subset of the listed
alternatives.
[0439] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.8 is hydrogen, halogen, --OH, --OMe, --NH.sub.2,
--NH(CH.sub.3), --N(CH.sub.3).sub.2, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl. In some embodiments of a compound of
Formula (I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.8 is hydrogen, halogen, --OH,
--NH.sub.2, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl. In
some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.8 is hydrogen, halogen, --OH, --NH.sub.2, or C.sub.1-C.sub.6
alkyl. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sub.8 is hydrogen or C.sub.1-C.sub.6 alkyl. In some embodiments
of a compound of Formula (I), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.8 is hydrogen.
[0440] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.9 and R.sup.10 are each independently hydrogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.9 and R.sup.10 are each hydrogen.
[0441] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
Q.sup.1 is N; and Q.sup.2 is CW. In some embodiments of a compound
of Formula (I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, Q.sup.1 is CW; and Q.sup.2 is N. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, Q.sup.1 is N;
and Q.sup.2 is N. In some embodiments of a compound of Formula (I),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, Q.sup.1 is CW; and Q.sup.2 is CW.
[0442] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each W is independently hydrogen, halogen, --CN, --OH, --OR,
--NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
C.sub.1-C.sub.6 alkyl, cycloalkyl, or heterocycloalkyl; wherein
each alkyl, cycloalkyl, and heterocycloalkyl, is independently
optionally substituted with one, two, or three R.sup.30. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each W is
independently hydrogen, halogen, --CN, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
C.sub.1-C.sub.6 alkyl, cycloalkyl, or heterocycloalkyl; wherein
each alkyl, cycloalkyl, and heterocycloalkyl, is independently
optionally substituted with one, two, or three R.sup.30; and each
R.sup.30 is independently halogen or C.sub.1-C.sub.6alkyl. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each W is
independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6alkyl, or C.sub.1-C.sub.6
haloalkyl. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each W is hydrogen.
[0443] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
A is --O--. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
A is --CH.sub.2--.
[0444] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
X is --O--. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
X is --NR.sup.11--. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, X is --NR.sup.11--; and R.sup.11 is hydrogen
or C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of
Formula (I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, X is --NR.sup.11--; and R.sup.11 is hydrogen
or methyl.
[0445] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
Y is --NR.sup.12--. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, Y is --NR.sup.12--; and R.sup.12 is hydrogen
or C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of
Formula (I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, Y is --NR.sup.12--; and R.sup.12 is hydrogen
or methyl. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
Y is --NR.sup.12--; and R.sup.12 is hydrogen. In some embodiments
of a compound of Formula (I), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, Y is --NR.sup.12--; and
R.sup.12 is C.sub.1-C.sub.6 alkyl.
[0446] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
Y is --(CR.sup.13R.sup.14).sub.v--. In some embodiments of a
compound of Formula (I), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, Y is
--(CR.sup.13R.sup.14).sub.v--; R.sup.13 and R.sup.14 are each
independently hydrogen, halogen, or C.sub.1-C.sub.6 alkyl; and v is
1 or 2. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
Y is --(CR.sup.13R.sup.14).sub.v--; R.sup.13 and R.sup.14 are each
independently hydrogen, halogen, or C.sub.1-C.sub.6 alkyl; and v is
2 or 3. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
Y is --(CR.sup.13R.sup.14).sub.v--; R.sup.13 and R.sup.14 are each
independently hydrogen, halogen, or C.sub.1-C.sub.6 alkyl; and v is
1. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
Y is --(CR.sup.13R.sup.14).sub.v--; R.sup.13 and R.sup.14 are each
independently hydrogen, halogen, or C.sub.1-C.sub.6 alkyl; and v is
2. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
Y is --(CR.sup.13R.sup.14).sub.v--; R.sup.13 and R.sup.14 are each
hydrogen; and v is 1 or 2. In some embodiments of a compound of
Formula (I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, Y is --(CR.sup.13R.sup.14).sub.v--; R.sup.13
and R.sup.14 are each hydrogen; and v is 2 or 3. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, Y is
--(CR.sup.13R.sup.14).sub.v--; R.sup.13 and R.sup.14 are each
hydrogen; and v is 1. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, Y is --(CR.sup.13R.sup.14).sub.v--; R.sup.13
and R.sup.14 are each hydrogen; and v is 2. In some embodiments of
a compound of Formula (I), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, Y is
--(CR.sup.13R.sup.14).sub.v--; R.sup.13 and R.sup.14 are each
halogen or C.sub.1-C.sub.6 alkyl; and v is 1 or 2. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, Y is
--(CR.sup.13R.sup.14).sub.v--; R.sup.13 and R.sup.14 are each
halogen or C.sub.1-C.sub.6 alkyl; and v is 2 or 3. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, Y is
--(CR.sup.13R.sup.14).sub.v--; R.sup.13 and R.sup.14 are each
halogen or C.sub.1-C.sub.6 alkyl; and v is 1. In some embodiments
of a compound of Formula (I), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, Y is
--(CR.sup.13R.sup.14).sub.v--; R.sup.13 and R.sup.14 are each
halogen or C.sub.1-C.sub.6 alkyl; and v is 2.
[0447] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
X is --O-- and Y is --NR.sup.12--. In some embodiments of a
compound of Formula (I), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, X is --O--; Y is --NR.sup.11--;
and R.sup.12 is hydrogen or C.sub.1-C.sub.6 alkyl. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, X is --O--; Y is
--NR.sup.12--; and R.sup.12 is hydrogen. In some embodiments of a
compound of Formula (I), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, X is --O--; Y is --NR.sup.12--;
and R.sup.12 is C.sub.1-C.sub.6 alkyl.
[0448] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
X is --NR.sup.11-- and Y is --(CR.sup.13R.sup.14).sub.v--. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, X is
--NR.sup.11--; Y is --(CR.sup.13R.sup.14).sub.v--; R.sup.11 is
hydrogen or C.sub.1-C.sub.6 alkyl; R.sup.13 and R.sup.14 are each
independently hydrogen, halogen, or C.sub.1-C.sub.6 alkyl; and v is
1 or 2. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
X is --NR.sup.11--; Y is --(CR.sup.13R.sup.14).sub.v--; R.sup.11 is
hydrogen; R.sup.13 and R.sup.14 are each hydrogen; and v is 1. In
some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
X is --NR.sup.11--; Y is --(CR.sup.13R.sup.14).sub.v--; R.sup.11 is
C.sub.1-C.sub.6 alkyl; R.sup.13 and R.sup.14 are each hydrogen; and
v is 1.
[0449] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
X is --NR.sup.11-- and Y is --NR.sup.12--. In some embodiments of a
compound of Formula (I), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, X is --NR.sup.11--; Y is
--NR.sup.11--; R.sup.11 is hydrogen or C.sub.1-C.sub.6 alkyl; and
R.sup.12 is hydrogen or C.sub.1-C.sub.6 alkyl. In some embodiments
of a compound of Formula (I), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, X is --NR.sup.11--; Y is
--NR.sup.12--; R.sup.11 is hydrogen; and R.sup.12 is hydrogen. In
some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
X is --NR.sup.11--; Y is --NR.sup.12--; R.sup.11 is C.sub.1-C.sub.6
alkyl; and R.sup.12 is C.sub.1-C.sub.6 alkyl. In some embodiments
of a compound of Formula (I), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, X is --NR.sup.11--; Y is
--NR.sup.12--; R.sup.11 is hydrogen; and R.sup.12 is
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, X is --NR.sup.11--; Y is --NR.sup.12--;
R.sup.11 is C.sub.1-C.sub.6 alkyl; and R.sup.12 is hydrogen.
[0450] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
X is --O--; Y is --(CR.sup.13R.sup.14).sub.v--. In some embodiments
of a compound of Formula (I), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, X is --O--; Y is
--(CR.sup.13R.sup.14).sub.v--; R.sup.13 and R.sup.14 are each
independently hydrogen, halogen, or C.sub.1-C.sub.6alkyl; and v is
2 or 3. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
X is --O--; Y is --(CR.sup.13R.sup.14).sub.v--; R.sup.13 and
R.sup.14 are each hydrogen; and v is 2. In some embodiments of a
compound of Formula (I), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, X is --O--; Y is
--(CR.sup.13R.sup.14).sub.v--; R.sup.13 and R.sup.14 are each
hydrogen; and v is 3.
[0451] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.5 and R.sup.6 are each independently hydrogen, halogen,
C.sub.1-C.sub.6 alkyl, or cycloalkyl; wherein each alkyl and
cycloalkyl is independently optionally substituted with one, two,
or three R.sup.30e. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.5 and R.sup.6 are each independently
hydrogen, halogen, C.sub.1-C.sub.6 alkyl, or cycloalkyl; wherein
each alkyl and cycloalkyl is independently optionally substituted
with one, two, or three R.sup.30e; and each R.sup.30e is
independently halogen or C.sub.1-C.sub.6 alkyl. In some embodiments
of a compound of Formula (I), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.5 and R.sup.6 are
each hydrogen.
[0452] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.4 and R.sup.7 are each independently hydrogen, halogen, --OH,
--OR.sup.15c, --NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.15c, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30d. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.4 and
R.sup.7 are each independently hydrogen, halogen, --OH,
--OR.sup.15c, --NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.15c, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30d; and each
R.sup.30d is independently halogen or C.sub.1-C.sub.6alkyl. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.4 and
R.sup.7 are each independently hydrogen, halogen, --OH,
--OR.sup.15c. --NR.sup.16cS(.dbd.O).sub.2R.sup.15c, or
--NR.sup.16cC(O)R.sup.15c. In some embodiments of a compound of
Formula (I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.4 and R.sup.7 are each independently
hydrogen, halogen. --OH, --OR.sup.15c,
--NR.sup.16cS(.dbd.O).sub.2R.sup.15c, or
--NR.sup.16cC(.dbd.O)R.sup.15c; R.sup.15c are each independently
C.sub.1-C.sub.6 alkyl or C.sub.1-C.sub.6 haloalkyl; and R.sup.16c
are each independently hydrogen, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl. In some embodiments of a compound of
Formula (I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.4 and R.sup.7 are each independently
hydrogen, halogen, --OH, --OR.sup.15c,
--NR.sup.16cS(.dbd.O).sub.2R.sup.15c, or
--NR.sup.16cC(.dbd.O)R.sup.15c; R.sup.15c are each independently
C.sub.1-C.sub.6 alkyl; and R.sup.16c are each independently
hydrogen or C.sub.1-C.sub.6 alkyl.
[0453] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.4 and R.sup.7 are each independently hydrogen, halogen, or
--OH. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.4 and R.sup.7 are each independently halogen or --OH. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof: R.sup.4 and
R.sup.7 are each --OH.
[0454] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
Z is --NR.sup.1R.sup.2.
[0455] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 is C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl),
C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--S(.dbd.O).sub.2R.sup.15a, --S(.dbd.O).sub.2NR.sup.16aR.sup.17a,
or --C(.dbd.O).sub.2R.sup.15a; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30a. In some embodiments
of a compound of Formula (I), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.1 is C.sub.1-C.sub.6
alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), C.sub.1-C.sub.6
alkyl(heterocycloalkyl), --S(O).sub.2R.sup.15a,
--S(.dbd.O).sub.2NR.sup.16aR.sup.17a, or
--C(.dbd.O).sub.2R.sup.15a; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30a; R.sup.15a is
C.sub.1-C.sub.6 alkyl, aryl, or C.sub.1-C.sub.6 alkyl (aryl);
wherein each alkyl and aryl is optionally substituted with one,
two, or three halogen; and R.sup.16a and R.sup.17a are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, aryl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl is
optionally substituted with one, two, or three halogen. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.1 is
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl),
C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--S(.dbd.O).sub.2R.sup.15a, --S(.dbd.O).sub.2NR.sup.16aR.sup.17a,
or --C(O)R.sup.15a; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30a; R.sup.15a is
C.sub.1-C.sub.6 alkyl; and R.sup.16a and R.sup.17a are each
independently hydrogen or C.sub.1-C.sub.6 alkyl.
[0456] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.15a is C.sub.1-C.sub.6 alkyl, aryl, or C.sub.1-C.sub.6
alkyl(aryl); wherein each alkyl and aryl is optionally substituted
with one, two, or three halogen; and R.sup.16a and R.sup.17a are
each independently hydrogen, C.sub.1-C.sub.6 alkyl, aryl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl is
optionally substituted with one, two, or three halogen. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.15a is
C.sub.1-C.sub.6 alkyl; and R.sup.16a and R.sup.17a are each
independently hydrogen or C.sub.1-C.sub.6 alkyl. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.15a is
C.sub.1-C.sub.6 alkyl, aryl, or C.sub.1-C.sub.6 alkyl(aryl);
wherein each alkyl and aryl is optionally substituted with one,
two, or three halogen. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.15a is C.sub.1-C.sub.6 alkyl. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.16a and
R.sup.17a are each independently hydrogen, C.sub.1-C.sub.6 alkyl,
aryl, or C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl
is optionally substituted with one, two, or three halogen. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.16a and
R.sup.17a are each independently hydrogen or C.sub.1-C.sub.6
alkyl.
[0457] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 is C.sub.1-C.sub.6 alkyl, cycloalkyl, C.sub.1-C.sub.6
alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30a. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 is C.sub.1-C.sub.6 alkyl, cycloalkyl,
or C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl, cycloalkyl, and
aryl is independently optionally substituted with one, two, or
three R.sup.30a. In some embodiments of a compound of Formula (I),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof: R.sup.1 is cycloalkyl or C.sub.1-C.sub.6 alkyl(aryl);
wherein each alkyl, cycloalkyl, and aryl is independently
optionally substituted with one, two, or three R.sup.30a. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.1 is
cycloalkyl optionally substituted with one, two, or three
R.sup.30a. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 is C.sub.1-C.sub.6 alkyl(aryl); wherein alkyl and aryl are
independently optionally substituted with one, two, or three
R.sup.30a.
[0458] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30a is independently halogen, --CN, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl; wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optimally substituted with one,
two, or three R.sup.31. In some embodiments of a compound of
Formula (I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, each R.sup.30a is independently halogen,
--CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optimally
substituted with one, two, or three R.sup.31; and each R.sup.31 is
independently halogen or C.sub.1-C.sub.6 alkyl. In some embodiments
of a compound of Formula (I), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.30a is
independently halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6
alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl; wherein each
alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.31; and each R.sup.31 is independently halogen. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each R.sup.30a
is independently halogen, --CN, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
C.sub.1-C.sub.6alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl; wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.31; and each R.sup.31 is independently
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, each R.sup.30a is independently halogen,
--CN, --OH, --OR.sup.a, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6haloalkyl. In some embodiments of a compound of
Formula (I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, each R.sup.30a is independently halogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof each R.sup.30a is independently halogen.
[0459] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 is cycloalkyl optionally substituted with one, two, or
three R.sup.30a; each R.sup.30a is independently halogen, --CN,
--OH, --OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.31; and each R.sup.31 is
independently halogen or C.sub.1-C.sub.6 alkyl. In some embodiments
of a compound of Formula (I), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.1 is cycloalkyl
optionally substituted with one, two, or three R.sup.30a; and each
R.sup.30a is independently halogen, --CN, --OH, --OR.sup.a,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.1 is
cycloalkyl optionally substituted with one, two, or three
R.sup.30a; and each R.sup.30a is independently halogen.
[0460] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 is C.sub.1-C.sub.6 alkyl(aryl); wherein alkyl and aryl are
independently optionally substituted with one, two, or three
R.sup.30a; each R.sup.30a is independently halogen, --CN, --OH,
--OR.sup.a, --NR.sup.cR.sup.d, --C(O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.31; and each R.sup.31 is
independently halogen or C.sub.1-C.sub.6 alkyl. In some embodiments
of a compound of Formula (I), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.1 is C.sub.1-C.sub.6
alkyl(aryl); wherein alkyl and aryl are independently optionally
substituted with one, two, or three R.sup.30a; and each R.sup.30a
is independently halogen, --CN, --OH, --OR.sup.a, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6 haloalkyl. In some embodiments of a
compound of Formula (I), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.1 is C.sub.1-C.sub.6
alkyl(aryl); wherein alkyl and aryl are independently optionally
substituted with one, two, or three R.sup.30a; and each R.sup.30a
is independently halogen.
[0461] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.2 is hydrogen or C.sub.1-C.sub.6 alkyl. In some embodiments
of a compound of Formula (I), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.2 is hydrogen. In
some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.2 is C.sub.1-C.sub.6 alkyl.
[0462] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 is cycloalkyl optionally substituted with one, two, or
three R.sup.30a; each R.sup.30a is independently halogen, --CN,
--OH, --OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.31; each R.sup.31 is
independently halogen or C.sub.1-C.sub.6 alkyl; and R.sup.2 is
hydrogen or C.sub.1-C.sub.6 alkyl. In some embodiments of a
compound of Formula (I), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.1 is cycloalkyl optionally
substituted with one, two, or three R.sup.30a; each R.sup.30a is
independently halogen, --CN, --OH, --OR.sup.a, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6 haloalkyl; and R.sup.2 is hydrogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 is cycloalkyl optionally substituted
with one, two, or three R.sup.30a; each R.sup.30a is independently
halogen; and R.sup.2 is hydrogen or C.sub.1-C.sub.6 alkyl.
[0463] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 is cycloalkyl optionally substituted with one, two, or
three R.sup.30a; each R.sup.30a is independently halogen, --CN,
--OH, --OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(O)NR.sup.cR.sup.d, C.sub.1-C.sub.6alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.31; each R.sup.31 is
independently halogen or C.sub.1-C.sub.6 alkyl; and R.sup.2 is
hydrogen. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 is cycloalkyl optionally substituted with one, two, or
three R.sup.30a, each R.sup.30a is independently halogen, --CN,
--OH, --OR.sup.a, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; and R.sup.2 is hydrogen. In some embodiments of a
compound of Formula (I), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.1 is cycloalkyl optionally
substituted with one, two, or three R.sup.30a; each R.sup.30a is
independently halogen; and R.sup.2 is hydrogen.
[0464] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 is cycloalkyl optionally substituted with one, two, or
three R.sup.30a; each R.sup.30a is independently halogen, --CN,
--OH, --OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.31; each R.sup.31 is
independently halogen or C.sub.1-C.sub.6 alkyl; and R.sup.2 is
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 is cycloalkyl optionally substituted
with one, two, or three R.sup.30a; each R.sup.30a is independently
halogen, --CN, --OH, --OR.sup.a, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl; and R.sup.2 is C.sub.1-C.sub.6 alkyl. In
some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 is cycloalkyl optionally substituted with one, two, or
three R.sup.30a; each R.sup.30a is independently halogen; and
R.sup.2 is C.sub.1-C.sub.6 alkyl.
[0465] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 is C.sub.1-C.sub.6 alkyl(aryl); wherein alkyl and aryl are
independently optionally substituted with one, two, or three
R.sup.30a; each R.sup.30a is independently halogen, --CN, --OH,
--OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.31; each R.sup.31 is
independently halogen or C.sub.1-C.sub.6 alkyl; and R.sup.2 is
hydrogen or C.sub.1-C.sub.6 alkyl. In some embodiments of a
compound of Formula (I), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.1 is C.sub.1-C.sub.6
alkyl(aryl); wherein alkyl and aryl are independently optionally
substituted with one, two, or three R.sup.30a; each R.sup.30a is
independently halogen, --CN, --OH, --OR.sup.a, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6 haloalkyl; and R.sup.2 is hydrogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 is C.sub.1-C.sub.6 alkyl(aryl);
wherein alkyl and aryl are independently optionally substituted
with one, two, or three R.sup.30a; each R.sup.30a is independently
halogen; and R.sup.2 is hydrogen or C.sub.1-C.sub.6 alkyl.
[0466] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 is C.sub.1-C.sub.6 alkyl(aryl); wherein alkyl and aryl are
independently optionally substituted with one, two, or three
R.sup.30a; each R.sup.30a is independently halogen, --CN, --OH,
--OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.31; each R.sup.31 is
independently halogen or C.sub.1-C.sub.6 alkyl; and R.sup.2 is
hydrogen. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R is C.sub.1-C.sub.6 alkyl(aryl); wherein alkyl and aryl are
independently optionally substituted with one, two, or three
R.sup.30a; each R.sup.30a is independently halogen, --CN, --OH,
--OR.sup.a, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
and R.sup.2 is hydrogen. In some embodiments of a compound of
Formula (I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 is C.sub.1-C.sub.6 alkyl(aryl);
wherein alkyl and aryl are independently optionally substituted
with one, two, or three R.sup.30a; each R.sup.30a is independently
halogen; and R.sup.2 is hydrogen.
[0467] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 is C.sub.1-C.sub.6 alkyl(aryl); wherein alkyl and aryl are
independently optionally substituted with one, two, or three
R.sup.30a; each R.sup.30a is independently halogen, --CN, --OH,
--OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.31; each R.sup.31 is
independently halogen or C.sub.1-C.sub.6 alkyl; and R.sup.2 is
C.sub.1-C.sub.6alkyl. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 is C.sub.1-C.sub.6alkyl(aryl);
wherein alkyl and aryl are independently optionally substituted
with one, two, or three R.sup.30a; each R.sup.30a is independently
halogen, --CN, --OH, --OR.sup.a, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl; and R.sup.1 is C.sub.1-C.sub.6 alkyl. In
some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 is C.sub.1-C.sub.6 alkyl(aryl); wherein alkyl and aryl are
independently optionally substituted with one, two, or three
R.sup.30a; each R.sup.30a is independently halogen; and R.sup.2 is
C.sub.1-C.sub.6 alkyl.
[0468] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 and R.sup.2 are taken together with the nitrogen atom to
which they are attached to form a heterocycloalkyl optionally
substituted with one, two, or three R.sup.30b. In some embodiments
of a compound of Formula (I), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.1 and R.sup.2 are
taken together with the nitrogen atom to which they are attached to
form a heterocycloalkyl optionally substituted with one, two, or
three R.sup.30b; each R.sup.30b is independently aryl optionally
substituted with one, two, or three R.sup.31; and each R.sup.31 is
independently halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 and R.sup.2 are taken together with the nitrogen atom to
which they are attached to form a heterocycloalkyl optionally
substituted with one, two, or three R.sup.30b; and R.sup.30b is
aryl. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 and R.sup.2 are taken together with the nitrogen atom to
which they are attached to form a heterocycloalkyl optionally
substituted with one R.sup.30b; and R.sup.30b is aryl.
[0469] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 and R.sup.2 are taken together with the nitrogen atom to
which they are attached to form a piperidine or a pyrrolidine
optionally substituted with one, two, or three R.sup.30b. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.1 and
R.sup.2 are taken together with the nitrogen atom to which they are
attached to form a piperidine or a pyrrolidine optionally
substituted with one, two, or three R.sup.30b; each R.sup.30b is
independently aryl optionally substituted with one, two, or three
R.sup.31; and each R.sup.31 is independently halogen,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.1 and
R.sup.2 are taken together with the nitrogen atom to which they are
attached to form a piperidine or a pyrrolidine optionally
substituted with one, two, or three R.sup.30b; and R.sup.30b is
aryl. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 and R.sup.2 are taken together with the nitrogen atom to
which they are attached to form a piperidine or a pyrrolidine
optionally substituted with one R.sup.30b; and R.sup.30b is
aryl.
[0470] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 and R.sup.2 are taken together with the nitrogen atom to
which they are attached to form a piperidine optionally substituted
with one, two, or three R.sup.30b. In some embodiments of a
compound of Formula (I), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.1 and R.sup.2 are taken
together with the nitrogen atom to which they are attached to form
a piperidine optionally substituted with one, two, or three
R.sup.30b; each R.sup.30b is independently aryl optionally
substituted with one, two, or three R.sup.31; and each R.sup.31 is
independently halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 and R.sup.2 are taken together with the nitrogen atom to
which they are attached to form a piperidine optionally substituted
with one, two, or three R.sup.30b; and R.sup.30b is aryl. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.1 and
R.sup.2 are taken together with the nitrogen atom to which they are
attached to form a piperidine optionally substituted with one
R.sup.30b; and R.sup.30b is aryl.
[0471] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 and R.sup.2 are taken together with the nitrogen atom to
which they are attached to form a pyrrolidine optionally
substituted with one, two, or three R.sup.30b. In some embodiments
of a compound of Formula (I), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.1 and R.sup.2 are
taken together with the nitrogen atom to which they are attached to
form a pyrrolidine optionally substituted with one, two, or three
R.sup.30b; each R.sup.30b is independently aryl optionally
substituted with one, two, or three R.sup.31; and each R.sup.31 is
independently halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 and R.sup.2 are taken together with the nitrogen atom to
which they are attached to form a pyrrolidine optionally
substituted with one, two, or three R.sup.30b; and R.sup.30b is
aryl. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 and R.sup.2 are taken together with the nitrogen atom to
which they are attached to form a pyrrolidine optionally
substituted with one R.sup.30b; and R.sup.30b is aryl.
[0472] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
Z is --OR.sup.60.
[0473] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.60 is hydrogen, --C(.dbd.O)R.sup.15e, --C(.dbd.O)OR.sup.16e,
--C(.dbd.O)NR.sup.16eR.sup.17e, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30m. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.60 is --C(.dbd.O)R.sup.15e,
--C(.dbd.O)OR.sup.16e, --C(.dbd.O)NR.sup.16eR.sup.17e,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl),
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30m. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.60 is
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30m.
[0474] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.60 is C.sub.1-C.sub.6 alkyl, cycloalkyl, C.sub.1-C.sub.6
alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30m. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.60 is C.sub.1-C.sub.6 alkyl,
cycloalkyl, or C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl,
cycloalkyl, and aryl is independently optionally substituted with
one, two, or three R.sup.30m. In some embodiments of a compound of
Formula (I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof: R.sup.60 is cycloalkyl or C.sub.1-C.sub.6
alkyl(aryl); wherein each alkyl, cycloalkyl, and aryl is
independently optionally substituted with one, two, or three
R.sup.30m. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.60 is cycloalkyl optionally substituted with one, two, or
three R.sup.30m. In some embodiments of a compound of Formula (I),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.60 is C.sub.1-C.sub.6 alkyl(aryl); wherein alkyl and
aryl are independently optionally substituted with one, two, or
three R.sup.30m.
[0475] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.15e is C.sub.1-C.sub.6 alkyl, aryl, or C.sub.1-C.sub.6
alkyl(aryl); wherein each alkyl and aryl is optionally substituted
with one, two, or three halogen; and R.sup.16e and R.sup.17e are
each independently hydrogen, C.sub.1-C.sub.6 alkyl, aryl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl is
optionally substituted with one, two, or three halogen. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.15e is
C.sub.1-C.sub.6 alkyl; and R.sup.16e and R.sup.17e are each
independently hydrogen or C.sub.1-C.sub.6 alkyl. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.15e is
C.sub.1-C.sub.6 alkyl, aryl, or C.sub.1-C.sub.6 alkyl(aryl);
wherein each alkyl and aryl is optionally substituted with one,
two, or three halogen. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.15e is C.sub.1-C.sub.6 alkyl. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.16e and
R.sup.17e are each independently hydrogen, C.sub.1-C.sub.6 alkyl,
aryl, or C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl
is optionally substituted with one, two, or three halogen. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.16e and
R.sup.17e are each independently hydrogen or C.sub.1-C.sub.6
alkyl.
[0476] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30m is independently halogen, --CN, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, --C(O)NR.sup.cR.sup.d,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl; wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.31. In some embodiments of a compound of
Formula (I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, each R.sup.30m is independently halogen,
--CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.31; and each R.sup.31 is
independently halogen or C.sub.1-C.sub.6 alkyl. In some embodiments
of a compound of Formula (I), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.30m is
independently halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6alkyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.31; and each
R.sup.31 is independently halogen. In some embodiments of a
compound of Formula (I), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, each R.sup.30m is independently
halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6
alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl; wherein each
alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.31; and each R.sup.31 is independently C.sub.1-C.sub.6 alkyl.
In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30m is independently halogen, --CN, --OH, --OR.sup.a,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each R.sup.30m
is independently halogen or C.sub.1-C.sub.6 alkyl. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each R.sup.30m
is independently halogen.
[0477] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
Z is --SR.sup.61.
[0478] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.61 is hydrogen, --C(.dbd.O)R.sup.15f, --C(.dbd.O)OR.sup.16f,
--C(.dbd.O)NR.sup.16fR.sup.17f, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30n. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.61 is --C(.dbd.O)R.sup.15f,
--C(.dbd.O)OR.sup.16f, --C(.dbd.O)NR.sup.16fR.sup.17f,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30n. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.61 is
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30o. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.61 is
C.sub.1-C.sub.6 alkyl, cycloalkyl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30a. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.61 is C.sub.1-C.sub.6 alkyl,
cycloalkyl, or C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl,
cycloalkyl, and aryl is independently optionally substituted with
one, two, or three R.sup.30n. In some embodiments of a compound of
Formula (I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.61 is cycloalkyl or C.sub.1-C.sub.6
alkyl(aryl); wherein each alkyl, cycloalkyl, and aryl is
independently optionally substituted with one, two, or three
R.sup.30n. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.61 is cycloalkyl optionally substituted with one, two, or
three R.sup.30n. In some embodiments of a compound of Formula (I),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.61 is C.sub.1-C.sub.6 alkyl(aryl); wherein alkyl and
aryl are independently optionally substituted with one, two, or
three R.sup.30n.
[0479] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.15f is C.sub.1-C.sub.6 alkyl, aryl, or C.sub.1-C.sub.6
alkyl(aryl); wherein each alkyl and aryl is optionally substituted
with one, two, or three halogen; and R.sup.16f and R.sup.17f are
each independently hydrogen, C.sub.1-C.sub.6 alkyl, aryl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl is
optionally substituted with one, two, or three halogen. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.15f is
C.sub.1-C.sub.6 alkyl; and R.sup.16f and R.sup.17f are each
independently hydrogen or C.sub.1-C.sub.6 alkyl. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.15f is
C.sub.1-C.sub.6 alkyl, aryl, or C.sub.1-C.sub.6 alkyl(aryl);
wherein each alkyl and aryl is optionally substituted with one,
two, or three halogen. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.15f is C.sub.1-C.sub.6 alkyl. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.16f and
R.sup.17f are each independently hydrogen, C.sub.1-C.sub.6 alkyl,
aryl, or C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl
is optionally substituted with one, two, or three halogen. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.16f and
R.sup.17f are each independently hydrogen or C.sub.1-C.sub.6
alkyl.
[0480] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30n is independently halogen, --CN, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl; wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.31. In some embodiments of a compound of
Formula (I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, each R.sup.30n is independently halogen,
--CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optimally
substituted with one, two, or three R.sup.31; and each R.sup.31 is
independently halogen or C.sub.1-C.sub.6 alkyl. In some embodiments
of a compound of Formula (I), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.30n is
independently halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6
alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl; wherein each
alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.31; and each R.sup.31 is independently halogen. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each R.sup.30a
is independently halogen, --CN, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
C.sub.1-C.sub.6alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl; wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.31; and each R.sup.31 is independently
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, each R.sup.30n is independently halogen,
--CN, --OH, --OR.sup.a, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30n is independently halogen or C.sub.1-C.sub.6 alkyl.
In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof
each R.sup.30n is independently halogen.
[0481] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
Z is --CR.sup.62R.sup.63R.sup.64.
[0482] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.62 is hydrogen, halogen, --CN, --OH, --OR.sup.15g,
--NR.sup.16gR.sup.17g, --C(.dbd.O)OR.sup.16g,
--C(.dbd.O)NR.sup.16gR.sup.17g, or C.sub.1-C.sub.6 alkyl optionally
substituted with one, two, or three R.sup.30o. In some embodiments
of a compound of Formula (I), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.62 is hydrogen,
halogen, --CN, --OH, --OR.sup.15g, --NR.sup.16gR.sup.17g,
--C(.dbd.O)OR.sup.16g, --C(O)NR.sup.16gR.sup.17g, or
C.sub.1-C.sub.6 alkyl optionally substituted with one, two, or
three R.sup.30o, R.sup.15g is C.sub.1-C.sub.6 alkyl; and R.sup.16g
and R.sup.17g are each independently hydrogen or C.sub.1-C.sub.6
alkyl. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.62 is hydrogen, halogen, or --OH. In some embodiments of a
compound of Formula (I), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.62 is hydrogen or halogen.
In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.62 is hydrogen.
[0483] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.43 is hydrogen, halogen, --CN, --OH, --OR.sup.15g,
--NR.sup.16gR.sup.17g, --C(.dbd.O)OR.sup.16g,
--C(O)NR.sup.16gR.sup.17g, or C.sub.1-C.sub.6 alkyl optionally
substituted with one, two, or three R.sup.30o. In some embodiments
of a compound of Formula (I), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.63 is hydrogen,
halogen, --CN, --OH, --OR.sup.15g, --NR.sup.16gR.sup.17g,
--C(.dbd.O)OR.sup.16g, --C(.dbd.O)NR.sup.16gR.sup.17g, or
C.sub.1-C.sub.6 alkyl optionally substituted with one, two, or
three R.sup.30o; R.sup.15g is C.sub.1-C.sub.6 alkyl; and R.sup.16g
and R.sup.17g are each independently hydrogen or C.sub.1-C.sub.6
alkyl. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.63 is hydrogen, halogen, or --OH. In some embodiments of a
compound of Formula (I), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.63 is hydrogen or halogen.
In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.63 is hydrogen.
[0484] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.64 is --OR.sup.15g, --SR.sup.15g, --S(.dbd.O)R.sup.15g,
--NR.sup.16gR.sup.17g, --S(.dbd.O).sub.2R.sup.15g,
--NHS(.dbd.O).sub.2R.sup.15g, --S(.dbd.O).sub.2NR.sup.16gR.sup.17g,
--C(.dbd.O)R.sup.15g, --C(.dbd.O)R.sup.16g,
--C(.dbd.O)NR.sup.16gR.sup.17g, cycloalkyl, heterocycloalkyl, aryl,
or heteroaryl; wherein each cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30o. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.64 is --OR.sup.15g, --SR.sup.15g,
--S(O)R.sup.15g, --NR.sup.16gR.sup.17g, --S(.dbd.O).sub.2R.sup.15g,
--NHS(.dbd.O).sub.2R.sup.15g, --S(.dbd.O).sub.2NR.sup.16gR.sup.17g,
--C(.dbd.O)R.sup.15g, --C(.dbd.O)OR.sup.16g,
--C(.dbd.O)NR.sup.16gR.sup.17g, cycloalkyl, heterocycloalkyl, aryl,
or heteroaryl; wherein each cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30o. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.64 is --OR.sup.15g,
--NR.sup.16gR.sup.17g, --C(.dbd.O)R.sup.15g, --C(.dbd.O)OR.sup.16g,
--C(.dbd.O)NR.sup.16gR.sup.17g, cycloalkyl, heterocycloalkyl, aryl,
or heteroaryl; wherein each cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30o. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.64 is --OR.sup.15g,
--NR.sup.16gR.sup.17g, cycloalkyl, heterocycloalkyl, aryl, or
heteroaryl; wherein each cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30o. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.64 is --OR.sup.15g or
--NR.sup.16gR.sup.17g. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.64 is cycloalkyl, heterocycloalkyl,
aryl, or heteroaryl; wherein each cycloalkyl, heterocycloalkyl,
aryl, and heteroaryl is independently optionally substituted with
one, two, or three R.sup.30o. In some embodiments of a compound of
Formula (I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.64 is cycloalkyl or heterocycloalkyl;
wherein each cycloalkyl and heterocycloalkyl is independently
optionally substituted with one, two, or three R.sup.30o. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.64 is
aryl, or heteroaryl; wherein each aryl, and heteroaryl is
independently optionally substituted with one, two, or three
Mo.
[0485] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.15g is C.sub.1-C.sub.6 alkyl, aryl, or C.sub.1-C.sub.6
alkyl(aryl); wherein each alkyl and aryl is optionally substituted
with one, two, or three halogen; and R.sup.16g and R.sup.17g are
each independently hydrogen. C.sub.1-C.sub.6 alkyl, aryl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl is
optionally substituted with one, two, or three halogen. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.15g is
C.sub.1-C.sub.6 alkyl; and R.sup.16g and R.sup.17g are each
independently hydrogen or C.sub.1-C.sub.6 alkyl. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.15g is
C.sub.1-C.sub.6 alkyl, aryl, or C.sub.1-C.sub.6 alkyl(aryl);
wherein each alkyl and aryl is optionally substituted with one,
two, or three halogen. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.15g is C.sub.1-C.sub.6 alkyl. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.16g and
R.sup.17g are each independently hydrogen, C.sub.1-C.sub.6 alkyl,
aryl, or C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl
is optionally substituted with one, two, or three halogen. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.16g and
R.sup.17g are each independently hydrogen or C.sub.1-C.sub.6
alkyl.
[0486] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30o is independently halogen, --CN, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl; wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optimally substituted with one,
two, or three R.sup.31. In some embodiments of a compound of
Formula (I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, each R.sup.30p is independently halogen,
--CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optimally
substituted with one, two, or three R.sup.31; and each R.sup.31 is
independently halogen or C.sub.1-C.sub.6 alkyl. In some embodiments
of a compound of Formula (I), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.30o is
independently halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6
alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl; wherein each
alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.31; and each R.sup.31 is independently halogen. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each R.sup.30o
is independently halogen, --CN, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl; wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.31; and each R.sup.31 is independently
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, each R.sup.30o is independently halogen,
--CN, --OH, --OR.sup.a, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30o is independently halogen or C.sub.1-C.sub.6 alkyl.
In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30o is independently halogen.
[0487] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.3 is halogen, --CN, --SR.sup.18b, --NR.sup.16bR.sup.17b,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30c. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.3 is
halogen, --CN, --SR.sup.18b, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30c. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.3 is halogen, --CN, --SR.sup.18b,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30c, and each
R.sup.30c is independently halogen or C.sub.1-C.sub.6 alkyl. In
some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.3 is halogen, --CN, --SR.sup.18b, C.sub.1-C.sub.6 alkyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6
alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optimally substituted with one, two, or
three R.sup.30c; and each R.sup.30c is independently halogen. In
some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.3 is halogen, --CN, --SR.sup.18b, C.sub.1-C.sub.6 alkyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6
alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30c; and each R.sup.30c is independently
C.sub.1-C.sub.6 alkyl.
[0488] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.3 is halogen, --CN, --SR.sup.18b, C.sub.1-C.sub.6 alkyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6
alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30c; and R.sup.18b is cycloalkyl or C.sub.1-C.sub.6
alkyl(cycloalkyl). In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.3 is halogen, --CN, --SR.sup.18b,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30c; R.sup.18b
is cycloalkyl or C.sub.1-C.sub.6 alkyl(cycloalkyl); and each
R.sup.30c is independently halogen or C.sub.1-C.sub.6 alkyl. In
some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.3 is halogen, --CN, --SR.sup.18b, C.sub.1-C.sub.6 alkyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6
alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl), Cif;
alkyl(cycloalkyl), or Cif; alkyl(heterocycloalkyl); wherein each
alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optimally substituted with one, two, or three
R.sup.31; R.sup.18b is cycloalkyl or C.sub.1-C.sub.6
alkyl(cycloalkyl); and each R.sup.30c is independently halogen. In
some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.3 is halogen, --CN, --SR.sup.18b, C.sub.1-C.sub.6 alkyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6
alkyl(aryl), alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl),
or C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optimally substituted with one, two, or three R.sup.30c; R.sup.18b
is cycloalkyl or C.sub.1-C.sub.6 alkyl(cycloalkyl); and each
R.sup.30c is independently C.sub.1-C.sub.6 alkyl.
[0489] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.3 is halogen, --CN, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
alkyl(cycloalkyl); wherein each alkyl, and cycloalkyl is
independently optionally substituted with one, two, or three
R.sup.30c. In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.3 is halogen, --CN, --SR.sup.18b, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 alkyl(cycloalkyl); wherein each alkyl, and
cycloalkyl is independently optionally substituted with one, two,
or three R.sup.30c; and each R.sup.30c is independently halogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof: R.sup.3 is halogen, --CN, --SR.sup.18b,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 alkyl(cycloalkyl);
wherein each alkyl, and cycloalkyl is independently optionally
substituted with ono two, or three R.sup.30c; and each R.sup.30c is
independently halogen. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.3 is halogen, --CN, --SR.sup.18b,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 alkyl(cycloalkyl);
wherein each alkyl, and cycloalkyl is independently optimally
substituted with one, two, or three R.sup.30c; and each R.sup.30c
is independently C.sub.1-C.sub.6 alkyl.
[0490] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.3 is halogen, --CN, --SR.sup.18b, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 alkyl(cycloalkyl); wherein each alkyl, and
cycloalkyl is independently optionally substituted with one, two,
or three R.sup.30c; and R.sup.18b is cycloalkyl or C.sub.1-C.sub.6
alkyl(cycloalkyl). In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.3 is halogen, --CN, --SR.sup.18b,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 alkyl(cycloalkyl);
wherein each alkyl, and cycloalkyl is independently optionally
substituted with one, two, or three R.sup.30c; R.sup.18b is
cycloalkyl or C.sub.1-C.sub.6 alkyl(cycloalkyl); and each R.sup.30c
is independently halogen or C.sub.1-C.sub.6 alkyl. In some
embodiments of a compound of Formula (I), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.3 is
halogen, --CN, --SR.sup.18b, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 alkyl(cycloalkyl); wherein each alkyl, and
cycloalkyl is independently optionally substituted with one, two,
or three R.sup.30c; R.sup.18b is cycloalkyl or C.sub.1-C.sub.6
alkyl(cycloalkyl); and each R.sup.30c is independently halogen. In
some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.3 is halogen, --CN, --SR.sup.18b, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 alkyl(cycloalkyl); wherein each alkyl, and
cycloalkyl is independently optionally substituted with one, two,
or three R.sup.30c; R.sup.18b is cycloalkyl or C.sub.1-C.sub.6
alkyl(cycloalkyl); and each R.sup.30c is independently
C.sub.1-C.sub.6 alkyl.
[0491] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.3 is --NH.sub.2. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.3 is halogen.
[0492] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.21 and R.sup.22 are each independently hydrogen, aryl, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25.
[0493] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.21 and R.sup.22 are each hydrogen.
[0494] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.21 and R.sup.22 are each
--(CR.sup.23R.sup.24).sup.wOC(.dbd.O)OR.sup.25. In some embodiments
of a compound of Formula (I), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.21 and R.sup.22 are
each --(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.15; w is 1 or 2;
each R.sup.23 and R.sup.24 are independently hydrogen, halogen, or
C.sub.1-C.sub.6 alkyl; and each R.sup.25 is independently hydrogen
or C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of
Formula (I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof: R.sup.21 and R.sup.22 are each
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25: w is 1; R.sup.23
and R.sup.24 are hydrogen; and each R.sup.25 is independently
hydrogen or C.sub.1-C.sub.6 alkyl. In some embodiments of a
compound of Formula (I), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.21 and R.sup.22 are each
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25; w is 1; R.sup.23
and R.sup.24 are hydrogen; and each R.sup.25 is C.sub.1-C.sub.6
alkyl.
[0495] In some embodiments of a compound of Formula (I), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.21 and R.sup.22 are taken together with the atoms to which
they are attached to form a heterocycloalkyl optionally substituted
with one, two, or three R.sup.30l. In some embodiments of a
compound of Formula (I), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.21 and R.sup.22 are taken
together with the atoms to which they are attached to form a
heterocycloalkyl optionally substituted with one, two, or three
R.sup.30l; and each R.sup.30l is independently halogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(I), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.21 and R.sup.22 are taken together with
the atoms to which they are attached to form a heterocycloalkyl
optionally substituted with one, two, or three R.sup.30l; and each
R.sup.30l is independently halogen.
[0496] Any combination of the groups described above for the
various variables is contemplated herein. Throughout the
specification, groups and substituents thereof are chosen by one
skilled in the field to provide stable moieties and compounds.
[0497] In some embodiments provided herein is a compound having the
structure of Formula (II), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof:
##STR00004##
wherein; [0498] A is --O-- or --CH.sub.2--; [0499] Q.sup.1 and
Q.sup.2 are independently N or CW; [0500] each W is independently
hydrogen, halogen, --CN, --OH, --OR.sup.a, --SH, --SR.sup.a,
--S(.dbd.O)R.sup.a, --NO.sub.2, --NR.sup.cR.sup.d,
--S(.dbd.O).sub.2R.sup.a, --NHS(.dbd.O).sub.2R.sup.a,
--S(.dbd.O).sub.2NR.sup.cR.sup.d, --C(.dbd.O)RR,
--OC(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b, --OC(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, --OC(O)NR.sup.cR.sup.d,
--NR.sup.bC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(.dbd.O)R.sup.a,
--NR.sup.bC(.dbd.O)OR.sup.b, alkyl, alkenyl, alkynyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, alkyl(aryl), alkyl(heteroaryl),
alkyl(cycloalkyl), or alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30; [0501] Z is --NR.sup.1R.sup.2, --OR.sup.60,
--SR.sup.61, or --CR.sup.62R.sup.63R.sup.64; [0502] R.sup.1 and
R.sup.2 are each independently hydrogen, alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkyl(aryl),
alkyl(heteroaryl), alkyl(cycloalkyl), alkyl(heterocycloalkyl),
--S(O).sub.2R.sup.15a, --S(.dbd.O).sub.2NR.sup.16aR.sup.17a, or
--C(.dbd.O).sub.2R.sup.15a; wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30a; [0503] or
R.sup.1 and R.sup.2 are taken together with the nitrogen atom to
which they are attached to form a heterocycloalkyl optionally
substituted with one, two, or three R.sup.30a; [0504] R.sup.60 is
hydrogen, --C(.dbd.O)R.sup.15e, --C(.dbd.O)OR.sup.16e,
--C(.dbd.O)NR.sup.16eR.sup.17e, alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkyl(aryl),
alkyl(heteroaryl), alkyl(cycloalkyl), alkyl(heterocycloalkyl);
wherein each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl,
aryl, and heteroaryl is independently optionally substituted with
one, two, or three R.sup.30m; [0505] R.sup.61 is hydrogen,
--C(.dbd.O)R.sup.15f, --C(.dbd.O)OR.sup.16f,
--C(.dbd.O)NR.sup.16fR.sup.17f, alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkyl(aryl),
alkyl(heteroaryl), alkyl(cycloalkyl), alkyl(heterocycloalkyl);
wherein each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl,
aryl, and heteroaryl is independently optionally substituted with
one, two, or three R.sup.30n; [0506] R.sup.62, R.sup.63, and
R.sup.64 are each independently hydrogen, halogen, --CN, --OH,
--OR.sup.15g, --SH, --SR.sup.15g, --S(.dbd.O)R.sup.15g, --NO.sub.2,
--NR.sup.16gR.sup.17g, --S(.dbd.O).sub.2R.sup.15g,
--NHS(.dbd.O).sub.2R.sup.15g, --S(.dbd.O).sub.2NR.sup.16gR.sup.17g,
--C(.dbd.O)R.sup.15g, --OC(.dbd.O)R.sup.15g, --C(.dbd.O)OR.sup.16g,
--OC(.dbd.O)OR.sup.16g, --C(.dbd.O)NR.sup.16gR.sup.17g,
--OC(.dbd.O)NR.sup.16gR.sup.17g,
--NR.sup.16gC(.dbd.O)NR.sup.16gR.sup.17g,
--NR.sup.16gC(.dbd.O)R.sup.15g, --NR.sup.16gC(.dbd.O)OR.sup.16g,
alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, alkyl(aryl), alkyl(heteroaryl), alkyl(cycloalkyl), or
alkyl(heterocycloalkyl); wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30o; [0507]
R.sup.3 is halogen, --CN, --OH, OR.sup.15b, SR.sup.18b,
--NR.sup.16bR.sup.17b, alkyl, alkenyl, alkynyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, alkyl(aryl), alkyl(heteroaryl),
alkyl(cycloalkyl), or alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30c; [0508] R.sup.4 and R.sup.7 are each
independently hydrogen, halogen, --OH, --OR.sup.15c,
--NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.15c, alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; wherein each
alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30d; [0509] R.sup.5 and R.sup.6 are each
independently hydrogen, halogen, --OH, --OR.sup.15d,
--NR.sup.16dS(.dbd.O).sub.2R.sup.15d,
--NR.sup.16dC(.dbd.O)R.sup.15d, alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; wherein each
alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30e; [0510] R.sup.8 is hydrogen, halogen, --OH,
--OR.sup.a, --NR.sup.cR.sup.d, alkyl, or haloalkyl; [0511] R.sup.9
and R.sup.10 are each independently hydrogen, halogen, alkyl, or
haloalkyl; [0512] X.sup.1 is bond, --C(.dbd.O)--,
--S(.dbd.O).sub.2--, or --CR.sup.40R.sup.41--; [0513] Y.sup.1 is
--(CR.sup.42R.sup.43).sup.v1--, --S(.dbd.O).sub.2--, --NR.sup.44--,
or --O--; [0514] Y.sup.2 is --(CR.sup.45R.sup.46).sub.v2--,
--NR.sup.47--, or --O--; [0515] Y.sup.3 is
--(CR.sup.48R.sup.49).sub.v3--, --NR.sup.50--, or --O--; [0516]
Y.sup.4 is --O--, --NH--, or --N(CH.sub.3)--; [0517] R.sup.40,
R.sup.41, R.sup.42, R.sup.43, R.sup.45, R.sup.46, R.sup.48, and
R.sup.49 are each independently hydrogen, halogen, --OH,
--OR.sup.a, --NR.sup.cR.sup.d, alkyl, or haloalkyl; [0518]
R.sup.44, R.sup.47, and R.sup.50 are each independently hydrogen,
--S(.dbd.O)R.sup.a, --S(.dbd.O).sub.2R.sup.a,
--S(.dbd.O).sub.2NR.sup.cR.sup.d, --C(.dbd.O)R.sup.a,
--C(.dbd.O)OR.sup.b, alkyl, alkenyl, alkynyl, cycloalkyl, or
heterocycloalkyl; wherein each alkyl, alkenyl, alkynyl, cycloalkyl,
and heterocycloalkyl is independently optionally substituted with
one, two, or three R.sup.30f; [0519] v1, v2, and v3 are each
independently 1-3; [0520] R.sup.15a, R.sup.15b, R.sup.15c,
R.sup.15d, R.sup.15e, R.sup.15f, R.sup.15g are each independently
alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, or
heteroaryl; wherein each alkyl, alkenyl, alkynyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optimally
substituted with one, two, or three R.sup.30g; [0521] R.sup.16a,
R.sup.16b, R.sup.16c, R.sup.16d, R.sup.16e, R.sup.16f, R.sup.16g
and R.sup.17a, R.sup.17b, R.sup.17b, R.sup.17e, R.sup.17f, and
R.sup.17g are each independently hydrogen, alkyl, alkenyl, alkynyl,
cycloalkyl, or heterocycloalkyl; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, and heterocycloalkyl is independently
optionally substituted with one, two, or three R.sup.30h; [0522] or
R.sup.16a and R.sup.17a or R.sup.16b and R.sup.17b or R.sup.16e and
R.sup.17e or R.sup.16f and R.sup.17f or R.sup.16g and R.sup.17g are
taken together with the nitrogen atom to which they are attached to
form a heterocycloalkyl optionally substituted with one, two, or
three halogen, alkyl, or haloalkyl; [0523] R.sup.18b is alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
alkyl(aryl), alkyl(heteroaryl), alkyl(cycloalkyl),
alkyl(heterocycloalkyl); wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30i; [0524]
R.sup.21 and R.sup.22 are each independently hydrogen, alkyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkyl(aryl),
alkyl(heteroaryl), alkyl(cycloalkyl), alkyl(heterocycloalkyl),
--(CR.sup.23R.sup.24).sub.wC(.dbd.O)OR.sup.25,
--(CR.sup.23R.sup.24).sub.wOC(O)R.sup.26,
--(CR.sup.23R.sup.24).sub.wSC(.dbd.O)R.sup.26, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30k; [0525] or
R.sup.21 and R.sup.22 are taken together with the atoms to which
they are attached to form a heterocycloalkyl optionally substituted
with one, two, or three R.sup.30l; [0526] each R.sup.23 and
R.sup.24 are independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, alkyl, or haloalkyl; [0527] each R.sup.25 is
independently hydrogen, alkyl, alkenyl, alkynyl, or heteroalkyl;
[0528] each R.sup.26 is independently alkyl, alkenyl, alkynyl, or
heteroalkyl; [0529] each w is independently 1-4; [0530] each
R.sup.30, R.sup.30a, R.sup.30b, R.sup.30c, R.sup.30d, R.sup.30e,
R.sup.30f, R.sup.30g and R.sup.30h, R.sup.30i, R.sup.30j,
R.sup.30k, R.sup.30l, R.sup.30n, R.sup.30m, and R.sup.30o are
independently halogen, --CN, --OH, --OR.sup.a, --SH, --SR.sup.a,
--S(.dbd.O)R.sup.a, --NO.sub.2, --NR.sup.cR.sup.d,
--S(.dbd.O).sub.2R.sup.a, --NHS(.dbd.O).sub.2R.sup.a,
--S(.dbd.O).sub.2NR.sup.cR.sup.d, --C(.dbd.O)R.sup.a,
--OC(O)R.sup.a, --C(.dbd.O)OR.sup.b, --OC(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, --OC(O)NR.sup.cR.sup.d,
NR.sup.bC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(.dbd.O)R.sup.a,
--NR.sup.bC(.dbd.O)OR.sup.b, alkyl, alkenyl, alkynyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, alkyl(aryl), alkyl(heteroaryl),
alkyl(cycloalkyl), or alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.31; [0531] each R.sup.31 is independently halogen,
--CN, --OH, --OR.sup.a, --SH, --SR.sup.a, --S(.dbd.O)R.sup.a,
--NO.sub.2, --NR.sup.cR.sup.d, --S(.dbd.O).sub.2R.sup.a,
--NHS(.dbd.O).sub.2R.sup.a, --S(O).sub.2NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --OC(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--OC(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
--OC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(.dbd.O)NR.sup.cR.sup.d,
--NR.sup.bC(.dbd.O)R.sup.a, --NR.sup.bC(.dbd.O)OR.sup.b, alkyl,
haloalkyl, hydroxyalkyl, heteroalkyl, or cycloalkyl optionally
substituted with one, two, or three halogen, alkyl, or haloalkyl;
[0532] each R.sup.a is independently alkyl, alkenyl, alkynyl,
heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl;
wherein the alkyl, alkenyl, alkynyl, heteroalkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three halogen, --OH, alkyl, or
haloalkyl; [0533] each R.sup.b is independently hydrogen, alkyl,
alkenyl, alkynyl, heteroalkyl, cycloalkyl, heterocycloalkyl, aryl,
or heteroaryl; wherein the alkyl, alkenyl, alkynyl, heteroalkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three halogen, --OH,
alkyl, or haloalkyl; [0534] R.sup.c and R.sup.d are each
independently hydrogen, alkyl, alkenyl, alkynyl, heteroalkyl,
cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; wherein the
alkyl, alkenyl, alkynyl, heteroalkyl, cycloalkyl, heterocycloalkyl,
aryl, and heteroaryl is independently optionally substituted with
one, two, or three halogen, --OH, alkyl, or haloalkyl; [0535] or
R.sup.c and R.sup.d are taken together with the nitrogen atom to
which they are attached to form a heterocycloalkyl optionally
substituted with one, two, or three halogen, alkyl, or haloalkyl;
[0536] n is 0 or 1; and [0537] m is 0 or 1.
[0538] In some embodiments provided herein is a compound having the
structure of Formula (II), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof wherein; [0539] A is --O-- or
--CH.sub.2--; [0540] Q.sup.1 and Q.sup.2 are independently N or CW;
[0541] each W is independently hydrogen, halogen, --CN, --OH,
--OR.sup.a, --SH, --SR.sup.a, --S(.dbd.O)R.sup.a, --NO.sub.2,
--NR.sup.cR.sup.d, --S(.dbd.O).sub.2R.sup.a,
--NHS(.dbd.O).sub.2R.sup.a, --S(O).sub.2NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --OC(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--OC(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
--OC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(.dbd.O)NR.sup.cR.sup.d,
--NR.sup.bC(.dbd.O)R.sup.a, --NR.sup.bC(.dbd.O)OR.sup.b,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30; [0542] Z
is --NR.sup.1R.sup.2, --OR.sup.60, --SR.sup.61, or
--CR.sup.62R.sup.63R.sup.64; [0543] R.sup.1 and R.sup.2 are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl),
C.sub.1-C.sub.6 alkyl(heterocycloalkyl), --S(O).sub.2R.sup.15a,
--S(.dbd.O).sub.2NR.sup.16aR.sup.17a, or
--C(.dbd.O).sub.2R.sup.15a; wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30a; [0544] or
R.sup.1 and R.sup.2 are taken together with the nitrogen atom to
which they are attached to form a heterocycloalkyl optionally
substituted with one, two, or three R.sup.30b; [0545] R.sup.60 is
hydrogen, --C(.dbd.O)R.sup.15e, --C(.dbd.O)OR.sup.16e,
--C(.dbd.O)NR.sup.16eR.sup.17e, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(acyl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.30m; [0546] R.sup.61 is hydrogen,
--C(.dbd.O)R.sup.15f, --C(.dbd.O)OR.sup.16f,
--C(.dbd.O)NR.sup.16fR.sup.17f; C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.30n; [0547] R.sup.62, R.sup.63, and R.sup.64
are each independently hydrogen, halogen, --CN, --OH, --OR.sup.15g,
--SH, --SR.sup.15g, --S(.dbd.O)R.sup.15g, --NO.sub.2,
--NR.sup.16gR.sup.17g, --S(.dbd.O).sub.2R.sup.15g,
--NHS(.dbd.O).sub.2R.sup.15g, --S(.dbd.O).sub.2NR.sup.16gR.sup.17g,
--C(.dbd.O)R.sup.15g, --OC(.dbd.O)R.sup.15g, --C(.dbd.O)OR.sup.16g,
--OC(.dbd.O)OR.sup.16g, --C(.dbd.O)NR.sup.16gR.sup.17g,
--OC(.dbd.O)NR.sup.16gR.sup.17g,
--NR.sup.16gC(.dbd.O)NR.sup.16gR.sup.17g,
--NR.sup.16gC(.dbd.O)R.sup.15g, --NR.sup.16gC(.dbd.O)OR.sup.16g,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6alkenyl, C.sub.2-C.sub.6
alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30o; [0548]
R.sup.3 is halogen, --CN, --OH, OR.sup.15b, SR.sup.15b,
--NR.sup.16bR.sup.17b, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30c; [0549] R.sup.4 and R.sup.7 are each
independently hydrogen, halogen, --OH, --OR.sup.15c,
--NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.15c, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.1-C.sub.6 cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.30d; [0550] R.sup.5 and R.sup.6 are each independently
hydrogen, halogen, --OH, --OR.sup.15d,
--NR.sup.16dS(.dbd.O).sub.2R.sup.15d,
--NR.sup.16dC(.dbd.O)R.sup.15d, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.30e; [0551] R.sup.8 is hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; [0552] R.sup.9 and R.sup.10 are each independently
hydrogen, halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; [0553] X.sup.1 is bond, --C(.dbd.O)--,
--S(.dbd.O).sub.2--, or --CR.sup.40R.sup.41--; [0554] Y.sup.1 is
--(CR.sup.42R.sup.43).sub.v1--, --S(.dbd.O).sub.2--, --NR.sup.44--,
or --O--; [0555] Y.sup.2 is --(CR.sup.45R.sup.46).sub.v2--,
--NR.sup.47--, or --O--; [0556] Y.sup.3 is
--(CR.sup.48R.sup.49).sub.v3--, --NR.sup.50--, or --O--; [0557]
Y.sup.4 is --O--, --NH--, or --N(CH.sub.3)--; [0558] R.sup.40,
R.sup.41, R.sup.42, R.sup.43, R.sup.45, R.sup.46, R.sup.48, and
R.sup.49 are each independently hydrogen, halogen, --OH,
--OR.sup.a, --NR.sup.cR.sup.d, C.sub.1-C.sub.4 alkyl, or
C.sub.1-C.sub.6 haloalkyl; [0559] R.sup.44, R.sup.47, and R.sup.50
are each independently hydrogen, --S(.dbd.O)R.sup.a,
--S(.dbd.O).sub.2R.sup.a, --S(.dbd.O).sub.2NR.sup.cR.sup.d,
--C(.dbd.O)OR.sup.b, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, or heterocycloalkyl;
wherein each alkyl, alkenyl, alkynyl, cycloalkyl, and
heterocycloalkyl is independently optionally substituted with one,
two, or three R.sup.30f; [0560] v1, v2, and v3 are each
independently 1-3; [0561] R.sup.15a, R.sup.15b, R.sup.15c,
R.sup.15d, R.sup.15e, R.sup.15f, R.sup.15g are each independently
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.30g. [0562] R.sup.16a, R.sup.16b, R.sup.16c,
R.sup.16d, R.sup.16e, R.sup.16f, R.sup.16g, R.sup.17a, R.sup.17b,
R.sup.17c, R.sup.17d, and R.sup.17g are each independently
hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, cycloalkyl, or heterocycloalkyl; wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, and heterocycloalkyl is
independently optionally substituted with one, two, or three
R.sup.30b; [0563] or R.sup.16a and R.sup.17a or R.sup.16b and
R.sup.17b or R.sup.16e and R.sup.17e or R.sup.16f and R.sup.17f or
R.sup.16g and R.sup.17g are taken together with the nitrogen atom
to which they are attached to form a heterocycloalkyl optionally
substituted with one, two, or three halogen, C.sub.1-C.sub.6 alkyl,
or C.sub.1-C.sub.6haloalkyl; [0564] R.sup.18b is C.sub.1-C.sub.6
alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6
alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.30i; [0565] R.sup.21 and R.sup.22 are each
independently hydrogen, C.sub.1-C.sub.20alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--(CR.sup.23R.sup.24).sub.wC(.dbd.O)OR.sup.25,
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)R.sup.26,
--(CR.sup.23R.sup.24).sub.wSC(.dbd.O)R.sup.26, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)R.sup.25; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30k; [0566] or
R.sup.21 and R.sup.22 are taken together with the atoms to which
they are attached to form a heterocycloalkyl optionally substituted
with one, two, or three R.sup.30l; [0567] each R.sup.23 and
R.sup.24 are independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; [0568] each R.sup.25 is independently hydrogen,
C.sub.1-C.sub.6alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0569] each R.sup.26 is
independently C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0570]
each w is independently 1-4; [0571] each R.sup.30, R.sup.30a,
R.sup.30b, R.sup.30c, R.sup.30d, R.sup.30e, R.sup.30f, R.sup.30g
and R.sup.30h, R.sup.30i, R.sup.30j, R.sup.30k, R.sup.30l,
R.sup.30m, R.sup.30n, and R.sup.30o are independently halogen,
--CN, --OH, --OR.sup.a, --SH, --SR.sup.a, --S(.dbd.O)R.sup.a,
--NO.sub.2, --NR.sup.cR.sup.d, --S(.dbd.O).sub.2R.sup.a,
--NHS(.dbd.O).sub.2R.sup.a, --S(.dbd.O).sub.2NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --OC(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--OC(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
--OC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(.dbd.O)NR.sup.cR.sup.d,
--NR.sup.bC(.dbd.O)R.sup.a, --NR.sup.bC(.dbd.O)OR.sup.b,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6alkenyl,
C.sub.2-C.sub.6alkynyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optimally substituted with one, two, or
three R.sup.31; [0572] each R.sup.31 is independently halogen,
--CN, --OH, --OR.sup.a, --SH, --SR.sup.a, --S(.dbd.O)R.sup.a,
--NO.sub.2, --NR.sup.cR.sup.d, --S(.dbd.O).sub.2R.sup.a,
--NHS(.dbd.O).sub.2R.sup.a, --S(O).sub.2NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --OC(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--OC(O)OR.sup.b, --C(O)NR.sup.cR.sup.d,
--OC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(.dbd.O)NR.sup.cR.sup.d,
--NR.sup.bC(O)R.sup.a, --NR.sup.bC(O)OR.sup.b, C.sub.1-C.sub.6
alkyl, C.sub.1-C.sub.6haloalkyl, C.sub.1-C.sub.6 hydroxyalkyl,
C.sub.1-C.sub.6 heteroalkyl, or cycloalkyl optimally substituted
with one, two, or three halogen, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl; [0573] each R.sup.a is independently
C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, C.sub.1-C.sub.6 heteroalkyl, cycloalkyl, heterocycloalkyl,
aryl, or heteroaryl; wherein the alkyl, alkenyl, alkynyl,
heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optimally substituted with one, two, or three
halogen, --OH, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[0574] each R.sup.b is independently hydrogen, C.sub.1-C.sub.6
alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl,
C.sub.1-C.sub.6 heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, or
heteroaryl; wherein the alkyl, alkenyl, alkynyl, heteroalkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three halogen, --OH,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl; [0575] R.sup.c
and R.sup.d are each independently hydrogen, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, C.sub.1-C.sub.6
heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl;
wherein the alkyl, alkenyl, alkynyl, heteroalkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three halogen, --OH, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6 haloalkyl; [0576] or R.sup.c and R.sup.d
are taken together with the nitrogen atom to which they are
attached to form a heterocycloalkyl optionally substituted with
one, two, or three halogen, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl; [0577] n is 0 or 1; and [0578] m is 0 or
1.
[0579] In some embodiments of a compound of Formula (II), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
at least one of n or m is 1. In some embodiments of a compound of
Formula (II), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, n is 1. In some embodiments of a compound of
Formula (II), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, n is 1 and m is 0. In some embodiments of a
compound of Formula (II), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, m is 1. In some embodiments of a
compound of Formula (II), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof m is 1 and n is 0.
[0580] In some embodiments of a compound of Formula (II), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof;
[0581] A is --O-- or --CH.sub.2--; [0582] Q.sup.1 and Q.sup.2 are
independently N or CW; [0583] each W is independently hydrogen,
halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30; [0584] Z
is --NR.sup.1R.sup.2; [0585] R.sup.1 and R.sup.2 are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30a; [0586] or R.sup.1 and R.sup.2 are taken
together with the nitrogen atom to which they are attached to form
a heterocycloalkyl optionally substituted with one, two, or three
R.sup.30a; [0587] R.sup.3 is halogen, --CN, --SR.sup.18b,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30c; [0588] R.sup.4 and
R.sup.7 are each independently hydrogen, halogen, --OH,
--OR.sup.15c, --NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.15c, C.sub.1-C.sub.6 alkyl, or
cycloalkyl; wherein each alkyl, and cycloalkyl is independently
optionally substituted with one, two, or three R.sup.30d; [0589]
R.sup.5 and R.sup.6 are each independently hydrogen, halogen,
C.sub.1-C.sub.6 alkyl, or cycloalkyl; wherein each alkyl, and
cycloalkyl is independently optionally substituted with one, two,
or three R.sup.30e; [0590] R.sup.8 is hydrogen, halogen, --OH,
--NH.sub.2, C.sub.1-C.sub.6alkyl, or C.sub.1-C.sub.6 haloalkyl;
[0591] R.sup.9 and R.sup.10 are each independently hydrogen,
halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6haloalkyl; [0592]
X.sup.1 is bond, --C(.dbd.O)--, --S(.dbd.O).sup.2--, or
--CR.sup.40R.sup.41--; [0593] Y.sup.1 is
--(CR.sup.42R.sup.43).sub.v1--, --S(.dbd.O).sub.2--, --NR.sup.44--,
or --O--; [0594] Y.sup.2 is --(CR.sup.45R.sup.46).sub.v2--,
--NR.sup.47--, or --O--; [0595] Y.sup.3 is
--(CR.sup.48R.sup.49).sub.v3-- or --NR.sup.50--, or --O--; [0596]
Y.sup.4 is --O-- or --NH--; [0597] R.sup.44, R.sup.47, and R.sup.50
are each independently hydrogen, --S(.dbd.O)RR,
--S(.dbd.O).sub.2R.sup.a, --S(.dbd.O).sub.2NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b, C.sub.1-C.sub.6 alkyl,
cycloalkyl, or heterocycloalkyl; wherein each alkyl, cycloalkyl,
and heterocycloalkyl is independently optionally substituted with
one, two, or three R.sup.30f; [0598] R.sup.40, R.sup.41, R.sup.42,
R.sup.43, R.sup.45, R.sup.46, R.sup.48, and R.sup.49 are each
independently hydrogen, halogen, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl; [0599] v1, v2, and v3 are each
independently 1-3; [0600] R.sup.15c is C.sub.1-C.sub.6 alkyl,
cycloalkyl, or heterocycloalkyl; wherein each alkyl, cycloalkyl,
and heterocycloalkyl is independently optionally substituted with
one, two, or three R.sup.30g; [0601] R.sup.16c is hydrogen or
C.sub.1-C.sub.6 alkyl optionally substituted with one, two, or
three R.sup.30h; [0602] R.sup.18b is C.sub.1-C.sub.6 alkyl,
cycloalkyl, C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, cycloalkyl, and
heterocycloalkyl is independently optionally substituted with one,
two, or three R.sup.30i; [0603] R.sup.21 and R.sup.22 are each
independently hydrogen, C.sub.1-C.sub.20alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--(CR.sup.23R.sup.24).sub.wC(.dbd.O)OR.sup.25,
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)R.sup.26,
--(CR.sup.23R.sup.24).sub.wSC(.dbd.O)R.sup.36, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30k; [0604] or
R.sup.21 and R.sup.22 are taken together with the atoms to which
they are attached to form a heterocycloalkyl optionally substituted
with one, two, or three R.sup.30l; [0605] each R.sup.23 and
R.sup.24 are independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; [0606] each R.sup.25 is independently hydrogen,
C.sub.1-C.sub.6alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0607] each R.sup.26 is
independently C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0608]
each w is independently 1-4; [0609] each R.sup.30, R.sup.30a,
R.sup.31b, R.sup.30c, R.sup.30d, R.sup.30e, R.sup.30f, R.sup.30g,
R.sup.30h, R.sup.30i, R.sup.30k, and R.sup.30l is independently
halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6alkyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.31, [0610]
each R.sup.31 is independently halogen, --OH, --OR.sup.a, or
--NR.sup.cR.sup.d; [0611] each R.sup.a is independently
C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6haloalkyl, C.sub.1-C.sub.6
hydroxyalkyl, or C.sub.1-C.sub.6 heteroalkyl; [0612] each R.sup.b
is independently hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6
haloalkyl, C.sub.1-C.sub.6 hydroxyalkyl, or C.sub.1-C.sub.6
heteroalkyl; [0613] R.sup.c and R.sup.d are each independently
hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 haloalkyl,
C.sub.1-C.sub.6 hydroxyalkyl, or C.sub.1-C.sub.6 heteroalkyl;
[0614] or R.sup.c and R.sup.d are taken together with the nitrogen
atom to which they are attached to form a heterocycloalkyl
optionally substituted with one, two, or three halogen,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl; [0615] n is 0
or 1; and [0616] m is 0 or 1; provided that at least one of n or m
is 1.
[0617] In some embodiments of a compound of Formula (II), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof;
[0618] A is --O-- or --CH.sub.2--; [0619] Q.sup.1 and Q.sup.2 are
independently N or CW; [0620] each W is hydrogen; [0621] Z is
--NR.sup.1R.sup.2; [0622] R.sup.1 and R.sup.2 are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, cycloalkyl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl, cycloalkyl, and
aryl is independently optionally substituted with one, two, or
three R.sup.30a; [0623] or R.sup.1 and R.sup.2 are taken together
with the nitrogen atom to which they are attached to form a
heterocycloalkyl optionally substituted with one, two, or three
R.sup.30b; [0624] R.sup.3 is halogen; [0625] R.sup.4 and R.sup.7
are each independently hydrogen, halogen, --OH, or --OR.sup.15c;
[0626] R.sup.5 and R.sup.6 are each hydrogen; [0627] R.sup.8 is
hydrogen; [0628] R.sup.9 and R.sup.10 are each hydrogen; [0629]
X.sup.1 is bond, --C(.dbd.O)--, --S(.dbd.O).sub.2--, or
--CR.sup.40R.sup.41--; [0630] Y.sup.1 is
--(CR.sup.42R.sup.43).sub.v1--, --S(.dbd.O).sub.2--, --NR.sup.44--,
or --O--; [0631] Y.sup.2 is --(CR.sup.45R.sup.46).sub.v2--,
--NR.sup.47--, or --O--; [0632] Y.sup.3 is
--(CR.sup.48R.sup.49).sub.v3-- or --NR.sup.50--; [0633] Y.sup.4 is
--O--; [0634] R.sup.44, R.sup.47, and R.sup.50 are each
independently hydrogen, --S(.dbd.O)R.sup.a,
--S(.dbd.O).sub.2R.sup.a, --S(.dbd.O).sub.2NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b, C.sub.1-C.sub.6 alkyl,
cycloalkyl, or heterocycloalkyl; wherein each alkyl, cycloalkyl,
and heterocycloalkyl is independently optionally substituted with
one, two, or three R.sup.30f; [0635] R.sup.40, R.sup.41, R.sup.42,
R.sup.43, R.sup.45, R.sup.46, R.sup.48 and R.sup.49 are each
independently hydrogen, halogen, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl; [0636] v1, v2, and v3 are each
independently 1 or 2; [0637] R.sup.15c is C.sub.1-C.sub.6 alkyl;
[0638] R.sup.21 and R.sup.22 are each hydrogen, C.sub.1-C.sub.20
alkyl, --(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25, or aryl
optionally substituted with one, two, or three R.sup.30k; [0639] or
R.sup.21 and R.sup.22 are taken together with the atoms to which
they are attached to form a heterocycloalkyl optionally substituted
with one, two, or three R.sup.30l; [0640] each R.sup.23 and
R.sup.24 are independently hydrogen; [0641] each R.sup.25 is
independently hydrogen or C.sub.1-C.sub.6 alkyl; [0642] each w is
independently 1 or 2; [0643] each R.sup.30a, R.sup.30b, R.sup.30f,
R.sup.30k, and R.sup.30l is independently halogen, --OH,
--OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, or
C.sub.1-C.sub.6 alkyl optionally substituted with one, two, or
three R.sup.31; [0644] each R.sup.31 is independently halogen,
--OH, --OR.sup.a, or --NR.sup.cR.sup.d; [0645] each R.sup.a is
independently C.sub.1-C.sub.6 alkyl; [0646] each R.sup.b is
independently hydrogen or C.sub.1-C.sub.6 alkyl; [0647] R.sup.c and
R.sup.d are each independently hydrogen or C.sub.1-C.sub.6 alkyl;
[0648] or R.sup.c and R.sup.d are taken together with the nitrogen
atom to which they are attached to form a heterocycloalkyl
optionally substituted with one, two, or three halogen or
C.sub.1-C.sub.6 alkyl [0649] n is 0 or 1; and [0650] m is 0 or 1;
provided that at least one of n or m is 1.
[0651] In some embodiments of a compound of Formula (II), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof;
[0652] A is --O-- or --CH.sub.2--; [0653] Q.sup.1 and Q.sup.2 are
independently N or CW; [0654] each W is independently hydrogen,
halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30; [0655] Z
is --NR.sup.1R.sup.2; [0656] R.sup.1 and R.sup.2 are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30a; [0657] or R.sup.1 and R.sup.2 are taken
together with the nitrogen atom to which they are attached to form
a heterocycloalkyl optionally substituted with one, two, or three
R.sup.30b; [0658] R.sup.3 is halogen, --CN, --SR.sup.18b,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-6 alkyl(cycloalkyl), or C.sub.1-6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30c; [0659] R.sup.4 and R.sup.7 are each
independently hydrogen, halogen, --OH, --OR.sup.15c,
--NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.15c, C.sub.1-C.sub.6 alkyl, or
cycloalkyl; wherein each alkyl, and cycloalkyl is independently
optionally substituted with one, two, or three R.sup.30d;
[0660] R.sup.5 and R.sup.6 are each independently hydrogen,
halogen, C.sub.1-C.sub.6 alkyl, or cycloalkyl; wherein each alkyl,
and cycloalkyl is independently optionally substituted with one,
two, or three R.sup.30e; [0661] R.sup.8 is hydrogen, halogen, --OH,
--NH.sub.2, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[0662] R.sup.9 and R.sup.10 are each independently hydrogen,
halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[0663] Y.sup.2 is --(CR.sup.45R.sup.46).sub.v2--, --NR.sup.47--, or
--O--; [0664] Y.sup.3 is --(CR.sup.48R.sup.49).sub.v3-- or
--NR.sup.50--, or --O--; [0665] Y.sup.4 is --O-- or --NH--; [0666]
R.sup.47 and R.sup.50 are each independently hydrogen,
--S(O)R.sup.a, --S(.dbd.O).sub.2R.sup.a,
--S(.dbd.O).sub.2NR.sup.cR.sup.d, --C(.dbd.O)R.sup.a,
--C(.dbd.O)OR.sup.b, C.sub.1-C.sub.6 alkyl, cycloalkyl, or
heterocycloalkyl; wherein each alkyl, cycloalkyl, and
heterocycloalkyl is independently optionally substituted with one,
two, or three R.sup.30f; [0667] R.sup.45, R.sup.46, R.sup.48 and
R.sup.49 are each independently hydrogen, halogen, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6 haloalkyl; [0668] v2 and v3 are each
independently 1-3; [0669] R.sup.15c is C.sub.1-C.sub.6 alkyl,
cycloalkyl, or heterocycloalkyl; wherein each alkyl, cycloalkyl,
and heterocycloalkyl is independently optionally substituted with
one, two, or three R.sup.30g; [0670] R.sup.16c is hydrogen or
C.sub.1-C.sub.6 alkyl optionally substituted with one, two, or
three R.sup.30h; [0671] R.sup.18b is C.sub.1-C.sub.6 alkyl,
cycloalkyl, C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, cycloalkyl, and
heterocycloalkyl is independently optionally substituted with one,
two, or three R.sup.30i; [0672] R.sup.21 and R.sup.22 are each
independently hydrogen, C.sub.1-C.sub.20 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--(CR.sup.23R.sup.24).sub.wC(.dbd.O)OR.sup.25,
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)R.sup.26,
--(CR.sup.23R.sup.24).sub.wSC(.dbd.O)R.sup.26, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30k; [0673] or
R.sup.21 and R.sup.22 are taken together with the atoms to which
they are attached to form a heterocycloalkyl optionally substituted
with one, two, or three R.sup.30l; [0674] each R.sup.23 and
R.sup.24 are independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; [0675] each R.sup.25 is independently hydrogen,
C.sub.1-C.sub.6alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0676] each R.sup.26 is
independently C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0677]
each w is independently 1-4; [0678] each R.sup.30, R.sup.30a,
R.sup.30b, R.sup.30c, R.sup.30d, R.sup.30e, R.sup.30f, R.sup.30g,
R.sup.30h, R.sup.30i, R.sup.30k, and R.sup.30l is independently
halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.31; [0679]
each R.sup.31 is independently halogen, --OH, --OR.sup.a, or
--NR.sup.cR.sup.d; [0680] each R.sup.a is independently
C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 haloalkyl, C.sub.1-C.sub.6
hydroxyalkyl, or C.sub.1-C.sub.6 heteroalkyl; [0681] each R.sup.b
is independently hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6
haloalkyl, C.sub.1-C.sub.6 hydroxyalkyl, or C.sub.1-C.sub.6
heteroalkyl; [0682] R.sup.c and R.sup.d are each independently
hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 haloalkyl,
C.sub.1-C.sub.6 hydroxyalkyl, or C.sub.1-C.sub.6 heteroalkyl;
[0683] or R.sup.c and R.sup.d are taken together with the nitrogen
atom to which they are attached to form a heterocycloalkyl
optionally substituted with one, two, or three halogen,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl; [0684] n is 1;
and [0685] m is 0.
[0686] In some embodiments of a compound of Formula (II), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof;
[0687] A is --O-- or --CH.sub.2--; [0688] Q.sup.1 and Q.sup.2 are
independently N or CW; [0689] each W is hydrogen; [0690] Z is
--NR.sup.1R.sup.2;
[0691] R.sup.1 and R.sup.2 are each independently hydrogen,
C.sub.1-C.sub.6 alkyl, cycloalkyl, or C.sub.1-C.sub.6 alkyl(aryl);
wherein each alkyl, cycloalkyl, and aryl is independently
optionally substituted with one, two, or three R.sup.30a; [0692] or
R.sup.1 and R.sup.2 are taken together with the nitrogen atom to
which they are attached to form a heterocycloalkyl optionally
substituted with one, two, or three R.sup.30b; [0693] R.sup.3 is
halogen; [0694] R.sup.4 and R.sup.7 are each independently
hydrogen, halogen, --OH, or --OR.sup.15c; [0695] R.sup.5 and
R.sup.6 are each hydrogen; [0696] R.sup.8 is hydrogen; [0697]
R.sup.9 and R.sup.10 are each hydrogen; [0698] Y.sup.2 is
--(CR.sup.45R.sup.46).sub.v2--, --NR.sup.47--, --O--; [0699]
Y.sup.3 is --(CR.sup.48R.sup.49).sub.v3-- or --NR.sup.50--; [0700]
Y.sup.4 is --O--; [0701] R.sup.47 and R.sup.50 are each
independently hydrogen, --S(O)R.sup.a, --S(.dbd.O).sub.2R.sup.a,
--S(.dbd.O).sub.2NR.sup.cR.sup.d, --C(.dbd.O)R.sup.a,
--C(.dbd.O)OR.sup.b, C.sub.1-C.sub.6 alkyl, cycloalkyl, or
heterocycloalkyl; wherein each alkyl, cycloalkyl, and
heterocycloalkyl is independently optionally substituted with one,
two, or three R.sup.30f; [0702] R.sup.45, R.sup.46, R.sup.48 and
R.sup.49 are each independently hydrogen, halogen, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6 haloalkyl; [0703] v2 and v3 are each
independently 1 or 2; [0704] R.sup.15c is C.sub.1-C.sub.6 alkyl;
[0705] R.sup.21 and R.sup.22 are each hydrogen, C.sub.1-C.sub.20
alkyl, --(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25, or aryl
optionally substituted with one, two, or three R.sup.30k; [0706] or
R.sup.21 and R.sup.22 are taken together with the atoms to which
they are attached to form a heterocycloalkyl optionally substituted
with one, two, or three R.sup.30l; [0707] each R.sup.23 and
R.sup.24 are independently hydrogen; [0708] each R.sup.25 is
independently hydrogen or C.sub.1-C.sub.6 alkyl; [0709] each w is
independently 1 or 2; [0710] each R.sup.30a, R.sup.30b, R.sup.30f,
R.sup.30k, and R.sup.30l is independently halogen, --OH,
--OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, or
C.sub.1-C.sub.6 alkyl optionally substituted with one, two, or
three R.sup.31; [0711] each R.sup.31 is independently halogen,
--OH, --OR.sup.a, or --NR.sup.cR.sup.d; [0712] each R.sup.a is
independently C.sub.1-C.sub.6 alkyl; [0713] each R.sup.b is
independently hydrogen or C.sub.1-C.sub.6 alkyl; [0714] R.sup.c and
R.sup.d are each independently hydrogen or C.sub.1-C.sub.6 alkyl;
[0715] or R.sup.c and R.sup.d are taken together with the nitrogen
atom to which they are attached to form a heterocycloalkyl
optionally substituted with one, two, or three halogen or
C.sub.1-C.sub.6 alkyl [0716] n is 1; and [0717] m is 0.
[0718] In some embodiments of a compound of Formula (II), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof;
[0719] A is --O-- or --CH.sub.2--; [0720] Q.sup.1 and Q.sup.2 are
independently N or CW; [0721] each W is independently hydrogen,
halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30; [0722] Z
is --NR.sup.1R.sup.2; [0723] R.sup.1 and R.sup.2 are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30c; [0724] or R.sup.1 and R.sup.2 are taken
together with the nitrogen atom to which they are attached to form
a heterocycloalkyl optionally substituted with one, two, or three
R.sup.30b; [0725] R.sup.3 is halogen, --CN, --SR.sup.18b,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30c; [0726] R.sup.4 and
R.sup.7 are each independently hydrogen, halogen, --OH,
--OR.sup.15c, --NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.15c, C.sub.1-C.sub.6 alkyl, or
cycloalkyl; wherein each alkyl, and cycloalkyl is independently
optionally substituted with one, two, or three R.sup.30d; [0727]
R.sup.5 and R.sup.6 are each independently hydrogen, halogen,
C.sub.1-C.sub.6 alkyl, or cycloalkyl; wherein each alkyl, and
cycloalkyl is independently optionally substituted with one, two,
or three R.sup.30e; [0728] R.sup.8 is hydrogen, halogen, --OH,
--NH.sub.2, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[0729] R.sup.9 and R.sup.10 are each independently hydrogen,
halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6haloalkyl; [0730]
X.sup.1 is bond, --C(.dbd.O)--, --S(.dbd.O).sub.2--, or
--CR.sup.40R.sup.41--; [0731] Y.sup.1 is
--(CR.sup.42R.sup.43).sub.v1--, --S(.dbd.O).sub.2--, --NR.sup.44--,
or --O--; [0732] Y.sup.2 is --(CR.sup.45R.sup.46).sub.v2--,
--NR.sup.47--, or --O--; [0733] Y.sup.4 is --O-- or --NH--; [0734]
R.sup.44 and R.sup.47 are each independently hydrogen,
--S(O)R.sup.a, --S(.dbd.O)R.sup.a,
--S(.dbd.O).sub.2NR.sup.cR.sup.d, --C(.dbd.O)R.sup.a,
--C(.dbd.O)OR.sup.b, C.sub.1-C.sub.6 alkyl, cycloalkyl, or
heterocycloalkyl; wherein each alkyl, cycloalkyl, and
heterocycloalkyl is independently optionally substituted with one,
two, or three R.sup.30f; [0735] R.sup.40, R.sup.41, R.sup.42,
R.sup.43, R.sup.45, and R.sup.46 are each independently hydrogen,
halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[0736] v1 and v2 are each independently 1-3; [0737] R.sup.15c is
C.sub.1-C.sub.6 alkyl, cycloalkyl, or heterocycloalkyl; wherein
each alkyl, cycloalkyl, and heterocycloalkyl is independently
optionally substituted with one, two, or three R.sup.30g; [0738]
R.sup.16c is hydrogen or C.sub.1-C.sub.6 alkyl optionally
substituted with one, two, or three R.sup.30h; [0739] R.sup.18b is
C.sub.1-C.sub.6 alkyl, cycloalkyl, C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, and heterocycloalkyl is
independently optionally substituted with one, two, or three
R.sup.30i;
[0740] R.sup.21 and R.sup.22 are each independently hydrogen,
C.sub.1-C.sub.20alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl),
C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--(CR.sup.23R.sup.24).sub.wC(.dbd.O)OR.sup.25,
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)R.sup.26,
--(CR.sup.23R.sup.24).sub.wSC(.dbd.O)R.sup.26, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.23; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.3: [0741] or
R.sup.21 and R.sup.22 are taken together with the atoms to which
they are attached to form a heterocycloalkyl optionally substituted
with one, two, or three R.sup.30l; [0742] each R.sup.23 and
R.sup.24 are independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; [0743] each R.sup.25 is independently hydrogen,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0744] each R.sup.26 is
independently C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0745]
each w is independently 1-4; [0746] each R.sup.30, R.sup.30a,
R.sup.30b, R.sup.30c, R.sup.30d, R.sup.30e, R.sup.30f, R.sup.30g,
R.sup.30h, R.sup.30i, R.sup.30k, and R.sup.30l is independently
halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.31; [0747]
each R.sup.31 is independently halogen, --OH, --OR.sup.a, or
--NR.sup.cR.sup.d; [0748] each R.sup.a is independently
C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 haloalkyl, C.sub.1-C.sub.6
hydroxyalkyl, or C.sub.1-C.sub.6 heteroalkyl; [0749] each R.sup.b
is independently hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6
haloalkyl, C.sub.1-C.sub.6 hydroxyalkyl, or C.sub.1-C.sub.4
heteroalkyl; [0750] R.sup.c and R.sup.d are each independently
hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 haloalkyl,
C.sub.1-C.sub.6 hydroxyalkyl, or C.sub.1-C.sub.6 heteroalkyl;
[0751] or R.sup.c and R.sup.d are taken together with the nitrogen
atom to which they are attached to form a heterocycloalkyl
optionally substituted with one, two, or three halogen,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl; [0752] n is 0;
and [0753] m is 1.
[0754] In some embodiments of a compound of Formula (II), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof;
[0755] A is --O-- or --CH.sub.2--; [0756] Q.sup.1 and Q.sup.2 are
independently N or CW; [0757] each W is hydrogen; [0758] Z is
--NR.sup.1R.sup.2; [0759] R.sup.1 and R.sup.2 are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, cycloalkyl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl, cycloalkyl, and
aryl is independently optionally substituted with one, two, or
three R.sup.30a; [0760] or R.sup.1 and R.sup.2 are taken together
with the nitrogen atom to which they are attached to form a
heterocycloalkyl optionally substituted with one, two, or three
R.sup.31b; [0761] R.sup.3 is halogen; [0762] R.sup.4 and R.sup.7
are each independently hydrogen, halogen, --OH, or --OR.sup.15c;
[0763] R.sup.5 and R.sup.6 are each hydrogen; [0764] R.sup.8 is
hydrogen; [0765] R.sup.9 and R.sup.10 are each hydrogen; [0766]
X.sup.1 is bond, --C(.dbd.O)--, --S(.dbd.O).sub.2--, or
--CR.sup.40R.sup.41--; [0767] Y.sup.1 is
--(CR.sup.42R.sup.43).sub.v1--, --S(.dbd.O).sub.2--, --NR.sup.44--,
or --O--; [0768] Y.sup.2 is --(CR.sup.45R.sup.46).sub.v2--,
--NR.sup.47--, or --O--; [0769] Y.sup.4 is --O--; [0770] R.sup.44
and R.sup.47 are each independently hydrogen, --S(O)R.sup.a,
--S(.dbd.O).sub.2R.sup.a, --S(.dbd.O).sub.2NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b, C.sub.1-C.sub.6 alkyl,
cycloalkyl, or heterocycloalkyl; wherein each alkyl, cycloalkyl,
and heterocycloalkyl is independently optionally substituted with
one, two, or three R.sup.30f; [0771] R.sup.40, R.sup.41, R.sup.42,
R.sup.43, R.sup.45, and R.sup.46 are each independently hydrogen,
halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[0772] v1 and v2 are each independently 1 or 2; [0773] R.sup.15c is
C.sub.1-C.sub.6 alkyl; [0774] R.sup.21 and R.sup.22 are each
hydrogen, C.sub.1-C.sub.20 alkyl,
--(CR.sup.23R.sup.24).sub.wCO(.dbd.O)OR.sup.25, or aryl optionally
substituted with one, two, or three R.sup.30k; [0775] or R.sup.21
and R.sup.22 are taken together with the atoms to which they are
attached to form a heterocycloalkyl optionally substituted with
one, two, or three R.sup.30l; [0776] each R.sup.23 and R.sup.24 are
independently hydrogen; [0777] each R.sup.25 is independently
hydrogen or C.sub.1-C.sub.6 alkyl; [0778] each w is independently 1
or 2; [0779] each R.sup.30a, R.sup.30b, R.sup.30f, R.sup.30k, and
R.sup.30l is independently halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, or C.sub.1-C.sub.6 alkyl
optionally substituted with one, two, or three R.sup.31; [0780]
each R.sup.31 is independently halogen, --OH, --OR.sup.a, or
--NR.sup.cR.sup.d; [0781] each R.sup.a is independently
C.sub.1-C.sub.6 alkyl; [0782] each R.sup.b is independently
hydrogen or C.sub.1-C.sub.6 alkyl; [0783] R.sup.c and R.sup.d are
each independently hydrogen or C.sub.1-C.sub.6 alkyl; [0784] or
R.sup.c and R.sup.d are taken together with the nitrogen atom to
which they are attached to form a heterocycloalkyl optionally
substituted with one, two, or three halogen or C.sub.1-C.sub.6
alkyl [0785] n is 0; and [0786] m is 1.
[0787] In some embodiments of a compound of Formula (II), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof;
[0788] A is --O-- or --CH.sub.2--; [0789] Q.sup.1 is N or CW;
[0790] Q.sup.2 is N; [0791] each W is independently hydrogen,
halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optimally substituted with one, two, or three R.sup.30; [0792] Z is
--NR.sup.1R.sup.2; [0793] R.sup.1 and R.sup.2 are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30a; [0794] or R.sup.1 and R.sup.2 are taken
together with the nitrogen atom to which they are attached to form
a heterocycloalkyl optionally substituted with one, two, or three
R.sup.30b; [0795] R.sup.3 is halogen, --CN, --SR.sup.18b,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each cycloalkyl, heterocycloalkyl,
aryl, and heteroaryl is independently optionally substituted with
one, two, or three R.sup.30c; [0796] R.sup.4 and R.sup.7 are each
independently hydrogen, halogen, --OH, --OR.sup.15c,
--NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.15c, C.sub.1-C.sub.6 alkyl, or
cycloalkyl; wherein each alkyl, and cycloalkyl is independently
optionally substituted with one, two, or three R.sup.30d; [0797]
R.sup.5 and R.sup.6 are each independently hydrogen, halogen,
C.sub.1-C.sub.6 alkyl, or cycloalkyl; wherein each alkyl, and
cycloalkyl is independently optionally substituted with one, two,
or three R.sup.30e; [0798] R.sup.8 is hydrogen, halogen, --OH,
--NH.sub.2, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[0799] R.sup.9 and R.sup.10 are each independently hydrogen,
halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6haloalkyl; [0800]
X.sup.1 is bond; [0801] Y.sup.1 is --O--; [0802] Y.sup.2 is
--(CR.sup.45R.sup.46).sub.v2--; [0803] Y.sup.4 is --O-- or --NH--;
R.sup.45 and R.sup.46 are each independently hydrogen, halogen,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl; [0804] v2 is
1-3; [0805] R.sup.15c is C.sub.1-C.sub.6 alkyl, cycloalkyl, or
heterocycloalkyl; wherein each alkyl, cycloalkyl, and
heterocycloalkyl is independently optionally substituted with one,
two, or three R.sup.30g; [0806] R.sup.16c is hydrogen or
C.sub.1-C.sub.6 alkyl optionally substituted with one, two, or
three R.sup.30h; [0807] R.sup.18b is C.sub.1-C.sub.6 alkyl,
cycloalkyl, C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, cycloalkyl, and
heterocycloalkyl is independently optionally substituted with one,
two, or three R.sup.30b; [0808] R.sup.21 and R.sup.22 are each
independently hydrogen, C.sub.1-C.sub.20 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--(CR.sup.23R.sup.24).sub.wC(O)OR.sup.25,
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)R.sup.26,
--(CR.sup.23R.sup.24).sub.wSC(.dbd.O)R.sup.26, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30k; [0809] or
R.sup.21 and R.sup.22 are taken together with the atoms to which
they are attached to form a heterocycloalkyl optionally substituted
with one, two, or three R.sup.30l; [0810] each R.sup.23 and
R.sup.24 are independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; [0811] each R.sup.25 is independently hydrogen,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0812] each
R.sup.26 is independently C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, or C.sub.1-C.sub.6 heteroalkyl;
[0813] each w is independently 1-4; [0814] each R.sup.30,
R.sup.30a, R.sup.30b, R.sup.30c, R.sup.30d, R.sup.30e, R.sup.30g,
R.sup.30h, R.sup.30i, R.sup.30k, and R.sup.30l is independently
halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b, --C(O)NR.sup.cR.sup.d,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl, or
heteroaryl; wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.31; [0815] each R.sup.31 is independently
halogen, --OH, --OR.sup.a, or --NR.sup.cR.sup.d; [0816] each
R.sup.a is independently C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6
haloalkyl, C.sub.1-C.sub.6 hydroxyalkyl, or C.sub.1-C.sub.6
heteroalkyl; [0817] each R.sup.b is independently hydrogen,
C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 haloalkyl, C.sub.1-C.sub.6
hydroxyalkyl, or C.sub.1-C.sub.6 heteroalkyl; [0818] R.sup.c and
R.sup.d are each independently hydrogen, C.sub.1-C.sub.6 alkyl,
C.sub.1-C.sub.6 haloalkyl, C.sub.1-C.sub.6 hydroxyalkyl, or
C.sub.1-C.sub.6 heteroalkyl; [0819] or R.sup.c and R.sup.d are
taken together with the nitrogen atom to which they are attached to
form a heterocycloalkyl optionally substituted with one, two, or
three halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[0820] n is 0 or 1; and [0821] m is 0 or 1; provided that at least
one of n or m is 1.
[0822] In some embodiments of a compound of Formula (II), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof;
[0823] A is --O-- or --CH.sub.2--; [0824] Q.sup.1 is N or CW;
[0825] Q.sup.2 is N; [0826] each W is hydrogen; [0827] Z is
--NR.sup.1R.sup.2; [0828] R.sup.1 and R.sup.2 are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, cycloalkyl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl, cycloalkyl, and
aryl is independently optionally substituted with one, two, or
three R.sup.30a; [0829] or R.sup.1 and R.sup.2 are taken together
with the nitrogen atom to which they are attached to form a
heterocycloalkyl optionally substituted with one, two, or three
R.sup.30b; [0830] R.sup.3 is halogen; [0831] R.sup.4 and R.sup.7
are each independently hydrogen, halogen, --OH, or --OR.sup.15c;
[0832] R.sup.5 and R.sup.6 are each hydrogen; [0833] R.sup.8 is
hydrogen; [0834] R.sup.9 and R.sup.10 are each hydrogen; [0835]
X.sup.1 is bond; [0836] Y.sup.1 is --O--; [0837] Y.sup.2 is
--(CR.sup.45R.sup.46).sub.v2--, [0838] Y.sup.4 is --O--; [0839]
R.sup.45 and R.sup.46 are each independently hydrogen, halogen,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6haloalkyl; [0840] v2 is 1
or 2; [0841] R.sup.15c is C.sub.1-C.sub.6 alkyl; [0842] R.sup.21
and R.sup.22 are each hydrogen, C.sub.1-C.sub.20 alkyl,
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25, or aryl optionally
substituted with one, two, or three R.sup.30k; [0843] or R.sup.21
and R.sup.22 are taken together with the atoms to which they are
attached to form a heterocycloalkyl optionally substituted with
one, two, or three R.sup.30l; [0844] each R.sup.23 and R.sup.24 are
independently hydrogen; [0845] each R.sup.25 is independently
hydrogen or C.sub.1-C.sub.6 alkyl; [0846] each w is independently 1
or 2; [0847] each R.sup.30a, R.sup.30b, R.sup.30k, and R.sup.30l is
independently halogen, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)OR.sup.b, or C.sub.1-C.sub.6alkyl optionally substituted
with one, two, or three R.sup.31; [0848] each R.sup.31 is
independently halogen, --OH, --OR.sup.a, or --NR.sup.cR.sup.d;
[0849] each R.sup.a is independently C.sub.1-C.sub.6 alkyl; [0850]
each R.sup.b is independently hydrogen or C.sub.1-C.sub.6 alkyl;
[0851] R.sup.c and R.sup.d are each independently hydrogen or
C.sub.1-C.sub.6 alkyl; [0852] or R.sup.c and R.sup.d are taken
together with the nitrogen atom to which they are attached to form
a heterocycloalkyl optionally substituted with one, two, or three
halogen or C.sub.1-C.sub.6 alkyl [0853] n is 0 or 1; and [0854] m
is 0 or 1; provided that at least one of n or m is 1.
[0855] In some embodiments of a compound of Formula (II), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof;
[0856] A is --O-- or --CH.sub.2--; [0857] Q.sup.1 is N or CW;
[0858] Q.sup.2 is N; [0859] each W is independently hydrogen,
halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --CH(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30; [0860] Z
is --NR.sup.1R.sup.2; [0861] R.sup.1 and R.sup.2 are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30a; [0862] or R.sup.1 and R.sup.2 are taken
together with the nitrogen atom to which they are attached to form
a heterocycloalkyl optionally substituted with one, two, or three
R.sup.30b; [0863] R.sup.3 is halogen, --CN, --SR.sup.18b,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30c; [0864] R.sup.4 and
R.sup.7 are each independently hydrogen, halogen, --OH,
--OR.sup.15c, --NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.15c, C.sub.1-C.sub.6 alkyl, or
cycloalkyl; wherein each alkyl, and cycloalkyl is independently
optionally substituted with one, two, or three R.sup.30d; [0865]
R.sup.5 and R.sup.6 are each independently hydrogen, halogen,
C.sub.1-C.sub.6 alkyl, or cycloalkyl; wherein each alkyl, and
cycloalkyl is independently optionally substituted with one, two,
or three R.sup.30e; [0866] R.sup.8 is hydrogen, halogen, --OH,
--NH.sub.2, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[0867] R.sup.9 and R.sup.10 are each independently hydrogen,
halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[0868] X.sup.1 is bond, --C(.dbd.O)--, --S(.dbd.O).sub.2--, or
--CR.sup.40R.sup.41--; [0869] Y.sup.1 is
--(CR.sup.42R.sup.43).sub.v1--, --S(.dbd.O).sub.2--, --NR.sup.44--,
or --O--; [0870] Y.sup.2 is --(CR.sup.45R.sup.46).sub.v2--,
--NR.sup.47--, or --O--; [0871] Y.sup.4 is --O-- or --NH--; [0872]
R.sup.44 and R.sup.47 are each independently hydrogen,
--S(.dbd.O)R.sup.a, --S(.dbd.O).sub.2R.sup.a,
--S(.dbd.O).sub.2NR.sup.cR.sup.d, --C(.dbd.O)R.sup.a,
--C(.dbd.O)OR.sup.b, C.sub.1-C.sub.6 alkyl, cycloalkyl, or
heterocycloalkyl; wherein each alkyl, cycloalkyl, and
heterocycloalkyl is independently optionally substituted with one,
two, or three R.sup.30f; [0873] R.sup.40, R.sup.41, R.sup.42,
R.sup.43, R.sup.45, and R.sup.46 are each independently hydrogen,
halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[0874] v1 and v2 are each independently 1-3; [0875] R.sup.15c is
C.sub.1-C.sub.6 alkyl, cycloalkyl, or heterocycloalkyl; wherein
each alkyl, cycloalkyl, and heterocycloalkyl is independently
optionally substituted with one, two, or three R.sup.30g; [0876]
R.sup.16c is hydrogen or C.sub.1-C.sub.6 alkyl optionally
substituted with one, two, or three R.sup.30h; [0877] R.sup.18b is
C.sub.1-C.sub.6 alkyl, cycloalkyl, C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, and heterocycloalkyl is
independently optionally substituted with one, two, or three
R.sup.30i; [0878] R.sup.21 and R.sup.22 are each independently
hydrogen, C.sub.1-C.sub.20alkyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl),
C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--(CR.sup.23R.sup.24).sub.wC(.dbd.O)OR.sup.25,
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)R.sup.26,
--(CR.sup.23R.sup.24).sub.wSC(.dbd.O)R.sup.26, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30k; [0879] or
R.sup.21 and R.sup.22 are taken together with the atoms to which
they are attached to form a heterocycloalkyl optionally substituted
with one, two, or three R.sup.30l; [0880] each R.sup.23 and
R.sup.24 are independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; [0881] each R.sup.25 is independently hydrogen,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0882] each R.sup.26 is
independently C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0883]
each w is independently 1-4; [0884] each R.sup.30, R.sup.30a,
R.sup.36b, R.sup.31c, R.sup.30d, R.sup.30e, R.sup.30f, R.sup.30g,
R.sup.30h, R.sup.30i, R.sup.30k, and R.sup.30l is independently
halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6alkyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.31; [0885]
each R.sup.31 is independently halogen, --OH, --OR.sup.a, or
--NR.sup.cR.sup.d; [0886] each R.sup.a is independently
C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6haloalkyl, C.sub.1-C.sub.6
hydroxyalkyl, or C.sub.1-C.sub.6 heteroalkyl; [0887] each R.sup.b
is independently hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6
haloalkyl, C.sub.1-C.sub.6 hydroxyalkyl, or C.sub.1-C.sub.6
heteroalkyl; [0888] R.sup.c and R.sup.d are each independently
hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 haloalkyl,
C.sub.1-C.sub.6 hydroxyalkyl, or C.sub.1-C.sub.6 heteroalkyl;
[0889] or R.sup.c and R.sup.d are taken together with the nitrogen
atom to which they are attached to form a heterocycloalkyl
optionally substituted with one, two, or three halogen,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl; [0890] n is 0;
and [0891] m is 1.
[0892] In some embodiments of a compound of Formula (II), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof;
[0893] A is --O-- or --CH.sub.2--; [0894] Q.sup.1 is N or CW;
[0895] Q.sup.2 is N; [0896] each W is hydrogen; [0897] Z is
--NR.sup.1R.sup.2; [0898] R.sup.1 and R.sup.2 are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, cycloalkyl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl, cycloalkyl, and
aryl is independently optionally substituted with one, two, or
three R.sup.30a; [0899] or R.sup.1 and R.sup.2 are taken together
with the nitrogen atom to which they are attached to form a
heterocycloalkyl optionally substituted with one, two, or three
R.sup.30b; [0900] R.sup.3 is halogen; [0901] R.sup.4 and R.sup.7
are each independently hydrogen, halogen, --OH, or --OR.sup.15c;
[0902] R.sup.5 and R.sup.6 are each hydrogen; [0903] R.sup.8 is
hydrogen; [0904] R.sup.9 and R.sup.10 are each hydrogen; [0905]
X.sup.1 is bond, --C(.dbd.O)--, --S(.dbd.O).sub.2--, or
--CR.sup.40R.sup.41--; [0906] Y.sup.1 is
--(CR.sup.42R.sup.43).sub.v1--, --S(.dbd.O).sub.2--, --NR.sup.44--,
or --O--; [0907] Y.sup.2 is --(CR.sup.45R.sup.46).sub.v2--,
--NR.sup.47--, or --O--; [0908] Y.sup.4 is --O--; [0909] R.sup.44
and R.sup.47 are each independently hydrogen, --S(O)R.sup.a,
--S(.dbd.O).sub.2R.sup.a, --S(.dbd.O).sub.2NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b, C.sub.1-C.sub.6 alkyl,
cycloalkyl, or heterocycloalkyl; wherein each alkyl, cycloalkyl,
and heterocycloalkyl is independently optionally substituted with
one, two, or three R.sup.30f; [0910] R.sup.40, R.sup.41, R.sup.42,
R.sup.43, R.sup.45, and R.sup.46 are each independently hydrogen,
halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[0911] v1 and v2 are each independently 1 or 2; [0912] R.sup.15c is
C.sub.1-C.sub.6 alkyl; [0913] R.sup.21 and R.sup.22 are each
hydrogen, C.sub.1-C.sub.20 alkyl.
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25, or aryl optionally
substituted with one, two, or three R.sup.30k; [0914] or R.sup.21
and R.sup.22 are taken together with the atoms to which they are
attached to form a heterocycloalkyl optionally substituted with
one, two, or three R.sup.30l; [0915] each R.sup.23 and R.sup.24 are
independently hydrogen; [0916] each R.sup.25 is independently
hydrogen or C.sub.1-C.sub.6 alkyl; [0917] each w is independently 1
or 2; [0918] each R.sup.30a, R.sup.30b, R.sup.30f, R.sup.30k, and
R.sup.30l is independently halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, or C.sub.1-C.sub.4 alkyl
optionally substituted with one, two, or three R.sup.31; [0919]
each R.sup.31 is independently halogen, --OH, --OR.sup.a, or
--NR.sup.cR.sup.d; [0920] each R.sup.a is independently
C.sub.1-C.sub.6 alkyl; [0921] each R.sup.b is independently
hydrogen or C.sub.1-C.sub.6 alkyl; [0922] R.sup.c and R.sup.d are
each independently hydrogen or C.sub.1-C.sub.6 alkyl; [0923] or
R.sup.c and R.sup.d are taken together with the nitrogen atom to
which they are attached to form a heterocycloalkyl optionally
substituted with one, two, or three halogen or C.sub.1-C.sub.6
alkyl [0924] n is 0; and [0925] m is 1.
[0926] For any and all of the embodiments of Formula (II),
substituents are selected from among a subset of the listed
alternatives.
[0927] In some embodiments of a compound of Formula (II), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.8 is hydrogen, halogen, --OH, --OMe, --NH.sub.1,
--NH(CH.sub.3), --N(CH.sub.3).sub.2, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl. In some embodiments of a compound of
Formula (II), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.8 is hydrogen, halogen, --OH,
--NH.sub.2, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl. In
some embodiments of a compound of Formula (II), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.8 is hydrogen, halogen, --OH, --NH.sub.2, or C.sub.1-C.sub.6
alkyl. In some embodiments of a compound of Formula (II), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof;
R.sup.8 is hydrogen or C.sub.1-C.sub.6 alkyl. In some embodiments
of a compound of Formula (II), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.8 is hydrogen.
[0928] In some embodiments of a compound of Formula (II), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.9 and R.sup.10 are each independently hydrogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(II), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.9 and R.sup.10 are each hydrogen.
[0929] In some embodiments of a compound of Formula (II), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
m is 1. In some embodiments of a compound of Formula (II), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
m is 1; and n is 0.
[0930] In some embodiments of a compound of Formula (II), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
Y.sup.4 is --O--. In some embodiments of a compound of Formula
(II), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, Y.sup.4 is --NH--. In some embodiments of a
compound of Formula (II), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, Y.sup.4 is --N(CH.sub.3)--.
[0931] In some embodiments of a compound of Formula (II), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
the compound of Formula (II) is of Formula (IIa):
##STR00005##
[0932] In some embodiments of a compound of Formula (IIa), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof;
[0933] A is --O-- or --CH.sub.2--; [0934] Q.sup.1 is CW and Q.sup.2
is N; or [0935] Q.sup.1 is N and Q.sup.2 is N; [0936] W is
hydrogen, halogen, --CN, --OH, --OR.sup.a, --SH, --SR.sup.a,
--S(.dbd.O)R.sup.a, --NO.sub.2, --NR.sup.cR.sup.d,
--S(.dbd.O).sub.2R.sup.a, --NHS(.dbd.O).sub.2R.sup.a,
--S(.dbd.O).sub.2NR.sup.CR.sup.d, --C(.dbd.O)R.sup.a,
--OC(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b, --OC(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, --OC(.dbd.O)NR.sup.cR.sup.d,
--NR.sup.bC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(.dbd.O)R.sup.a,
--NR.sup.bC(.dbd.O)OR.sup.b, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30; [0937] Z is --NR.sup.1R.sup.2, --OR.sup.60,
--SR.sup.61, or --CR.sup.62R.sup.63R.sup.64; [0938] R.sup.1 and
R.sup.2 are each independently hydrogen, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--S(.dbd.O).sub.2R.sup.15a, --S(.dbd.O).sub.2NR.sup.16aR.sup.17a,
or --C(.dbd.O).sub.2R.sup.15a; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.30a; [0939] or R.sup.1 and R.sup.2 are taken together with
the nitrogen atom to which they are attached to form a
heterocycloalkyl optionally substituted with one, two, or three
R.sup.30b; [0940] R.sup.60 is hydrogen, --C(.dbd.O)R.sup.15e,
--C(.dbd.O)OR.sup.16e, --C(.dbd.O)NR.sup.16eR.sup.17e,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30m; [0941]
R.sup.61 is hydrogen, --C(.dbd.O)R.sup.15f, --C(.dbd.O)OR.sup.16f,
--C(.dbd.O)NR.sup.16fR.sup.17f, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.4-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.30n; [0942] R.sup.62, R.sup.63, and R.sup.64
are each independently hydrogen, halogen, --CN, --OH, --OR.sup.15g,
--SH, --SR.sup.15g, --S(.dbd.O)R.sup.15g, --NO.sub.2,
--NR.sup.16gR.sup.17g, --S(.dbd.O).sub.2R.sup.15g,
--NHS(.dbd.O).sub.2R.sup.15g, --S(.dbd.O).sub.2NR.sup.16gR.sup.17g,
--C(.dbd.O)R.sup.15g, --OC(.dbd.O)R.sup.15g, --C(.dbd.O)OR.sup.16g,
--OC(.dbd.O)R.sup.16g, --C(.dbd.O)NR.sup.16gR.sup.17g,
--OC(.dbd.O)NR.sup.16gR.sup.17g,
--NR.sup.15gC(.dbd.O)NR.sup.16gR.sup.17g,
--NR.sup.16hC(.dbd.O)R.sup.15g, --NR.sup.16gC(.dbd.O)OR.sup.16g,
C.sub.1-C.sub.6alkyl, C.sub.2-C.sub.6alkenyl, C.sub.2-C.sub.6
alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30o; [0943]
R.sup.3 is halogen, --CN, --OH, --OR.sup.15b, --SR.sup.18b,
--NR.sup.16bR.sup.17b, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30c; [0944] R.sup.4 and R.sup.7 are each
independently hydrogen, halogen, --OH, --OR.sup.15c,
--NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.15c, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.30d; [0945] R.sup.5 and R.sup.6 are each independently
hydrogen, halogen, --OH, --OR.sup.15d,
--NR.sup.16cS(.dbd.O).sub.2R.sup.15d, --NR.sup.16dC(O)R.sup.15d,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.30e; [0946] X.sup.1 is a bond; [0947] Y.sup.1
is --S(.dbd.O).sub.2--; [0948] Y.sup.2 is
--(CR.sup.45R.sup.46).sub.v2--; [0949] R.sup.45 and R.sup.46 are
each independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; [0950] v2 is 1-3; [0951] R.sup.15a, R.sup.15b,
R.sup.15c, R.sup.15d, R.sup.15e, R.sup.15f, R.sup.15g are each
independently C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl, aryl, or
heteroaryl; wherein each alkyl, alkenyl, alkynyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30g; [0952] R.sup.16a,
R.sup.16b, R.sup.16c, R.sup.16d, R.sup.16e, R.sup.16f, R.sup.17a,
R.sup.17b, R.sup.17e, R.sup.17f, and R.sup.17g are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, or heterocycloalkyl;
wherein each alkyl, alkenyl, alkynyl, cycloalkyl, and
heterocycloalkyl is independently optionally substituted with one,
two, or three R.sup.30h; [0953] or R.sup.16a and R.sup.17a or
R.sup.16b and R.sup.17b or R.sup.16e and R.sup.17e or R.sup.16f and
R.sup.17f or R.sup.16g and R.sup.17g are taken together with the
nitrogen atom to which they are attached to form a heterocycloalkyl
optionally substituted with one, two, or three halogen,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl; [0954]
R.sup.18b is C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30i; [0955] R.sup.21 and R.sup.22 are each
independently hydrogen, C.sub.1-C.sub.20alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--(CR.sup.23R.sup.24).sub.wC(.dbd.O)OR.sup.25,
--(CR.sup.23R.sup.24).sub.wCO(.dbd.O)R.sup.26,
--(CR.sup.23R.sup.24).sub.wSC(.dbd.O)R.sup.26, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optimally substituted with one, two, or three R.sup.30k; [0956] or
R.sup.21 and R.sup.22 are taken together with the atoms to which
they are attached to form a heterocycloalkyl optionally substituted
with one, two, or three R.sup.30l; [0957] each R.sup.23 and
R.sup.24 are independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; [0958] each R.sup.25 is independently hydrogen,
C.sub.1-C.sub.6alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0959] each R.sup.26 is
independently C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [0960]
each w is independently 1-4; [0961] each R.sup.30, R.sup.30a,
R.sup.30b, R.sup.30c, R.sup.30d, R.sup.30e, R.sup.30g and
R.sup.30h, R.sup.30i, R.sup.30j, R.sup.30k, R.sup.30l, R.sup.30m,
R.sup.30n, and R.sup.30o are independently halogen, --CN, --OH,
--OR.sup.a, --SH, --SR.sup.a, --S(.dbd.O)R.sup.a, --NO.sub.2,
--NR.sup.cR.sup.d, --S(.dbd.O).sub.2R.sup.a,
--NHS(.dbd.O).sub.2R.sup.a, --S(.dbd.O).sub.2NR.sup.cR.sup.d,
--C(O)R.sup.a, --OC(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--OC(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
--OC(.dbd.O)--NR.sup.cNR.sup.d, --NR.sup.bC(.dbd.O)NR.sup.cR.sup.d,
--NR.sup.bC(.dbd.O)R.sup.a, --NR.sup.bC(.dbd.O)OR.sup.6,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.31; [0962]
each R.sup.31 is independently halogen, --CN, --OH, --OR.sup.a,
--SH, --SR.sup.a, --S(.dbd.O)R.sup.a, --NO.sub.2,
--NR.sup.cR.sup.d, --S(.dbd.O).sub.2R, --NHS(.dbd.O).sub.2R.sup.a,
--S(.dbd.O).sub.2NR.sup.cR.sup.d, --C(.dbd.O)R.sup.a,
--OC(CO)R.sup.a, --C(.dbd.O)OR.sup.b, --OC(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, --OC(.dbd.O)NR.sup.cR.sup.d,
--NR.sup.bC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(.dbd.O)R.sup.a,
--NR.sup.bC(.dbd.O)OR.sup.b, C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6
haloalkyl, C.sub.1-C.sub.6 hydroxyalkyl, C.sub.1-C.sub.6
heteroalkyl, or cycloalkyl optionally substituted with one, two, or
three halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[0963] each R.sup.a is independently C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, C.sub.1-C.sub.6
heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl;
wherein the alkyl, alkenyl, alkynyl, heteroalkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three halogen, --OH, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6 haloalkyl; [0964] each R.sup.b is
independently hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, C.sub.1-C.sub.6 heteroalkyl,
cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; wherein the
alkyl, alkenyl, alkynyl, heteroalkyl, cycloalkyl, heterocycloalkyl,
aryl, and heteroaryl is independently optionally substituted with
one, two, or three halogen, --OH, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl; and [0965] R.sup.c and R.sup.d are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, C.sub.1-C.sub.6 heteroalkyl,
cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; wherein the
alkyl, alkenyl, alkynyl, heteroalkyl, cycloalkyl, heterocycloalkyl,
aryl, and heteroaryl is independently optionally substituted with
one, two, or three halogen, --OH, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl; [0966] or R.sup.c and R.sup.d are taken
together with the nitrogen atom to which they are attached to form
a heterocycloalkyl optionally substituted with one, two, or three
halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl.
[0967] In some embodiments of a compound of Formula (II) or (IIa),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, Y.sup.1 is --(CR.sup.42R.sup.43).sub.v1--. In some
embodiments of a compound of Formula (II) or (IIa), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
Y.sup.1 is --(CR.sup.42R.sup.43).sub.v1--; and v1 is 1 or 2. In
some embodiments of a compound of Formula (II) or (IIa), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
Y.sup.1 is --(CR.sup.42R.sup.43).sub.v1--; and v1 is 1. In some
embodiments of a compound of Formula (II) or (IIa), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
Y.sup.1 is --(CR.sup.42R.sup.43).sub.v1--; and v1 is 2. In some
embodiments of a compound of Formula (II) or (IIa), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof;
Y.sup.1 is --(CR.sup.42R.sup.43).sub.v1--; and R.sup.42 and
R.sup.43 are each independently hydrogen, halogen, or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(II) or (IIa), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, Y.sup.1 is --(CR.sup.42R.sup.43).sub.v1--;
and R.sup.42 and R.sup.43 are each hydrogen. In some embodiments of
a compound of Formula (II) or (IIa), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, Y.sup.1 is
--(CR.sup.42R.sup.43).sub.v1--; R.sup.42 and R.sup.43 are each
independently hydrogen, halogen, or C.sub.1-C.sub.6 alkyl; and v1
is 1 or 2. In some embodiments of a compound of Formula (II) or
(IIa), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, Y.sup.1 is --(CR.sup.42R.sup.43).sub.v1--;
R.sup.42 and R.sup.43 are each hydrogen; and v1 is 1.
[0968] In some embodiments of a compound of Formula (II) or (IIa),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, Y.sup.1 is --NR.sup.44--. In some embodiments of a
compound of Formula (II) or (IIa), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, Y.sup.1 is --NR.sup.44--;
and R.sup.44 is hydrogen or C.sub.1-C.sub.6 alkyl. In some
embodiments of a compound of Formula (II) or (IIa), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
Y.sup.1 is --NR.sup.44--; and R.sup.44 is hydrogen. In some
embodiments of a compound of Formula (II) or (IIa), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof:
Y.sup.1 is --NR.sup.44--; and R.sup.44 is C.sub.1-C.sub.6
alkyl.
[0969] In some embodiments of a compound of Formula (II) or (IIa),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, Y.sup.1 is --O--.
[0970] In some embodiments of a compound of Formula (II) or (IIa),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, Y.sup.1 is --S(.dbd.O).sub.2--.
[0971] In some embodiments of a compound of Formula (II) or (IIa),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, X.sup.1 is bond. In some embodiments of a compound of
Formula (II) or (IIa), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, X.sup.1 is --C(.dbd.O)--. In some
embodiments of a compound of Formula (II) or (IIa), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
X.sup.1 is --S(.dbd.O).sub.2--.
[0972] In some embodiments of a compound of Formula (II) or (IIa),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, X.sup.1 is --CR.sup.40R.sup.41--. In some embodiments of a
compound of Formula (II) or (IIa), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, X.sup.1 is
--CR.sup.40R.sup.41--; and R.sup.40 and R.sup.41 are each
independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl. In some embodiments of a compound of Formula (II) or
(IIa), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, X.sup.1 is --CR.sup.40R.sup.41--; and
R.sup.40 and R.sup.41 are each independently hydrogen, halogen,
--OH, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl. In some
embodiments of a compound of Formula (II) or (IIa), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
X.sup.1 is --CR.sup.40R.sup.41--; and R.sup.40 and R.sup.31 are
each independently C.sub.1-C.sub.6 alkyl or --OH.
[0973] In some embodiments of a compound of Formula (II) or (IIa),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, X.sup.1 is bond, --C(.dbd.O)--, --S(.dbd.O).sub.2--, or
--CR.sup.40R.sup.41--; Y.sup.1 is --(CR.sup.42R.sup.43).sub.v1--,
--NR.sup.44--, or --O--; and Y.sup.2 is
--(CR.sup.45R.sup.46).sub.v2--, --NR.sup.47--, or --O--.
[0974] In some embodiments of a compound of Formula (II) or (IIa),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, X.sup.1 is bond or --CR.sup.40R.sup.41--; Y.sup.1 is
--(CR.sup.42R.sup.43).sub.v1--, --S(.dbd.O).sup.2--, --NR.sup.44--,
or --O--; and Y.sup.2 is --(CR.sup.45R.sup.46).sub.v2--,
--NR.sup.47--, or --O--.
[0975] In some embodiments of a compound of Formula (II) or (IIa),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, X.sup.1 is --C(.dbd.O)--; Y.sup.1 is
--(CR.sup.42R.sup.43)O--; and Y.sup.2 is
--(CR.sup.45R.sup.46).sub.v2--. In some embodiments of a compound
of Formula (II) or (IIa), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, X.sup.1 is --C(.dbd.O)--; Y.sup.1
is --(CR.sup.42R.sup.43).sub.v1--: Y.sup.2 is
--(CR.sup.43R.sup.46)O--; R.sup.42 and R.sup.43 are each
independently hydrogen, halogen, or C.sub.1-C.sub.6 alkyl; v1 is 1
or 2; R.sup.45 and R.sup.46 are each independently hydrogen,
halogen, or C.sub.1-C.sub.6 alkyl; and v2 is 1 or 2. In some
embodiments of a compound of Formula (II) or (IIa), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
X.sup.1 is --C(.dbd.O)--; Y.sup.1 is
--(CR.sup.42R.sup.43).sub.v1--; Y.sup.2 is
--(CR.sup.45R.sup.46).sub.v2--; R.sup.42 and R.sup.43 are each
hydrogen; v1 is 1; R.sup.45 and R.sup.46 are each hydrogen; and v2
is 1.
[0976] In some embodiments of a compound of Formula (II) or (IIa),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, X.sup.1 is --CR.sup.40R.sup.41--; Y.sup.1 is
--(CR.sup.42R.sup.43).sub.v1--; and Y.sup.2 is
--(CR.sup.45R.sup.46).sub.v2--. In some embodiments of a compound
of Formula (II) or (IIa), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, X.sup.1 is --CR.sup.40R.sup.41--;
Y.sup.1 is --(CR.sup.42R.sup.43).sub.v1--; Y.sup.2 is
--(CR.sup.43R.sup.46).sub.v2--; R.sup.40 and R.sup.41 are each
independently hydrogen, halogen, --OH, or C.sub.1-C.sub.6 alkyl;
R.sup.42 and R.sup.43 are each independently hydrogen, halogen, or
C.sub.1-C.sub.6 alkyl: v1 is 1 or 2; R.sup.45 and R.sup.46 are each
independently hydrogen, halogen, or C.sub.1-C.sub.6 alkyl; and v2
is 1 or 2. In some embodiments of a compound of Formula (II) or
(IIa), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, X.sup.1 is --CR.sup.40R.sup.41--; Y.sup.1 is
--(CR.sup.42R.sup.43).sub.v1--; Y.sup.2 is
--(CR.sup.45R.sup.46).sub.v2--; R.sup.40 and R.sup.41 are each
independently hydrogen, --OH, or C.sub.1-C.sub.6 alkyl; R.sup.42
and R.sup.43 are each hydrogen; v1 is 1; R.sup.45 and R.sup.46 are
each hydrogen; and v2 is 1.
[0977] In some embodiments of a compound of Formula (II) or (IIa),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, X.sup.1 is --C(.dbd.O)--; Y.sup.1 is --O--; and Y.sup.2 is
--NR.sup.47--. In some embodiments of a compound of Formula (II) or
(IIa), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, X.sup.1 is --C(.dbd.O)--; Y.sup.1 is --O--;
Y.sup.2 is --NR.sup.47--; and R.sup.47 is hydrogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(II) or (IIa), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, X.sup.1 is --C(.dbd.O)--; Y.sup.1 is --O--;
Y.sup.2 is --NR.sup.47--; and R.sup.47 is hydrogen. In some
embodiments of a compound of Formula (II) or (IIa), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
X.sup.1 is --C(.dbd.O)--: Y.sup.1 is --O--; Y.sup.2 is
--NR.sup.47--; and R.sup.47 is C.sub.1-C.sub.6 alkyl.
[0978] In some embodiments of a compound of Formula (II) or (IIa),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, X.sup.1 is --S(.dbd.O).sub.2--; Y.sup.1 is
--(CR.sup.42R.sup.43).sub.v1--; and Y.sup.2 is
--(CR.sup.45R.sup.46).sub.v2--. In some embodiments of a compound
of Formula (II) or (IIa), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, X.sup.1 is --S(.dbd.O).sub.2--:
Y.sup.1 is --(CR.sup.45R.sup.46).sub.v1--; Y.sup.2 is
--(CR.sup.45R.sup.46).sub.v2--; R.sup.42 and R.sup.43 are each
independently hydrogen, halogen, or C.sub.1-C.sub.6 alkyl; v1 is 1
or 2; R.sup.45 and R.sup.46 are each independently hydrogen,
halogen, or C.sub.1-C.sub.6 alkyl; and v2 is 1 or 2. --. In some
embodiments of a compound of Formula (II) or (IIa), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
X.sup.1 is --S(.dbd.O).sub.2--; Y.sup.1 is
--(CR.sup.42R.sup.43).sub.v1--; Y.sup.2 is
--(CR.sup.45R.sup.46).sub.v2--; R.sup.42 and R.sup.43 are each
hydrogen; v1 is 1; R.sup.45 and R.sup.46 are each hydrogen; and v2
is 1.
[0979] In some embodiments of a compound of Formula (II) or (IIa),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, X.sup.1 is --S(.dbd.O).sub.2--; Y.sup.1 is --NR.sup.44--;
and Y.sup.2 is --(CR.sup.45R.sup.46).sub.v2--. In some embodiments
of a compound of Formula (II) or (IIa), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, X.sup.1 is
--S(.dbd.O).sub.v--; Y.sup.1 is --NR.sup.44--; Y.sup.2 is
--(CR.sup.45R.sup.46).sub.v2--; R.sup.44 is hydrogen or
C.sub.1-C.sub.6 alkyl; R.sup.45 and R.sup.46 are each independently
hydrogen, halogen, or C.sub.1-C.sub.6 alkyl; and v2 is 1 or 2. In
some embodiments of a compound of Formula (II) or (IIa), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
X.sup.1 is --S(.dbd.O).sub.2--; Y.sup.1 is --NR.sup.44--; Y.sup.2
is --(CR.sup.45R.sup.46).sup.v2--; R.sup.44 is hydrogen; R.sup.45
and R.sup.46 are each hydrogen; and v2 is 1. In some embodiments of
a compound of Formula (II) or (IIa), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, X.sup.1 is
--S(.dbd.O).sub.2--; Y.sup.1 is --NR.sup.44--; Y.sup.2 is
--(CR.sup.45R.sup.46).sub.v2--; R.sup.44 is C.sub.1-C.sub.6 alkyl;
R.sup.45 and R.sup.46 are each hydrogen; and v2 is 1.
[0980] In some embodiments of a compound of Formula (II) or (IIa),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, X.sup.1 is --S(.dbd.O).sub.2--; Y.sup.1 is
--(CR.sup.42R.sup.43).sub.v1--; and Y.sup.2 is --NR.sup.47--. In
some embodiments of a compound of Formula (II) or (IIa), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
X.sup.1 is --S(.dbd.O).sub.2--; Y.sup.1 is
--(CR.sup.42R.sup.43).sub.v1--: Y.sup.2 is --NR.sup.47--; R.sup.42
and R.sup.43 are each independently hydrogen, halogen, or
C.sub.1-C.sub.6 alkyl: v1 is 1 or 2; and R.sup.47 is hydrogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(II) or (IIa), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, X.sup.1 is --S(.dbd.O).sub.2--; Y.sup.1 is
--(CR.sup.02R.sup.43).sub.v1--; Y.sup.2 is --NR.sup.47--; R.sup.42
and R.sup.03 are each hydrogen; v1 is 1; and R.sup.47 is hydrogen.
In some embodiments of a compound of Formula (II) or (IIa), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
X.sup.1 is --S(.dbd.O).sub.2--; Y.sup.1 is
--(CR.sup.42R.sup.43).sub.v1--; Y.sup.2 is --NR.sup.47--; R.sup.42
and R.sup.43 are each hydrogen; v1 is 1; and R.sup.47 is
C.sub.1-C.sub.6 alkyl.
[0981] In some embodiments of a compound of Formula (II) or (IIa),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, X.sup.1 is --S(.dbd.O).sub.2--; Y.sup.1 is --NR.sup.44--;
and Y.sup.2 is --NR.sup.47--. In some embodiments of a compound of
Formula (II) or (IIa), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, X.sup.1 is --S(.dbd.O).sub.2--;
Y.sup.1 is --NR.sup.44--; Y.sup.2 is --NR.sup.47--; R.sup.44 is
hydrogen or C.sub.1-C.sub.6 alkyl; and R.sup.47 is hydrogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(II) or (IIa), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, X.sup.1 is --S(.dbd.O).sub.2--; Y.sup.1 is
--NR.sup.44--; Y.sup.2 is --NR.sup.47--; R.sup.44 is hydrogen; and
R.sup.47 is hydrogen. In some embodiments of a compound of Formula
(II) or (IIa), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, X.sup.1 is --S(.dbd.O).sub.2--; Y.sup.1 is
--NR.sup.44--; Y.sup.2 is --NR.sup.47--; R.sup.44 is
C.sub.1-C.sub.6 alkyl; and R.sup.47 is C.sub.1-C.sub.6 alkyl. In
some embodiments of a compound of Formula (II) or (IIa), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
X.sup.1 is --S(.dbd.O).sub.2--; Y.sup.1 is --NR.sup.44--; Y.sup.2
is --NR.sup.47--; R.sup.44 is hydrogen; and R.sup.47 is
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(II) or (IIa), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, X.sup.1 is --S(.dbd.O).sub.2--; Y.sup.1 is
--NR.sup.44--; Y.sup.2 is --NR.sup.47--; R.sup.44 is
C.sub.1-C.sub.6 alkyl; and R.sup.47 is hydrogen.
[0982] In some embodiments of a compound of Formula (II) or (IIa),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, X.sup.1 is bond; Y.sup.1 is --O--; and Y.sup.2 is
--(CR.sup.45R.sup.46).sub.v2--. In some embodiments of a compound
of Formula (II) or (IIa), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, X.sup.1 is bond; Y.sup.1 is
--O--; Y.sup.2 is --(CR.sup.45R.sup.46).sub.v2--; R.sup.45 and
R.sup.46 are each independently hydrogen, halogen, or
C.sub.1-C.sub.6 alkyl; and v2 is 1 or 2. In some embodiments of a
compound of Formula (II) or (IIa), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, X.sup.1 is bond; Y.sup.1 is
--O--; Y.sup.2 is --(CR.sup.45R.sup.46).sub.v2--; R.sup.45 and
R.sup.46 are each hydrogen; and v2 is 1.
[0983] In some embodiments of a compound of Formula (II) or (IIa),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, X.sup.1 is bond; Y.sup.1 is --S(.dbd.O).sub.2--; and
Y.sup.2 is --(CR.sup.45R.sup.46).sub.v2--. In some embodiments of a
compound of Formula (II) or (IIa), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, X.sup.1 is bond: Y.sup.1 is
--S(.dbd.O).sub.2--; Y.sup.2 is --(CR.sup.45R.sup.46).sub.v2--;
R.sup.45 and R.sup.46 are each independently hydrogen, halogen, or
C.sub.1-C.sub.6 alkyl; and v2 is 1 or 2. In some embodiments of a
compound of Formula (II) or (IIa), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, X.sup.1 is bond; Y.sup.1 is
--S(.dbd.O).sub.2--; Y.sup.2 is --(CR.sup.45R.sup.46).sub.v2--;
R.sup.45 and R.sup.46 are each hydrogen; and v2 is 1.
[0984] In some embodiments of a compound of Formula (II) or (IIa),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, X.sup.1 is bond; Y.sup.1 is --NR.sup.44--; and Y.sup.1 is
--(CR.sup.45R.sup.46).sub.v2--. In some embodiments of a compound
of Formula (II) or (IIa), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, X.sup.1 is bond; Y is
--NR.sup.44--; Y.sup.2 is --(CR.sup.45SR.sup.46).sub.v2--; R.sup.44
is hydrogen, C.sub.1-C.sub.6 alkyl, --S(.dbd.O).sub.2R.sup.a, or
--C(.dbd.O)R.sup.a; R.sup.45 and R.sup.46 are each independently
hydrogen, halogen, or C.sub.1-C.sub.6 alkyl; and v2 is 1 or 2. In
some embodiments of a compound of Formula (II) or (IIa), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
X.sup.1 is bond; Y.sup.1 is --NR.sup.44--; Y.sup.2 is
--(CR.sup.45R.sup.46).sub.v2--; R.sup.44 is hydrogen or
C.sub.1-C.sub.6 alkyl, R.sup.45 and R.sup.46 are each hydrogen; and
v2 is 1. In some embodiments of a compound of Formula (II) or
(IIa), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, X.sup.1 is bond: Y.sup.1 is --NR.sup.44--;
Y.sup.2 is --(CR.sup.45R.sup.46).sub.r: R.sup.44 is
--S(.dbd.O).sub.2R.sup.a or --C(.dbd.O)R.sup.a, R.sup.45 and
R.sup.46 are each hydrogen; and v2 is 1. In some embodiments of a
compound of Formula (II) or (IIa), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, X.sup.1 is bond; Y.sup.1 is
--NR.sup.44--; Y.sup.2 is --(CR.sup.45R.sup.46).sub.v2--; R.sup.44
is --C(.dbd.O)R.sup.a, R.sup.45 and R.sup.46 are each hydrogen; and
v2 is 1. In some embodiments of a compound of Formula (II) or
(IIa), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, X.sup.1 is bond; Y.sup.1 is --NR.sup.44--;
Y.sup.1 is --(CR.sup.45R.sup.46).sub.v2--; R.sup.44 is
--C(.dbd.O)R.sup.a, R.sup.45 and R.sup.46 are each hydrogen; and v2
is 1.
[0985] In some embodiments of a compound of Formula (II), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
the compound of Formula (II) is of Formula (IIb):
##STR00006##
[0986] In some embodiments of a compound of Formula (II) or (IIb),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, Y.sup.3 is --(CR.sup.48R.sup.49).sub.v3--. In some
embodiments of a compound of Formula (II) or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
Y.sup.3 is --(CR.sup.48R.sup.49).sub.v3--; R.sup.48 and R.sup.49
are each independently hydrogen, halogen, or C.sub.1-C.sub.6 alkyl;
and v3 is 1 or 2. In some embodiments of a compound of Formula (II)
or (IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, Y.sup.3 is --(CR.sup.48R.sup.46).sub.v3--;
R.sup.48 and R.sup.49 are each hydrogen; and v3 is 1.
[0987] In some embodiments of a compound of Formula (II) or (IIb),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, Y.sup.3 is --NR.sup.50--. In some embodiments of a
compound of Formula (II) or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, Y.sup.3 is --NR.sup.50--;
and R.sup.50 is hydrogen or C.sub.1-C.sub.6 alkyl. In some
embodiments of a compound of Formula (II) or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
Y.sup.3 is --NR.sup.50--; and R.sup.50 is hydrogen. In some
embodiments of a compound of Formula (II) or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
Y.sup.3 is --NR.sup.50--; and R.sup.50 is C.sub.1-C.sub.6
alkyl.
[0988] In some embodiments of a compound of Formula (II) or (IIb),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, Y.sup.3 is --O--.
[0989] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, Y.sup.1 is --(CR.sup.45R.sup.46).sub.v2--. In
some embodiments of a compound of Formula (II), (IIa), or (IIb), or
a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, Y.sup.2 is --(CR.sup.45R.sup.46).sub.v2--; R.sup.45 and
R.sup.46 are each independently hydrogen, halogen, or
C.sub.1-C.sub.6 alkyl; and v2 is 1 or 2. In some embodiments of a
compound of Formula (II), (IIa), or (IIb), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, Y.sup.2 is
--(CR.sup.45R).sub.v2--; R.sup.45 and R.sup.46 are each hydrogen;
and v2 is 1.
[0990] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, Y.sup.1 is --NR.sup.47--. In some embodiments
of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
Y.sup.2 is --NR.sup.47--; and R.sup.47 is hydrogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, Y.sup.2 is --NR.sup.47--; and
R.sup.47 is hydrogen. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, Y.sup.2 is --NR.sup.47--; and
R.sup.47 is C.sub.1-C.sub.6 alkyl.
[0991] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, Y.sup.2 is --O--.
[0992] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, Y.sup.2 is --O-- and Y.sup.3 is
--(CR.sup.48R.sup.49).sub.v3--. In some embodiments of a compound
of Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, Y.sup.2 is --O--; Y.sup.3
is --(CR.sup.48R.sup.49).sub.3--; R.sup.48 and R.sup.49 are each
independently hydrogen, halogen, or C.sub.1-C.sub.6 alkyl; and v3
is 1 or 2. In some embodiments of a compound of Formula (II),
(IIa), or (IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, Y.sup.2 is --O--; Y.sup.3 is
--(CR.sup.48R.sup.49).sub.v3--; R.sup.48 and R.sup.39 are each
hydrogen; and v3 is 1.
[0993] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, Q.sup.1 is N; and Q.sup.2 is CW. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
Q.sup.1 is CW; and Q.sup.2 is N. In some embodiments of a compound
of Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, Q.sup.1 is N; and Q.sup.2
is N. In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, Q.sup.1 is CW; and Q.sup.2 is CW.
[0994] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, each W is independently hydrogen, halogen,
--CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6alkyl, cycloalkyl, or
heterocycloalkyl; wherein each alkyl, cycloalkyl, and
heterocycloalkyl, is independently optionally substituted with one,
two, or three R.sup.30. In some embodiments of a compound of
Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each W is independently
hydrogen, halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6
alkyl, cycloalkyl, or heterocycloalkyl; wherein each alkyl,
cycloalkyl, and heterocycloalkyl, is independently optionally
substituted with one, two, or three R.sup.30; and each R.sup.30 is
independently halogen or C.sub.1-C.sub.6 alkyl. In some embodiments
of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each W is independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl. In some embodiments of a compound of Formula (II),
(IIa), or (IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, each W is hydrogen.
[0995] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, A is --O--. In some embodiments of a compound
of Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, A is --CH.sub.2--.
[0996] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.5 and R.sup.6 are each independently
hydrogen, halogen, C.sub.1-6 alkyl, or cycloalkyl; wherein each
alkyl and cycloalkyl is independently optionally substituted with
one, two, or three R.sup.30e. In some embodiments of a compound of
Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.5 and R.sup.6 are
each independently hydrogen, halogen, C.sub.1-C.sub.6 alkyl, or
cycloalkyl; wherein each alkyl and cycloalkyl is independently
optionally substituted with one, two, or three R.sup.30e; and each
R.sup.30e is independently halogen or C.sub.1-C.sub.6 alkyl. In
some embodiments of a compound of Formula (II), (IIa), or (IIb), or
a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.5 and R.sup.6 are each hydrogen.
[0997] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.4 and R.sup.7 are each independently
hydrogen, halogen, --OH, --OR.sup.15c,
--NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.15c, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30d. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.4 and R.sup.7 are each independently hydrogen, halogen, --OH,
--OR.sup.15c, --NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.15c, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30d; and each
R.sup.30d is independently halogen or C.sub.1-C.sub.6 alkyl. In
some embodiments of a compound of Formula (II), (IIa), or (IIb), or
a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.4 and R.sup.7 are each independently hydrogen,
halogen. --OH, --OR.sup.15c, --NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
or --NR.sup.16cC(.dbd.O)R.sup.15c. In some embodiments of a
compound of Formula (II), (IIa), or (IIb), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.4 and
R.sup.7 are each independently hydrogen, halogen, --OH,
--OR.sup.15c, --NR.sup.16cS(.dbd.O).sub.2R.sup.15c, or
--NR.sup.16cC(.dbd.O)R.sup.15c; R.sup.15c are each independently
C.sub.1-C.sub.6 alkyl or C.sub.1-C.sub.6 haloalkyl; and R.sup.16c
are each independently hydrogen, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl. In some embodiments of a compound of
Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.4 and R.sup.7 are
each independently hydrogen, halogen, --OH, --OR.sup.15c,
--NR.sup.16cS(.dbd.O).sub.2R.sup.15c, or
--NR.sup.16cC(.dbd.O)R.sup.15c; R.sup.15c are each independently
C.sub.1-C.sub.6 alkyl; and R.sup.16 are each independently hydrogen
or C.sub.1-C.sub.6 alkyl.
[0998] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.4 and R.sup.7 are each independently
hydrogen, halogen, or --OH. In some embodiments of a compound of
Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.4 and R.sup.7 are
each independently halogen or --OH. In some embodiments of a
compound of Formula (II), (IIa), or (IIb), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.4 and
R.sup.7 are each --OH.
[0999] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, Z is --NR.sup.1R.sup.2.
[1000] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, one of R.sup.1 or R.sup.2 is not
hydrogen.
[1001] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 is C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--S(.dbd.O).sub.2R.sup.15a, --S(.dbd.O).sub.2NR.sup.16aR.sup.17a,
or --C(.dbd.O).sub.2R.sup.15a; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30a. In some embodiments
of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 is C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl),
C.sub.1-C.sub.6 alkyl(heterocycloalkyl), --S(O).sub.2R.sup.15a,
--S(.dbd.O).sub.2NR.sup.16aR.sup.17a, or
--C(.dbd.O).sub.2R.sup.13a; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30a; R.sup.15a is
C.sub.1-C.sub.6 alkyl, aryl, or C.sub.1-C.sub.6 alkyl(aryl);
wherein each alkyl and aryl is optionally substituted with one,
two, or three halogen; and R.sup.16a and R.sup.17a are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, aryl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl is
optionally substituted with one, two, or three halogen. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 is C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl),
C.sub.1-C.sub.6 alkyl(heterocycloalkyl), --S(O).sub.2R.sup.15a,
--S(.dbd.O).sub.2NR.sup.16aR.sup.17a, or --C(.dbd.O)--R.sup.15a;
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optimally substituted with one, two, or
three R.sup.34'; Ma is C.sub.1-C.sub.6 alkyl; and R.sup.16a and
R.sup.17a are each independently hydrogen or C.sub.1-C.sub.6
alkyl.
[1002] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 is cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl),
C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--S(.dbd.O).sub.2R.sup.15a, --S(.dbd.O).sub.2NR.sup.16aR.sup.17a,
or --C(.dbd.O).sub.2R.sup.15a; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30A. In some embodiments
of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 is cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), C.sub.1-C.sub.6
alkyl(heterocycloalkyl), --S(.dbd.O).sub.2R.sup.15A,
--S(.dbd.O).sub.2NR.sup.16aR.sup.17a, or
--C(.dbd.O).sub.2R.sup.15a; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30a; R.sub.15a is
C.sub.1-C.sub.6 alkyl, aryl, or C.sub.1-C.sub.6 alkyl(aryl);
wherein each alkyl and aryl is optionally substituted with one,
two, or three halogen; and R.sup.16a and R.sup.17a are each
independently hydrogen. C.sub.1-C.sub.6 alkyl, aryl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl is
optionally substituted with one, two, or three halogen. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 is cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), C.sub.1-C.sub.6
alkyl(heterocycloalkyl), --S(.dbd.O).sub.2R.sup.15a,
--S(.dbd.O).sub.2NR.sup.16aR.sup.17a, or
--C(.dbd.O).sub.2R.sup.15a; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30a; R.sup.15a is
C.sub.1-C.sub.6 alkyl; and R.sup.16a and R.sup.17a are each
independently hydrogen or C.sub.1-C.sub.6 alkyl.
[1003] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.15a is C.sub.1-C.sub.6 alkyl, aryl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl is
optionally substituted with one, two, or three halogen; and
R.sup.16a and R.sup.17a are each independently hydrogen,
C.sub.1-C.sub.6 alkyl, aryl, or C.sub.1-C.sub.6 alkyl(aryl);
wherein each alkyl and aryl is optionally substituted with one,
two, or three halogen. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.15 is C.sub.1-C.sub.6
alkyl; and R.sup.16a and R.sup.17a are each independently hydrogen
or C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of
Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.15a is
C.sub.1-C.sub.6 alkyl, aryl, or C.sub.1-C.sub.6 alkyl(aryl);
wherein each alkyl and aryl is optionally substituted with one,
two, or three halogen. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.15a is C.sub.1-C.sub.6
alkyl. In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.16a and R.sup.17a are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, aryl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl is
optionally substituted with one, two, or three halogen. In some
embodiments of a compound of Formula (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.16a and R.sup.17a are each independently hydrogen or
C.sub.1-C.sub.6 alkyl.
[1004] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 is C.sub.1-C.sub.6 alkyl, cycloalkyl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.31%. In some embodiments
of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 is C.sub.1-C.sub.6 alkyl, cycloalkyl, or C.sub.1-C.sub.6
alkyl(aryl); wherein each alkyl, cycloalkyl, and aryl is
independently optionally substituted with one, two, or three
R.sup.30a. In some embodiments of a compound of Formula (II),
(IIa), or (IIb), or a pharmaceutically acceptable salt, solvate; or
stereoisomer thereof, R.sup.1 is cycloalkyl or C.sub.1-C.sub.6
alkyl(aryl); wherein each alkyl, cycloalkyl, and aryl is
independently optionally substituted with one, two, or three
R.sup.30a. In some embodiments of a compound of Formula (II),
(IIa), or (IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 is cycloalkyl optionally substituted
with one, two, or three R.sup.30a. In some embodiments of a
compound of Formula (II), (IIa), or (IIb), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R is
C.sub.1-C.sub.6 alkyl(aryl); wherein alkyl and aryl are
independently optionally substituted with one, two, or three
R.sup.30a.
[1005] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, each R.sup.30a is independently halogen,
--CN, --OH. --OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.31. In some embodiments
of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30a is independently halogen, --CN, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl; wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.31; and each R.sup.31 is independently halogen
or C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of
Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.30a is
independently halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6
alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl; wherein each
alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.31; and each R.sup.31 is independently halogen. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30a is independently halogen, --CN, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, --C(O)NR.sup.cR.sup.d,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl; wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.31; and each R.sup.31 is independently
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(II), (ha), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, each R.sup.30a is independently
halogen, --CN, --OH, --OR.sup.a, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl. In some embodiments of a compound of
Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.30a is
independently halogen or C.sub.1-C.sub.6 alkyl. In some embodiments
of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30a is independently halogen.
[1006] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 is cycloalkyl optionally substituted
with one, two, or three R.sup.30a; each R.sup.30a is independently
halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6
alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl; wherein each
alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.31; and each R.sup.31 is independently halogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R is cycloalkyl optionally
substituted with one, two, or three R.sup.30a; and each R.sup.30a
is independently halogen, --CN, --OH, --OR.sup.a, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6 haloalkyl. In some embodiments of a
compound of Formula (II), (IIa), or (IIb), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.1 is
cycloalkyl optionally substituted with one, two, or three
R.sup.30a; and each R.sup.30a is independently halogen.
[1007] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 is C.sub.1-C.sub.6 alkyl(aryl);
wherein alkyl and aryl are independently optionally substituted
with one, two, or three R.sup.30a; each R.sup.30a is independently
halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6
alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl; wherein each
alkyl, cycloalkyl, heterocycloalkaryl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.31; and each R.sup.31 is independently halogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.1 is C.sub.1-C.sub.6
alkyl(aryl); wherein alkyl and aryl are independently optionally
substituted with one, two, or three R.sup.30a; and each R.sup.20a
is independently halogen, --CN, --OH, --OR.sup.a, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6 haloalkyl. In some embodiments of a
compound of Formula (II), (IIa), or (IIb), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof: R.sup.1 is
C.sub.1-C.sub.6 alkyl(aryl); wherein alkyl and aryl are
independently optionally substituted with one, two, or three
R.sup.30a; and each R.sup.30a is independently halogen.
[1008] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.2 is hydrogen or C.sub.1-C.sub.6 alkyl.
In some embodiments of a compound of Formula (II), (IIa), or (IIb),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.2 is hydrogen. In some embodiments of a compound of
Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.2 is C.sub.1-C.sub.6
alkyl.
[1009] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 is cycloalkyl optionally substituted
with one, two, or three R.sup.30a; each R.sup.30a is independently
halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6
alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl; wherein each
alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.31; each R.sup.31 is independently halogen or C.sub.1-C.sub.6
alkyl; and R.sup.2 is hydrogen or C.sub.1-C.sub.6 alkyl. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 is cycloalkyl optionally substituted with one, two, or
three R.sup.30a; each R.sup.30a is independently halogen, --CN,
--OH, --OR.sup.a, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; and R.sup.2 is hydrogen or C.sub.1-C.sub.6 alkyl. In
some embodiments of a compound of Formula (II), (IIa), or (IIb), or
a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.1 is cycloalkyl optionally substituted with one,
two, or three R.sup.30a; each R.sup.30a is independently halogen;
and R.sup.2 is hydrogen or C.sub.1-C.sub.6 alkyl.
[1010] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 is cycloalkyl optionally substituted
with one, two, or three R.sup.30a; each R.sup.30a is independently
halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6
alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl; wherein each
alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.31; each R.sup.31 is independently halogen or C.sub.1-C.sub.6
alkyl; and R.sup.2 is hydrogen. In some embodiments of a compound
of Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.1 is cycloalkyl
optionally substituted with one, two, or three R.sup.30a; each
R.sup.30a is independently halogen, --CN, --OH, --OR.sup.a,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl; and R.sup.1 is
hydrogen. In some embodiments of a compound of Formula (II), (IIa),
or (IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 is cycloalkyl optionally substituted
with one, two, or three R.sup.30a; each R.sup.30a is independently
halogen; and R.sup.2 is hydrogen.
[1011] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 is cycloalkyl optionally substituted
with one, two, or three R.sup.30a; each R.sup.10a is independently
halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6
alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl; wherein each
alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.31; each R.sup.31 is independently halogen or C.sub.1-C.sub.6
alkyl; and R.sup.2 is C.sub.1-C.sub.6 alkyl. In some embodiments of
a compound of Formula (II), (IIa), or (IIb), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.1 is
cycloalkyl optionally substituted with one, two, or three
R.sup.30a; each R.sup.30a is independently halogen, --CN, --OH,
--OR.sup.a, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
and R.sup.2 is C.sub.1-C.sub.6 alkyl. In some embodiments of a
compound of Formula (II), (IIa), or (IIb), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.1 is
cycloalkyl optionally substituted with one, two, or three
R.sup.30a; each R.sup.30a is independently halogen; and R.sup.2 is
C.sub.1-C.sub.6 alkyl.
[1012] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 is C.sub.1-C.sub.6 alkyl(aryl);
wherein alkyl and aryl are independently optionally substituted
with one, two, or three R.sup.30a; each R.sup.30a is independently
halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6
alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl; wherein each
alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.31; each R.sup.31 is independently halogen or C.sub.1-C.sub.6
alkyl; and R.sup.2 is hydrogen or C.sub.1-C.sub.6 alkyl. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 is C.sub.1-C.sub.6 alkyl(aryl); wherein alkyl and aryl are
independently optionally substituted with one, two, or three
R.sup.30a; each R.sup.30a is independently halogen, --CN, --OH,
--OR.sup.a, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
and R.sup.2 is hydrogen or C.sub.1-C.sub.6 alkyl. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 is C.sub.1-C.sub.6 alkyl(aryl); wherein alkyl and aryl are
independently optionally substituted with one, two, or three
R.sup.30a; each R.sup.30a is independently halogen; and R.sup.2 is
hydrogen or C.sub.1-C.sub.6 alkyl.
[1013] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 is C.sub.1-C.sub.6 alkyl(aryl);
wherein alkyl and aryl are independently optionally substituted
with one, two, or three R.sup.30a; each R.sup.30a is independently
halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)OR.sup.b, --C(O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.31; each
R.sup.31 is independently halogen or C.sub.1-C.sub.6 alkyl; and
R.sup.2 is hydrogen. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.1 is C.sub.1-C.sub.6
alkyl(aryl); wherein alkyl and aryl are independently optionally
substituted with one, two, or three R.sup.30a; each R.sup.30a is
independently halogen, --CN, --OH, --OR.sup.a, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6 haloalkyl; and R.sup.2 is hydrogen. In
some embodiments of a compound of Formula (II), (IIa), or (IIb), or
a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.1 is C.sub.1-C.sub.6 alkyl(aryl); wherein alkyl and
aryl are independently optionally substituted with one, two, or
three R.sup.30a; each R.sup.30a is independently halogen; and
R.sup.2 is hydrogen.
[1014] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 is C.sub.1-C.sub.6 alkyl(aryl);
wherein alkyl and aryl are independently optionally substituted
with one, two, or three R.sup.30a; each R.sup.30a is independently
halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6
alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl; wherein each
alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.31; each R.sup.31 is independently halogen or C.sub.1-C.sub.6
alkyl; and R.sup.2 is C.sub.1-C.sub.6 alkyl. In some embodiments of
a compound of Formula (II), (IIa), or (IIb), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.1 is
C.sub.1-C.sub.6 alkyl(aryl); wherein alkyl and aryl are
independently optionally substituted with one, two, or three
R.sup.30a; each R.sup.30a is independently halogen, --CN, --OH,
--OR.sup.a, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
and R.sup.2 is C.sub.1-C.sub.6 alkyl. In some embodiments of a
compound of Formula (II), (IIa), or (IIb), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.1 is
C.sub.1-C.sub.6 alkyl(aryl); wherein alkyl and aryl are
independently optionally substituted with one, two, or three
R.sup.30a; each R.sup.30a is independently halogen; and R.sup.2 is
C.sub.1-C.sub.6 alkyl.
[1015] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 and R.sup.2 are taken together with
the nitrogen atom to which they are attached to form a
heterocycloalkyl optionally substituted with one, two, or three
R.sup.30b. In some embodiments of a compound of Formula (II),
(IIa), or (IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 and R.sup.2 are taken together with
the nitrogen atom to which they are attached to form a
heterocycloalkyl optionally substituted with one, two, or three
R.sup.30b; each R.sup.30b is independently aryl optionally
substituted with one, two, or three R.sup.31; and each R.sup.31 is
independently halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl. In some embodiments of a compound of Formula (II),
(IIa), or (IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 and R.sup.2 are taken together with
the nitrogen atom to which they are attached to form a
heterocycloalkyl optionally substituted with one, two, or three
R.sup.30b; and R.sup.30b is aryl. In some embodiments of a compound
of Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.1 and R.sup.2 are
taken together with the nitrogen atom to which they are attached to
form a heterocycloalkyl optionally substituted with one R.sup.30b;
and R.sup.30 is aryl.
[1016] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 and R.sup.2 are taken together with
the nitrogen atom to which they are attached to form a piperidine
or a pyrrolidine optionally substituted with one, two, or three
R.sup.30b. In some embodiments of a compound of Formula (II),
(IIa), or (IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 and R.sup.2 are taken together with
the nitrogen atom to which they are attached to form a piperidine
or a pyrrolidine optionally substituted with one, two, or three
R.sup.30b; each R.sup.30b is independently aryl optionally
substituted with one, two, or three R.sup.31; and each R.sup.31 is
independently halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl. In some embodiments of a compound of Formula (II),
(IIa), or (IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 and R.sup.2 are taken together with
the nitrogen atom to which they are attached to form a piperidine
or a pyrrolidine optionally substituted with one, two, or three
R.sup.30b; and R.sup.30b is aryl. In some embodiments of a compound
of Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.1 and R.sup.2 are
taken together with the nitrogen atom to which they are attached to
form a piperidine or a pyrrolidine optionally substituted with one
R.sup.30b; and R.sup.30b is aryl.
[1017] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 and R.sup.2 are taken together with
the nitrogen atom to which they are attached to form a piperidine
optionally substituted with one, two, or three R.sup.30b. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate or stereoisomer thereof,
R.sup.1 and R.sup.2 are taken together with the nitrogen atom to
which they are attached to form a piperidine optionally substituted
with one, two, or three R.sup.30b; each R.sup.30b is independently
aryl optionally substituted with one, two, or three R.sup.31; and
each R.sup.31 is independently halogen, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl. In some embodiments of a compound of
Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.1 and R.sup.2 are
taken together with the nitrogen atom to which they are attached to
form a piperidine optionally substituted with one, two, or three
R.sup.30b; and R.sup.30b is aryl. In some embodiments of a compound
of Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.1 and R.sup.2 are
taken together with the nitrogen atom to which they are attached to
form a piperidine optionally substituted with one R.sup.30b; and
R.sup.30b is aryl.
[1018] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 and R.sup.2 are taken together with
the nitrogen atom to which they are attached to form a pyrrolidine
optionally substituted with one, two, or three R.sup.30b. In some
embodiments of a compound of Formula (II). (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate or stereoisomer thereof,
R.sup.1 and R.sup.2 are taken together with the nitrogen atom to
which they are attached to form a pyrrolidine optionally
substituted with one, two, or three R.sup.30b; each R.sup.30b is
independently aryl optionally substituted with one, two, or three
R.sup.31; and each R.sup.31 is independently halogen,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 and R.sup.2 are taken together with the nitrogen atom to
which they are attached to form a pyrrolidine optionally
substituted with one, two, or three R.sup.30b; and R.sup.30b is
aryl. In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.1 and R.sup.2 are taken together with
the nitrogen atom to which they are attached to form a pyrrolidine
optionally substituted with one R.sup.30b; and R.sup.30b is
aryl.
[1019] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, Z is --OR.sup.60.
[1020] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.60 is hydrogen. --C(.dbd.O)R.sup.15e,
--C(.dbd.O)OR.sup.16e, --C(.dbd.O)NR.sup.16eR.sup.17e.
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optimally substituted with one, two, or three R.sup.30m. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.60 is --C(.dbd.O)R.sup.15e, --C(.dbd.O)OR.sup.16e,
--C(.dbd.O)NR.sup.16eR.sup.17e, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein
each alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.30m. In some embodiments of a compound of Formula (II),
(IIa), or (IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.60 is C.sub.1-C.sub.6 alkyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6
alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30m.
[1021] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.60 is C.sub.1-C.sub.6 alkyl,
cycloalkyl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30m. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.60 is C.sub.1-C.sub.6 alkyl, cycloalkyl, or C.sub.1-C.sub.6
alkyl(aryl); wherein each alkyl, cycloalkyl, and aryl is
independently optionally substituted with one, two, or three
R.sup.30m. In some embodiments of a compound of Formula (II),
(IIa), or (IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.60 is cycloalkyl or C.sub.1-C.sub.6
alkyl(aryl); wherein each alkyl, cycloalkyl, and aryl is
independently optionally substituted with one, two, or three
R.sup.30m. In some embodiments of a compound of Formula (II),
(IIa), or (IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.60 is cycloalkyl optionally substituted
with one, two, or three R.sup.30m. In some embodiments of a
compound of Formula (II), (IIa), or (IIb), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.60 is
C.sub.1-C.sub.6 alkyl(aryl); wherein alkyl and aryl are
independently optionally substituted with one, two, or three
R.sup.30m.
[1022] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.15e is C.sub.1-C.sub.6 alkyl, aryl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl is
optionally substituted with one, two, or three halogen; and
R.sup.16e and R.sup.17e are each independently hydrogen,
C.sub.1-C.sub.6 alkyl, aryl, or C.sub.1-C.sub.6 alkyl(aryl);
wherein each alkyl and aryl is optionally substituted with one,
two, or three halogen. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.15e is C.sub.1-C.sub.6
alkyl; and R.sup.16e and R.sup.17e are each independently hydrogen
or C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of
Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.15e is
C.sub.1-C.sub.6 alkyl, aryl, or C.sub.1-C.sub.6 alkyl(aryl);
wherein each alkyl and aryl is optionally substituted with one,
two, or three halogen. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.15e is C.sub.1-C.sub.6
alkyl. In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.16e and R.sup.17c are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, aryl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl is
optionally substituted with one, two, or three halogen. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.16e and R.sup.17e are each independently hydrogen or
C.sub.1-C.sub.6 alkyl.
[1023] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, each R.sup.30m is independently halogen,
--CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.31. In some embodiments
of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30m is independently halogen, --CN, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl; wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.31; and each R.sup.31 is independently halogen
or C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of
Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.30m is
independently halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6
alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl; wherein each
alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.31; and each R.sup.31 is independently halogen. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30m is independently halogen, --CN, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, --C(O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
C.sub.1-C.sub.6alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl; wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.31; and each R.sup.31 is independently
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, each R.sup.30m is independently
halogen, --CN, --OH, --OR.sup.a, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl. In some embodiments of a compound of
Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.30m is
independently halogen or C.sub.1-C.sub.6 alkyl. In some embodiments
of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30m is independently halogen.
[1024] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, Z is --SR.sup.61.
[1025] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.61 is hydrogen, --C(.dbd.O)R.sup.15f,
--C(.dbd.O)OR.sup.16f, --C(.dbd.O)NR.sup.16fR.sup.17f,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30n. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.61 is --C(.dbd.O)R.sup.15f, --C(.dbd.O)OR.sup.16f,
--C(.dbd.O)NR.sup.16fR.sup.17f, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30a. In some embodiments of a compound of Formula
(II). (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.61 is C.sub.1-C.sub.6
alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30n. In some embodiments
of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.61 is C.sub.1-C.sub.6 alkyl, cycloalkyl, C.sub.1-C.sub.6
alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30n. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.61 is C.sub.1-C.sub.6
alkyl, cycloalkyl, or C.sub.1-C.sub.6 alkyl(aryl); wherein each
alkyl, cycloalkyl, and aryl is independently optionally substituted
with one, two, or three R.sup.30n. In some embodiments of a
compound of Formula (II), (IIa), or (IIb), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.61 is
cycloalkyl or C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl,
cycloalkyl, and aryl is independently optimally substituted with
one, two, or three R.sup.30n. In some embodiments of a compound of
Formula (II), (IIa), or (Lib), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.61 is cycloalkyl
optionally substituted with one, two, or three R.sup.30n. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.61 is C.sub.1-C.sub.6 alkyl(aryl); wherein alkyl and aryl are
independently optionally substituted with one, two, or three
R.sup.30n.
[1026] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.15f is C.sub.1-C.sub.6 alkyl, aryl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl is
optionally substituted with one, two, or three halogen; and
R.sup.16f and R.sup.17f are each independently hydrogen,
C.sub.1-C.sub.6 alkyl, aryl, or C.sub.1-C.sub.6 alkyl(aryl);
wherein each alkyl and aryl is optionally substituted with one,
two, or three halogen. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, Rim is C.sub.1-C.sub.6 alkyl; and
R.sup.16f, and R.sup.17f are each independently hydrogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.15f is C.sub.1-C.sub.6
alkyl, aryl, or C.sub.1-C.sub.4 alkyl(aryl); wherein each alkyl and
aryl is optionally substituted with one, two, or three halogen. In
some embodiments of a compound of Formula (II), (IIa), or (IIb), or
a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.15f is C.sub.1-C.sub.6 alkyl. In some embodiments of
a compound of Formula (II), (IIa), or (IIb), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.16f and
R.sup.17f are each independently hydrogen, C.sub.1-C.sub.6 alkyl,
aryl, or C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl
is optionally substituted with one, two, or three halogen. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.16f and R.sup.17f are each independently hydrogen or
C.sub.1-C.sub.6 alkyl.
[1027] In some embodiments of a compound of Formula (II), (IIa), or
(Lib), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, each R.sup.30n is independently halogen,
--CN, --OH. --OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.31. In some embodiments
of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30n is independently halogen, --CN, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl; wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.31; and each R.sup.31 is independently halogen
or C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of
Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.30n is
independently halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.b, --C(O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.31; and each
R.sup.31 is independently halogen. In some embodiments of a
compound of Formula (II), (IIa), or (IIb), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each R.sup.30n
is independently halogen, --CN, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, C.sub.1-C.sub.6 alkyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.31; and each
R.sup.31 is independently C.sub.1-C.sub.6 alkyl. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30n is independently halogen, --CN, --OH, --OR.sup.a,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30n is independently halogen or C.sub.1-C.sub.6 alkyl.
In some embodiments of a compound of Formula (II), (IIa), or (IIb),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, each R.sup.30n is independently halogen.
[1028] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, Z is --CR.sup.62R.sup.63R.sup.64.
[1029] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.62 is hydrogen, halogen, --CN, --OH,
--OR.sup.15g, --NR.sup.16gR.sup.17g, --C(.dbd.O)OR.sup.16g,
--C(.dbd.O)NR.sup.16gR.sup.17g, or C.sub.1-C.sub.6 alkyl optionally
substituted with one, two, or three R.sup.30o. In some embodiments
of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.61 is hydrogen, halogen, --CN, --OH, --OR.sup.15g,
--NR.sup.16gR.sup.17g, --C(.dbd.O)OR.sup.16g,
--C(.dbd.O)NR.sup.16gR.sup.17g, or C.sub.1-C.sub.6 alkyl optionally
substituted with one, two, or three R.sup.30o; R.sup.15g is
C.sub.1-C.sub.6 alkyl; and R.sup.15g and R.sup.17g are each
independently hydrogen or C.sub.1-C.sub.6 alkyl. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, sol vale, or stereoisomer
thereof, R.sup.62 is hydrogen, halogen, or --OH. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.62 is hydrogen or halogen. In some embodiments of a compound
of Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.62 is hydrogen.
[1030] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.63 is hydrogen, halogen, --CN, --OH,
--OR.sup.15g, --NR.sup.16gR.sup.17g, --C(O)OR.sup.16g,
--C(.dbd.O)NR.sup.16gR.sup.17g, or C.sub.1-C.sub.6 alkyl optionally
substituted with one, two, or three R.sup.30o. In some embodiments
of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.63 is hydrogen, halogen, --CN, --OH, --OR.sup.15g,
--NR.sup.16gR.sup.17g, --C(.dbd.O)OR.sup.16g,
--C(.dbd.O)NR.sup.16gR.sup.17g, or C.sub.1-C.sub.6 alkyl optionally
substituted with one, two, or three R.sup.30o; R.sup.15g is
C.sub.1-C.sub.6 alkyl; and R.sup.16g and R.sup.17g are each
independently hydrogen or C.sub.1-C.sub.6 alkyl. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.63 is hydrogen, halogen, or --OH. In some embodiments of a
compound of Formula (II), (IIa), or (IIb), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof: R.sup.63 is
hydrogen or halogen. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.63 is hydrogen.
[1031] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.64 is --OR.sup.15g, --SR.sup.15g,
--S(.dbd.O)R.sup.15g, --NR.sup.16gR.sup.17g,
--S(.dbd.O).sub.2R.sup.15g, --NHS(.dbd.O).sub.2R.sup.15g,
--S(.dbd.O).sub.2NR.sup.16gR.sup.17g, --C(.dbd.O)R.sup.15g,
--C(.dbd.O)OR.sup.16g, --C(.dbd.O)NR.sup.16gR.sup.17g, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30o. In some embodiments
of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.64 is --OR.sup.15g, --SR.sup.15g, --S(.dbd.O)R.sup.15g,
--NR.sup.16gR.sup.17g, --S(.dbd.O).sub.2R.sup.15g,
--NHS(.dbd.O).sub.2R.sup.15g, --S(.dbd.O).sub.2NR.sup.16gR.sup.17g,
--C(.dbd.O)R.sup.15g, --C(O)OR.sup.16g,
--C(.dbd.O)NR.sup.16gR.sup.17g, cycloalkyl, heterocycloalkyl, aryl,
or heteroaryl; wherein each cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optimally substituted with one, two, or
three R.sup.30o. In some embodiments of a compound of Formula (II),
(IIa), or (IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.64 is --OR.sup.15g,
--NR.sup.16gR.sup.17g, --C(.dbd.O)R.sup.15g, --C(.dbd.O)OR.sup.16g,
--C(.dbd.O)NR.sup.16gR.sup.17g, cycloalkyl, heterocycloalkyl, aryl,
or heteroaryl; wherein each cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30o. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.64 is --OR.sup.15g,
--NR.sup.16gR.sup.17g, cycloalkyl, heterocycloalkyl, aryl, or
heteroaryl; wherein each cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.31o. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.64 is --OR.sup.15g or
--NR.sup.16gR.sup.17g. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.64 is cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30o. In some embodiments
of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.64 is cycloalkyl or heterocycloalkyl; wherein each cycloalkyl
and heterocycloalkyl is independently optionally substituted with
one, two, or three R.sup.30o. In some embodiments of a compound of
Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.64 is aryl, or
heteroaryl; wherein each aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30o.
[1032] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.15g is C.sub.1-C.sub.6 alkyl, aryl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl is
optionally substituted with one, two, or three halogen; and
R.sup.16g and R.sup.17g are each independently hydrogen,
C.sub.1-C.sub.6 alkyl, aryl, or C.sub.1-C.sub.6 alkyl(aryl);
wherein each alkyl and aryl is optionally substituted with one,
two, or three halogen. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.15g is C.sub.1-C.sub.6
alkyl; and R.sup.16g and R.sup.17g are each independently hydrogen
or C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of
Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.15g is
C.sub.1-C.sub.6 alkyl, aryl, or C.sub.1-C.sub.6 alkyl(aryl);
wherein each alkyl and aryl is optionally substituted with one,
two, or three halogen. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.15g is C.sub.1-C.sub.6
alkyl. In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.16g and R.sup.17g are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, aryl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl is
optionally substituted with one, two, or three halogen. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.16g and R.sup.17g are each independently hydrogen or
C.sub.1-C.sub.6 alkyl.
[1033] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, each R.sup.30o is independently halogen,
--CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.31. In some embodiments
of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30o is independently halogen, --CN, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl; wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.31; and each R.sup.31 is independently halogen
or C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of
Formula (II). (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.30o is
independently halogen, --CN, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.b, --C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6
alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl; wherein each
alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.31; and each R.sup.31 is independently halogen. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30o is independently halogen, --CN, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl; wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.31; and each R.sup.31 is independently
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, each R.sup.30o is independently
halogen, --CN, --OH, --OR.sup.a, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl. In some embodiments of a compound of
Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.30o is
independently halogen or C.sub.1-C.sub.6 alkyl. In some embodiments
of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30o is independently halogen.
[1034] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.3 is halogen, --CN, --SR.sup.18b,
--NR.sup.16bR.sup.17b, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30c. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.3 is halogen, --CN,
--SR.sup.18b, C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30c. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.3 is halogen. --CN. --SR.sup.18b, C.sub.1-C.sub.6 alkyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6
alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30c; and each R.sup.30c is independently halogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.3 is halogen, --CN,
--SR.sup.18b, C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30c; and each
R.sup.30c is independently halogen. In some embodiments of a
compound of Formula (II), (IIa), or (IIb), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.3 is
halogen, --CN, --SR.sup.18b, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30c; and each R.sup.30c is independently
C.sub.1-C.sub.6 alkyl.
[1035] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.3 is halogen, --CN, --SR.sup.18b,
--NR.sup.16bR.sup.17b, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30c. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.3 is halogen, --CN,
--SR.sup.18b, C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30c. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.3 is halogen, --CN, --SR.sup.18b, C.sub.1-C.sub.6 alkyl,
cycloalkyl, heterocycloalkyl, heteroaryl, C.sub.1-C.sub.6
alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30c; and each R.sup.30c is independently halogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.3 is halogen, --CN,
--SR.sup.18b, C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30c; and each
R.sup.30c is independently halogen. In some embodiments of a
compound of Formula (II), (IIa), or (IIb), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.3 is
halogen, --CN, --SR.sup.18b, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30c; and each R.sup.30c is independently
C.sub.1-C.sub.6 alkyl.
[1036] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.3 is halogen, --CN, --SR.sup.18b,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30c; and R.sup.18b is cycloalkyl or C.sub.1-C.sub.6
alkyl(cycloalkyl). In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.3 is halogen, --CN,
--SR.sup.18b, C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30c; R.sup.18b
is cycloalkyl or C.sub.1-C.sub.6 alkyl(cycloalkyl); and each
R.sup.30c is independently halogen or C.sub.1-C.sub.6 alkyl. In
some embodiments of a compound of Formula (II), (IIa), or (IIb), or
a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.3 is halogen, --CN, --SR.sup.18b, C.sub.1-C.sub.6
alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30c; R.sup.18b is
cycloalkyl or C.sub.1-C.sub.6 alkyl(cycloalkyl); and each R.sup.30c
is independently halogen. In some embodiments of a compound of
Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.3 is halogen, --CN,
--SR.sup.18b, C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30c; R.sup.18b
is cycloalkyl or C.sub.1-C.sub.6 alkyl(cycloalkyl); and each
R.sup.30c is independently C.sub.1-C.sub.6 alkyl.
[1037] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.3 is halogen, --CN, --SR.sup.18b,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 alkyl(cycloalkyl);
wherein each alkyl, and cycloalkyl is independently optionally
substituted with one, two, or three R.sup.30c. In some embodiments
of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 is halogen, --CN. --SR.sup.18b, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 alkyl(cycloalkyl); wherein each alkyl, and
cycloalkyl is independently optionally substituted with one, two,
or three R.sup.30c; and each R.sup.30c is independently halogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.3 is halogen, --CN,
--SR.sup.18b, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
alkyl(cycloalkyl); wherein each alkyl, and cycloalkyl is
independently optionally substituted with one, two, or three
R.sup.30c; and each R.sup.30c is independently halogen. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.3 is halogen, --CN, --SR.sup.18b, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 alkyl(cycloalkyl); wherein each alkyl, and
cycloalkyl is independently optionally substituted with one, two,
or three R.sup.30c; and each R.sup.30c is independently
C.sub.1-C.sub.6 alkyl.
[1038] In some embodiments of a compound of Formula (II), (IIa), or
Mb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.3 is halogen, --CN, --SR.sup.18b,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 alkyl(cycloalkyl);
wherein each alkyl, and cycloalkyl is independently optionally
substituted with one, two, or three R.sup.30c; and R.sup.18b is
cycloalkyl or C.sub.1-C.sub.6 alkyl(cycloalkyl). In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.3 is halogen, --CN, --SR.sup.18b, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 alkyl(cycloalkyl); wherein each alkyl, and
cycloalkyl is independently optionally substituted with one, two,
or three R.sup.30c; R.sup.18b is cycloalkyl or C.sub.1-C.sub.6
alkyl(cycloalkyl); and each R.sup.30c is independently halogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(II), (IIa), or (IIb), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.3 is halogen, --CN,
--SR.sup.18b, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
alkyl(cycloalkyl); wherein each alkyl, and cycloalkyl is
independently optionally substituted with one, two, or three
R.sup.30c; R.sup.18b is cycloalkyl or C.sub.1-C.sub.6
alkyl(cycloalkyl); and each R.sup.30c is independently halogen. In
some embodiments of a compound of Formula (II), (IIa), or (IIb), or
a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.1 is halogen, --CN, --SR.sup.18b, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6 alkyl(cycloalkyl); wherein each alkyl,
and cycloalkyl is independently optionally substituted with one,
two, or three R.sup.30c; R.sup.18b is cycloalkyl or C.sub.1-C.sub.6
alkyl(cycloalkyl); and each R.sup.30c is independently
C.sub.1-C.sub.6 alkyl.
[1039] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.3 is halogen. In some embodiments of a
compound of Formula (II), (IIa), or (IIb), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.3 is
--NH.sub.2.
[1040] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.21 and R.sup.22 are each independently
hydrogen, aryl, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25.
[1041] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.21 and R.sup.22 are each hydrogen.
[1042] In some embodiments of a compound of Formula (II), (IIa), or
(IIb), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.21 and R.sup.22 are each
--(CR.sup.23R.sup.14).sub.wOC(.dbd.O)OR.sup.25. In some embodiments
of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.21 and R.sup.22 are each
--(CR.sup.23R.sup.24)OC(.dbd.O)OR.sup.25; w is 1 or 2; each
R.sup.23 and R.sup.24 are independently hydrogen, halogen, or
C.sub.1-C.sub.6 alkyl; and each R.sup.23 is independently hydrogen
or C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of
Formula (II), (IIa), or (IIb), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.21 and R.sup.22 are
each --(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25; w is 1:
R.sup.23 and R.sup.24 are hydrogen; and each R.sup.25 is
independently hydrogen or C.sub.1-C.sub.6 alkyl. In some
embodiments of a compound of Formula (II), (IIa), or (IIb), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.21 and R.sup.22 are each
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25; w is 1; R.sup.23
and R.sup.24 are hydrogen; and each R.sup.25 is C.sub.1-C.sub.6
alkyl.
[1043] In some embodiments of a compound of Formula (II) or (IIa),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.21 and R.sup.22 are taken together with the atoms to
which they are attached to form a heterocycloalkyl optionally
substituted with one, two, or three R.sup.30l. In some embodiments
of a compound of Formula (II) or (IIa), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof: R.sup.21 and
R.sup.22 are taken together with the atoms to which they are
attached to form a heterocycloalkyl optionally substituted with
one, two, or three R.sup.30l; and each R.sup.30l is independently
halogen or C.sub.1-C.sub.6 alkyl. In some embodiments of a compound
of Formula (II) or (IIa), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.21 and R.sup.22 are taken
together with the atoms to which they are attached to form a
heterocycloalkyl optionally substituted with one, two, or three
R.sup.30l; and each R.sup.30l is independently halogen.
[1044] In some embodiments provided herein is a compound having the
structure of Formula (III), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof:
##STR00007##
wherein; [1045] Q.sup.3 and Q.sup.4 are independently N or
CW.sup.1; provided that at least one of Q.sup.3 or Q.sup.4 is N;
[1046] W.sup.1 is hydrogen, halogen, --CN, --OH, --OR.sup.a,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl; [1047] A is
--O-- or --CH.sub.2--; [1048] Z is --NR.sup.1R.sup.2, --OR.sup.60,
--SR.sup.61, or --CR.sup.62R.sup.63R.sup.64; [1049] R.sup.1 and
R.sup.2 are each independently hydrogen, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--S(.dbd.O).sub.2R.sup.15a, --S(C)).sub.2NR.sup.16aR.sup.17a, or
--C(.dbd.O).sub.2R.sup.15a; wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30a; [1050] or
R.sup.1 and R.sup.2 are taken together with the nitrogen atom to
which they are attached to form a heterocycloalkyl optionally
substituted with one, two, or three R.sup.30b; [1051] R.sup.60 is
hydrogen, --C(.dbd.O)R.sup.15e, --C(.dbd.O)OR.sup.16e,
--C(.dbd.O)NR.sup.16eR.sup.17e, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.30m; [1052] R.sup.61 is hydrogen.
--C(.dbd.O)R.sup.15f, --C(.dbd.O)OR.sup.16f,
--C(.dbd.O)NR.sup.16fR.sup.17f, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.30n; [1053] R.sup.62, R.sup.63, and R.sup.64
are each independently hydrogen, halogen, --CN, --OH, --OR.sup.15g,
--SH, --SR.sup.15g, --S(.dbd.O)R.sup.15g, --NO.sub.2,
--NR.sup.16gR.sup.17g, --S(.dbd.O)R.sup.15g,
--NHS(.dbd.O).sub.2R.sup.15g, --S(O).sub.2NR.sup.16gR.sup.17g,
--C(.dbd.O)R.sup.15g, --OC(O)R.sup.15g, --C(.dbd.O)OR.sup.16g,
--OC(.dbd.O)OR.sup.16g, --C(O)NR.sup.16gR.sup.17g,
--OC(.dbd.O)NR.sup.16gR.sup.17g,
--NR.sup.16gC(.dbd.O)NR.sup.16gR.sup.17g,
--NR.sup.16gC(.dbd.O)R.sup.15g, --NR.sup.16gC(.dbd.O)OR.sup.16g,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6alkenyl, C.sub.2-C.sub.6
alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30o; [1054]
R.sup.3 is halogen, --CN, --OH, --OR.sup.15b, --SR.sup.18b,
--NR.sup.16bR.sup.17b, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30o; [1055] R.sup.4 and R.sup.7 are each
independently hydrogen, halogen, --OH, --OR.sup.15c,
--NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.15c, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.30d; [1056] R.sup.5 and R.sup.6 are each independently
hydrogen, halogen, --OH, --OR.sup.15d,
--NR.sup.16dS(.dbd.O).sub.2R.sup.15d, --NR.sup.16dC(O)R.sup.15d,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.30e; [1057] R.sup.8 is hydrogen, halogen, --OH,
--OR.sup.a, --NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl; [1058] R.sup.9 and R.sup.10 are each
independently hydrogen, halogen, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl; [1059] X.sup.1 is bond, --C(.dbd.O)--,
--S(.dbd.O).sub.2--, --O--, or --CR.sup.30R.sup.41--; [1060]
Y.sup.1 is --C(.dbd.O)--, --(CR.sup.42R.sup.43).sub.v1--,
--S(.dbd.O).sub.2--, --NR.sup.44--, --S--, or --O--; [1061] Y.sup.2
is --(CR.sup.45R.sup.46).sub.v2--, --NR.sup.47--, or --O--; [1062]
R.sup.40, R.sup.41, R.sup.42, R.sup.43, R.sup.45, and R.sup.46 are
each independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, cycloalkyl, or heterocycloalkyl; wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, and heterocycloalkyl is
independently optionally substituted with one, two, or three
R.sup.30p; [1063] R.sup.44 and R.sup.47 are each independently
hydrogen, --S(.dbd.O)R.sup.a, --S(.dbd.O).sub.2R.sup.a,
--S(.dbd.O).sub.2NR.sup.cR.sup.d, --C(.dbd.O)R.sup.a,
--C(.dbd.O)OR.sup.b, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, or heterocycloalkyl;
wherein each alkyl, alkenyl, alkynyl, cycloalkyl, and
heterocycloalkyl is independently optionally substituted with one,
two, or three R.sup.30f; [1064] v1 and v2 are each independently
1-3; [1065] R.sup.15a, R.sup.15b, R.sup.15c, R.sup.15d, R.sup.15e,
R.sup.15f, R.sup.15g are each independently C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.30g; [1066] R.sup.16a, R.sup.16b, R.sup.16c, R.sup.16d,
R.sup.16e, R.sup.16f, R.sup.16g and R.sup.17a, R.sup.17b,
R.sup.17e, R.sup.17f, and R.sup.17g are each independently
hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, cycloalkyl, or heterocycloalkyl; wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, and heterocycloalkyl is
independently optionally substituted with one, two, or three
R.sup.30h; [1067] or R.sup.16a and R.sup.17a or R.sup.1b6 and
R.sup.17b or R.sup.16e and R.sup.17e or R.sup.16f and R.sup.17f or
R.sup.16g and R.sup.17g are taken together with the nitrogen atom
to which they are attached to form a heterocycloalkyl optionally
substituted with one, two, or three halogen, C.sub.1-C.sub.6 alkyl,
or C.sub.1-C.sub.6haloalkyl; [1068] R.sup.18b is C.sub.1-C.sub.6
alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6
alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl,
aryl, and heteroaryl is independently optionally substituted with
one, two, or three R.sup.30i; [1069] R.sup.21 and R.sup.22 are each
independently hydrogen, C.sub.1-C.sub.20alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--(CR.sup.23R.sup.24).sub.wC(.dbd.O)OR.sup.25,
--(CR.sup.23R.sup.24).sub.wCO(.dbd.O)R.sup.26,
--(CR.sup.23R.sup.24).sub.wSC(.dbd.O)R.sup.26, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30k; [1070] or
R.sup.21 and R.sup.22 are taken together with the atoms to which
they are attached to form a heterocycloalkyl optionally substituted
with one, two, or three R.sup.30l; [1071] each R.sup.23 and
R.sup.24 are independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; [1072] each R.sup.25 is independently hydrogen,
C.sub.1-C.sub.6alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [1073] each R.sup.26 is
independently C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [1074]
each w is independently 1-4; [1075] each R.sup.30a, R.sup.30b,
R.sup.30c, R.sup.30d, R.sup.30e, R.sup.30f, R.sup.30g, R.sup.30h,
R.sup.30i, R.sup.30j, R.sup.30k, R.sup.30l, R.sup.30m, R.sup.30n,
R.sup.30o, and R.sup.30p are independently halogen, --CN, --OH,
--OR.sup.a, --SH, --SR.sup.a, --S(.dbd.O)R.sup.a, --NO.sub.2,
--NR.sup.cR.sup.d, --S(.dbd.O).sub.2R.sup.a,
--NHS(.dbd.O).sub.2R.sup.a, --S(.dbd.O).sub.2NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --OC(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--OC(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
--OC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(O)NR.sup.cR.sup.d,
--NR.sup.bC(.dbd.O)R.sup.a, --NR.sup.bC(.dbd.O)OR.sup.6,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl and heteroaryl is independently
optionally substituted with one, two, or three R.sup.31; [1076]
each R.sup.31 is independently halogen, --CN, --OH, --OR.sup.a,
--SH, --SR.sup.a, --S(.dbd.O)R.sup.a, --NO.sub.2,
--NR.sup.cR.sup.d, --S(.dbd.O).sub.2R.sup.a,
--NHS(.dbd.O).sub.2R.sup.a, --S(.dbd.O).sub.2NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --OC(O)R.sup.a, --C(.dbd.O)OR.sup.b,
--OC(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
--OC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(.dbd.O)NR.sup.cR.sup.d,
--NR.sup.bC(.dbd.O)R.sup.a, --NR.sup.bC(O)OR.sup.b, C.sub.1-C.sub.6
alkyl, C.sub.1-C.sub.6haloalkyl, C.sub.1-C.sub.6 hydroxyalkyl,
C.sub.1-C.sub.6 heteroalkyl, or cycloalkyl optionally substituted
with one, two, or three halogen, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6haloalkyl; [1077] each R.sup.a is independently
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, C.sub.1-C.sub.6 heteroalkyl, cycloalkyl, heterocycloalkyl,
aryl, or heteroaryl; wherein the alkyl, alkenyl, alkynyl,
heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
halogen, --OH, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[1078] each R.sup.b is independently hydrogen, C.sub.1-C.sub.6
alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl,
C.sub.1-C.sub.6 heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, or
heteroaryl; wherein the alkyl, alkenyl, alkynyl, heteroalkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three halogen, --OH,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl; and [1079]
R.sup.c and R.sup.d are each independently hydrogen,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, C.sub.1-C.sub.6 heteroalkyl, cycloalkyl, heterocycloalkyl,
aryl, or heteroaryl; wherein the alkyl, alkenyl, alkynyl,
heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
halogen, --OH, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[1080] or R.sup.c and R.sup.d are taken together with the nitrogen
atom to which they are attached to form a heterocycloalkyl
optionally substituted with one, two, or three halogen,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl.
[1081] In some embodiments provided herein is a compound having the
structure of Formula (IV), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof:
##STR00008##
wherein; [1082] Q.sup.1 and Q.sup.2 are independently N or CW;
[1083] Q.sup.3 and Q.sup.4 are independently N or CW.sup.1;
provided that at least one of Q.sup.3 or Q.sup.4 is N; [1084] each
W is independently hydrogen, halogen, --CN, --OH, --OR.sup.a, --SH,
--SR.sup.a, --S(.dbd.O)R.sup.a, --NO.sub.2. --NR.sup.cR.sup.d,
--S(.dbd.O).sub.2R.sup.a, --NHS(.dbd.O).sub.2R.sup.a,
--S(.dbd.O).sub.2NR.sup.cR.sup.d, --C(.dbd.O)R.sup.a,
--OC(O)R.sup.a, --C(.dbd.O)OR.sup.b, --OC(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, --OC(.dbd.O)NR.sup.cR.sup.d,
--NR.sup.bC(O)NR.sup.cR.sup.d, --NR.sup.bC(.dbd.O)R.sup.a,
--NR.sup.bC(.dbd.O)OR.sup.b, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30; [1085] W.sup.1 is hydrogen, halogen, --CN, --OH,
--OR.sup.a, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[1086] A is --O-- or --CH.sub.2--; [1087] Z is --NR.sup.1R.sup.2,
--OR.sup.60, --SR.sup.61, or --CR.sup.62R.sup.63R.sup.64; [1088]
R.sup.1 and R.sup.2 are each independently hydrogen,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), C.sub.1-C.sub.6
alkyl(heterocycloalkyl), --S(.dbd.O).sub.2R.sup.15a,
--S(.dbd.O).sub.2NR.sup.16aR.sup.17a, or
--C(.dbd.O).sub.2R.sup.15a; wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30a; [1089] or
R.sup.1 and R.sup.2 are taken together with the nitrogen atom to
which they are attached to form a heterocycloalkyl optionally
substituted with one, two, or three R.sup.30b; [1090] R.sup.60 is
hydrogen, --C(.dbd.O)R.sup.15e, --C(.dbd.O)OR.sup.16e,
--C(.dbd.O)NR.sup.16eR.sup.17e, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.30m; [1091] R.sup.61 is hydrogen,
--C(.dbd.O)R.sup.15f, --C(.dbd.O)OR.sup.16f,
--C(.dbd.O)NR.sup.16fR.sup.17f, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.30n; [1092] R.sup.62, R.sup.63, and R.sup.64
are each independently hydrogen, halogen, --CN, --OH, --OR.sup.15g,
--SH, --SR.sup.15g, --S(.dbd.O)R.sup.15g, --NO.sub.2,
--NR.sup.16gR.sup.17g, --S(.dbd.O).sub.2R.sup.15g,
--NHS(.dbd.O).sub.2R.sup.15g, --S(O).sub.2NR.sup.16aR.sup.17a,
--C(.dbd.O)R.sup.15g, --OC(.dbd.O)R.sup.15g, --C(.dbd.O)OR.sup.16g,
--OC(.dbd.O)OR.sup.16g, --C(.dbd.O)NR.sup.16gR.sup.17g,
--OC(.dbd.O)NR.sup.16gR.sup.17g,
--NR.sup.16gC(.dbd.O)NR.sup.16gR.sup.17g,
--N.sup.16gC(.dbd.O)R.sup.15g, --NR.sup.16gC(.dbd.O)OR.sup.16g,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6alkenyl, C.sub.2-C.sub.6
alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, alkenyl, alkynyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30c; [1093]
R.sup.3 is halogen, --CN, --OH, --OR.sup.15b, --SR.sup.18b,
--NR.sup.16bR.sup.17b, C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30c; [1094] R.sup.4 and R.sup.7 are each
independently hydrogen, halogen, --OH, --OR.sup.15c,
--NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.15c, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.30d; [1095] R.sup.5 and R.sup.6 are each independently
hydrogen, halogen, --OH, --OR.sup.15d,
--NR.sup.16dS(.dbd.O).sub.2R.sup.15d,
--NR.sup.16dC(.dbd.O)R.sup.15d, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.30e; [1096] R.sup.8 is hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; [1097] R.sup.9 and R.sup.10 are each independently
hydrogen, halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; [1098] X.sup.1 is bond, --C(.dbd.O)--,
--S(.dbd.O).sub.2--, --O--, or --CR.sup.40R.sup.41--; [1099]
Y.sup.1 is --C(.dbd.O)--, --(CR.sup.42R.sup.43).sub.v1--,
--S(.dbd.O).sub.2--, --NR.sup.44--, --S--, or --O--; [1100] Y.sup.1
is --(CR.sup.45R.sup.46).sub.v2--, --NR.sup.47-- or --O--; [1101]
R.sup.40, R.sup.41, R.sup.42, R.sup.43, R.sup.45, and R.sup.46 are
each independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.1-C.sub.6 alkynyl, cycloalkyl, or heterocycloalkyl; wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, and heterocycloalkyl is
independently optionally substituted with one, two, or three
R.sup.30p; [1102] R.sup.44 and R.sup.47 are each independently
hydrogen, --S(.dbd.O)R.sup.a, --S(.dbd.O)--R.sup.a,
--S(.dbd.O).sub.2NR.sup.cR.sup.d, --C(.dbd.O)R.sup.a,
--C(.dbd.O)OR.sup.b, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, or heterocycloalkyl;
wherein each alkyl, alkenyl, alkynyl, cycloalkyl, and
heterocycloalkyl is independently optionally substituted with one,
two, or three R.sup.30f; [1103] v1 and v2 are each independently
1-3; [1104] R.sup.15a, R.sup.15b, R.sup.15c, R.sup.15d, R.sup.15e,
R.sup.15f, R.sup.15g are each independently C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl,
alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.30g; [1105] R.sup.16a, R.sup.16b, R.sup.16c, R.sup.16d,
R.sup.16e, R.sup.16f, R.sup.16g and R.sup.17a, R.sup.17b,
R.sup.17e, R.sup.17f, and R.sup.17g are each independently
hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, cycloalkyl, or heterocycloalkyl; wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, and heterocycloalkyl is
independently optionally substituted with one, two, or three
R.sup.30h; [1106] or R.sup.16a and R.sup.17a or R.sup.16b and
R.sup.17b, or R.sup.16e and R.sup.17e or R.sup.16f and R.sup.17f or
R.sup.16g and R.sup.17g are taken together with the nitrogen atom
to which they are attached to form a heterocycloalkyl optionally
substituted with one, two, or three halogen, C.sub.1-C.sub.6 alkyl,
or C.sub.1-C.sub.6 haloalkyl; [1107] R.sup.18b is C.sub.1-C.sub.6
alkyl, C.sub.2-C.sub.8 alkenyl, C.sub.2-C.sub.6 alkynyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6
alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl,
aryl, and heteroaryl is independently optionally substituted with
one, two, or three R.sup.30i; [1108] R.sup.21 and R.sup.22 are each
independently hydrogen, C.sub.1-C.sub.20alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--(CR.sup.23R.sup.24).sub.wC(.dbd.O)OR.sup.25,
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)R.sup.26,
--(CR.sup.23R.sup.24).sub.wSC(.dbd.O)R.sup.26, or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30k; [1109] or
R.sup.21 and R.sup.22 are taken together with the atoms to which
they are attached to form a heterocycloalkyl optionally substituted
with one, two, or three R.sup.30l; [1110] each R.sup.23 and
R.sup.24 are independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl; [1111] each R.sup.25 is independently hydrogen,
C.sub.1-C.sub.6alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [1112] each R.sup.26 is
independently C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, or C.sub.1-C.sub.6 heteroalkyl; [1113]
each w is independently 1-4; [1114] each R.sup.30, R.sup.30a,
R.sup.30b, R.sup.30c, R.sup.30d, R.sup.30e, R.sup.30f, R.sup.30g
and R.sup.30h, R.sup.30i, R.sup.30j, R.sup.30k, R.sup.30l,
R.sup.30m, R.sup.30n, R.sup.30o, and R.sup.30p are independently
halogen, --CN, --OH, --OR.sup.a, --SH, --SR.sup.a,
--S(.dbd.O)R.sup.a, --NO.sub.2, --NR.sup.cR.sup.d,
--S(.dbd.O).sub.2R.sup.a, --NHS(.dbd.O).sub.2R.sup.a,
--S(.dbd.O).sub.3NR.sup.cR.sup.d, --C(.dbd.O)R.sup.a,
--OC(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b, --OC(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, --OC(.dbd.O)NR.sup.cR.sup.d,
--NR.sup.bC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(.dbd.O)R.sup.a,
--NR.sup.bC(.dbd.O)OR.sup.b, C.sub.1-C.sub.6alkyl, C.sub.1-C.sub.6
alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, heterocycloalkyl,
aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.31; [1115] each R.sup.31 is independently halogen,
--CN, --OH, --OR.sup.a, --SH, --SR.sup.a, --S(.dbd.O)R.sup.a,
--NO.sub.2, --NR.sup.cR.sup.d, --S(.dbd.O).sub.2R.sup.a,
--NHS(.dbd.O).sub.2R.sup.a, --S(.dbd.O).sub.2NR.sup.cR.sup.d,
--C(.dbd.O)R.sup.a, --OC(.dbd.O)R.sup.a, --C(.dbd.O)OR.sup.b,
--OC(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
--OC(.dbd.O)NR.sup.cR.sup.d, --NR.sup.bC(.dbd.O)NR.sup.cR.sup.d,
--NR.sup.bC(O)R.sup.a, --NR.sup.bC(O)OR.sup.b, C.sub.1-C.sub.6
alkyl, C.sub.1-C.sub.6haloalkyl, C.sub.1-C.sub.6 hydroxyalkyl,
C.sub.1-C.sub.6 heteroalkyl, or cycloalkyl optimally substituted
with one, two, or three halogen, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl; [1116] each R.sup.a is independently
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, C.sub.1-C.sub.6 heteroalkyl, cycloalkyl, heterocycloalkyl,
aryl, or heteroaryl; wherein the alkyl, alkenyl, alkynyl,
heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optimally substituted with one, two, or three
halogen, --OH, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[1117] each R.sup.b is independently hydrogen, C.sub.1-C.sub.6
alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl,
C.sub.1-C.sub.6 heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, or
heteroaryl; wherein the alkyl, alkenyl, alkynyl, heteroalkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three halogen, --OH,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl; and [1118]
R.sup.c and R.sup.d are each independently hydrogen,
C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6
alkynyl, C.sub.1-C.sub.6 heteroalkyl, cycloalkyl, heterocycloalkyl,
aryl, or heteroaryl; wherein the alkyl, alkenyl, alkynyl,
heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
halogen, --OH, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl;
[1119] or R.sup.c and R.sup.d are taken together with the nitrogen
atom to which they are attached to form a heterocycloalkyl
optionally substituted with one, two, or three halogen,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl.
[1120] For any and all of the embodiments of Formula (III) or (IV),
substituents are selected from among a subset of the listed
alternatives.
[1121] In some embodiments of a compound of formula (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
when
##STR00009##
then one of R.sup.45 or R.sup.46 is not hydrogen.
[1122] In some embodiments of a compound of Formula (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
the compound is not
(1-((5-(2-chloro-6-(methylamino)-9H-purin-9-yl)-3,4-dihydroxytetrahydrofu-
ran-2-yl)methoxy)-2,2,2-trifluoroethyl)phosphonic acid or any
stereoisomers thereof.
[1123] In some embodiments of a compound of Formula (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
Q.sup.1 is N; and Q.sup.2 is CW. In some embodiments of a compound
of Formula (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, Q.sup.1 is CW; and Q.sup.2 is N. In some
embodiments of a compound of Formula (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, Q.sup.1 is CW;
and Q.sup.2 is CW. In some embodiments of a compound of Formula
(IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, Q.sup.1 is N; and Q.sup.2 is N. In some
embodiments of a compound of Formula (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof.
##STR00010##
In some embodiments of a compound of Formula (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer
thereof,
##STR00011##
[1124] In some embodiments of a compound of Formula (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each W is independently hydrogen, halogen, --CN, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
C.sub.1-C.sub.6 alkyl, cycloalkyl, or heterocycloalkyl; wherein
each alkyl, cycloalkyl, and heterocycloalkyl, is independently
optionally substituted with one, two, or three R.sup.30. In some
embodiments of a compound of Formula (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each W is
independently hydrogen, halogen, --CN, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b, --C(.dbd.O)NR.sup.cR.sup.d,
C.sub.1-C.sub.6alkyl, cycloalkyl, or heterocycloalkyl; wherein each
alkyl, cycloalkyl, and heterocycloalkyl, is independently
optionally substituted with one, two, or three R.sup.30. In some
embodiments of a compound of Formula (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each W is
independently hydrogen, halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl. In some embodiments of a compound of Formula (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each W is hydrogen.
[1125] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, each R.sup.30 is independently halogen, --CN, --OH,
--OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.31. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each R.sup.30 is
independently halogen, --CN, --OH, --OR.sup.a, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6 haloalkyl. In some embodiments of a
compound of Formula (III) or (IV), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.30 is
independently halogen, --OH, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl. In some embodiments of a compound of
Formula (III) or (IV), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, each R.sup.30 is independently
halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl. In
some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30 is independently halogen, or C.sub.1-C.sub.6 alkyl.
In some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30 is independently halogen.
[1126] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.8 is hydrogen, halogen, --OH, --OMe, --NH.sub.2,
--NH(CH.sub.3), --N(CH.sub.3).sub.2, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl. In some embodiments of a compound of
Formula (III) or (IV), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.8 is hydrogen, halogen,
--OH, --NH.sub.2, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl. In some embodiments of a compound of Formula (III) or
(IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.8 is hydrogen, halogen, --OH,
--NH.sub.2, or C.sub.1-C.sub.6 alkyl. In some embodiments of a
compound of Formula (III) or (IV), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.8 is hydrogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(III) or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.8 is hydrogen.
[1127] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.9 and R.sup.10 are each independently hydrogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(III) or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.9 and R.sup.10 are each hydrogen.
[1128] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, Q.sup.3 is N and Q.sup.4 is CW.sup.1. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, Q.sup.4 is N and
Q.sup.3 is CW.sup.1. In some embodiments of a compound of Formula
(III) or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, Q.sup.3 is N and Q.sup.4 is N.
[1129] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, W.sup.1 is hydrogen, halogen, or C.sub.1-C.sub.6 alkyl. In
some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
W.sup.1 is hydrogen.
[1130] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, A is --O--. In some embodiments of a compound of Formula
(III) or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, A is --CH.sub.2--.
[1131] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, v1 is 1 or 2. In some embodiments of a compound of Formula
(III) or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, v1 is 1. In same embodiments of a compound of
Formula (III) or (IV), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, v1 is 2.
[1132] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, v2 is 1 or 2. In some embodiments of a compound of Formula
(III) or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof: v2 is 1. In some embodiments of a compound of
Formula (III) or (IV), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, v2 is 2.
[1133] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof,
##STR00012##
[1134] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof,
##STR00013##
[1135] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof,
##STR00014##
In some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer
thereof,
##STR00015##
In some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer
thereof,
##STR00016##
[1136] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof.
##STR00017##
and when
##STR00018##
then [1137] R.sup.45 is halogen, --OH, --OR.sup.a,
--NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl,
C.sub.2-C.sub.6 alkynyl, cycloalkyl, or heterocycloalkyl; wherein
each alkyl, alkenyl, alkynyl, cycloalkyl, and heterocycloalkyl is
independently optionally substituted with one, two, or three
R.sup.31p; and [1138] R.sup.46 is hydrogen, halogen, --OH,
--OR.sup.a, --NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, or
heterocycloalkyl; wherein each alkyl, alkenyl, alkynyl, cycloalkyl,
and heterocycloalkyl is independently optionally substituted with
one, two, or three R.sup.30p.
[1139] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.40 and R.sup.41 are each independently hydrogen,
halogen, --OH, --OR.sup.a, --NR.sup.cR.sup.d, C.sub.1-C.sub.6
alkyl, cycloalkyl, or heterocycloalkyl; wherein each alkyl,
cycloalkyl, and heterocycloalkyl is independently optionally
substituted with one, two, or three R.sup.30p. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.40 and
R.sup.41 are each independently hydrogen, halogen. --OH,
--OR.sup.a, --NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl. In some embodiments of a compound of
Formula (III) or (IV), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.40 and R.sup.41 are each
independently hydrogen, halogen, --OH, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl. In some embodiments of a compound of
Formula (III) or (IV), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.40 and R.sup.41 are each
independently hydrogen, halogen, or C.sub.1-C.sub.6 alkyl. In some
embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.40 and R.sup.41 are each independently hydrogen or halogen.
In some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.40 and R.sup.41 are each hydrogen.
[1140] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.42 and R.sup.43 are each independently hydrogen,
halogen, --OH, --OR.sup.a, --NR.sup.cR.sup.d, C.sub.1-C.sub.6
alkyl, cycloalkyl, or heterocycloalkyl; wherein each alkyl,
cycloalkyl, and heterocycloalkyl is independently optionally
substituted with one, two, or three R.sup.30p. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.42 and
R.sup.43 are each independently hydrogen, halogen, --OH,
--OR.sup.a, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl. In
some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.42 and R.sup.43 are each independently hydrogen, halogen,
--OH, --OR.sup.a, or C.sub.1-C.sub.6 alkyl. In some embodiments of
a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.42 and
R.sup.43 are each hydrogen.
[1141] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.44 is hydrogen, --S(.dbd.O).sub.2R.sup.a,
--C(.dbd.O)R.sup.a, C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6
haloalkyl, or C.sub.1-C.sub.6 alkyl(aryl). In some embodiments of a
compound of Formula (III) or (IV), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.44 is hydrogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(III) or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.44 is hydrogen. In some embodiments of
a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.44 is
C.sub.1-C.sub.6 alkyl.
[1142] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.45 and R.sup.46 are each independently hydrogen,
halogen, --OH, --OR.sup.a, --NR.sup.cR.sup.d, C.sub.1-C.sub.6
alkyl, cycloalkyl, or heterocycloalkyl; wherein each alkyl,
cycloalkyl, and heterocycloalkyl is independently optionally
substituted with one, two, or three R.sup.30p. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.45 and
R.sup.46 are each independently hydrogen, halogen, C.sub.1-C.sub.6
alkyl, or cycloalkyl; wherein each alkyl and cycloalkyl is
independently optionally substituted with one, two, or three
R.sup.30p. In some embodiments of a compound of Formula (III) or
(IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.45 and R.sup.46 are each independently
hydrogen, halogen, C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6
hydroxyalkyl, C.sub.1-C.sub.6 haloalkyl, C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(aryl), or cycloalkyl. In
some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.45 and R.sup.46 are each independently hydrogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(III) or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.45 and R.sup.46 are each hydrogen.
[1143] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.45 is halogen, --OH, --OR.sup.a, --NR.sup.cR.sup.d,
C.sub.1-C.sub.6 alkyl, cycloalkyl, or heterocycloalkyl; wherein
each alkyl, cycloalkyl, and heterocycloalkyl is independently
optionally substituted with one, two, or three R.sup.30p; and
T.sup.46 is hydrogen or C.sub.1-C.sub.6 alkyl. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.45 is
halogen, C.sub.1-C.sub.6 alkyl, or cycloalkyl; wherein each alkyl
and cycloalkyl is independently optionally substituted with one,
two, or three R.sup.30p; and R.sup.46 is hydrogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(III) or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.45 is halogen, C.sub.1-C.sub.6 alkyl,
C.sub.1-C.sub.6 hydroxyalkyl, C.sub.1-C.sub.6 haloalkyl,
C.sub.1-C.sub.6 alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(aryl), or
cycloalkyl; and R.sup.46 is hydrogen or C.sub.1-C.sub.6 alkyl. In
some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.45 is C.sub.1-C.sub.6 alkyl; and R.sup.46 is hydrogen or
C.sub.1-C.sub.6 alkyl.
[1144] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.30p is halogen, --CN, --OH, --OR.sup.a,
C.sub.1-C.sub.6alkyl, cycloalkyl, heterocycloalkyl, aryl, or
heteroaryl; wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl,
and heteroaryl is independently optionally substituted with one,
two, or three R.sup.31. In some embodiments of a compound of
Formula (III) or (IV), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.30p is halogen, --OH,
--OR.sup.a, C.sub.1-C.sub.6 alkyl, cycloalkyl, or aryl; wherein
each alkyl, cycloalkyl, and aryl is independently optionally
substituted with one, two, or three R.sup.31. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.30p is
--OH, cycloalkyl, or aryl; wherein each alkyl, cycloalkyl, and aryl
is independently optionally substituted with one, two, or three
R.sup.31. In some embodiments of a compound of Formula (III) or
(IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.30p is --OH, cycloalkyl, or aryl.
[1145] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, each R.sup.30p is independently halogen, --CN, --OH,
--OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.31. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each R.sup.30p
is independently halogen, --CN, --OH, --OR.sup.a, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6 haloalkyl. In some embodiments of a
compound of Formula (III) or (IV), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.30p is
independently halogen, --OH, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl. In some embodiments of a compound of
Formula (III) or (IV), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, each R.sup.30p is independently
halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl. In
some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30p is independently halogen, or C.sub.1-C.sub.6 alkyl.
In some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30p is independently halogen.
[1146] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.47 is hydrogen. --S(.dbd.O).sub.2R.sup.a,
--C(.dbd.O)R.sup.a, C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6
haloalkyl, or C.sub.1-C.sub.6 alkyl(aryl). In some embodiments of a
compound of Formula (III) or (IV), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.47 is hydrogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(III) or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.47 is hydrogen. In some embodiments of
a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.47 is
C.sub.1-C.sub.6 alkyl.
[1147] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.5 and R.sup.6 are each independently hydrogen,
halogen, C.sub.1-C.sub.6 alkyl, or cycloalkyl; wherein each alkyl
and cycloalkyl is independently optionally substituted with one,
two, or three R.sup.30e. In some embodiments of a compound of
Formula (III) or (IV), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.5 and R.sup.6 are each
independently hydrogen, halogen, C.sub.1-C.sub.6 alkyl, or
cycloalkyl; wherein each alkyl and cycloalkyl is independently
optionally substituted with one, two, or three R.sup.30e. In some
embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.5 and R.sup.6 are each hydrogen.
[1148] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.15d is C.sub.1-C.sub.6 alkyl, aryl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl is
optionally substituted with one, two, or three halogen. In some
embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.15d is C.sub.1-C.sub.6 alkyl or C.sub.1-C.sub.6 haloalkyl. In
some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.15d is C.sub.1-C.sub.6 alkyl.
[1149] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.16d is hydrogen, C.sub.1-C.sub.6 alkyl, aryl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl is
optionally substituted with one, two, or three halogen. In some
embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.16d is hydrogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl. In some embodiments of a compound of Formula (III) or
(IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.16d is hydrogen or C.sub.1-C.sub.6
alkyl.
[1150] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, each R.sup.30C is independently halogen, --CN, --OH,
--OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.31. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each R.sup.30e
is independently halogen, --CN, --OH, --OR.sup.a, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6 haloalkyl. In some embodiments of a
compound of Formula (III) or (IV), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.30e is
independently halogen, --OH, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl. In some embodiments of a compound of
Formula (III) or (IV), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, each R.sup.30e is independently
halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl. In
some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30e is independently halogen, or C.sub.1-C.sub.6 alkyl.
In some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30e is independently halogen.
[1151] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.4 and R.sup.7 are each independently hydrogen,
halogen, --OH, --OR.sup.15c, --NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.15c, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30d. In some
embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.4 and R.sup.7 are each independently hydrogen, halogen, --OH,
--OR.sup.15c, --NR.sup.16cS(.dbd.O).sub.2R.sup.15c,
--NR.sup.16cC(.dbd.O)R.sup.15c, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30d. In some
embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.4 and R.sup.7 are each independently hydrogen, halogen, --OH,
--OR.sup.15c, --NR.sup.16cS(.dbd.O).sub.2R.sup.15c, or
--NR.sup.16cC(.dbd.O)R.sup.15c.
[1152] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.4 and R.sup.7 are each independently hydrogen,
halogen, or --OH. In some embodiments of a compound of Formula
(III) or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.4 and R.sup.7 are each independently
halogen or --OH. In some embodiments of a compound of Formula (III)
or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.4 and R.sup.7 are each --OH.
[1153] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.15c is C.sub.1-C.sub.6 alkyl, aryl, or
C.sub.1-C.sub.4 alkyl(aryl); wherein each alkyl and aryl is
optionally substituted with one, two, or three halogen. In some
embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.15c is C.sub.1-C.sub.6 alkyl or C.sub.1-C.sub.6 haloalkyl. In
some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.15c is C.sub.1-C.sub.6 alkyl.
[1154] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.16c is hydrogen, C.sub.1-C.sub.6 alkyl, aryl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl is
optionally substituted with one, two, or three halogen. In some
embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.16c is hydrogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl. In some embodiments of a compound of Formula (III) or
(IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.16c is hydrogen or C.sub.1-C.sub.6
alkyl.
[1155] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, each R.sup.30d is independently halogen, --CN, --OH,
--OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.1,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.31. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each R.sup.30d
is independently halogen, --CN, --OH, --OR.sup.a, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6haloalkyl. In some embodiments of a
compound of Formula (III) or (IV), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.30d is
independently halogen, --OH, C.sub.1-C.sub.6 alkyl, or CI-CG
haloalkyl. In some embodiments of a compound of Formula (III) or
(IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, each R.sup.30d is independently halogen,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl. In some
embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30d is independently halogen, or C.sub.1-C.sub.6 alkyl.
In some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30d is independently halogen.
[1156] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, Z is --NR.sup.1R.sup.2. In some embodiments of a compound
of Formula (III) or (IV), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof one of R.sup.1 or R.sup.2 is not
hydrogen.
[1157] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.1 is C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl),
--S(.dbd.O).sub.2R.sup.15a, --S(.dbd.O).sub.2NR.sup.16aR.sup.17a,
or --C(.dbd.O).sub.2R.sup.15a; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30a.
[1158] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.1 is cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), C.sub.1-C.sub.6
alkyl(heterocycloalkyl), --S(.dbd.O).sub.2R.sup.15a,
--S(.dbd.O).sub.2NR.sup.16aR.sup.17a or --C(.dbd.O).sub.2R.sup.15a;
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.31a.
[1159] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.15a is C.sub.1-C.sub.6 alkyl, aryl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl is
optionally substituted with one, two, or three halogen. In some
embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.15a is C.sub.1-C.sub.6 alkyl or C.sub.1-C.sub.6 haloalkyl. In
some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.15a is C.sub.1-C.sub.6 alkyl.
[1160] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.15a and R.sup.17a are each independently hydrogen,
C.sub.1-C.sub.6 alkyl, aryl, or C.sub.1-C.sub.6 alkyl(aryl);
wherein each alkyl and aryl is optionally substituted with one,
two, or three halogen. In some embodiments of a compound of Formula
(III) or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.16a and R.sup.17a are each
independently C.sub.1-C.sub.6 alkyl or C.sub.1-C.sub.6 haloalkyl.
In some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate or stereoisomer thereof,
R.sup.16a and R.sup.17a are each independently hydrogen or
C.sub.1-C.sub.6 alkyl.
[1161] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.1 is C.sub.1-C.sub.6 alkyl, cycloalkyl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optimally
substituted with one, two, or three R.sup.30a. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate a stereoisomer thereof, R.sup.1 is
C.sub.1-C.sub.6 alkyl, cycloalkyl, or C.sub.1-C.sub.6 alkyl(aryl);
wherein each alkyl, cycloalkyl, and aryl is independently
optionally substituted with one, two, or three R.sup.10a. In some
embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 is cycloalkyl or C.sub.1-C.sub.6 alkyl(aryl); wherein each
alkyl, cycloalkyl, and aryl is independently optionally substituted
with one, two, or three R.sup.30a. In some embodiments of a
compound of Formula (III) or (IV), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.1 is cycloalkyl
optionally substituted with one, two, or three R.sup.30a. In some
embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.1 is C.sub.1-C.sub.6 alkyl(aryl); wherein alkyl and aryl are
independently optionally substituted with one, two, or three
R.sup.30a.
[1162] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.1 is cycloalkyl optionally substituted with one,
two, or three R.sup.30a. In some embodiments of a compound of
Formula (III) or (IV), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.1 is C.sub.1-C.sub.6
alkyl(aryl); wherein alkyl and aryl are independently optionally
substituted with one, two, or three R.sup.30a.
[1163] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, each R.sup.30a is independently halogen, --CN, --OH,
--OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three Rif. In some embodiments of a
compound of Formula (III) or (IV), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.30a is
independently halogen, --CN, --OH, --OR.sup.a, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6 haloalkyl. In some embodiments of a
compound of Formula (III) or (IV), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.30a is
independently halogen, --OH, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl. In some embodiments of a compound of
Formula (III) or (IV), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, each R.sup.30a is independently
halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl. In
some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30a is independently halogen, or C.sub.1-C.sub.6 alkyl.
In some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30a is independently halogen.
[1164] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.2 is hydrogen or C.sub.1-C.sub.6 alkyl. In some
embodiments of a compound of Formula (III) or (aV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.2 is hydrogen. In some embodiments of a compound of Formula
(III) or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.2 is C.sub.1-C.sub.6 alkyl.
[1165] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.1 and R.sup.2 are taken together with the nitrogen
atom to which they are attached to form a heterocycloalkyl
optionally substituted with one, two, or three R.sup.30b.
[1166] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.1 and R.sup.2 are taken together with the nitrogen
atom to which they are attached to form an azetidine, a piperidine,
a morpholine, or a pyrrolidine, each optionally substituted with
one, two, or three R.sup.30b.
[1167] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.1 and R.sup.2 are taken together with the nitrogen
atom to which they are attached to form a piperidine optionally
substituted with one, two, or three R.sup.30b. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.1 and
R.sup.2 are taken together with the nitrogen atom to which they are
attached to form a pyrrolidine optionally substituted with one,
two, or three R.sup.30b.
[1168] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, each R.sup.30b is independently halogen, C.sub.1-C.sub.6
alkyl, C.sub.1-C.sub.6 haloalkyl, or aryl; wherein the alkyl and
aryl are optionally substituted with one, two, or three R.sup.31.
In some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30b is independently aryl optionally substituted with
one, two, or three R.sup.31. In some embodiments of a compound of
Formula (III) or (IV), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, each R.sup.30b is aryl.
[1169] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, each R.sup.30b is independently halogen, --CN, --OH,
--OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.31. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each R.sup.30b
is independently halogen, --CN, --OH, --OR.sup.a, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6 haloalkyl. In some embodiments of a
compound of Formula (III) or (IV), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.30b is
independently halogen, --OH, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl. In some embodiments of a compound of
Formula (III) or (IV), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, each R.sup.30b is independently
halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl. In
some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30b is independently halogen, or C.sub.1-C.sub.6 alkyl.
In some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30b is independently halogen.
[1170] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, Z is --OR.sup.60.
[1171] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.60 is hydrogen, --C(.dbd.O)R.sup.15e,
--C(.dbd.O)OR.sup.16e, --C(.dbd.O)NR.sup.16eR.sup.17e,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30m. In some
embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate or stereoisomer thereof,
R.sup.60 is --C(.dbd.O)R.sup.15e, --C(.dbd.O)OR.sup.16e,
--C(.dbd.O)NR.sup.16eR.sup.17e, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein
each alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is
independently optionally substituted with one, two, or three
R.sup.30m. In some embodiments of a compound of Formula (III) or
(IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.60 is C.sub.1-C.sub.6 alkyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6
alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30m.
[1172] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.60 is C.sub.1-C.sub.6 alkyl, cycloalkyl,
C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl),
C.sub.1-C.sub.6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30m. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate or stereoisomer thereof, R.sup.60 is
C.sub.1-C.sub.6 alkyl, cycloalkyl, or C.sub.1-C.sub.6 alkyl(aryl);
wherein each alkyl, cycloalkyl, and aryl is independently
optionally substituted with one, two, or three R.sup.30m. In some
embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.60 is cycloalkyl or C.sub.1-C.sub.6 alkyl(aryl); wherein each
alkyl, cycloalkyl, and aryl is independently optionally substituted
with one, two, or three R.sup.30m. In some embodiments of a
compound of Formula (III) or (IV), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.60 is cycloalkyl
optionally substituted with one, two, or three R.sup.30m. In some
embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.60 is C.sub.1-C.sub.6 alkyl(aryl); wherein alkyl and aryl are
independently optionally substituted with one, two, or three
R.sup.30m.
[1173] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.15e is C.sub.1-C.sub.6 alkyl, aryl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl is
optionally substituted with one, two, or three halogen. In some
embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.15e is C.sub.1-C.sub.6 alkyl or C.sub.1-C.sub.6 haloalkyl. In
some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof:
R.sup.15e is C.sub.1-C.sub.6 alkyl.
[1174] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.16e and R.sup.17c are each independently hydrogen,
C.sub.1-C.sub.6 alkyl, aryl, or C.sub.1-C.sub.6 alkyl(aryl);
wherein each alkyl and aryl is optionally substituted with one,
two, or three halogen. In some embodiments of a compound of Formula
(III) or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.16e and R.sup.17e are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl. In some embodiments of a compound of Formula (III) or
(IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.16e and R.sup.17e are each
independently hydrogen or C.sub.1-C.sub.6 alkyl.
[1175] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, each R.sup.30m is independently halogen, --CN, --OH,
--OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.31. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each R.sup.30m
is independently halogen, --CN, --OH, --OR.sup.a, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6 haloalkyl. In some embodiments of a
compound of Formula (III) or (IV), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.30m is
independently halogen or C.sub.1-C.sub.6 alkyl. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each R.sup.30m
is independently halogen.
[1176] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, Z is --SR.sup.61.
[1177] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.61 is hydrogen, --C(.dbd.O)R.sup.15f,
--C(.dbd.O)OR.sup.16f, --C(.dbd.O)NR.sup.16fR.sup.17f,
C.sub.1-C.sub.6 alkyl, cycloalkyl, heterocycloalkyl, aryl,
heteroaryl, C.sub.1-C.sub.6 alkyl(aryl), C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-6 alkyl(cycloalkyl), or C.sub.1-C.sub.6
alkyl(heterocycloalkyl); wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30n. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate or stereoisomer thereof, R.sup.61 is
--C(.dbd.O)R.sup.15f, --C(.dbd.O)OR.sup.16f,
--C(.dbd.O)NR.sup.16fR.sup.17f, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(acyl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30n. In some embodiments of a compound of Formula
(III) or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.61 is C.sub.1-C.sub.6 alkyl,
cycloalkyl, heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6
alkyl(aryl), C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30n. In some embodiments of a compound of Formula
(III) or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.61 is C.sub.1-C.sub.6 alkyl,
cycloalkyl, C.sub.1-C.sub.6 alkyl(aryl). C.sub.1-C.sub.6
alkyl(heteroaryl), C.sub.1-C.sub.6 alkyl(cycloalkyl), or
C.sub.1-C.sub.6 alkyl(heterocycloalkyl); wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.30n. In some
embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof:
R.sup.61 is C.sub.1-C.sub.6 alkyl, cycloalkyl, or C.sub.1-C.sub.6
alkyl(aryl); wherein each alkyl, cycloalkyl, and aryl is
independently optionally substituted with one, two, or three
R.sup.30n. In some embodiments of a compound of Formula (III) or
(IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.61 is cycloalkyl or C.sub.1-C.sub.6
alkyl(aryl); wherein each alkyl, cycloalkyl, and aryl is
independently optionally substituted with one, two, or three
R.sup.30n. In some embodiments of a compound of Formula (III) or
(IV), or a pharmaceutically acceptable salt, solvate; or
stereoisomer thereof, R.sup.61 is cycloalkyl optionally substituted
with one, two, or three R.sup.30n. In some embodiments of a
compound of Formula (III) or (IV), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.61 is C.sub.1-C.sub.6
alkyl(aryl); wherein alkyl and aryl are independently optionally
substituted with one, two, or three R.sup.30n.
[1178] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.15f is C.sub.1-C.sub.6 alkyl, aryl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl is
optionally substituted with one, two, or three halogen. In some
embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.15f is C.sub.1-C.sub.6 alkyl or C.sub.1-C.sub.6 haloalkyl. In
some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.15f is C.sub.1-C.sub.6 alkyl.
[1179] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.16f and R.sup.17f are each independently hydrogen,
C.sub.1-C.sub.6 alkyl, aryl, or C.sub.1-C.sub.6 alkyl(aryl);
wherein each alkyl and aryl is optionally substituted with one,
two, or three halogen. In some embodiments of a compound of Formula
(III) or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.16f and R.sup.17f are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl. In some embodiments of a compound of Formula (III) or
(IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.16f and R.sup.17f are each
independently hydrogen or C.sub.1-C.sub.6 alkyl.
[1180] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, each R.sup.30n is independently halogen, --CN, --OH,
--OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.31. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each R.sup.30n
is independently halogen, --CN, --OH, --OR.sup.a, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6 haloalkyl. In some embodiments of a
compound of Formula (III) or (IV), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.30n is
independently halogen or C.sub.1-C.sub.6 alkyl. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each R.sup.30n
is independently halogen.
[1181] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, Z is --CR.sup.62R.sup.63R.sup.64.
[1182] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.62 is hydrogen, halogen, --CN, --OH, --OR.sup.15g,
--NR.sup.16gR.sup.17g, --C(O)OR.sup.16g,
--C(.dbd.O)NR.sup.16gR.sup.17g, or C.sub.1-C.sub.6 alkyl optionally
substituted with one, two, or three R.sup.30o. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.62 is
hydrogen, halogen, --CN, --OH, --OR.sup.15g, --NR.sup.16gR.sup.17g,
--C(.dbd.O)OR.sup.16g, --C(.dbd.O)NR.sup.16gR.sup.17g, or
C.sub.1-C.sub.6 alkyl optionally substituted with one, two, or
three R.sup.30o. In some embodiments of a compound of Formula (III)
or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.61 is hydrogen, halogen, or --OH. In
some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.62 is hydrogen or halogen. In some embodiments of a compound
of Formula (III) or (IV), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.62 is hydrogen.
[1183] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.63 is hydrogen, halogen, --CN, --OH, --OR.sup.15g,
--NR.sup.16gR.sup.17g, --C(.dbd.O)OR.sup.16g,
--C(.dbd.O)NR.sup.16gR.sup.17g, or C.sub.1-C.sub.6 alkyl optionally
substituted with one, two, or three R.sup.30o. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.63 is
hydrogen, halogen, --CN, --OH, --OR.sup.15g, --NR.sup.16gR.sup.17g,
--C(.dbd.O)OR.sup.16g, --C(.dbd.O)NR.sup.16gR.sup.17g, or
C.sub.1-C.sub.6 alkyl optionally substituted with one, two, or
three R.sup.30o. In some embodiments of a compound of Formula (III)
or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.63 is hydrogen, halogen, or --OH. In
some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.63 is hydrogen or halogen. In some embodiments of a compound
of Formula (III) or (IV), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.63 is hydrogen.
[1184] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.64 is --OR.sup.15g, --SR.sup.15g,
--S(.dbd.O)R.sup.15g, --NR.sup.16gR.sup.17g,
--S(.dbd.O).sub.2R.sup.15g, --NHS(.dbd.O).sub.2R.sup.15g,
--S(.dbd.O).sub.2NR.sup.16gR.sup.17g, --C(.dbd.O)R.sup.15g,
--C(.dbd.O)OR.sup.16g, --C(.dbd.O)NR.sup.16gR.sup.17g, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.30o. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.64 is
--OR.sup.15g, --SR.sup.15g, --S(.dbd.O)R.sup.15g,
--NR.sup.16gR.sup.17g, --S(.dbd.O).sub.2R.sup.15g,
--NHS(.dbd.O).sub.2R.sup.15g, --S(.dbd.O).sub.2NR.sup.16gR.sup.17g,
--C(.dbd.O)R.sup.15g, --C(.dbd.O)R.sup.16g,
--C(.dbd.O)NR.sup.16gR.sup.17g, cycloalkyl, heterocycloalkyl, aryl,
or heteroaryl; wherein each cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30o. In some embodiments of a compound of Formula
(III) or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.64 is --OR.sup.15g,
--NR.sup.16gR.sup.17s, --C(.dbd.O)R.sup.15g, --C(O)OR.sup.16g,
--C(.dbd.O)NR.sup.16gR.sup.17g, cycloalkyl, heterocycloalkyl, aryl,
or heteroaryl; wherein each cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30o. In some embodiments of a compound of Formula
(III) or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.64 is --OR.sup.15g,
--NR.sup.16gR.sup.17g, cycloalkyl, heterocycloalkyl, aryl, or
heteroaryl; wherein each cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30o. In some embodiments of a compound of Formula
(III) or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.64 is --OR.sup.15g or
--NR.sup.16gR.sup.17g. In some embodiments of a compound of Formula
(III) or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.64 is cycloalkyl, heterocycloalkyl,
aryl, or heteroaryl; wherein each cycloalkyl, heterocycloalkyl,
aryl, and heteroaryl is independently optionally substituted with
one, two, or three R.sup.30o. In some embodiments of a compound of
Formula (III) or (IV), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sub.64 is cycloalkyl or
heterocycloalkyl; wherein each cycloalkyl and heterocycloalkyl is
independently optionally substituted with one, two, or three
R.sup.30o. In some embodiments of a compound of Formula (III) or
(IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.64 is aryl, or heteroaryl; wherein each
aryl, and heteroaryl is independently optionally substituted with
one, two, or three R.sup.30o.
[1185] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.15g is C.sub.1-C.sub.6 alkyl, aryl, or
C.sub.1-C.sub.6 alkyl(aryl); wherein each alkyl and aryl is
optionally substituted with one, two, or three halogen. In some
embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.15g is C.sub.1-C.sub.6 alkyl or C haloalkyl. In some
embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.15g is C.sub.1-C.sub.6 alkyl.
[1186] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.16g and R.sup.17g are each independently hydrogen,
C.sub.1-C.sub.6 alkyl, aryl, or C.sub.1-C.sub.6 alkyl(aryl);
wherein each alkyl and aryl is optionally substituted with one,
two, or three halogen. In some embodiments of a compound of Formula
(III) or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.16g and R.sup.17g are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl. In some embodiments of a compound of Formula (III) or
(IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.16g and R.sup.17g are each
independently hydrogen or C.sub.1-C.sub.6 alkyl.
[1187] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, each R.sup.30o is independently halogen, --CN, --OH,
--OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.31. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each R.sup.30o
is independently halogen, --CN, --OH, --OR.sup.a, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6 haloalkyl. In some embodiments of a
compound of Formula (III) or (IV), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.30o is
independently halogen or C.sub.1-C.sub.6 alkyl. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each R.sup.30o
is independently halogen.
[1188] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.3 is halogen, --CN, --OR.sup.15b, --SR.sup.18b,
--NR.sup.16bR.sup.17b, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl);
wherein each alkyl, cycloalkyl, heterocycloalkyl, aryl, and
heteroaryl is independently optionally substituted with one, two,
or three R.sup.30c. In some embodiments of a compound of Formula
(III) or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.3 is halogen, --CN, --OR.sup.15b,
--NR.sup.16bR.sup.17b, C.sub.1-C.sub.6 alkyl, cycloalkyl, or
heterocycloalkyl; wherein each alkyl, cycloalkyl, and
heterocycloalkyl is independently optionally substituted with one,
two, or three R.sup.30c. In some embodiments of a compound of
Formula (III) or (IV), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.3 is halogen.
[1189] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.15b is C.sub.1-C.sub.6 alkyl optionally substituted
with one, two, or three halogen. In some embodiments of a compound
of Formula (III) or (IV), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.15b is C.sub.1-C.sub.6
alkyl or C.sub.1-C.sub.6 haloalkyl. In some embodiments of a
compound of Formula (III) or (IV), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, R.sup.15b is
C.sub.1-C.sub.6 alkyl.
[1190] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.16b and R.sup.17b are each independently hydrogen,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl optionally
substituted with one, two, or three halogen. In some embodiments of
a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.16b and
R.sup.17b are each independently hydrogen or C.sub.1-C.sub.6
alkyl.
[1191] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.18b is C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl, C.sub.1-C.sub.6 alkyl(aryl),
C.sub.1-C.sub.6 alkyl(heteroaryl), C.sub.1-C.sub.6
alkyl(cycloalkyl), or C.sub.1-C.sub.6 alkyl(heterocycloalkyl). In
some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.18b is cycloalkyl or C.sub.1-C.sub.6 alkyl(cycloalkyl).
[1192] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, each R.sup.30c is independently halogen, --CN, --OH,
--OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.31. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each R.sup.30c
is independently halogen, --CN, --OH, --OR.sup.a, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6 haloalkyl. In some embodiments of a
compound of Formula (III) or (IV), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.30c is
independently halogen or C.sub.1-C.sub.6 alkyl. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each R.sup.30c
is independently halogen.
[1193] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.21 and R.sup.22 are each independently hydrogen,
aryl, or --(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.23. In some
embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.21 and R.sup.22 are each hydrogen or
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.21 and
R.sup.22 are each hydrogen. In some embodiments of a compound of
Formula (III) or (IV), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.21 and R.sup.22 are each
--(CR.sup.23R.sup.24).sub.wOC(.dbd.O)OR.sup.25.
[1194] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, w is 1 or 2. In some embodiments of a compound of Formula
(III) or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, w is 2. In some embodiments of a compound of
Formula (III) or (IV), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, w is 1.
[1195] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, each R.sup.23 and R.sup.24 are independently hydrogen,
halogen, or C.sub.1-C.sub.6 alkyl. In some embodiments of a
compound of Formula (III) or (IV), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.23 and R.sup.24
are hydrogen.
[1196] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, each R.sup.25 is independently hydrogen or C.sub.1-C.sub.6
alkyl. In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, each R.sup.25 is independently C.sub.1-C.sub.6 alkyl.
[1197] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.21 and R.sup.22 are taken together with the atoms to
which they are attached to form a heterocycloalkyl optionally
substituted with one, two, or three R.sup.30l. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.21 and
R.sup.22 are taken together with the atoms to which they are
attached to form a heterocycloalkyl optionally substituted with
one, two, or three R.sup.30l.
[1198] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, R.sup.30l is C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl,
cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently
optionally substituted with one, two, or three R.sup.31. In some
embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.30l is aryl optionally substituted with one, two, or three
R.sup.31.
[1199] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, each R.sup.30l is independently halogen, --CN, --OH,
--OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6 alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.31. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each R.sup.30l
is independently halogen, --CN, --OH, --OR.sup.a, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6 haloalkyl. In some embodiments of a
compound of Formula (III) or (IV), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.30l is
independently halogen or C.sub.1-C.sub.6 alkyl. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each R.sup.30l
is independently halogen.
[1200] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, each R.sup.30l, R.sup.30g, R.sup.30h, R.sup.30i,
R.sup.30j, and R.sup.30k is independently halogen, --CN, --OH,
--OR.sup.a, --NR.sup.cR.sup.d, --C(.dbd.O)OR.sup.b,
--C(.dbd.O)NR.sup.cR.sup.d, C.sub.1-C.sub.6alkyl, cycloalkyl,
heterocycloalkyl, aryl, heteroaryl; wherein each alkyl, cycloalkyl,
heterocycloalkyl, aryl, and heteroaryl is independently optionally
substituted with one, two, or three R.sup.31. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each R.sup.30f,
R.sup.30g, R.sup.30h, R.sup.30i, R.sup.30j, and R.sup.30k is
independently halogen, --CN, --OH, --OR.sup.a, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6 haloalkyl. In some embodiments of a
compound of Formula (III) or (IV), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.30d is
independently halogen, --OH, C.sub.1-C.sub.6 alkyl, or
C.sub.1-C.sub.6 haloalkyl. In some embodiments of a compound of
Formula (III) or (IV), or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof each R.sup.30l, R.sup.30g,
R.sup.30h, R.sup.30i, R.sup.30j, and R.sup.30k is independently
halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl. In
some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30f, R.sup.30g, R.sup.30h, R.sup.30i, R.sup.30j, and
R.sup.30k is independently halogen, or C.sub.1-C.sub.6 alkyl. In
some embodiments of a compound of Formula (III) or (IV), or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.30f, R.sup.30g, R.sup.30h, R.sup.30i, R.sup.30j, and
R.sup.30k is independently halogen.
[1201] In some embodiments of a compound of Formula (III) or (IV),
or a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof, each R.sup.31 is independently halogen, C.sub.1-C.sub.6
alkyl, or C.sub.1-C.sub.6 haloalkyl. In some embodiments of a
compound of Formula (III) or (IV), or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof, each R.sup.31 is
independently halogen or C.sub.1-C.sub.6 alkyl. In some embodiments
of a compound of Formula (III) or (IV), or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, each R.sup.31 is
independently halogen. In some embodiments of a compound of Formula
(III) or (IV), or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, each R.sup.31 is independently
C.sub.1-C.sub.6 alkyl.
[1202] In some embodiments of a compound of Formula (I), (II),
(IIa), (IIb), (III), or (IV) or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, each R.sup.a is independently
C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 haloalkyl, C.sub.1-C.sub.6
hydroxyalkyl, C.sub.1-C.sub.6 heteroalkyl, cycloalkyl,
heterocycloalkyl, aryl, or heteroaryl. In some embodiments of a
compound of Formula (I), (II), (IIa), (IIb), (III), or (IV) or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.a is independently C.sub.1-C.sub.6 alkyl,
C.sub.1-C.sub.6 haloalkyl, or cycloalkyl. In some embodiments of a
compound of Formula (I), (OI), (IIa), (IIb), (III), or (IV) or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.a is independently C.sub.1-C.sub.6 alkyl or
C.sub.1-C.sub.6 haloalkyl. In some embodiments of a compound of
Formula (I), (II), (IIa), (IIb), (III), or (IV) or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
each R.sup.a is independently C.sub.1-C.sub.6 alkyl.
[1203] In some embodiments of a compound of Formula (I), (II),
(IIa), (IIb), (III), or (IV) or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, each R.sup.b is independently
hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 haloalkyl,
C.sub.1-C.sub.6 hydroxyalkyl, C.sub.1-C.sub.6 heteroalkyl,
cycloalkyl, heterocycloalkyl, aryl, or heteroaryl. In some
embodiments of a compound of Formula (I), (II), (IIa), (IIb),
(III), or (IV) or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, each R.sup.b is independently hydrogen,
C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 haloalkyl, or cycloalkyl. In
some embodiments of a compound of Formula (I), (II), (IIa), (IIb),
(III), or (IV) or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, each R.sup.b is independently hydrogen,
C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl. In some
embodiments of a compound of Formula (I), (II), (IIa), (IIb),
(III), or (IV) or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof; each R.sup.b is independently hydrogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(I), (II), (IIa), (IIb), (III), or (IV) or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof each R.sup.b is
hydrogen. In some embodiments of a compound of Formula (I), (II),
(IIa), (IIb), (III), or (IV) or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, each R.sup.b is independently
C.sub.1-C.sub.6 alkyl.
[1204] In some embodiments of a compound of Formula (I), (II),
(IIa), (IIb), (III), or (IV) or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof: R.sup.c and R.sup.d are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6
haloalkyl, C.sub.1-C.sub.6 hydroxyalkyl, C.sub.1-C.sub.6
heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl. In
some embodiments of a compound of Formula (I), (II), (IIa), (IIb),
(III), or (IV) or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.c and R.sup.d are each independently
hydrogen, C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 haloalkyl, or
cycloalkyl. In some embodiments of a compound of Formula (I), (II),
(IIa), (IIb), (III), or (IV) or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.c and R.sup.d are each
independently hydrogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6
haloalkyl. In some embodiments of a compound of Formula (I), (II),
(IIa), (IIb), (III), or (IV) or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.c and R.sup.d are each
independently hydrogen or C.sub.1-C.sub.6 alkyl. In some
embodiments of a compound of Formula (I), (II), (IIa), (IIb),
(III), or (IV) or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.c and R.sup.d are each hydrogen. In
some embodiments of a compound of Formula (I), (II), (IIa), (IIb),
(III), or (IV) or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.c and R.sup.d are each independently
C.sub.1-C.sub.6 alkyl.
[1205] In some embodiments of a compound of Formula (I), (II),
(IIa), (IIb), (III), or (IV) or a pharmaceutically acceptable salt,
solvate, or stereoisomer thereof, R.sup.c and R.sup.d are taken
together with the nitrogen atom to which they are attached to form
a heterocycloalkyl optionally substituted with one, two, or three
halogen, C.sub.1-C.sub.6 alkyl, or C.sub.1-C.sub.6 haloalkyl. In
some embodiments of a compound of Formula (I), (II), (IIa), (IIb),
(III), or (IV) or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof, R.sup.c and R.sup.d are taken together with
the nitrogen atom to which they are attached to form a pyrrolidine
optionally substituted with one, two, or three halogen or
C.sub.1-C.sub.6 alkyl. In some embodiments of a compound of Formula
(I), (II), (IIa), (IIb), (III), or (IV) or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, R.sup.c and
R.sup.d are taken together with the nitrogen atom to which they are
attached to form a piperidine optionally substituted with one, two,
or three halogen or C.sub.1-C.sub.6 alkyl. In some embodiments of a
compound of Formula (I), (II), (IIa), (IIb), (III), or (IV) or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof,
R.sup.c and R.sup.d are taken together with the nitrogen atom to
which they are attached to form a piperazine optionally substituted
with one, two, or three halogen or C.sub.1-C.sub.6 alkyl.
[1206] Any combination of the groups described above for the
various variables is contemplated herein. Throughout the
specification, groups and substituents thereof are chosen by one
skilled in the field to provide stable moieties and compounds.
[1207] In some embodiments is a compound, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, having a
structure selected from:
TABLE-US-00001 Ex. STRUCTURE NAME 1 ##STR00019##
(2-(((2R,3S,4R,5R)-5-(6-chloro-4-((2-
chlorobenzyl)amino)-1H-pyrazolo[3,4- d]dipyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)-2-oxoethyl)phosphonic acid
2 ##STR00020## (2-((((2R,3S,4R,5R)-5-(6-chloro-4-((2-
chlorobenzyl)amino)-1H-pyrazolo[3,4- d]dipyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methyl)amino)-2-oxoethyl)phosphonic
acid 3 ##STR00021## ((N-(((2R,3S,4R,5R)-5-(6-chloro-4-((2-
chlorobenzyl)amino)-1H-pyrazolo[3,4- d]dipyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methyl)sulfamoyl)methyl)phosphonic
acid 4 ##STR00022## (2-((2R,3S,4R,5R)-5-(6-chloro-4-(((S)-2,3-
dihydro-1H-inden-1-yl)(methyl)amino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)ethyl)phosphonic acid 5 ##STR00023## (2-(((2R,3S,4R,5R)-5-(4-
(benzyl(methyl)amino)-6-chloro-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)ethyl)phosphonic acid 6 ##STR00024##
(2-(((2R,3S,4R,5R)-5-(4- (benzyl(methyl)amino)-6-chloro-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)ethyl)phosphonic acid 7 ##STR00025##
((((2R,3S,4R,5R)-5-(4- (benzyl(methyl)amino)-6-chloro-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 8 ##STR00026##
(2-(((2R,3S,4R,5R)-5-(6-chloro-4-(((S)-2,3-
dihydro-1H-inden-1-yl)(methyl)amino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2-yl)methoxy)-2- oxoethyl)phosphonic acid
9 ##STR00027## (2-((((2R,3S,4R,5R)-5-(6-chloro-4-((2-
chlorobenzyl)amino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methyl)(methyl)amino)-2-
oxoethyl)phosphonic acid 10 ##STR00028##
((((2R,3S,4R,5R)-5-(6-chloro-4-((2-
chlorobenzyl)amino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 11
##STR00029## (2-(((2R,3S,4R,5R)-5-(5-chloro-7-(((S)-2,3-
dihydro-1H-inden-1-yl)(methyl)amino)-3H-
[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)-3,4-
dihydroxytetrahydrofuran-2-yl)methoxy)-2- oxoethyl)phosphonic acid
12 ##STR00030## ((((2R,3S,4R,5R)-5-(5-chloro-7-(((S)-2,3-
dihydro-1H-inden-1-yl)amino)-3H-
[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 13
##STR00031## (((((2R,3S,4R,5R)-5-(6-chloro-4-((2-
chlorobenzyl)amino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)thio)methyl)phosphonic acid
14 ##STR00032## (((((2R,3S,4R,5R)-5-(6-chloro-4-((2-
chlorobenzyl)amino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2-yl) methyl)sulfonyl)methyl)phosphonic
acid 15 ##STR00033## ((((2R,3S,4R,5R)-5-(2-chloro-4-
((cyclopropylmethyl)amino)-7H- pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2-yl) methoxy)methyl)phosphonic acid 16
##STR00034## ((((2R,3S,4R,5R)-5-(5-chloro-7-
((cyclopropylmethyl)amino)-3H-
[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 17
##STR00035## ((((2R,3S,4R,5R)-5-(4-((2-
chlorobenzyl)amino)-6-(hydroxymethyl)-
1H-pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 18 ##STR00036##
((((2R,3S,4R,5R)-5-(4-((3- chlorobenzyl)amino)-6-cyano-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 19 ##STR00037##
((((2R,3S,4R,5R)-5-(6-chloro-4-((2-
chlorobenzyl)amino)-1H-pyrazolo[3,4-
d]pyrimidin-1-yl)-3,4-dihydroxy-3- methyltetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 20 ##STR00038##
(2-((((2R,3S,4R,5R)-5-(6-chloro-4-((2-
chlorobenzyl)amino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methyl)(isobutyl)amino)-2-
oxoethyl)phosphonic acid 23 ##STR00039##
((((1R,2R,3S,4R)-4-(5-chloro-7-(((S)-2,3-
dihydro-1H-inden-1-yl)amino)-3H-
[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)-2,3-
dihydroxycyclopentyl)methoxy)methyl) phosphonic acid 24
##STR00040## ((((2R,3S,4R,5R)-5-(5-chloro-7-((3-
chlorobenzyl)amino)-3H-[1,2,3] triazolo[4,5- d]pyrimidin-3-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 25
##STR00041## ((((2R,3S,4R,5R)-5-(6-chloro-4-(((S)-2,3-
dihydro-1H-inden-1-yl)amino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 26 ##STR00042##
((((2R,3S,4R,5R)-5-(5-chloro-7-(((S)-2,3-
dihydro-1H-inden-1-yl)(methyl)amino)-3H-
[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 27
##STR00043## ((((2R,3S,4R,5R)-5-(6-chloro-4-((3-
chlorobenzyl)amino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 28
##STR00044## (2-(benzyl(((2R,3S,4R,5R)-5-(6-chloro-4-
((3-chlorobenzyl)amino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 29
##STR00045## ((((2R,3S,4R,5R)-5-(6-chloro-4-((3-
fluorobenzyl)amino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 30
##STR00046## ((((2R,3S,4R,5R)-5-(5-chloro-7-((2-
chlorobenzyl)amino)-3H-[1,2,3] triazolo[4,5- d]pyrimidin-3-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 31
##STR00047## ((((2R,3S,4R,5R)-5-(6-chloro-4-(((S)-2,3-
dihydro-1H-inden-1-yl)(methyl)amino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 32 ##STR00048##
((((2R,3S,4R,5R)-5-(6-chloro-4-((3-
(trifluoromethyl)benzyl)amino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 33 ##STR00049##
((((2R,3S,4R,5R)-5-(6-chloro-4-(((S)-1-(2-
chlorophenyl)ethyl)amino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 34
##STR00050## ((((2R,3S,4R,5R)-5-(6-chloro-4-(((S)-1-
(3-chlorophenyl)ethyl)amino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 35 ##STR00051##
((((2R,3S,4R,5R)-5-(6-chloro-4-(((S)-
1-(3-chlorophenyl)ethyl)amino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 36 ##STR00052##
((((2R,3S,4R,5R)-5-(6-chloro-4-(((S)-1-(3-
chlorophenyl)ethyl)(methyl)amino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 37 ##STR00053##
((((2R,3S,4R,5R)-5-(6-chloro-4-((3- chlorobenzyl)(methyl)amino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 38 ##STR00054##
((((2R,3S,4R,5R)-5-(6-chloro-4- ((cyclopropylmethyl)amino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 39 ##STR00055##
((((2R,3S,4R,5R)-5-(5-chloro-7-((3- chlorobenzyl)(methyl)amino)-3H-
[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 40
##STR00056## ((((2R,3S,4R,5R)-5-(2-chloro-4-((2-
chlorobenzyl)amino)-7H-pyrazolo[2,3- d]pyrimidin-7-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 41
##STR00057## ((((2R,3S,4R,5R)-5-(6-chloro-4-((3-
methylbenzyl)amino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 42
##STR00058## ((((2R,3S,4R,5R)-5-(6-chloro-4- morpholino-
1H-pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 43 ##STR00059##
((((2R,3S,4R,5R)-5-(6-chloro-4- (ethylamino)-
1H-pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 44 ##STR00060##
((((2R,3S,4R,5R)-5-(4-((3- chlorobenzyl)amino)-6-methyl-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 45 ##STR00061##
((((2R,3S,4R,5R)-5-(6-chloro-4-((((R)-
tetrahydrofuran-3-yl)methyl)amino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 46 ##STR00062##
((((2R,3S,4R,5R)-5-(6-chloro-4-((3-
cyanobenzyl)amino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 47
##STR00063## ((((2R,3S,4R,5R)-5-(6-chloro-4-((2,3-
dichlorobenzyl)amino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 48
##STR00064## ((((2R,3S,4R,5R)-5-(6-chloro-4-(((1- methyl-
1H-indazol-7-yl)methyl)amino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 49 ##STR00065##
((((2R,3S,4R,5R)-5-(6-chloro-4- ((naphthalen-
1-ylmethyl)amino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 50
##STR00066## (((S)-1-((2S,3S,4R,5R)-5-(6-chloro-4-
((2-chlorobenzyl)amino)-1H- pyrazolo[3,4-d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 51
##STR00067## ((((2R,3S,4R,5R)-5-(6-chloro-4- ((quinolin-5-
ylmethyl)amino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 52
##STR00068## ((((2R,3S,4R,5R)-5-(6-chloro-4-
(methylamino)-1H-pyrazolo[3,4- d]pyrimidin-
1-yl)-3,4-dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic
acid 53 ##STR00069## ((((2R,3S,4R,5R)-5-(6-chloro-4-
(cyclopentyl(methyl)amino)- 1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 54
##STR00070## ((((2R,3S,4R,5R)-5-(4-((3-
chlorobenzyl)amino)-6-isobutoxy-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 55 ##STR00071##
((((2R,3S,4R,5R)-5-(4-((3- chlorobenzyl)amino)-6-
(pyrrolidin-1-yl)-1H- pyrazolo[3,4-d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 56
##STR00072## ((((2R,3S,4R,5R)-5-(4-((3- chlorobenzyl)amino)-6-
(methylamino)-1H- pyrazolo[3,4-d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 57
##STR00073## ((((2R,3S,4R,5R)-5-(4-amino-6- chloro-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 58 ##STR00074##
((((2R,3S,4R,5R)-5-(6-chloro-4-((3- chloro-2-
fluorobenzyl)amino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 59
##STR00075## ((((2R,3S,4R,5R)-5-(5-chloro-7-((2-
chlorobenzyl)(methyl)amino)-3H-
[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 60
##STR00076## (((R)-1-((2S,3S,4R,5R)-5-(6-chloro-4-((2-
chlorobenzyl)amino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)ethoxy)methyl)phosphonic acid 61
##STR00077## (((((2S,3S,4R,5R)-5-(6-chloro-4-((3-
chlorobenzyl)amino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methyl)sulfonyl)methyl)phosphonic
acid 62 ##STR00078## (((((2S,3S,4R,5R)-5-(6-chloro-4-
((cyclopropylmethyl)amino)-1H- pyrazolo[3,4-d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methyl)sulfonyl)methyl)phosphonic
acid 63 ##STR00079## ((((2R,3S,4R,5R)-5-(6-chloro-4-
(isobutylamino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 64
##STR00080## ((((2R,3S,4R,5R)-5-(6-chloro-4-((2-
chlorobenzyl)(methyl)amino)-1H- pyrazolo[3,4-d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 65
##STR00081## ((((2R,3S,4R,5R)-5-(6-chloro-4-((3-
chlorobenzyl)oxy)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 66
##STR00082## (((((2S,3S,4R,5R)-5-(6-chloro-4-
((cyclopentylamino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methyl)sulfonyl)methyl)phosphonic
acid 67 ##STR00083## ((((2R,3S,4R,5R)-5-(4-((3-
chlorobenzyl)amino)-6- (isobutylamino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 68 ##STR00084##
((((2R,3S,4R,5R)-5-(6-chloro-4- ((cyclobutylmethyl)amino)-1H-
pyrazolo[3,4- d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 69 ##STR00085##
((((2R,3S,4R,5R)-5-(6-chloro-4-((((S)-
tetrahydrofuran-2-yl)methyl)amino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 70 ##STR00086##
((((2R,3S,4R,5R)-5-(6-chloro-4-((((R)-
tetrahydrofuran-2-yl)methyl)amino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 71 ##STR00087##
((((2R,3S,4R,5R)-5-(6-chloro-4-((((S)-
tetrahydrofuran-2-yl)methyl)amino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 72 ##STR00088##
((((2R,3S,4R,5R)-5-(6-chloro-4-
((cyclopropylmethyl)(methyl)amino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 73 ##STR00089##
((((2R,3S,4R,5R)-5-(6-chloro-4- ((tetrahydro-
2H-pyran-4-yl)amino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 74
##STR00090## ((((2R,3S,4R,5R)-5-(6-chloro-4-
(isopropylamino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 75
##STR00091## ((((2R,3S,4R,5R)-5-(6-chloro-4-
(phenylamino)-1H-pyrazolo[3,4- d]pyrimidin-
1-yl)-3,4-dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic
acid 76 ##STR00092## ((((2R,3S,4R,5R)-5-(6-chloro-4-
(cyclopropylamino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 77
##STR00093## ((((2R,3S,4R,5R)-5-(6-chloro- 4-(((1s,3S)-3-
hydroxy-3-methylcyclobutyl)amino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 78 ##STR00094##
((((2R,3S,4R,5R)-5-(6-chloro-4- (pentan-3-ylamino)-1H-pyrazolo[3,4-
d]pyrimidin-1-yl)- 3,4-dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 79 ##STR00095##
((((2R,3S,4R,5R)-5-(6-chloro-4- (cyclobutylamino)-1H-pyrazolo[3,4-
d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 80 ##STR00096##
((((2R,3S,4R,5R)-5-(6-chloro-4-(((R)-
tetrahydrofuran-3-yl)amino)-1H- pyrazolo[3,4-d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 81
##STR00097## ((((2R,3S,4R,5R)-5-(6-chloro-4- (pyrrolidin-
1-yl)-1H-pyrazolo[3,4-d]pyrimidin-1-
yl)-3,4-dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic
acid 82 ##STR00098## ((((2R,3S,4R,5R)-5-(4-
((cyclopropylmethyl)amino)-6-methoxy-
1H-pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 83 ##STR00099##
((((2R,3S,4R,5R)-5-(4-(azetidin-1-yl)-6-
cyclo-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-
3,4-dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid
84 ##STR00100## (((((2R,3S,4R,5R)-5-(6-chloro-4-
((cyclopropylmethyl)(methyl)amino-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)sulfonyl)methyl)phosphonic acid 85 ##STR00101##
((2-((2R,3S,4R,5R)-5-(6-chloro-4- ((cyclopropylmethyl)amino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)ethoxy)methyl)phosphonic acid 86 ##STR00102##
((((2R,3S,4R,5R)-5-(6-chloro-4-(((3,3-
difluorocyclobutyl)methyl)amino-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 87 ##STR00103##
((((2R,3S,4R,5R)-5-(6-chloro-4-((3,3- difluorocyclobutyl)amino-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 88 ##STR00104##
(((2-((2R,3S,4R,5R)-5-(6-chloro-4- ((cyclopropylmethyl)amino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)ethyl)sulfonyl)methyl)phosphonic acid 89 ##STR00105##
((((2R,3S,4R,5R)-5-(6-chloro-4- ((((1s,3S)-3-hydroxy-3-
methylcyclobutyl)methyl)amino)-
1H-pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 90 ##STR00106##
((((2R,3S,4R,5R)-5-(6-chloro-4-((pyridin-
2-ylmethyl)amino-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 91
##STR00107## ((((2R,3S,4R,5R)-5-(6-chloro-4-(((S)-1-
cyclopropylmethyl)amino)-1H- pyrazolo[3,4-d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 92
##STR00108## ((((2R,3S,4R,5R)-5-(6-chloro-4-(((R)-1-
cyclopropylethyl)amino)-1H- pyrazolo[3,4-d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 93
##STR00109## ((((2R,3S,4R,5R)-5-(6-chloro-4-
(cyclohexylamino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 94
##STR00110## ((((2R,3S,4R,5R)-5-(6-chloro-4-((2-
cyclopropylethyl)amino)-1H- pyrazolo[3,4-d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 95
##STR00111## ((((2R,3S,4R,5R)-5-(5-chloro-7- (cyclohexylamino)-3H-
[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 96
##STR00112## ((((2R,3S,4R,5R)-5-(6-chloro-4-(((1-
methylcyclopropyl)methyl)amino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 97 ##STR00113##
((((2R,3S,4R,5R)-5-(2-chloro-4-
((cyclopropylmethyl)amino)-6-methyl-
7H-pyrrolo[2,3-d]pyrimidin-7-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 98 ##STR00114##
((N-(((2R,3S,4R,5R)-5-(6-chloro-4-
(cyclopentylamino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2-yl)methyl)-N-
methylsulfamoyl)methyl)phosphonic acid 99 ##STR00115##
((((2R,3S,4R,5R)-5-(6-chloro-4-(N-
cyclopentylacetamido)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 100
##STR00116## ((((2R,3S,4R,5R)-5-(6-chloro-4-(5-
methylfuran-2-yl)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 101
##STR00117## (3-((2R,3S,4R,5R)-5-(6-chloro-4-
(cyclopentylamino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)propyl)phosphonic acid 102
##STR00118## ((((2R,3S,4R,5R)-5-(6-chloro-4-(((S)-
2,2-dimethylcyclopentyl)amino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 103 ##STR00119##
((((2R,3S,4R,5R)-5-(6-chloro-4-(((R)-2,2-
dimethylcyclopentyl)amino)-1H- pyrazolo[3,4-d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 104
##STR00120## ((((2R,3S,4R,5R)-5-(6-chloro-4-
(((1S,2R)-2-methylcyclopropyl)amino)-
1H-pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 105 ##STR00121##
((((2R,3S,4R,5R)-5-(6-chloro-4- (((1S,2R)-2-
methylcyclopropyl)amino)- 1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 106
##STR00122## (((((2R,3S,4R,5R)-5-(5-chloro-7-
(cyclopentylamino)-3H-[1,2,3] triazolo[4,5- d]pyrimidin-3-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphoryl)
methyl)phosphonic acid 107 ##STR00123##
(((((2R,3S,4R,5R)-5-(6-chloro-4- (cyclobutylamino)-1H-pyrazolo[3,4-
d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methyl)sulfonyl)methyl)phosphonic acid 108 ##STR00124##
(((((2S,3S,4R,5R)-5-(6-chloro-7- (cyclobutylamino)-3H-
[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methyl)sulfonyl)methyl)phosphonic
acid 109 ##STR00125## (2-((((2R,3S,4R,5R)-5-(6-chloro-4-
(cyclobutylamino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methyl)(methyl)amino)-2-
oxoethyl)phosphonic acid 110 ##STR00126##
(((((2S,3S,4R,5R)-5-(5-chloro-7-
(cyclobutylamino)-3H-[1,2,3]triazolo[4,5- d]pyrimidin-3-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methyl)sulfonyl)methyl)phosphonic
acid 111 ##STR00127## (((((2S,3S,4R,5R)-5-(6-chloro-4-
((cyclobutylmethyl)amino)-1H- pyrazolo[3,4-d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methyl)sulfonyl)methyl)phosphonic
acid 112 ##STR00128## (((((2S,3S,4R,5R)-5-(2-chloro-6-
(cyclopentylamino)-9H-purin-9-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methyl)sulfonyl)methyl)phosphonic acid 113 ##STR00129##
(((((2S,3S,4R,5R)-5-(5-chloro-7-
((cyclobutylmethyl)amino)-3H-[1,2,3]
triazolo[4,5-d]pyrimidin-3-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methyl)sulfonyl)methyl)phosphonic acid 114 ##STR00130##
(((((2S,3S,4R,5R)-5-(5-chloro-7-(((S)-
1-(4-fluorophenyl)ethyl)amino)-3H-
[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)-
3,4-dihydroxytetrahydrofuran-2-
yl)methyl)sulfonyl)methyl)phosphonic acid 115 ##STR00131##
(2-((((2R,3S,4R,5R)-5-(5-chloro-7- (cyclopentylamino)-3H-
[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)-
3,4-dihydroxytetrahydrofuran-2- yl)methyl)(methyl)amino)-2-
oxoethyl)phosphonic acid 116 ##STR00132##
(((((2S,3S,4R,5R)-5-(6-chloro-4- (((S)-1-(4-fluorophenyl)
ethyl)amino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methyl)sulfonyl)methyl)phosphonic
acid 117 ##STR00133## (((((2S,3S,4R,5R)-5-(6-chloro-4-((4-
fluorobenzyl)amino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methyl)sulfonyl)methyl)phosphonic
acid 118 ##STR00134## (((((2S,3S,4R,5R)-5-(5-chloro-7-((2-
chlorobenzyl)amino)-3H- [1,2,3]triazolo[4,5- d]pyrimidin-3-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methyl)sulfonyl)methyl)phosphonic
acid 119 ##STR00135## (((((2S,3S,4R,5R)-5-(5-chloro-7-((4-
fluorobenzyl)amino)-3H- [1,2,3]triazolo[4,5- d]pyrimidin-3-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methyl)sulfonyl)methyl)phosphonic
acid 120 ##STR00136## (((((2S,3S,4R,5R)-5-(5-chloro-7-((4-
chlorobenzyl)amino)-3H- [1,2,3]triazolo[4,5- d]pyrimidin-3-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methyl)sulfonyl)methyl)phosphonic
acid
121 ##STR00137## (((((2S,3S,4R,5R)-5-(5-chloro-7-((2,3-
dihydro-1H-inden-2-yl)amino)-3H-
[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)-
3,4-dihydroxytetrahydrofuran-2-
yl)methyl)sulfonyl)methyl)phosphonic acid 122 ##STR00138##
(((((2S,3S,4R,5R)-5-(5-chloro-7-((3- chlorobenzyl)amino)-3H-
[1,2,3]triazolo[4,5- d]pyrimidin-3-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methyl)sulfonyl)methyl)phosphonic
acid 123 ##STR00139## (((((2S,3S,4R,5R)-5-(6-chloro-4-(((S)-
2,3-dihydro-1H-inden-1-yl)amino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methyl)sulfonyl)methyl)phosphonic acid 124 ##STR00140##
(((((2S,3S,4R,5R)-5-(6-chloro-4- ((cyclobutylmethyl)amino)-1H-
pyrazolo[3,4- d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methyl)sulfonyl)methyl)phosphonic acid 125 ##STR00141##
(((((2S,3S,4R,5R)-5-(4- (cyclopentylamino)-6-
(hydroxymethyl)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methyl)sulfonyl)methyl)phosphonic
acid 126 ##STR00142## (((((2S,3S,4R,5R)-5-(6-chloro-4-((2,3-
dihydro-1H-inden-2-yl)amino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methyl)sulfonyl)methyl)phosphonic acid 127 ##STR00143##
(((((2S,3S,4R,5R)-5-(6-chloro-4-((4- chlorobenzyl)amino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methyl)sulfonyl)methyl)phosphonic acid 128 ##STR00144##
(((((2S,3S,4R,5R)-5-(6-chloro-4-((2- methylcyclopentyl)amino)-1H-
pyrazolo[3,4- d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methyl)sulfonyl)methyl)phosphonic acid 129 ##STR00145##
(((((2S,3S,4R,5R)-5-(6-chloro-4- (((S)-1-(2-chlorophenyl)ethyl)
amino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methyl)sulfonyl)methyl)phosphonic
acid 130 ##STR00146## (((((2S,3S,4R,5R)-5-(5-chloro-7-(((S)-
2,3-dihydro-1H-inden-2-yl)amino)-3H-
[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)-
3,4-dihydroxytetrahydrofuran-2-
yl)methyl)sulfonyl)methyl)phosphonic acid 131 ##STR00147##
(4S)-2-(((((2S,3S,4R,5R)-5-(6-chloro-4-
(cyclobutylmethyl)amino)-1H- pyrazolo[3,4-d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methyl)sulfonyl)methyl)-4-(3-
chlorophenyl)-1,2,3- dioxaphosphinane 2-oxide 132 ##STR00148##
((((2R,3S,4R,5R)-5-(4- chloropentylamino)-
6-(2-hydroxypropan-2-yl)-1H- pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methoxy)methyl)phosphonic acid 133
##STR00149## (((((2S,3S,4R,5R)-5-(6-chloro-4-
(cyclopentyl(2-methoxyethyl)amino)-
1H-pyrazolo[3,4-d]pyrimidin-1-yl)- 3,4-dihydroxytetrahydrofuran-2-
yl)methyl)sulfonyl)methyl)phosphonic acid 134 ##STR00150##
(((((2S,3S,4R,5R)-5-(6-chloro-4-
(((1R,2S)-2-methylcyclopentyl)amino)-
1H-pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methyl)sulfonyl)methyl)phosphonic acid 135 ##STR00151##
(((((2S,3S,4R,5R)-5-(6-chloro-4- (((1S,2R)-2-methylcyclopentyl)
amino)-1H-pyrazolo[3,4- d]pyrimidin-1-yl)-3,4-
dihydroxytetrahydrofuran-2- yl)methyl)sulfonyl)methyl)phosphonic
acid 136 ##STR00152## (((((2S,3S,4R,5R)-5-(6-chloro-4-(((R)-
2,3-dihydro-1H-inden-1-yl)amino)-
1H-pyrazolo[3,4-d]pyrimidin-1-yl)- 3,4-dihydroxytetrahydrofuran-2-
yl)methyl)sulfonyl)methyl)phosphonic acid 137 ##STR00153##
((((2R,3S,4R,5R)-5-(6-chloro-4- (cyclopentylamino)-7H-pyrrolo[2,3-
d]pyrimidin-7-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid 138 ##STR00154##
((((2R,3S,4R,5R)-5-(6-chloro-4-(((1-
cyanocyclopropyl)methyl)amino)-1H-
pyrazolo[3,4-d]pyrimidin-1-yl)-3,4- dihydroxytetrahydrofuran-2-
yl)methoxy)methyl)phosphonic acid
[1208] In some embodiments is a compound, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, having a
structure selected from:
##STR00155## ##STR00156## ##STR00157## ##STR00158## ##STR00159##
##STR00160## ##STR00161## ##STR00162## ##STR00163## ##STR00164##
##STR00165## ##STR00166## ##STR00167## ##STR00168## ##STR00169##
##STR00170## ##STR00171## ##STR00172## ##STR00173## ##STR00174##
##STR00175## ##STR00176## ##STR00177## ##STR00178## ##STR00179##
##STR00180## ##STR00181## ##STR00182##
##STR00183## ##STR00184## ##STR00185## ##STR00186## ##STR00187##
##STR00188## ##STR00189## ##STR00190## ##STR00191## ##STR00192##
##STR00193## ##STR00194## ##STR00195## ##STR00196## ##STR00197##
##STR00198## ##STR00199## ##STR00200## ##STR00201## ##STR00202##
##STR00203## ##STR00204## ##STR00205## ##STR00206## ##STR00207##
##STR00208## ##STR00209## ##STR00210## ##STR00211##
[1209] In some embodiments is a compound, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, having a
structure selected from:
##STR00212## ##STR00213##
[1210] In some embodiments is a compound, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof, having a
structure selected from;
##STR00214## ##STR00215##
Further Forms of Compounds Disclosed Herein
Isomers Stereoisomers
[1211] In some embodiments, the compounds described herein exist as
geometric isomers. In some embodiments, the compounds described
herein possess one or more double bonds. The compounds presented
herein include all cis, trans, syn, anti, entgegen (E), and
zusammen (Z) isomers as well as the corresponding mixtures thereof.
In some situations, the compounds described herein possess one or
more chiral centers and each center exists in the R configuration,
or S configuration. The compounds described herein include all
diastereomeric, enantiomeric, and epimeric forms as well as the
corresponding mixtures thereof. In additional embodiments of the
compounds and methods provided herein, mixtures of enantiomers
and/or diastereoisomers, resulting from a single preparative step,
combination, or interconversion are useful for the applications
described herein. In some embodiments, the compounds described
herein are prepared as their individual stereoisomers by reacting a
racemic mixture of the compound with an optically active resolving
agent to form a pair of diastereoisomeric compounds, separating the
diastereomers and recovering the optically pure enantiomers. In
some embodiments, dissociable complexes are preferred. In some
embodiments, the diastereomers have distinct physical properties
(e.g., melting points, boiling points, solubilities, reactivity,
etc.) and are separated by taking advantage of these
dissimilarities. In some embodiments, the diastereomers are
separated by chiral chromatography, or preferably, by
separation/resolution techniques based upon differences in
solubility. In some embodiments, the optically pure enantiomer is
then recovered, along with the resolving agent.
Labeled Compounds
[1212] In some embodiments, the compounds described herein exist in
their isotopically-labeled forms. In some embodiments, the methods
disclosed herein include methods of treating diseases by
administering such isotopically-labeled compounds. In some
embodiments, the methods disclosed herein include methods of
treating diseases by administering such isotopically-labeled
compounds as pharmaceutical compositions. Thus, in some
embodiments, the compounds disclosed herein include
isotopically-labeled compounds, which are identical to those
recited herein, but for the fact that one or more atoms are
replaced by an atom having an atomic mass or mass number different
from the atomic mass or mass number usually found in nature.
Examples of isotopes that can be incorporated into compounds
disclosed herein, or a solvate, or stereoisomer thereof, include
isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorous,
sulfur, fluorine, and chloride, such as .sup.2H, .sup.3H, .sup.13C,
.sup.14O, .sup.15N, .sup.18O, .sup.17O, .sup.31P, .sup.32P,
.sup.35S, .sup.18F, and .sup.36Cl, respectively. Compounds
described herein, and the metabolites, pharmaceutically acceptable
salts, esters, prodrugs, solvate, hydrates or derivatives thereof
which contain the aforementioned isotopes and/or other isotopes of
other atoms are within the scope of this invention. Certain
isotopically-labeled compounds, for example those into which
radioactive isotopes such as .sup.3H and .sup.14C are incorporated,
are useful in drug and/or substrate tissue distribution assays.
Tritiated, i.e., .sup.3H and carbon-14, i.e., .sup.14C, isotopes
are particularly preferred for their ease of preparation and
detectability. Further, substitution with heavy isotopes such as
deuterium, i.e., .sup.2H, produces certain therapeutic advantages
resulting from greater metabolic stability, for example increased
in vivo half-life or reduced dosage requirements. In some
embodiments, the isotopically labeled compound or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof
is prepared by any suitable method.
[1213] In some embodiments, the compounds described herein are
labeled by other means, including, but not limited to, the use of
chromophores or fluorescent moieties, bioluminescent labels, or
chemiluminescent labels.
Pharmaceutically Acceptable Salts
[1214] In some embodiments, the compounds described herein exist as
their pharmaceutically acceptable salts. In some embodiments, the
methods disclosed herein include methods of treating diseases by
administering such pharmaceutically acceptable salts. In some
embodiments, the methods disclosed herein include methods of
treating diseases by administering such pharmaceutically acceptable
salts as pharmaceutical compositions.
[1215] In some embodiments, the compounds described herein possess
acidic or basic groups and therefor react with any of a number of
inorganic or organic bases, and inorganic and organic acids, to
form a pharmaceutically acceptable salt. In some embodiments, these
salts are prepared in situ during the final isolation and
purification of the compounds disclosed herein, or by separately
reacting a purified compound in its free form with a suitable acid
or base, and isolating the salt thus formed.
[1216] Examples of pharmaceutically acceptable salts include those
salts prepared by reaction of the compounds described herein with a
mineral, organic acid, or inorganic base, such salts including
acetate, acrylate, adipate, alginate, aspartate, benzoate,
benzenesulfonate, bisulfate, bisulfate, bromide, butyrate,
butyn-1,4-dioate, camphorate, camphorsulfonate, caproate,
caprylate, chlorobenzoate, chloride, citrate,
cyclopentanepropionate, decanoate, digluconate,
dihydrogenphosphate, dinitrobenzoate, dodecylsulfate,
ethanesulfonate, formate, fumarate, glucoheptanoate,
glycerophosphate, glycolate, hemisulfate, heptanoate, hexanoate,
hexyne-1,6-dioate, hydroxy benzoate, .gamma.-hydroxybutyrate,
hydrochloride, hydrobromide, hydroiodide, 2-hydroxyethanesulfonate,
iodide, isobutyrate, lactate, maleate, malonate, methanesulfonate,
mandelate metaphosphate, methanesulfonate, methoxybenzoate,
methylbenzoate, monohydrogenphosphate, 1-napthalenesulfonate,
2-napthalenesulfonate, nicotinate, nitrate, palmoate, pectinate,
persulfate, 3-phenylpropionate, phosphate, picrate, pivalate,
propionate, pyrosulfate, pyrophosphate, propiolate, phthalate,
phenylacetate, phenylbutyrate, propanesulfonate, salicylate,
succinate, sulfate, sulfite, succinate, suberate, sebacate,
sulfonate, tartrate, thiocyanate, tosylateundeconate, and
xylenesulfonate.
[1217] Further, the compounds described herein can be prepared as
pharmaceutically acceptable salts formed by reacting the free base
form of the compound with a pharmaceutically acceptable inorganic
or organic acid, including, but not limited to, inorganic acids
such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric
acid, phosphoric acid, metaphosphoric acid, and the like; and
organic acids such as acetic acid, propionic acid, hexanoic acid,
cyclopentanepropionic acid, glycolic acid, pyruvic acid, lactic
acid, malonic acid, succinic acid, malic acid, maleic acid, fumaric
acid, p-toluenesulfonic acid, tartaric acid, trifluoroacetic acid,
citric acid, benzoic acid, 3-(4-hydroxybenzoyl)benzoic acid,
cinnamic acid, mandelic acid, arylsulfonic acid, methanesulfonic
acid, ethanesulfonic acid, 1,2-ethanedisulfonic acid,
2-hydroxyethanesulfonic acid, benzenesulfonic acid,
2-naphthalenesulfonic acid,
4-methylbicyclo-[2.2.2]oct-2-ene-1-carboxylic acid, glucoheptonic
acid, 4,4'-methylenebis-(3-hydroxy-2-ene-1-carboxyl is acid),
3-phenylpropionic acid, trimethylacetic acid, tertiary butylacetic
acid, lauryl sulfuric acid, gluconic acid, glutamic acid,
hydroxynaphthoic acid, salicylic acid, stearic acid, and muconic
acid.
[1218] In some embodiments, those compounds described herein which
comprise a free acid group react with a suitable base, such as the
hydroxide, carbonate, bicarbonate, sulfate, of a pharmaceutically
acceptable metal cation, with ammonia, or with a pharmaceutically
acceptable organic primary, secondary, tertiary, or quaternary
amine. Representative salts include the alkali or alkaline earth
salts, like lithium, sodium, potassium, calcium, and magnesium, and
aluminum salts and the like. Illustrative examples of bases include
sodium hydroxide, potassium hydroxide, choline hydroxide, sodium
carbonate, N.sup.+(C.sub.1-4 alkyl).sub.4, and the like.
[1219] Representative organic amines useful for the formation of
base addition salts include ethylamine, diethylamine,
ethylenediamine, ethanolamine, diethanolamine, piperazine, and the
like. It should be understood that the compounds described herein
also include the quaternization of any basic nitrogen-containing
groups they contain. In some embodiments, water or oil-soluble or
dispersible products are obtained by such quaternization.
Solvates
[1220] In some embodiments, the compounds described herein exist as
solvates. The invention provides for methods of treating diseases
by administering such solvates. The invention further provides for
methods of treating diseases by administering such solvates as
pharmaceutical compositions.
[1221] Solvates contain either stoichiometric or non-stoichiometric
amounts of a solvent, and, in some embodiments, are formed during
the process of crystallization with pharmaceutically acceptable
solvents such as water, ethanol, and the like. Hydrates are formed
when the solvent is water, or alcoholates are formed when the
solvent is alcohol. Solvates of the compounds described herein can
be conveniently prepared or formed during the processes described
herein. By way of example only, hydrates of the compounds described
herein can be conveniently prepared by recrystallization from an
aqueous/organic solvent mixture, using organic solvents including,
but not limited to, dioxane, tetrahydrofuran, or methanol. In
addition, the compounds provided herein can exist in unsolvated as
well as solvated forms. In general, the solvated forms are
considered equivalent to the unsolvated forms for the purposes of
the compounds and methods provided herein.
Tautomers
[1222] In some situations, compounds exist as tautomers. The
compounds described herein include all possible tautomers within
the formulas described herein. Tautomers are compounds that are
interconvertible by migration of a hydrogen atom, accompanied by a
switch of a single bond and adjacent double bond. In bonding
arrangements where tautomerization is possible, a chemical
equilibrium of the tautomers will exist. All tautomeric forms of
the compounds disclosed herein are contemplated. The exact ratio of
the tautomers depends on several factors, including temperature,
solvent, and pH. Some examples of tautomeric interconversions
include:
##STR00216##
Preparation of the Compounds
[1223] The compounds used in the reactions described herein are
made according to organic synthesis techniques known to those
skilled in this art, starting from commercially available chemicals
and/or from compounds described in the chemical literature.
"Commercially available chemicals" are obtained from standard
commercial sources including Acros Organics (Pittsburgh, Pa.),
Aldrich Chemical (Milwaukee, Wis., including Sigma Chemical and
Fluka), Apin Chemicals Ltd. (Milton Park, UK), Avocado Research
(Lancashire, U.K), BDH Inc. (Toronto, Canada), Bionet (Cornwall,
U.K.), Chemservice Inc. (West Chester, Pa.), Crescent Chemical Co.
(Hauppauge, N.Y.), Eastman Organic Chemicals, Eastman Kodak Company
(Rochester, N.Y.), Fisher Scientific Co. (Pittsburgh, Pa.), Fisons
Chemicals (Leicestershire, UK), Frontier Scientific (Logan, Utah),
ICN Biomedicals, Inc. (Costa Mesa. Calif.), Key Organics (Cornwall,
U.K.), Lancaster Synthesis (Windham, N.H.), Maybridge Chemical Co.
Ltd. (Cornwall, U.K), Parish Chemical Co. (Orem Utah), Pfaltz &
Bauer, Inc. (Waterbury, Conn.), Polyorganix (Houston, Tex.), Pierce
Chemical Co. (Rockford, Ill.), Riedel de Haen AG (Hanover,
Germany), Spectrum Quality Product, Inc. (New Brunswick, N.J.), TCI
America (Portland, Oreg.), Trans World Chemicals, Inc. (Rockville,
Md.), and Wako Chemicals USA, Inc. (Richmond, Va.).
[1224] Suitable reference books and treatise that detail the
synthesis of reactants useful in the preparation of compounds
described herein, or provide references to articles that describe
the preparation, include for example, "Synthetic Organic
Chemistry", John Wiley & Sons, Inc., New York; S. R. Sander et
al., "Organic Functional Group Preparations," 2nd Ed., Academic
Press, New York, 1983; H. O. House, "Modem Synthetic Reactions",
2nd Ed., W. A. Benjamin, Inc. Menlo Palk, Calif. 1972; T. L.
Gilchrist, "Heterocyclic Chemistry", 2nd Ed., John Wiley &
Sons. New York, 1992; J. March, "Advanced Organic Chemistry:
Reactions, Mechanisms and Structure", 4th Ed., Wiley-Interscience,
New York, 1992. Additional suitable reference books and treatise
that detail the synthesis of reactants useful in the preparation of
compounds described herein, or provide references to articles that
describe the preparation, include for example, Fuhrhop, J, and
Penzlin G. "Organic Synthesis: Concepts, Methods, Starting
Materials", Second, Revised and Enlarged Edition (1994) John Wiley
& Sons ISBN: 3-527-29074-5; Hoffman, R. V. "Organic Chemistry,
An Intermediate Text" (1996) Oxford University Press, ISBN
0-19-509618-5; Larock, R. C. "Comprehensive Organic
Transformations: A Guide to Functional Group Preparations" 2nd
Edition (1999) Wiley-VCH, ISBN: 0-471-19031-4; March, J. "Advanced
Organic Chemistry: Reactions, Mechanisms, and Structure" 4th
Edition (1992) John Wiley & Sons, ISBN: 0-471-60180-2; Otera.
J. (editor) "Modem Carbonyl Chemistry" (2000) Wiley-VCH, ISBN:
3-527-29871-1; Patai. S. "Patai's 1992 Guide to the Chemistry of
Functional Groups" (1992) Interscience ISBN: 0-471-93022-9;
Solomans, T. W. G. "Organic Chemistry" 7th Edition (2000) John
Wiley & Sons, ISBN: 0-471-19095-0: Stowell, J. C.,
"Intermediate Organic Chemistry" 2nd Edition (1993)
Wiley-Interscience, ISBN: 0-471-57456-2: "Industrial Organic
Chemicals: Starting Materials and Intermediates; An Ullmann's
Encyclopedia" (1999) John Wiley & Sons, ISBN: 3-527-29635-X, in
8 volumes; "Organic Reactions" (1942-200) John Wiley & Sons, in
over 55 volumes; and "Chemistry of Functional Groups" John Wiley
& Sons, in 73 volumes.
[1225] Specific and analogous reactants are optionally identified
through the indices of known chemicals prepared by the Chemical
Abstract Service of the American Chemical Society, which are
available in most public and university libraries, as well as
through on-line databases (contact the American Chemical Society,
Washington, D.C. for more details). Chemicals that are known but
not commercially available in catalogs are optionally prepared by
custom chemical synthesis houses, where many of the standard
chemical supply houses (e.g., those listed above) provide custom
synthesis services. A reference for the preparation and selection
of pharmaceutical salts of the compounds described herein is P. H.
Stahl & C. G. Wemuth "Handbook of Pharmaceutical Salts", Verlag
Helvetica Chimica Acta, Zurich, 2002.
[1226] In some embodiments, the compounds described herein are
prepared as outlined in Schemes 1-9.
##STR00217## ##STR00218##
##STR00219##
##STR00220##
##STR00221## ##STR00222##
##STR00223##
##STR00224## ##STR00225##
##STR00226## ##STR00227##
##STR00228## ##STR00229##
##STR00230##
Pharmaceutical Compositions
[1227] In certain embodiments, the compound disclosed herein is
administered as a pure chemical. In some embodiments, the compound
disclosed herein is combined with a pharmaceutically suitable or
acceptable carrier (also referred to herein as a pharmaceutically
suitable (or acceptable) excipient, physiologically suitable (or
acceptable) excipient, or physiologically suitable (or acceptable)
carrier) selected on the basis of a chosen route of administration
and standard pharmaceutical practice as described, for example, in
Remington: The Science and Practice of Pharmacy (Gennaro, 21.sup.st
Ed. Mack Pub. Co., Easton, Pa. (2005)).
[1228] Accordingly, provided herein is a pharmaceutical composition
comprising at least one compound disclosed herein, or a
pharmaceutically acceptable salt, solvate, or steroisomer thereof,
together with one or more pharmaceutically acceptable carriers. The
carrier(s) (or excipient(s)) is acceptable or suitable if the
carrier is compatible with the other ingredients of the composition
and not deleterious to the recipient (i.e., the subject) of the
composition.
[1229] One embodiment provides a pharmaceutical composition
comprising a pharmaceutically acceptable excipient and a compound
disclosed herein, or a pharmaceutically acceptable salt, solvate,
or steroisomer thereof.
[1230] In certain embodiments, the compound disclosed herein is
substantially pure, in that it contains less than about 5%, or less
than about 1%, or less than about 0.1%, of other organic small
molecules, such as unreacted intermediates or synthesis by-products
that are created, for example, in one or more of the steps of a
synthesis method.
[1231] Pharmaceutical compositions are administered in a manner
appropriate to the disease to be treated (or prevented). An
appropriate dose and a suitable duration and frequency of
administration will be determined by such factors as the condition
of the patient, the type and severity of the patient's disease, the
particular form of the active ingredient, and the method of
administration. In general, an appropriate dose and treatment
regimen provides the composition(s) in an amount sufficient to
provide therapeutic and/or prophylactic benefit (e.g., an improved
clinical outcome, such as more frequent complete or partial
remissions, or longer disease-free and/or overall survival, or a
lessening of symptom severity. Optimal doses are generally
determined using experimental models and/or clinical trials. The
optimal dose depends upon the body mass, weight, or blood volume of
the patient.
[1232] Oral doses typically range from about 1.0 mg to about 1000
mg, one to four times, or more, per day.
Methods of Treatment
[1233] The compounds disclosed herein, or a pharmaceutically
acceptable salt, solvate, or steroisomer thereof, are useful as
inhibitors of CD73 and, therefore, useful in the treatment of
diseases or disorders in which it is believed CD73 activity plays a
role. In some embodiments, the disease or disorder is cancer. In
some embodiments, the disease or disorder is an infection. In some
embodiments, the disease or disorder is a neurodegenerative
disease. In some embodiments, the disease or disorder is a
psychiatric disorder.
[1234] Disclosed herein are methods of treating a subject with a
disorder mediated by CD73 comprising the step of administering to
the subject an effective amount of a compound disclosed herein, or
a pharmaceutically acceptable salt, solvate, or stereoisomer
thereof.
Cancer
[1235] CD73 has been found to be overexpressed in many cancer cell
lines and tumor types including breast cancer, colorectal cancer,
ovarian cancer, gastric cancer, and gallbladder cancer and
associated with poor prognosis. Increasing evidence suggests that
CD73 is a key protein molecule in cancer development.
[1236] Higher expression levels of CD73 are associated with tumor
neovascularization, invasiveness, resistance to chemotherapy and
metastasis, and with shorter patient survival time in cancer. In
some embodiments, the compounds disclosed herein are useful in
reducing tumor neovascularization, invasiveness, resistance to
chemotherapy and metastasis, as well as to lengthen patient
survival time in cancer patients. In some embodiments, the CD73
inhibitors disclosed herein are used to control tumor
neovascularization, progression, resistance to chemotherapy, and
metastasis.
[1237] One embodiment provides a method of treating cancer in a
subject in need thereof, comprising administering to the subject a
compound of disclosed herein, or a pharmaceutically acceptable
salt, solvate, or stereoisomer thereof.
[1238] In some embodiments, the cancer is chemoresistant cancer,
radio resistant cancer, anti-hormonal therapy resistant cancer, or
treatment refractory cancer. In some embodiments, the cancer is
relapsed cancer, persistent cancer, or recurrent cancer. Another
embodiment provided herein describes a method of reducing
incidences of cancer recurrence. Also provided here in some
embodiments, is a method for treating a therapy-resistant cancer.
In some embodiments, the cancer is metastasic cancer.
[1239] In certain embodiments, the cancer treatable with the
methods provided herein includes, but is not limited to, (1)
leukemias, including, but not limited to, acute leukemia, acute
lymphocytic leukemia, acute myelocytic leukemias such as
myeloblastic, promyelocytic, myelomonocytic, monocytic,
erythroleukemia leukemias and myelodysplastic syndrome or a symptom
thereof (such as anemia, thrombocytopenia, neutropenia,
bicytopenia, or pancytopenia), refractory anemia (RA), RA with
ringed sideroblasts (RARS), RA with excess blasts (RAEB), RAEB in
transformation (RAEB-T), preleukemia, and chronic myelomonocytic
leukemia (CMML); (2) chronic leukemias, including, but not limited
to, chronic myelocytic (granulocytic) leukemia, chronic lymphocytic
leukemia, and hairy cell leukemia; (3) polycythemia vera; (4)
lymphomas, including, but not limited to, Hodgkin's disease and
non-Hodgkin's disease; (5) multiple myelomas, including, but not
limited to, smoldering multiple myeloma, non-secretory myeloma
osteosclerotic myeloma, plasma cell leukemia, solitary
plasmacytoma, and extramedullary plasmacytoma; (6) Waldenstrom's
macroglobulinemia; (7) monoclonal gammopathy of undetermined
significance; (8) benign monoclonal gammopathy; (9) heavy chain
disease: (10) bone and connective tissue sarcomas, including, but
not limited to, bone sarcoma, osteosarcoma, chondresarcoma, Ewing's
sarcoma, malignant giant cell tumor, fibrosarcoma of bone,
chordoma, periosteal sarcoma, soft-tissue sarcomas, angiosarcoma
(hemangiosarcoma), fibrosarcoma, Kaposi's sarcoma, leiomyosarcoma,
liposarcoma, lymphangiosarcoma, metastatic cancers, neurilemmoma,
rhabdomyosarcoma, and synovial sarcoma; (11) brain tumors,
including, but not limited to, glioma, astrocytoma, brain stem
glioma, ependymoma, aligodendroglioma, nonglial tumor, acoustic
neurinoma, craniopharyngioma, medulloblastoma, meningioma,
pineocytoma, pineoblastoma, and primary brain lymphoma; (12) breast
cancer, including, but not limited to, adenocarcinoma, lobular
(small cell) carcinoma, intraductal carcinoma, medullary breast
cancer, mutinous breast cancer, tubular breast cancer, papillary
breast cancer, primary cancers, Paget's disease, and inflammatory
breast cancer; (13) adrenal cancer, including but not limited to,
pheochromocytom and adrenocortical carcinoma; (14) thyroid cancer,
including, but not limited to, papillary or follicular thyroid
cancer, medullary thyroid cancer, and anaplastic thyroid cancer;
(15) pancreatic cancer, including, but not limited to, insulinoma,
gastrinoma, glucagonoma, vipoma, somatostatin-secreting tumor, and
carcinoid or islet cell tumor; (16) pituitary cancer, including,
but limited to, Cushing's disease, prol actin-secreting tumor,
acromegaly, and diabetes insipius; (17) eye cancer, including, but
not limited, to ocular melanoma such as iris melanoma, choroidal
melanoma, and cilliary body melanoma, and retinoblastoma: (18)
vaginal cancer, including, but not limited to, squamous cell
carcinoma, adenocarcinoma, and melanoma; (19) vulvar cancer,
including, but not limited to, squamous cell carcinoma, melanoma,
adenocarcinoma, basal cell carcinoma, sarcoma, and Paget's disease;
(20) cervical cancers, including, but not limited to, squamous cell
carcinoma, and adenocarcinoma; (21) uterine cancer, including, but
not limited to, endometrial carcinoma and uterine sarcoma; (22)
ovarian cancer, including, but not limited to, ovarian epithelial
carcinoma, borderline tumor, germ cell tumor, and stromal tumor;
(23) esophageal cancer, including, but not limited to, squamous
cancer, adenocarcinoma, adenoid cystic carcinoma, mucoepidermoid
carcinoma, adenosquamous carcinoma, sarcoma, melanoma,
plasmacytoma, verrucous carcinoma, and oat cell (small cell)
carcinoma; (24) stomach cancer, including, but not limited to,
adenocarcinoma, fungating (polypoid), ulcerating, superficial
spreading, diffusely spreading, malignant lymphoma, liposarcoma,
fibrosarcoma, and carcinosarcoma; (25) colon cancer; (26) rectal
cancer; (27) liver cancer, including, but not limited to,
hepatocellular carcinoma and hepatoblastoma; (28) gallbladder
cancer, including, but not limited to, adenocarcinoma; (29)
cholangiocarcinomas, including, but not limited to, pappillary,
nodular, and diffuse; (30) lung cancer, including, but not limited
to, non-small cell lung cancer, squamous cell carcinoma (epidermoid
carcinoma), adenocarcinoma, large-cell carcinoma, and small-cell
lung cancer; (31) testicular cancer, including, but not limited to,
germinal tumor, seminoma, anaplastic, classic (typical),
spermatocytic, nonserninoma, embryonal carcinoma, teratoma
carcinoma, and choriocarcinoma (yolk-sac tumor); (32) prostate
cancer, including, but not limited to, adenocarcinoma,
leiomyosarcoma, and rhabdomyosarcorna; (33) penal cancer; (34) oral
cancer, including, but not limited to, squamous cell carcinoma;
(35) basal cancer; (36) salivary gland cancer, including, but not
limited to, adenocarcinoma, mucoepidermoid carcinoma, and
adenoidcystic carcinoma; (37) pharynx cancer, including, but not
limited to, squamous cell cancer and verrucous; (38) skin cancer,
including, but not limited to, basal cell carcinoma, squamous cell
carcinoma and melanoma, superficial spreading melanoma, nodular
melanoma, lentigo malignant melanoma, and acral lentiginous
melanoma; (39) kidney cancer, including, but not limited to, renal
cell cancer, adenocarcinoma, hypemephroma, fibrosarcoma, and
transitional cell cancer (renal pelvis and/or uterer); (40) Wilms'
tumor, (41) bladder cancer, including, but not limited to,
transitional cell carcinoma, squamous cell cancer, adenocarcinoma,
and carcinosarcoma; (42) reproductive cancers, such as cervical
cancer, uterus cancer, ovarian cancer, or testicular cancer; (43)
esophagus cancer; (44) laryngeal cancer; (45) head and neck cancers
(including mouth, nose, throat, larynx, sinuses, or salivary glands
cancers); and other cancer, including, not limited to, myxosarcoma,
osteogenic sarcoma, endotheliosarcoma,
lymphangio-endotheliosarcoma, mesothelioma, synovioma,
hemangioblastoma, epithelial carcinoma, cystadenocarcinoma,
bronchogenic carcinoma, sweat gland carcinoma, sebaceous gland
carcinoma, papillary carcinoma, and papillary adenocarcinomas (See
Fishman et al., 1985, Medicine, 2d Ed., J.B. Lippincott Co.,
Philadelphia and Murphy et al., 1997, Informed Decisions: The
Complete Book of Cancer Diagnosis, Treatment, and Recovery, Viking
Penguin, Penguin Books U.S.A., Inc., United States of America).
[1240] In certain embodiments, the cancer treatable with the
methods provided herein is a hematological malignancy. In certain
embodiments, the hematological malignancy is a T-cell malignancy.
In certain embodiments, T-cell malignancies include peripheral
T-cell lymphoma not otherwise specified (PTCL-NOS), anaplastic
large cell lymphoma, angioimmunoblastic lymphoma, cutaneous T-cell
lymphoma, adult T-cell leukemia/lymphoma (ATLL), blastic NK-cell
lymphoma, enteropathy-type T-cell lymphoma, hematosplenic
gamma-delta T-cell lymphoma, lymphoblastic lymphoma, nasal NUT-cell
lymphomas, or treatment-related T-cell lymphomas.
[1241] In certain embodiments, the hematological malignancy is a
B-cell malignancy. In certain embodiments, B-cell malignancies
include acute lymphoblastic leukemia (ALL), acute myelogenous
leukemia (AML), chronic myelogenous leukemia (CML), acute monocytic
leukemia (AMoL), chronic lymphocytic leukemia (CLL), high-risk
chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma
(SLL), high-risk small lymphocytic lymphoma (SLL), follicular
lymphoma (FL), diffuse large B-cell lymphoma (DLBCL), mantle cell
lymphoma (MCL), Waldenstrom's macroglobulinemia, multiple myeloma,
extranodal marginal zone B cell lymphoma, nodal marginal zone B
cell lymphoma, Burkitfs lymphoma, non-Burkitt high grade B cell
lymphoma, primary mediastinal B-cell lymphoma (PMBL), immunoblastic
large cell lymphoma, precursor B-lymphoblastic lymphoma, B cell
prolymphocytic leukemia, lymphoplasmacytic lymphoma, splenic
marginal zone lymphoma, plasma cell myeloma, plasmacytoma,
mediastinal (thymic) large B cell lymphoma, intravascular large B
cell lymphoma, primary effusion lymphoma, or lymphomatoid
granulomatosis. In certain embodiments, the B-cell malignancy is
diffuse large B-cell lymphoma (DLBCL). In certain embodiments, the
DLBCL is an activated B-cell DLBCL (ABC-DLBCL), a germinal center
B-cell like DLBCL (GBC-DLBCL), a double hit DLBCL (DH-DLBCL), or a
triple hit DLBCL (TH-DLBCL).
[1242] In certain embodiments, the cancer treatable with the
methods provided herein is lung cancer, melanoma, breast cancer,
ovarian cancer, colorectal cancer, gastric cancer, gallbladder
cancer, or prostate cancer.
Infections
[1243] A number of studies have shown changes in the activity of
the CD39/CD73 axis during infections induced by a variety of
microorganisms. One embodiment provides a method of treating an
infection in a subject in need thereof, comprising administering to
the subject a compound of disclosed herein, or a pharmaceutically
acceptable salt, solvate, or stereoisomer thereof.
[1244] In some embodiments, the infection is a viral infection, a
bacterial infection, or a parasitic infection.
Parasitic Infections
[1245] In some embodiments, the infection is a parasitic infection.
In some embodiments, the parasitic infection is caused by infection
of the subject with a protozoan organism. In some embodiments, the
protozoan organism selected from the group consisting of the genera
Acanthamoeba, Babesia, Balantidium, Cryptosporidium, Dientamoeba,
Eimeria, Entamoeba, Giardia, Isospora, Leishmania, Naegleria,
Neospora, Plasmodium, Sarcocystis, Theileria, Toxoplasma,
Trichomonas, Trypanosoma, or any combinations thereof. In some
embodiments, the parasitic infection is caused by an infection with
Toxoplasma gondii (T. gondii). In some embodiments, the parasitic
infection is toxoplasmosis. In some embodiments, the toxoplasmosis
is acute toxoplasmosis, latent toxoplasmosis, or cutaneous
toxoplasmosis.
[1246] Acute toxoplasmosis: acute toxoplasmosis is often
asymptomatic in healthy adults. However, symptoms may manifest and
are often influenza-like: swollen lymph nodes, headaches, fever,
fatigue, or muscle aches and pains that last for a month or more.
Rarely will a human with a fully functioning immune system develop
severe symptoms following infection. People with weakened immune
systems are likely to experience headache, confusion, poor
coordination, seizures, lung problems that may resemble
tuberculosis or Pneumocystis jiroveci pneumonia (a common
opportunistic infection that occurs in people with AIDS), or
blurred vision caused by severe inflammation of the retina (ocular
toxoplasmosis). Young children and immunocompromised people, such
as those with HIV/AIDS, those taking certain types of chemotherapy,
or those who have recently received an organ transplant, may
develop severe toxoplasmosis. In some instances, toxoplasmosis
causes damage to the brain (encephalitis) or the eyes (necrotizing
retinochoroiditis). Infants infected via placental transmission may
be born with either of these problems, or with nasal malformations,
although these complications are rare in newborns. The toxoplasmic
trophozoites causing acute toxoplasmosis are referred to as
tachyzoites, and are typically found in bodily fluids.
[1247] Latent toxoplasmosis: due to its asymptomatic nature, it is
easy for a host to become infected with Toxoplasma gondii and
develop toxoplasmosis without knowing it. Although mild, flu-like
symptoms occasionally occur during the first few weeks following
exposure, infection with T. gondii produces no readily observable
symptoms in healthy human adults. In most immunocompetent people,
the infection enters a latent phase, during which only bradyzoites
(tissue cysts) are present; these tissue cysts and even lesions can
occur in the retinas, alveolar lining of the lungs (where an acute
infection may mimic a Pneumocystis jirovecii infection), heart,
skeletal muscle, and the central nervous system (CNS), including
the brain. Cysts form in the CNS (brain tissue) upon infection with
T. gondii and persist for the lifetime of the host. Most infants
who are infected while in the womb have no symptoms at birth, but
may develop symptoms later in life.
[1248] Cutaneous toxoplasmosis: in some embodiments, skin lesions
occur in the acquired form of the disease, including roseola and
erythema multiforme-like eruptions, prurigo-like nodules,
urticaria, and maculopapular lesions. Newborns may have punctate
macules or ecchymoses. Diagnosis of cutaneous toxoplasmosis is
based on the tachyzoite form of T. gondii being found in the
epidermis.
Viral Infections
[1249] In some embodiments, the infection is a viral infection. In
certain embodiments, the viral infection treatable with the methods
provided herein includes, but is not limited to, chickenpox, the
flu (influenza), herpes, human immunodeficiency virus (HIV/AIDS),
human papillomavirus (HPV), Infectious mononucleosis, mumps,
measles, rubella, shingles, viral gastroenteritis (stomach flu),
viral hepatitis, viral meningitis, and viral pneumonia.
Neurodegenerative Diseases
[1250] In the central nervous system, adenosine plays a critical
role in controlling a multitude of neural functions. Through the
activation of P1 receptors, adenosine is involved in diverse
physiological and pathological processes such as regulation of
sleep, general arousal state and activity, local neuronal
excitability, and coupling of the cerebral blood flow to the energy
demand. In some embodiments, the manipulation of adenosine
production via CD73 inhibitors has therapeutic potential in
neurodegenerative diseases. One embodiment provides a method of
treating a neurodegenerative disease in a subject in need thereof,
comprising administering to the subject a compound of disclosed
herein, or a pharmaceutically acceptable salt, solvate, or
stereoisomer thereof. In certain embodiments, the neurodegenerative
disease treatable with the methods provided herein includes, but is
not limited to, Alzheimer's disease, Parkinson's disease, and
Huntington's disease. One embodiment provides a method of treating
a psychiatric disorder in a subject in need thereof, comprising
administering to the subject a compound of disclosed herein, or a
pharmaceutically acceptable salt, solvate, or stereoisomer thereof.
In some embodiments, the psychiatric disorder is schizophrenia or
autism.
Combination Therapy
[1251] In certain instances, the compound disclosed herein, or a
pharmaceutically acceptable salt, solvate, or steroisomer thereof,
is administered in combination with a second therapeutic agent.
[1252] In some embodiments, the benefit experienced by a patient is
increased by administering one of the compounds described herein
with a second therapeutic agent (which also includes a therapeutic
regimen) that also has therapeutic benefit.
[1253] In one specific embodiment, a compound disclosed herein, or
a pharmaceutically acceptable salt, solvate, or steroisomer
thereof, is co-administered with a second therapeutic agent,
wherein the compound disclosed herein, or a pharmaceutically
acceptable salt, solvate, or steroisomer thereof, and the second
therapeutic agent modulate different aspects of the disease,
disorder or condition being treated, thereby providing a greater
overall benefit than administration of either therapeutic agent
alone.
[1254] In any case, regardless of the disease, disorder or
condition being treated, the overall benefit experienced by the
patient is simply additive of the two therapeutic agents or the
patient experiences a synergistic benefit.
[1255] In certain embodiments, different therapeutically-effective
dosages of the compounds disclosed herein will be utilized in
formulating a pharmaceutical composition and/or in treatment
regimens when the compounds disclosed herein are administered in
combination with a second therapeutic agent.
Therapeutically-effective dosages of drugs and other agents for use
in combination treatment regimens are optionally determined by
means similar to those set forth hereinabove for the actives
themselves. Furthermore, the methods of prevention/treatment
described herein encompasses the use of metronomic dosing, i.e.,
providing more frequent, lower doses in order to minimize toxic
side effects. In some embodiments, a combination treatment regimen
encompasses treatment regimens in which administration of a
compound disclosed herein, or a pharmaceutically acceptable salt,
solvate, or steroisomer thereof, is initiated prior to, during, or
after treatment with a second agent described herein, and continues
until any time during treatment with the second agent or after
termination of treatment with the second agent. It also includes
treatments in which a compound disclosed herein, or a
pharmaceutically acceptable salt, solvate, or steroisomer thereof,
and the second agent being used in combination are administered
simultaneously or at different times and/or at decreasing or
increasing intervals during the treatment period. Combination
treatment further includes periodic treatments that start and stop
at various times to assist with the clinical management of the
patient.
[1256] It is understood that the dosage regimen to treat, prevent,
or ameliorate the condition(s) for which relief is sought, is
modified in accordance with a variety of factors (e.g., the
disease, disorder or condition from which the subject suffers; the
age, weight, sex, diet, and medical condition of the subject).
Thus, in some instances, the dosage regimen actually employed
varies and, in some embodiments, deviates from the dosage regimens
set forth herein.
[1257] For combination therapies described herein, dosages of the
co-administered compounds vary depending on the type of co-drug
employed, on the specific drug employed, on the disease or
condition being treated, and so forth. In additional embodiments,
when co-administered with a second therapeutic agent, the compound
provided herein is administered either simultaneously with the
second therapeutic agent, or sequentially.
[1258] In combination therapies, the multiple therapeutic agents
(one of which is one of the compounds described herein) are
administered in any order or even simultaneously. If administration
is simultaneous, the multiple therapeutic agents are, by way of
example only, provided in a single, unified form, or in multiple
forms (e.g., as a single pill or as two separate pills).
[1259] The compounds disclosed herein, or a pharmaceutically
acceptable salt, solvate, or steroisomer thereof, as well as
combination therapies, are administered before, during or after the
occurrence of a disease or condition, and the timing of
administering the composition containing a compound varies. Thus,
in one embodiment, the compounds described herein are used as a
prophylactic and are administered continuously to subjects with a
propensity to develop conditions or diseases in order to prevent
the occurrence of the disease or condition. In another embodiment,
the compounds and compositions are administered to a subject during
or as soon as possible after the onset of the symptoms. In specific
embodiments, a compound described herein is administered as soon as
is practicable after the onset of a disease or condition is
detected or suspected, and for a length of time necessary for the
treatment of the disease. In some embodiments, the length required
for treatment varies, and the treatment length is adjusted to suit
the specific needs of each subject. For example, in specific
embodiments, a compound described herein or a formulation
containing the compound is administered for at least 2 weeks, about
1 month to about 5 years.
[1260] In certain embodiments, the second therapeutic agent is an
adjuvant. In certain embodiments, the second therapeutic agent is
an anti-cancer agent. In certain embodiments, the second
therapeutic agent is an antiemetic. In certain embodiments, the
second therapeutic agent is an anti-infective agent. In certain
embodiments, the second therapeutic agent is an antiviral agent. In
certain embodiments, the second therapeutic agent is an
antibacterial agent.
[1261] In some embodiments, the compound disclosed herein, or a
pharmaceutically acceptable salt, solvate, or steroisomer thereof,
is administered in combination with an adjuvant. In one embodiment,
the therapeutic effectiveness of one of the compounds described
herein is enhanced by administration of an adjuvant (i.e., by
itself the adjuvant has minimal therapeutic benefit, but in
combination with another therapeutic agent, the overall therapeutic
benefit to the patient is enhanced).
In some embodiments, the compound disclosed herein, or a
pharmaceutically acceptable salt, solvate, or steroisomer thereof,
is administered in combination with an anti-cancer agent.
[1262] In some embodiments, the anti-cancer agent is a hormone
blocking therapy. Hormone blocking therapy includes the use of
agents that block the production of estrogens or block the estrogen
receptors. In some embodiments, hormone blocking therapy includes
the use of estrogen receptor modulators and/aromatase inhibitors.
Estrogen receptor modulators include triphenylethylene derivatives
(e.g., tamoxifen, toremifene, droloxifene, 3-hydroxytamoxifen,
idoxifene, TAT-59 (a phosphorylated derivative of
4-hydroxytamoxifen) and GW5638 (a carboxylic acid derivative of
tamoxifen)); non-steroidal estrogen receptor modulators (e.g.,
raloxifene, LY353381 (SERM3) and LY357489); steroidal estrogen
receptor modulators (e.g., ICI-182.780). Aromatase inhibitors
include steroidal aromatase inhibitors and non-steroidal aromatase
inhibitors. Steroidal aromatase inhibitors include, but are not
limited to, exemestane. Non-steroidal aromatase inhibitors include,
but are not limited to, anastrozole and letrozole.
[1263] In certain embodiments, compounds disclosed herein are used
in combination with one or more passive immunotherapies, including
but not limited to, naked monoclonal antibody drugs and conjugated
monoclonal antibody drugs. Examples of naked monoclonal antibody
drugs that can be used include, but are not limited to, rituximab,
an antibody against the CD20 antigen; trastuzumab, an antibody
against the HER2 protein; alemtuzumab, an antibody against the CD52
antigen: cetuximab, an antibody against the EGFR protein; and
bevacizumab which is an anti-angiogenesis inhibitor of VEGF
protein.
[1264] Examples of conjugated monoclonal antibodies include, but
are not limited to, radiolabeled antibody ibritumomab tiuxetan;
radiolabeled antibody tositumomab; and immunotoxin gemtuzumab
ozogamicin which contains calicheamicin: BL22, an anti-CD22
monoclonal antibody-immunotoxin conjugate; radiolabeled antibodies
such as OncoScint (Registered trademark) and ProstaScint
(Registered trademark): brentuximab vedotin; and ado-trastuzumab
emtansine.
[1265] Further examples of therapeutic antibodies that can be used
include, but are not limited to, abciximab, an antibody against the
glycoprotein IIb/IIIa receptor on platelets; daclizumab, an
immunosuppressive, humanized anti-CD25 monoclonal antibody;
edrecolomab, a murine anti-17-IA cell surface antigen igG2a
antibody; BEC2, a murine anti-idiotype (GD3 epitope) IgG antibody;
IMC-C225, a chimeric anti-EGFR IgG antibody; VITAXIN (Registered
Trademark) a humanized anti-aVbeta 3 integrin antibody; Campath
1H/LDP-03, a humanized anti CD52 IgG1 antibody; Smart M195, a
humanized anti-CD33 IgG antibody; epratuzumab, a humanized
anti-CD22 IgG antibody; Lymphoscan; visilizumab; CM3, a humanized
anti-ICAM3 antibody; IDEC-114 a primatized anti-CD80 antibody;
IDEC-131 a humanized anti-CD40L antibody; IDEC-151 a primatized
anti-CD4 antibody; IDEC-152 a primatized anti-CD23 antibody; SMART
anti-CD3, a humanized anti-CD3 IgG; 5G1.1, a humanized
anti-complement factor 5 (C5) antibody; D2E7, a humanized
anti-TNF-alpha antibody; CDP870, a humanized anti-TNF-alpha Fab
fragment; IDEC-151, a primatized anti-CD4 IgG1 antibody; MDX-CD4, a
human anti-CD4 IgG antibody; CD20-streptdavidin (+biotin-yttrium
90); CDP571, a humanized anti-TNF-alpha IgG4 antibody; LDP-02, a
humanized anti-alpha 4beta 7 antibody; OrthoClone OKT4A, a
humanized anti-CD4 IgG antibody; ANTOVA (Registered Trademark), a
humanized anti-CD40L IgG antibody; ANTEGREN (Registered Trademark),
a humanized anti-VLA-4 IgG antibody; and CAT-152, a human
anti-TGF-beta 2 antibody.
[1266] In some embodiments, the second therapeutic agent for use in
combination with a compound disclosed herein, or a pharmaceutically
acceptable salt, solvate, or steroisomer thereof, include one or
more of the following: abiraterone; abarelix; adriamycin;
actinomycin; acivicin; aclarubicin; acodazole hydrochloride;
acronine; adozelesin; aldesleukin; alemtuzumab; allopurinol:
alitretinoin; altretamine; ambomycin: ametantrone acetate;
aminoglutethimide; aminolevulinic acid; amifostine; amsacrine;
anastrozole: anthramycin: aprepitant: arsenic trioxide:
asparaginase: asperlin: azacitidine; azetepa; azotomycin;
batimastat; bendamustine hydrochloride; benzodepa; bevacizumab;
bexarotene; bicalutamide; bisantrene hydrochloride; bi snail de
dimesylate: bizelesin; bleomycin; bleomycin sulfate; bortezomib;
brequinar sodium; bropirimine; busulfan; cactinomycin; calusterone;
caracemide; carbetimer, carboplatin; carmustine; carubicin
hydrochloride; carzelesin; capecitabine; cedefingol; cetuximab;
chlorambucil; cirolemycin; cisplatin: cladribine; clofarabine:
crisnatol mesylate; cyclophosphamide; cytarabine: dacarbazine;
dasatinib; daunorubicin hydrochloride; dactinomycin; darbepoetin
alfa; decitabine; degarelix; denileukin diftitox; dexormaplatin;
dexrazoxane hydrochloride; dezaguanine; dezaguanine mesylate;
diaziquone; docetaxel; doxorubicin; doxorubicin hydrochloride;
droloxifene; droloxifene citrate; dromostanolone propionate:
duazomycin; edatrexate: eflomithine hydrochloride; elsamitrucin;
eltrombopag olamine: enloplatin; enpromate: epipropidine:
epirubicin hydrochloride: epoetin alfa: erbulozole: erlotinib
hydrochloride; esorubicin hydrochloride: estramustine: estramustine
phosphate sodium: etanidazole; etoposide; etoposide phosphate;
etoprine; everolimus; exemestane; fadrozole hydrochloride;
fazarabine; fenretinide; filgrastim: floxuridine; fludarabine
phosphate: fluorouracil; fluorocitabine; fosquidone; fostriecin
sodium; fulvestrant; gefitinib: gemcitabine; gemcitabine
hydrochloride; gemcitabine cisplatin; gemtuzumab ozogamicin;
goserelin acetate; histrelin acetate; hydroxyurea: idarubicin
hydrochloride; ifosfamide; iimofosine; ibritumomab tiuxetan;
idarubicin; ifosfamide: imatinib mesylate; imiquimod; interleukin
I1 (including recombinant interleukin IL or rlL2), interferon
alfa-2a; interferon alfa-2b; interferon alfa-n1; interferon
alfa-n3; interferon beta-1a; interferon gamma-1b: iproplatin;
irinotecan hydrochloride; ixabepilone; lanreotide acetate;
lapatinib; lenalidomide; letrozole; leuprolide acetate; leucovorin
calcium; leuprolide acetate; levamisole; liposomal cytarabine;
liarozole hydrochloride; lometrexol sodium; lomustine; losoxantrone
hydrochloride; masoprocol; maytansine; mechlorethamine
hydrochloride; megestrol acetate; melengestrol acetate; melphalan;
menogaril; mercaptopurine; methotrexate; methotrexate sodium;
methoxsalen; metoprine; meturedepa; mitindomide; mitocarcin;
mitocromin; mitogillin; mitomalcin; mitomycin C; mitosper;
mitotane; mitoxantrone hydrochloride; mycophendic acid; nandrolone
phenpropionate; nelarabine; nilotinib; nocodazoie; nofetumomab;
nogalamycin; ofatumuntb; oprelvekin; ormaplatin; oxaliplatin;
oxisuran; paclitaxel; palifermin; palonosetron hydrochloride;
pamidronate; pegfilgrastim; pemetrexed di sodium; pentostatin;
panitumumab; pazopanib hydrochloride; pemetrexed disodium;
plerixafor; pralatrexate; pegaspargase; peliomycin; pentamustine;
peplomycin sulfate; perfosfamide; pipobroman; piposulfan;
piroxantrone hydrochloride; plicamycin; plomestane; porfimer
sodium; porfiromycin; prednimustine; procarbazine hydrochloride;
puromycin; puromycin hydrochloride; pyrazofurin; quinacrine;
raloxifene hydrochloride; rasburicase; recombinant HPV bivalent
vaccine; recombinant HPV quadrivalent vaccine; riboprine;
rogletimide; rituximab; romidepsin; romiplostim; safingol; safingol
hydrochloride; sargramostim; semustine; simtrazene; sipuleucel-T;
sorafenib; sparfosate sodium; sparsomycin; spirogermanium
hydrochloride; spiromustine; spiroplatin; streptonigrin;
streptozocin; sulofenur; sunitinib malate; talisomycin; tamoxifen
citrate; tecogalan sodium; tegafur; teloxantrone hydrochloride;
temozolomide; temoporfin; temsirolinus; teniposide; teroxirone;
testolactone; thalidomide; thiamiprine; thioguanine; thiotepa;
tiazofunn; tirapazamine; topotecan hydrochloride; toremifene;
tositumomab and I 131 Iodine tositumomab; trastuzumab; trestolone
acetate; tretinoin; tricinbine phosphate; trimetrexate;
trimetrexate glucuronate; triptorelin; tubuiozole hydrochloride;
uracil mustard; uredepa; valrubicin; vapreotide; verteporfin;
vinblastine; vinblastine sulfate; vincristine sulfate; vindesine;
vindesine sulfate; vinepidine sulfate; vinglycinate sulfate;
vinleurosine sulfate; vinorelbine tartrate; vinrosidine sulfate;
vinzolidine sulfate; vorinostat; vorozole; zeniplatin; zinostatin;
zoledronic acid; and zorubicin hydrochloride.
[1267] In some embodiments, the second therapeutic agent is an
alkylating agent. Examples of alkylating agents for use in
combination with a compound disclosed herein, or a pharmaceutically
acceptable salt, solvate, or steroisomer thereof, include, but are
not limited to, nitrogen mustards (e.g., mechloroethamine,
cyclophosphamide, chlorambucil, meiphalan, etc.), ethylenimine and
methylmelamines (e.g., hexamethlymelamine, thiotepa), alkyl
sulfonates (e.g., busulfan), nitrosoureas (e.g., carmustine,
lomusitne, semustine, streptozocin, etc.), or triazenes
(decarbazine, etc.).
[1268] Other agents that are optionally used in the methods and
compositions described herein for the treatment or prevention of
cancer include platinum coordination complexes (e.g., cisplatin,
carbobiatin), anthracenedione (e.g., mitoxantrone), substituted
urea (e.g., hydroxyurea), methyl hydrazine derivative (e.g.,
procarbazine), adrenocortical suppressant (e.g., mitotane,
aminoglutethimide).
[1269] In some embodiments, the second therapeutic agent is an
immunotherapy agent. Examples of immunotherapy agents for use in
combination with a compound disclosed herein, or a pharmaceutically
acceptable salt, solvate, or steroisomer thereof, include, but are
not limited to, checkpoint inhibitors (e.g., anti-PD1 and
anti-PD-L1 inhibitors), cancer vaccines (e.g., sipuleucel-T),
oncolytic viruses (e.g., talimogene laherparepvec), cytokines
(e.g., IL-2 and INF-alpha), CAR-T cells.
[1270] In some embodiments, a compound disclosed herein, or a
pharmaceutically acceptable salt, solvate, or steroisomer thereof,
is used in combination with anti-emetic agents to treat nausea or
emesis, which results from the use of a compound disclosed herein,
or a pharmaceutically acceptable salt, solvate, or steroisomer
thereof, anti-cancer agent(s) and/or radiation therapy. Anti-emetic
agents include, but are not limited to: neurokinin-1 receptor
antagonists, 5HT3 receptor antagonists (such as ondansetron,
granisetron, tropisetron, palonosetron, and zatisetron), GABAB
receptor agonists (such as baclofen), corticosteroids (such as
dexamethasone, prednisone, prednisolone, or others), dopamine
antagonists (such as, but not limited to, domperidone, droperidol,
haloperidol, chlorpromazine, promethazine, prochlorperazine,
metoclopramide), antihistamines (H1 histamine receptor antagonists,
such as but not limited to, cyclizine, diphenhydramine,
dimenhydrinate, meclizine, promethazine, hydroxyzine), cannabinoids
(such as but not limited to, cannabis, marinol, dronabinol), and
others (such as, but not limited to, trimethobenzamide; ginger,
emetrol, propofol).
[1271] In some embodiments, a compound disclosed herein, or a
pharmaceutically acceptable salt, solvate, or steroisomer thereof,
is used in combination with an agent useful in the treatment of
anemia. Such an anemia treatment agent is, for example, a
continuous eythropoiesis receptor activator (such as
epoetin-.alpha.).
[1272] In some embodiments, a compound disclosed herein, or a
pharmaceutically acceptable salt, solvate, or steroisomer thereof,
is used in combination with an agent useful in the treatment of
neutropenia. Examples of agents useful in the treatment of
neutropenia include, but are not limited to, a hematopoietic growth
factor which regulates the production and function of neutrophils
such as a human granulocyte colony stimulating factor, (G-CSF).
Examples of a G-CSF include filgrastim.
[1273] In one embodiment, a compound disclosed herein, or a
pharmaceutically acceptable salt, solvate, or steroisomer thereof,
is administered to a mammal in combination with a non-steroidal
anti-inflammatory drug (NSAID). NSAIDs include, but are not limited
to: aspirin, salicylic acid, gentisic acid, choline magnesium
salicylate, choline salicylate, choline magnesium salicylate,
choline salicylate, magnesium salicylate, sodium salicylate,
diflunisal, carprofen, fenoprofen, fenoprofen calcium,
fluorobiprofen, ibuprofen, ketoprofen, nabutone, ketolorac,
ketorolac tromethamine, naproxen, oxaprozin, diclofenac, etodolac,
indomethacin, sulindac, tolmetin, meclofenamate, meclofenamate
sodium, mefenamic acid, piroxicam, meloxicam, COX-2 specific
inhibitors (such as, but not limited to, celecoxib, rofecoxib,
valdecoxib, parecoxib, etoricoxib, lumiracoxib, CS-502, TIE-522
L-745 337, and NS398).
[1274] In some embodiments, a compound disclosed herein, or a
pharmaceutically acceptable salt, solvate, or steroisomer thereof,
is used in combination with radiation therapy (or radiotherapy).
Radiation therapy is the treatment of cancer and other diseases
with ionizing radiation. Radiation therapy is optionally used to
treat localized solid tumors, such as cancers of the skin, tongue,
larynx, brain, breast, prostate, colon uterus, and/or cervix. It is
also optionally used to treat leukemia and lymphoma (cancers of the
blood-forming cells and lymphatic system, respectively).
EXAMPLES
I. Chemical Synthesis
[1275] Unless otherwise noted, reagents and solvents were used as
received from commercial suppliers. Anhydrous solvents and
oven-dried glassware were used for synthetic transformations
sensitive to moisture and/or oxygen. Yields were not optimized.
Reaction times are approximate and were not optimized. Column
chromatography and thin layer chromatography (MC) were performed on
silica gel unless otherwise noted.
Example 1.
(2-(((2R,3S,4R,5R)-5-(6-Chloro-4-((2-chlorobenzyl)amino)-1H-pyr-
azolo[3,4-d]pyrimidin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)-2-o-
xoethyl)phosphonic Acid (1)
##STR00231##
[1276] Step A.
(2R,3R,4R,5R)-2-(Acetoxymethyl)-5-(4,6-dichloro-1H-pyrazolo[3,4-d]pyrimid-
in-1-yl)tetrahydrofuran-3,4-diyl Diacetate (1a)
##STR00232##
[1278] .beta.-D-Ribofuranose 1,2,3,5-tetraacetate (5.73 g, 18.0
mmol) was heated at 90.degree. C. for 10 min,
4,6-dichloro-1H-pyrazolo[3,4-d]pyrimidine (1.5 g, 18.0 mmol) and
SnCl.sub.4 (60 mg) was added successively. After the mixture was
heated at 130.degree. C. for 15 min under reduced pressure, it was
cooled to rt, diluted with water and extracted with DCM. The
combined organics were washed with water, brine, dried, and
concentrated. The residue was purified by column chromatography
(petroleum ether/ethyl acetate: 10:1 to 5:1) to give the title
compound (1a) (2.4 g, 68% yield) as a yellow solid.
Step B.
(2R,3R,4R,5R)-2-(Acetoxymethyl)-S-(6-chloro-4-(2-chlorobenzylamino-
)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)tetrahydrofuran-3,4-diyl
Diacetate (1b)
##STR00233##
[1280] A mixture of 1a (2.4 g, 5.37 mmol),
(2-chlorophenyl)methanamine (912 mg, 6.44 mmol), trimethylamine
(813 mg) and EtOH (40 mL) was heated at 50.degree. C. for 1 h. The
mixture was cooled to rt and concentrated. The residue was purified
by column chromatography (petroleum ether/ethyl acetate: 5:1) to
provide the title compound (1b) (1.7 g, 58% yield) as a yellow
solid.
Step C.
(2R,3R,4S,5R)-2-(6-Chloro-4-(2-chlorobenzylamino)-1H-pyrazolo[3,4--
d]pyrimidin-1-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol
(1c)
##STR00234##
[1282] A mixture of 1b (240 mg, 3.8 mmol), SnO(n-Bu).sub.2 (3.07 g,
12.3 mmol) and methanol (40 ml) was heated at 65.degree. C.
overnight. The mixture was cooled to rt and concentrated. The
residue was purified by column chromatography (DCM/MeOH: 50:1 to
20:1) to give the title compound (1c) (1.0 g. 77% yield).
Step D.
((3aR,4R,6R,6aR)-6-(6-Chloro-4-((2-chlorobenzyl)amino)-1H-pyrazolo-
l-[3,4-d]pyrimidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl-
)methanol (1d)
##STR00235##
[1284] To a solution of
(2R,3R,4S,5R)-2-[6-chloro-4-[(2-chlorophenyl)methylamino]pyrazolo[3,4-d]p-
yrimidin-1-yl]-5-(hydroxymethyl)tetrahydrofuran-3,4-diol (1c) (3.00
g, 7.04 mmol) in DMF (32 mL) was added 2,2-dimethoxypropane (2.59
mL, 21.1 mmol) followed by p-toluenesulfonic acid monohydrate (268
mg, 1.41 mmol). The mixture was heated to 70.degree. C. for 1 h.
The reaction mixture was cooled to rt and concentrated. The residue
was purified by column chromatography (SiO.sub.2, 0-100%
EtOAc/hexanes) to give the title compound (1d) (2.79 g. 85% yield)
as a white solid.
Step E.
((3aR,4R,6R,6aR)-6-(6-Chloro-4-((2-chlorobenzyl)amino)-1H-pyrazolo-
[3,4-d]pyrimidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)m-
ethyl 2-(diethoxyphosphoryl)acetate (1e)
##STR00236##
[1286] To a slurry of
((3aR,4R,6R,6aR)-6-(6-chloro-4-((2-chlorobenzyl)amino)-1H-pyrazolo[3,4-d]-
pyrimidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methanol
(1d) (100 mg, 0.21 mmol) and diethoxyphosphoryl acetic acid (0.07
mL, 0.43 mmol) in DCM (2 mL) was added dicyclohexylcarbodiimide (88
mg, 0.43 mmol) and 4-dimethylaminopyridine (1.3 mg, 0.010 mmol).
The reaction mixture was allowed to stir overnight. The reaction
mixture was filtered over Celite and the filtrate was concentrated.
The residue was purified by column chromatography (SiO.sub.2,
0-100% EtOAc/hexanes) to provide the title compound (1e) (118 mg,
85% yield) as a white solid.
Step F.
(2-(((2R,3S,4R,5R)-5-(6-Chloro-4-((2-chlorobenzyl)amino)-1H-pyrazo-
lo[3,4-d]pyrimidin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)-2-oxoe-
thyl)phosphonic Acid (1)
##STR00237##
[1288] To a solution of
((3aR,4R,6R,6aR)-6-(6-chloro-4-((2-chlorobenzyl)amino)-1H-pyrazolo[3,4-d]-
pyrimidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methyl
2-(diethoxyphosphoryl)acetate (1e) (118 mg, 0.18 mmol) in DCM (6.5
mL) was added bromo(trimethyl)silane (0.14 mL, 1.1 mmol) at rt. The
mixture was stirred overnight. The reactions was concentrated and
dissolved in MeOH (5 mL). The mixture was stirred for 30 min and
was then concentrated again. The residue was dissolved in
hexafluoro-2-propanol (2.3 mL) and water (0.11 mL) and hydrochloric
acid (2 M in dioxane, 0.11 mL, 0.44 mmol) was added dropwise. After
the mixture was stirred for 1 h, it was quenched with sat.
NH.sub.4OH (0.3 mL) and was concentrated. The residue was purified
by reverse phase HPLC (C18 column, 0 to 65% acetonitrile/water with
0.1% TFA) to provide the title compound (1) as a white solid in the
TFA salt form (43 mg, 35% yield). .sup.1H NMR (400 MHz, DMSO-d6)
.delta. ppm 9.32 (t, J=5.55 Hz, 1H), 8.30 (s, 1H), 7.47-7.56 (m,
1H), 7.41-7.47 (m, 1H), 7.31-7.38 (m, 2H), 6.05 (d, J=3.51 Hz, 1H),
5.49-5.62 (br s, 1H), 4.77 (d, J=5.55 Hz, 2H), 4.50 (t, J=4.0 Hz,
1H), 4.26-4.37 (m, 2H), 4.05-4.11 (m, 1H), 3.92-3.99 (m, 1H),
2.76-2.81 (m, 2H), m/z (ESI, +ve ion)=548.0 [M+H].sup.+.
Example 2.
(2-((((2R,3S,4R,5R)-5-(6-Chloro-4-((2-chlorobenzyl)amino)-1H-py-
razolo[3,4-d]pyrimidin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl)amin-
o)-2-oxoethyl)phosphonic Acid (2)
##STR00238##
[1289] Step A.
1-((3aR,4R,6R,6aR)-6-(Azidomethyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]-
dioxol-4-yl)-6-chloro-N-(2-chlorobenzyl)-1H-pyrazolo[3,4-d]pyrimidin-4-ami-
ne (2a)
##STR00239##
[1291] To a solution of
((3aR,4R,6R,6aR)-6-(6-chloro-4-((2-chlorobenzyl)amino)-1H-pyrazolo[3,4-d]-
pyrimidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4
yl)methanol (1d) (228 mg, 0.49 mmol) in THF (2.3 mL) was added
triphenylphosphine (154 mg, 0.59 mmol) and DIAD (0.12 mL, 0.59
mmol) dropwise. The reaction mixture was cooled to 0.degree. C.,
and stirred for 10 min before diphenyl phosphorazidate (0.13 mL,
0.59 mmol) was added dropwise. The mixture was warmed to rt
overnight. The mixture was concentrated and the resulting residue
was purified by column chromatography (SiO.sub.2, 0-100%
EtOAc/hexanes) to provide the title compound (2a) (144 mg, 60%
yield) as a foamy solid.
Step B.
1-((3aR,4R,6R,6aR)-6-(Aminomethyl)-2,2-dimethyltetrahydrofuro[3,4--
d][1,3]dioxol-4-yl)-6-chloro-N-(2-chlorobenzyl)-1H-pyrazolo[3,4-d]pyrimidi-
n-4-amine (2b)
##STR00240##
[1293] To a solution of
1-((3aR,4R,6R,6aR)-6-(azidomethyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]-
dioxol-4-yl)-6-chloro-N-(2-chlorobenzyl)-1H-pyrazolo[3,4-d]pyrimidin-4-ami-
ne (2a) (144 mg, 0.29 mmol) in pyridine (3 mL) was added
triphenylphosphine (115 mg, 0.44 mmol). After the mixture was
stirred for 2 h, sat. NH.sub.4OH (7 mL) was added and the mixture
was allowed to stir overnight. The reaction mixture was
concentrated and the residue was purified by column chromatography
(SiC.sub.2, 0-10% MeOH/DCM with 0.1% TEA) to provide the title
compound (2b) (130 mg, 95% yield) as a white solid.
Step C. Diethyl
(2-((((3aR,4R,6R,6aR)-6-(6-chloro-44(2-chlorobenzyl)amino)-1H-pyrazolo[3,-
4-d]pyrimidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)meth-
yl)amino)-2-oxoethyl)phosphonate (2c)
##STR00241##
[1295] To a solution of
1-((3aR,4R,6R,6aR)-6-(aminomethyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]-
dioxol-4-yl)-6-chloro-N-(2-chlorobenzyl)-1H-pyrazolo[3,4-d]pyrimidin-4-ami-
ne (2b) (130 mg, 0.28 mmol) and diethoxyphosphorylacetic acid (0.09
mL, 0.56 mmol) in DCM (3 mL) was added dicyclohexylcarbodiimide
(115 mg, 0.56 mmol) and 4-dimethylaminopyridine (1.7 mg, 0.01
mmol). The mixture was allowed to stir overnight. The reaction
mixture was filtered through Celite and the filtrate was
concentrated. The resulting residue was purified by column
chromatography (SiO.sub.2, 0-6% MeOH/DCM) to provide the title
compound (2c) (120 mg, 67% yield) as a white solid.
Step D.
(2-((((2R,3S,4R,5R)-5-(6-Chloro-4-((2-chlorobenzyl)amino)-1H-pyraz-
olo[3,4-d]pyrimidin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl)amino)--
2-oxoethyl)phosphonic acid (2)
##STR00242##
[1297] To solution of diethyl
(2-((((3aR,4R,6R,6aR)-6-(6-chloro-4-((2-chlorobenzyl)amino)-1H-pyrazolo[3-
,4-d]pyrimidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)met-
hyl)amino)-2-oxoethyl)phosphonate (2c) (120 mg, 0.19 mmol) in DCM
(6.5 mL) was added bromo(trimethyl)silane (0.15 mL, 1.1 mmol) and
the mixture was stirred overnight. The reaction mixture was
concentrated and the residue was dissolved in 5 mL MeOH. After 30
min, the mixture was concentrated. The residue was dissolved in
hexafluoro-2-propanol (2.34 mL) and water (0.11 mL) and
hydrochloric acid (2M in dioxane, 0.11 mL, 0.45 mmol) was added
dropwise. After the mixture was stirred for 1 h, it was quenched
with sat. NH.sub.4OH (0.3 mL). The mixture was concentrated. The
residue was purified by reverse phase HPLC (C18 column, 0 to 65%
gradient of acetonitrile and water with 0.1% TFA) to provide the
product (2) (34 mg, 28% yield) as a white solid in the TFA salt
form. .sup.1H NMR (400 MHz, DMSO-d6) .delta. ppm 9.29-9.34 (m, 1H),
8.32 (s, 1H), 7.84-7.90 (m, 1H), 7.47-7.53 (m, 1H), 7.40-7.47 (m,
1H), 7.30-7.39 (m, 2H), 6.03 (d, J=3.95 Hz, 1H), 5.33-5.51 (br s,
1H), 4.77 (d, J=5.55 Hz, 2H), 4.54 (t, J=4.40 Hz, 1H), 4.20 (t,
J=4.80 Hz, 1H), 3.85-3.98 (m, 1H), 3.42-3.58 (m, 1H), 3.00-3.13 (m,
1H), 2.54-2.64 (m, 2H), m/z (ESI, +ve ion)=547.1 [M+H].sup.+.
Example 3.
((N-(((2R,3S,4R,5R)-5-(6-Chloro-4-((2-chlorobenzyl)amino)-1H-py-
razolo[3,4-d]pyrimidin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl)sulf-
amoyl)methyl)phosphonic Acid (3)
##STR00243##
[1298] Step A.
N-(((3aR,4R,6R,6aR)-6-(6-Chloro-4-((2-chlorobenzyl)amino)-1H-pyrazolo[3,4-
-d]pyrimidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methy-
l)methanesulfonamide (3a)
##STR00244##
[1300] To a solution of
1-((3aR,4R,6R,6aR)-6-(aminomethyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]-
(dioxol-4-yl)-6-chloro-N-(2-chlorobenzyl)-1H-pyrazolo[3,4-d]pyrimidin-4-am-
ine (2b) (250 mg, 0.54 mmol) in DCM (2.5 mL) was added
triethylamine (0.22 mL, 1.6 mmol) followed by addition of
methanesulfonyl chloride (0.05 mL, 0.64 mmd) and
4-dimethylaminopyridine (13 mg, 0.11 mmd). The mixture was allowed
to stir overnight. The reaction mixture was concentrated and the
residue was purified by column chromatography (SiO.sub.2, 0-6%
MeOH/DCM) to provide the product (3a) (242 mg, 83% yield) as a
white solid.
Step B. Diethyl
((N-(((3aR,4R,6R,6aR)-6-(6-chloro-4-((2-chlorobenzyl)amino)-1H-pyrazolo[3-
,4-d]pyrimidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)met-
hyl)sulfamoyl)methyl)phosphonate (3b)
##STR00245##
[1302] To a solution of diisopropylamine (0.11 mL, 0.79 mmd) in THE
(3 mL) at -78.degree. C. was added n-butyllithium (1.6 M in
hexanes, 0.46 mL, 0.73 mmol) over 5 min. The solution slowly warmed
to 0.degree. C. over 30 min and the mixture was cooled to
-78.degree. C. To the reaction mixture was added
N-(((3aR,4R,6R.sup.6aR)-6-(6-chloro-4-((2-chlorobenzyl)amino)-1-
H-pyrazolo[3,4-d]pyrimidin-13.1)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dio-
xol-4-yl)methyl)methanesulfonamide (3a) (120 mg, 0.22 mmol)
dissolved in THF (2 mL) dropwise over 5 min. The mixture allowed to
stir for 30 min at -78.degree. C. Diethyl chlorophosphate (0.04 mL,
0.24 mmol) was added dropwise and the mixture was allowed to stir
for 15 min. The solution was slowly warmed to 0.degree. C. over 1
h. The reaction mixture was quenched with sat. NH.sub.4C.sub.1 (1.0
mL) and was partitioned between EtOAc (25 mL) and water (25 mL).
The aqueous layer was extracted two additional times with EtOAc (25
mL) and the combined organic layers were dried with MgSO.sub.4,
filtered, and concentrated. The resulting residue was purified by
column chromatography (SiO.sub.2, 20-100% EtOAc/hexanes) to provide
the product (3b) (36 mg, 24% yield) as a white solid.
Step C.
((N-(((2R,3S,4R,5R)-5-(6-Chloro-4-((2-chlorobenzyl)amino)-1H-pyraz-
olo[3,4-d]pyrimidin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl)sulfamo-
yl)methyl)phosphonic Acid (3)
##STR00246##
[1304] To solution of diethyl
((N-(((3aR,4R,6R,6aR)-6-(6-chloro-4-((2-chlorobenzyl)amino)-1H-pyrazolo[3-
,4-d]pyrimidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)met-
hyl)sulfamoyl)methyl)phosphonate (3b) (36 mg, 0.05 mmol) in DCM (2
mL) was added bromo(trimethyl)silane (0.04 mL, 0.32 mmol) and the
mixture was allowed to stir overnight. The reaction mixture was
concentrated and dissolved in MeOH (5 mL). After 30 min, the
mixture was concentrated. The residue was dissolved in
hexafluoro-2-propanol (0.67 mL) and water (0.03 mL) followed by
hydrochloric acid (2 M in dioxane, 0.03 mL, 0.13 mmol). After the
mixture was stirred for 1 h, it was quenched with sat. NH.sub.4OH
(1 mL) and concentrated. The residue was purified by reverse phase
HPLC (C18 column, 0 to 65% acetonitrile/water with 0.1% TFA) to
provide the product (3) (13 mg, 31% yield) as a white solid.
.sup.1H NMR (400 MHz, DMSO-d6) .delta. ppm 9.31-9.35 (m, 1H), 8.31
(s, 1H), 7.47-7.57 (m, 1H), 7.39-7.47 (m, 1H), 7.30-7.39 (m, 2H),
6.96-7.01 (m, 1H), 6.03 (d, J=4.40 Hz. 1H), 5.35-5.56 (br s, 1H),
4.77 (d, J=5.20 Hz, 2H), 4.56 (t, J=4.60 Hz, 1H), 4.23 (t, J=4.40
Hz, 1H), 3.89-4.02 (m, 1H), 3.43-3.56 (m, 2H), 3.20-3.32 (m, 1H),
3.03-3.17 (m, 1H), m/z (ESI, +ve ion)=583.0 [M+H].sup.+.
Example 4. (2-((2R,3S,4R,5R)-5-(6-Chloro-4
(((S)-2,3-dihydro-1H-inden-1-yl)(methyl)amino)-1H-pyrazolo[3,4-d]pyrimidi-
n-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)ethyl)phosphonic Acid
(4)
##STR00247##
[1305] Step A.
(3aR,6R,6aR)-6-Methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxole-4-ca-
rbaldehyde (4a)
##STR00248##
[1307] Oxalyl chloride (10.4 g) was added dropwise to a solution of
DMSO (7.5 g) in DCM (100 ml) at -78.degree. C. After the resulting
solution was stirred for 15 min, a solution of
((3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-
-yl)methanol (15.2 g) in DCM (20 ml) was added dropwise. The
reaction mixture was stirred for 20 min at -78.degree. C. DIPEA (48
g) was added and the mixture was stirred at -78.degree. C. for
another 30 min, then allowed to warm to rt for 2 h. The solution
was quenched with water and extracted with DCM. The organic layer
was dried, concentrated to afford the title compound (4a) (10 g,
66% yield) as a yellow liquid.
Step B. Diethyl
((E)-2-((3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]d-
ioxol-4-yl)vinyl)phosphonate (4b)
##STR00249##
[1309] Tetraethyl methylenediphosphonate was (500 mg, 1.74 mmol)
was added to potassium tert-butoxide solution (1 M in THF, 20 ml)
at 0.degree. C., and the reaction mixture was stirred for 10 min,
then warm to rt. After being stirred at rt for another 30 min, the
reaction was cooled to 0.degree. C., and 4a (174 mg, 0.87 mmol) was
added. The mixture was then stirred at 0.degree. C. for 1 h and
quenched with sat. NH.sub.4Cl (1.0 mL). The aqueous layer was
extracted with EtOAc and the combined organic layers were dried
with MgSO.sub.4, filtered, and concentrated. The residue was
purified by column chromatography to provide the title compound
(4b) (211 mg, 25% yield).
Step C. Diethyl
(2-((3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxo-
l-4-yl)ethyl)phosphonate (4c)
##STR00250##
[1311] Palladium on carbon (10% wt, 100 mg) was added to a solution
of 4b (700 mg) in MeOH (20 ml). After the mixture was stirred under
hydrogen (1 atm) for 2 h, it was filtered and filtrate was
concentrated to afford the title compound (4c) (640 mg, 92% yield)
as a crude oil.
Step D. Diethyl
(2-((2R,3S,4R)-3,4,5-trihydroxytetrahydrofuran-2-yl)ethyl)phosphonate
(4d)
##STR00251##
[1313] A solution of 4c (4.0 g, 11.83 mmol) in sulfuric acid (0.1
N, 40 mL) and dioxane (16 mL) was refluxed for 2 h. After the
reaction was cooled to rt, it was adjusted to PH-7 and concentrated
to dryness. The residue was evaporated with pyridine twice to
afford the crude product (3.4 g), which was used in the next step
without purification.
Step E.
(3R,4R,5R)-5-(2-(Diethoxyphosphoryl)ethyl)tetrahydrofuran-2,3,4-tr-
iyl triacetate (4e)
##STR00252##
[1315] To a solution of 4d (3.4 g, 11.83 mmol) in dry pyridine (45
mL) was added dropwise acetic anhydride (6.8 g, 66.7 mmol) at
0.degree. C. After the reaction mixture was stirred at rt
overnight, it was concentrated to dryness. The residue was treated
with EtOAc (100 mL)/water (100 mL) and the organic layer was
separated, washed with brine (50 mL), dried, and concentrated. The
residue was purified by column chromatography (SiO.sub.2, 33%
EtOAc/petroleum) to afford the title compound (4e) (3.2 g, 66%
yield over two steps).
Step F.
(2R,3R,4R,5R)-2-(4,6-Dichloro-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-5--
(2-(diethoxyphosphoryl)ethyl)tetrahydrofuran-3,4-diyldiacetate
(4f)
##STR00253##
[1317] To a solution of 4e (2 g, 4.88 mmol),
4,6-dichloro-1H-pyrazolo[3,4-d]pyrimidine (922 mg, 4.88 mmol), and
TMSOTf (4.33 g, 19.6 mmol) in dry MeCN (60 mL) was added dropwise
DBU (2.24 g, 14.7 mmol). The mixture was stirred at rt for 2 h and
was poured into sat. aq. NaHCO.sub.3 and the solution was extracted
with EtOAc. The organic layer was washed with brine, dried, and
concentrated in vacuo. The residue was purified by column
chromatography (SiO.sub.2, 50% EtOAc petroleum) to afford the title
compound (4f) (1.4 g, 53% yield).
Step G.
(2R,3R,4R,5R)-2-(6-Chloro-4-(((S)-2,3-dihydro-1H-inden-1-yl)(methy-
l)amino)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-5-(2-(diethoxyphosphoryl)ethyl)-
tetrahydrofuran-3,4-diyl Diacetate (4 g)
##STR00254##
[1319] A mixture of 4f (1.4 g, 2.6 mmol),
(S)--N-methyl-2,3-dihydro-1H-inden-1-amine hydrochloride (477 mg,
2.6 mmol) and TEA (656 mg, 6.5 mmol) in ethanol (40 mL) was stirred
at 55.degree. C. for 1 h and then concentrated in vacuo. The
residue was purified by column chromatography (SiO.sub.2, 25%
EtOAc/petroleum) to afford the title compound (4g) (912 mg, 54%
yield).
Step H.
(2-((2R,3S,4R,5R)-5-(6-Chloro-4-(((S)-2,3-dihydro-1H-inden-1-yl)(m-
ethyl)amino)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-3,4-dihydroxytetrahydrofura-
n-2-yl)ethyl)phosphonic Acid (4)
##STR00255##
[1321] To a solution of 4 g (230 mg, 0.35 mmol) and TEA (1.43 g,
14.16 mmol) in dry MeCN (25 mL) was added bromo(trimethyl)silane
(1.62 g, 10.6 mmol). After the reaction mixture was stirred at rt
overnight, it was concentrated to dryness. The residue was treated
with methanol (3 mL) and 1 N NaOH (3 mL) and the mixture was
stirred overnight at rt. The solution was directly purified by
reverse phase HPLC (C18 column, 0 to 65% acetonitrile/water with
0.1% TFA) to afford the title compound (4) (30 mg, 14% yield) as a
TFA salt. .sup.1H NMR (400 MHz; D.sub.2O) .delta. 8.14 (m, 1H),
7.22-7.02 (m, 4H), 5.90 (m, 1H), 5.04 (m, 1H), 4.33-4.09 (m, 2H),
3.99-3.87 (m, 1H), 2.97-2.76 (m, 5H), 2.55-2.34 (m, 1H), 2.1-1.92
(m, 1H), 1.72-1.70 (m, 2H), 1.27 (m, 2H), m/z (ESI, +ve ion)=510.3
[M+H].sup.+.
Examples 5.
(2-(((2R,3S,4R,5R)-5-(4-(Benzyl(methyl)amino)-6-chloro-1H-pyrazolo[3,4-d]-
pyrimidin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)ethyl)phosphonic
Acid (5)
##STR00256##
[1322] Step A. Diethyl
(2-(((3aR,4R,6aR)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol--
4-yl)methoxy)ethyl)phosphonate (5a)
##STR00257##
[1324] Cesium carbonate (830 mg, 2.55 mmol) was added to a mixture
of
((3aR,4R,6aR)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl-
)methanol (26 g, 12.7 mmol) and diethyl vinylphosphonate (2 g, 12.7
mmol). After the mixture was stirred at 50.degree. C. overnight, it
was directly purified by column chromatography (SiO.sub.2, 50%
EtOAc/petroleum ether) to afford the title compound (5a) (2.36 g,
50% yield).
Step B.
(3R,4R,5R)-5-((2-(Diethoxyphosphoryl)ethoxy)methyltetrahydrofuran--
2,3,4-triyl Triacetate (5b)
##STR00258##
[1326] Concentrated sulfuric acid (0.72 mL) was added dropwise to a
solution of 5a (1.3 g, 3.53 mmol) in acetic acid (3 mL) and acetic
anhydride (2.14 mL) at 0.degree. C. The mixture was allowed to stir
at rt overnight and poured into aq. NaHCO.sub.3. The solution was
extracted with EtOAc and the organic layer was washed with brine,
dried and concentrated. The residue was purified by column
chromatography (SiO.sub.2, 100% EtOAc) to afford the title compound
(5b) (520 mg, 33% yield) as a mixture of two diastereomers.
Step C.
(3R,4R,5R)-2-(4,6-Dichloro-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-5-((2-
-(diethoxyphosphoryl)ethoxy)methyl)tetrahydrofuran-3,4-diyl
Diacetate (5c)
##STR00259##
[1328] TMSOTf (1.04 g, 4.72 mmol) and DBU (532 mg, 3.54 mmol) were
added to a solution of 5b (520 mg, 1.18 mmol) and
4,6-dichloro-1H-pyrazolo[3,4-d]pyrimidine (220 mg, 1.18 mmol) in
MeCN (14 mL) successively. After the reaction mixture was stirred
at rt for 2 h, it was poured into sat.aq. NaHCO.sub.3 and extracted
with EtOAc. The organic layer was washed with brine, dried and
concentrated in vacuo. The residue was purified by column
chromatography (SiO.sub.2, 33% EtOAc/petroleum ether) to afford the
title compound (5c) (250 mg, 38% yield) as a mixture of two
diastereomers.
Step D.
(3R,4R,5R)-2-(4-(Benzyl(methyl)amino)-6-chloro-1H-pyrazolo[3,4-d]p-
yrimidin-1-yl)-5-((2-(diethoxyphosphoryl)ethoxy)methyl)tetrahydrofuran-3,4-
-diyl Diacetate (5d)
##STR00260##
[1330] A mixture of 5c (250 mg, 0.44 mmol), Et.sub.3N (58 mg, 0.53
mmol) and N-methyl-1-phenylmethanamine (70 mg, 0.53 mmol) in EtOH
(8 mL) was stirred at 55.degree. C. for 1 h. The mixture was then
concentrated in vacuo and purified by column chromatography
(SiO.sub.2, 25% EtOAc/petroleum ether) to afford the title compound
(5d) (200 mg, 70% yield).
Step E. Diethyl (2-(((2R,3S,4R,5R)
5-(4-(benzyl(methyl)amino)-6-chloro-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-3,4-
-dihydroxytetrahydrofuran-2-yl)methoxy)ethyl)phosphonate (5e-1) and
Diethyl
(2-(((2R,3S,4R,5S)-5-(4-(benzyl(methyl)amino)-6-chloro-1H-pyrazol-
o[3,4-d]pyrimidin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)ethyl)ph-
osphonate (5e-2)
##STR00261##
[1332] To a solution of 5d (200 mg, 0.306 mmol) in methanol (8 mL)
was added potassium carbonate (220 mg, 0.917 mmol). After the
reaction mixture was stirred at 40.degree. C. for 30 min, it was
concentrated in vacuo and the residue was purified by column
chromatography (SiO.sub.2, 100% EtOAc) to afford the crude product
as a mixture of two diastereomers (110 mg, 63% yield), which was
separated by reverse phase HPLC (C18 column, 0 to 65%
acetonitrile/water with 0.1% TFA) to afford 5e-1 (50 mg) and 5e-2
(50 mg), respectively.
Step F.
(2-(((2R,3S,4R,5R)-5-(4-(Benzyl(methyl)amino)-6-chloro-1H-pyrazolo-
[3,4-d]pyrimidin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)ethyl)pho-
sphonic Acid (5)
##STR00262##
[1334] To a solution of 5e-1 (50 mg, 0.088 mmol) and TEA (354 mg,
3.51 mmol) in dry MeCN (4 mL) was added bromo(trimethyl)silane (403
mg, 2.63 mmol). After the mixture was stirred at rt overnight, it
was concentrated in vacuo and the residue was purified by reverse
phase HPLC (C18 column, 0 to 65% acetonitrile/water with 0.1% TFA)
to afford title compound (5) (34 mg, 61% yield) as a TFA salt.
.sup.1H NMR (400 MHz, 1320) S 8.14-7.7 (m, 1H), 7.25-7.20 (m, 5H),
5.93 (m, 1H), 4.87 (m, 2H), 4.65-4.4 (m, 1H), 4.07-4.01 (m, 2H),
3.65-3.52 (m, 4H), 3.25-3.20 (m, 3H), 1.65-1.61 (m, 2H), m/z (ESI,
+ve ion)=514.3 [M+H].sup.+.
Example 6.
(2-(((2R,3S,4R,5S)-5-(4-(Benzyl(methyl)amino)-6-chloro-1H-pyraz-
olo[3,4-d]pyrimidin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)ethyl)-
phosphonic Acid (6)
##STR00263##
[1336] Compound 6 was prepared from 5e-2 (Example 5, Step E) by
procedure similar to that described in Example 5, Step F. .sup.1H
NMR (400 MHz, D.sub.2O) S 7.74-7.46 (m, 1H), 6.96-6.87 (m, 5H),
5.98 (s, 1H), 4.58-4.37 (m, 3H), 4.19-3.99 (m, 2H), 3.66-3.42 (m,
4H), 2.88 (br s, 3H), 1.89-1.85 (m, 2H). m/z (ESI, +ve ion)=514.5
[M+H].sup.+.
Example 7. ((((2R,3S,4R,5R)
5-(4-(Benzyl(methyl)amino)-6-chloro-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-3,4-
-dihydroxytetrahydrofuran-2-yl)methoxy)methyl)phosphonic Acid
(7)
##STR00264##
[1337] Step A.
((3aR,4R,6R,6aR)-6-(4-(benzyl(methyl)amino)-6-chloro-1H-pyrazolo[3,4-d]py-
rimidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methanol
(7a)
##STR00265##
[1339] The starting material 7a was prepared from
(2R,3R,4R,5R)-2-(acetoxymethyl)-5-(4,6-dichloro-1H-pyrazolo[3,4-d]pyrimid-
in-1-yl)tetrahydrofuran-3,4-diyl diacetate (1a) (Example 1, Step A)
by procedures similar to those described in Example 1, Steps B, C
and D, substituting benzylmethylamine for 2-chlorobenzylamine in
Step B.
Step B. Diethyl
((((3aR,4R,6R,6aR)-6-(4-(benzyl(methyl)amino)-6-chloro-1H-pyrazolo[3,4-d]-
pyrimidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1.3]dioxol-4-yl)methoxy)-
methyl)phosphonate (7b)
##STR00266##
[1341] To a solution of 7a (300 mg, 0.67 mmol) in dry DMF (10 mL)
was added sodium hydride (60% in mineral oil. 80 mg, 2.02 mmol) at
0.degree. C. The mixture was stirred for 10 min at the same
temperature and (diethoxyphosphoryl)methyl 4-methylbenzenesulfonate
(433 mg, 1.34 mind) was added. After the reaction mixture was
stirred at rt overnight, it was poured into water and extracted
with ethyl acetate. The organic layer was washed with brine, dried
and concentrated in vacuo. The residue was purified by column
chromatography (SiO.sub.2, 33% EtOAc/petroleum ether) to afford the
title compound (7b) (200 mg, 50% yield).
Step C.
((((2R,3S,4R,5R)-5-(4-(Benzyl(methyl)amino)-6-chloro-1H-pyrazolo[3-
,4-d]pyrimidin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)methyl)phos-
phonic Acid (7)
##STR00267##
[1343] To a solution of 7b (140 mg, 0.235 mmol) and TEA (951 mg,
9.41 mmol) in dry MeCN (6 mL) was added bromo(trimethyl)silane
(1.08 g, 7.06 mmol) and the mixture was stirred at rt overnight.
The mixture was concentrated in vacuo and the residue was treated
with aq. TFA (50% aqueous solution, 6 mL). Alter the mixture was
stirred for 1 h, it was concentrated and the residue was purified
by reverse phase HPLC (C18 column, 0 to 65% acetonitrile/water with
0.1% TFA) to afford the title compound (7) (20 mg, 14% yield) as a
TFA salt. .sup.1H NMR (400 MHz, D.sub.2O) .delta. 8.17-7.71 (m,
1H), 7.27-7.21 (m, 5H), 5.98 (br s, 1H), 4.95 (m, 2H), 4.25-4.10
(m, 2H), 3.70-3.53 (m, 2H), 3.38-3.16 (m, 6H), m/z (ESI, +ve
ion)=500.5 [M+H].sup.+.
Example 8.
(2-(((2R,3S,4R,5R)-5-(6-Chloro-4-(((S)-2,3-dihydro-1H-inden-1-y-
l)(methyl)amino)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-3,4-dihydroxytetrahydro-
furan-2-yl)methoxy)-2-oxoethyl)phosphonic Acid (8)
##STR00268##
[1345] Example 8 was prepared from
(2R,3R,4R,5R)-2-(acetoxymethyl)-5-(4,6-dichloro-1H-pyrazolo[3,4-d]pyrimid-
in-1-yl)tetrahydrofuran-3,4-diyl diacetate (1a) (Example 1, Step A)
by procedures similar to those described in Example 1, Steps B, C,
D, E and F, substituting (S)--N-methyl-2,3-dihydro-1H-inden-1-amine
for 2-chlorobenzylamine in Step B. .sup.1H NMR (400 MHz, DMSO-d6)
.delta. ppm 8.36-8.56 (m, 1H), 7.07-7.40 (m, 4H), 6.62 (t, J=8.19
Hz, 1H), 6.08-6.15 (m, 1H), 4.52 (t, J=4.40 Hz, 1H), 4.37 (t,
J=5.19 Hz, 1H), 4.23-4.31 (m, 1H), 4.07-4.14 (m, 1H), 3.93-4.02 (m,
1H), 3.02-3.08 (m, 3H), 2.93-3.02 (m, 1H), 2.84 (brs, 1H),
2.70-2.65 (m, 2H), 2.41-2.44 (m, 1H), 2.02-2.07 (m, 1H).
[1346] The following examples were made according to the procedures
described in Examples 1-8 using the appropriate starting
material.
TABLE-US-00002 Ex. LC-MS 9 561.01 [M + H].sup.+ 10 520.1 [M +
H].sup.+ 11 555.0 [M + H].sup.+ 12 511.1 [M - H].sup.-
Example 13. (((((2S,3S,4R,5R)
5-(6-Chloro-4-((2-chlorobenzyl)amino)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-3-
,4-dihydroxytetrahydrofuran-2-yl)methyl)thio)methyl)phosphonic Acid
(13)
##STR00269##
[1347] Step A.
S-(((3aS,4S,6R,6aR)-6-(6-Chloro-4-((2-chlorobenzyl)amino)-1H-pyrazolo[3,4-
-d]pyrimidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methy-
l) ethanethioate (13a)
##STR00270##
[1349] To a dried flask charged with (E)-diisopropyl
azodicarboxylate (0.46 mL, 2.4 mmol) and THE (12 mL) was added
triphenylphosphine (619 mg, 2.36 mmol) at 0.degree. C. After the
mixture was stirred for 5 min,
[(3aR,4R,6R,6aR)-4-[6-chloro-4-[(2-chlorophenyl)methylamino]pyrazolo[3,4--
d]pyrimidin-1-yl]-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol--
1-yl]methanol (1d) (500 mg, 1.07 mmol) and thioacetic acid (0.17
mL, 2.4 mmol) were added successively. The mixture was stirred
overnight and slowly allowed to warm to rt. The mixture was
quenched with TEA (0.1 mL) and concentrated. The residue was
partitioned between EtOAc and water. Aqueous layer was extracted
(EtOAc) and combined organic layers were dried (MgSO.sub.4) and
concentrated. The residue was purified by flash column
chromatography (SiO.sub.2. 0-100% EtOAc/hexanes, gradient elution)
to give the title compound (13a). The crude product was used in the
next step without further purification. m/z (ESI, +ve ion)=524.0
[M+H].sup.+.
Step B. ((3aS,4S,6R,6aR)-6-(6-Chloro-4
((2-chlorobenzyl)amino)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-2,2-dimethyltet-
rahydrofuro[3,4-d][1,3]dioxol-4-yl)methanethiol (13b)
##STR00271##
[1351] To a flask containing 13a (562 mg, 1.07 mmol) was added
methanol (24 mL), triethylamine (1.69 mL, 12.1 mmol), followed by
addition of DL-dithiothreitol (165 mg, 1.07 mmol). After the
mixture was stirred at rt for 3 h, it was concentrated. The residue
was purified by flash column chromatography (SiO.sub.2, 0-50%
EtOAc/hexanes, a gradient elution) to provide the title compound
(13b) (505 mg, 97.6%). .sup.1H NMR (400 MHz, Chloroform-d) .delta.
8.19-7.22 (m, 5H), 6.48 (s, 2H), 5.39-5.20 (m, 1H), 5.04-4.80 (m,
3H), 4.24 (td, J=7.05, 1.97 Hz, 1H), 2.71 (t, J=7.31 Hz, 2H), 1.56
(s, 3H), 1.47 (t, J=8.48 Hz: 1H), 1.36 (s, 3H), m/z (ESI, +ve
ion)=482.0 [M+H].sup.+.
Step C. Di-tert-butyl
(((((3aS,4S,6R,6aR)-6-(6-chloro-4-((2-chlorobenzyl)amino)-1H-pyrazolo[3,4-
-d]pyrimidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methy-
l)thio)methyl)phosphonate (13c)
##STR00272##
[1353] To an oven dried flask was added sodium hydride (60%
dispersion in mineral oil, 41.9 mg, 1.05 mmol) and 4 mL of DMF. At
-10.degree. C., a solution of 13b (505 mg, 1.05 mmol) in DMF (6 mL)
was added. 30 min later, a solution of
ditert-butoxyphosphorylmethyl trifluoromethanesulfonate* (410 mg,
1.15 mmol) in DMF (1 mL) was added. The mixture was allowed to warm
tort and stirred for 1 h, it was quenched (sat. ammonium chloride)
and extracted (EtOAc). The organic layer was dried (MgSO.sub.4),
and concentrated. The residue was purified by flash column
chromatography (SiO.sub.2, 30-10% EtOAc/hexanes, a gradient
elution) to provide the title compound (13c) (500 mg, 69.4% yield).
.sup.1H NMR (400 MHz. Chloroform-d) .delta. 7.86-7.19 (m, 6H), 6.46
(d, J=1.46 Hz, 1H), 5.23 (s, 1H), 4.93-4.80 (m, 3H), 4.33-4.28 (m,
1H), 2.81 (d, J=7.60 Hz, 2H), 2.62-2.44 (m, 2H), 1.52 (s, 3H), 1.40
(s, 9H), 1.38 (s, 9H), 1.30 (s, 3H), m/z (ESI, +ve ion)=686.2
[M+H].sup.+.
*Synthesis of Ditert-butoxyphosphorylmethyl
Trifluoromethanesulfonate
##STR00273##
[1355] Step 1. To an oven dried flask was added di-t-butyl
phosphite (3.24 mL, 16 mmol) and water (1 mL) followed by addition
of triethylamine (2.68 mL, 19.22 mmol) and formaldehyde (37%
aqueous solution, 1.2 mL, 16 mmol). After the mixture was stirred
overnight, it was co-evaporated three times with MeOH (10 mL) and
one time with DCM (10 mL). The resulting white solid (3.5 g) was
placed under high vacuum for 30 min. The crude product was used in
the next step without further purification.
[1356] Step 2. The crude ditert-butoxyphosphorylmethanol (3.5 g,
15.61 mmol) in the original flask was dissolved in anhydrous DCM
(50 mL). To the reaction mixture was added 2,6-lutidine (3.64 mL,
31.2 mmol) and the flask was cooled to -78.degree. C. Using a
syringe pump, triflic anhydride (2.83 mL, 17.3 mmol) was added
dropwise over 30 min. After the mixture was warmed to 0.degree. C.,
and stirred for 3 h, it was cooled to -78.degree. C., and then
diluted with Et.sub.2O (100 mL). The solids were filtered over
Celite and the filtrate was partitioned with water (75 mL). The
solution was extracted (Et.sub.2O) and the combined organics were
washed (water and brine), dried (MgSO.sub.4), filtered, and
concentrated to provide ditert-butoxyphosphorylmethyl
trifluoromethanesulfonate (4.6 g, 12.9 mmol, 83%) as a red oil.
Step D.
(((((2S,3S,4R,5R)-5-(6-Chloro-4-((2-chlorobenzyl)amino)-1H-pyrazol-
o[3,4-d]pyrimidin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl)thiomethy-
l)phosphonic Acid (13)
##STR00274##
[1358] To an oven dried flask was added 13c (82 mg, 0.12 mmol) and
hexafluoro-2-propanol (1.48 mL) followed by addition of water (0.07
mL, 4 mmol) and hydrochloric acid (4 M in dioxane, 0.07 mL, 0.29
mmol). After the mixture was stirred at rt for 25 min, it was
quenched (sat. ammonium hydroxide) and concentrated. The residue
was dissolved in MeOH (1 mL) and DMF (1 mL), filtered through a
syringe filter. The solution was purified by reverse preparative
HPLC (0-65% ACN/H.sub.2O with 0.1% TFA) to afford the title
compound (13) (41 mg, 0.063 mmol, 53%) as a trifluoroacetate salt.
.sup.1H NMR (400 MHz, DMSO-d6) .delta. ppm 9.31 (t, J=5.55 Hz, 1H),
8.30 (s, 1H), 7.54-7.47 (m, 1H), 7.46-7.40 (m, 1H), 7.37-7.28 (m,
2H), 6.02 (d, J=4.24 Hz, 1H), 4.77 (d, J=5.55 Hz; 2H), 4.57 (t,
J=4.80 Hz, 1H), 4.21 (t, J=4.80 Hz, 1H), 4.09-3.99 (m, 1H),
3.02-2.90 (m, 1H), 2.87-2.76 (m, 1H), 2.64-2.53 (m, 2H), m/z (ESI,
+ve ion)=536.0 [M+H].sup.+.
Example 14.
(((((2S,3S,4R,5R)-5(6-Chloro-4-((2-chlorobenzyl)amino)-1H-pyrazolo[3,4-d]-
pyrimidin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl)sulfonyl)methyl)p-
hosphonic Acid (14)
##STR00275##
[1359] Step A. Di-tert-Butyl
(((((3aS,4S,6R,6aR)-6-(6-chloro-4-((2-chlorobenzyl)amino)-1H-pyrazolo[3,4-
-d]pyrimidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methy-
l)sulfonyl)methyl)phosphonate (14a)
##STR00276##
[1361] To an oven dried flask was added 13c (235 mg, 0.34 mmol)
followed by addition of MeOH (2 mL), water (2 mL), and THE (4.0
mL). To this mixture was added potassium peroxymonosulfate (519 mg,
3.41 mmol). After the mixture was stirred at rt for 24 h, it was
quenched (sat. sodium bicarbonate) and extracted (EtOAc). The
combined organic layers were dried (MgSO.sub.4), and concentrated.
The crude product (14a) was used in the next step without further
purification. .sup.1H NMR (400 MHz, DMSO-d6) .delta. 9.34 (t,
J=5.63 Hz, 1H), 8.32 (s, 1H), 7.54-7.48 (m, 1H), 7.47-7.42 (m, 1H),
7.37-7.31 (m, 2H), 6.06 (d, J=3.51 Hz, 1H), 4.77 (d, J=5.85 Hz;
2H), 4.48 (t, J=4.09, 1H), 4.40-4.28 (m, 2H), 3.74-3.56 (m, 4H),
m/z (ESI, +ve ion)=718.2 [M+H].sup.+.
Step B.
(((((2S,3S,4R,5R)-5-(6-Chloro-4-((2-chlorobenzyl)amino)-1H-pyrazol-
o[3,4-d]pyrimidin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl)sulfonyl)-
methyl)phosphonic Acid (14)
##STR00277##
[1363] To a flask was added 14a (246 mg, 0.34 mmol) and
hexafluoro-2-propanol (4.24 mL, 40.3 mmol) followed by addition of
water (0.2 mL, 11 mmol) and hydrochloric acid (4 M in dioxane, 0.2
mL, 0.82 mmol). After the mixture was stirred for 25 min, it was
quenched with sat. ammonium hydroxide (0.2 mL) and concentrated.
The residue was dissolved in DMF (6 mL) and purified by reverse
preparative HPLC (0-65% ACN/H.sub.2O with 0.1% TFA) to provide the
title compound (14) (127 mg, 0.224 mmol). .sup.1H NMR (400 MHz,
DMSO-d6) .delta. 9.34 (t, J=5.63 Hz, 1H), 8.32 (s, 1H), 7.54-7.48
(m, 1H), 7.47-7.42 (m, 1H), 7.37-7.31 (m, 2H), 6.06 (d, J=3.51 Hz,
1H), 4.77 (d, J=5.85 Hz, 2H), 4.48 (t, J=4.09, 1H), 4.40-4.28 (m,
2H), 3.74-3.56 (m, 4H), m/z (ESI, +ve ion)=568.0 [M+H].sup.+.
Example 15.
((((2R,3S,4R,5R)-5-(2-Chloro-4-((cyclopropylmethyl)amino)-7H-pyrrolo[2,3--
d]pyrimidin-7-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)methyl)phospho-
nic Acid (15)
##STR00278##
[1364] Step A.
(3aR,6R,6aR)-6-(Hydroxymethyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]diox-
ol-4-ol (15a)
##STR00279##
[1366] Concentrated sulfuric acid (0.3 mL) was added to a
suspension of D-ribose (12.5 g, 83 mmol) in acetone (125 mL). The
mixture was stirred at rt for 90 min to a clear solution which was
neutralized with saturated aqueous sodium carbonate. The solution
was filtered over Celite and the filtrate was concentrated to
afford the crude product (16 g), which was used in next step
without purification.
Step B.
((3aR,4R,6aR)-6-Hydroxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]diox-
ol-4-yl)methyl Benzoate (15b)
##STR00280##
[1368] To a solution of 15a (16 g, 83 mmol) in pyridine (60 mL) was
added dropwise BzCl (12.9 g, 91 mmol) at 0.degree. C. After the
reaction was stirred at rt overnight, it was concentrated and the
residue was diluted (EtOAc) and washed (5% aq. citric acid). The
organic layer was dried and concentrated and the residue was
purified by flash column chromatography (SiO.sub.2, 20%
EtOAc/petroleum ether) to provide the title compound (15b) (12 g,
49% yield for the two steps), m/z (ESI, +ve ion)=316.4
[M+Na].sup.+.
Step C.
((3aR,4R,6aR)-6-Bromo-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-
-4-yl)methyl Benzoate (15c)
##STR00281##
[1370] To a solution of 15b (2 g, 6.8 mmol) in dry DCM (60 mL) was
added dropwise TMSBr (2.1 g, 13.6 mmol) at 0.degree. C. After the
mixture was allowed to warm to rt and stirred for 2 h, it was
concentrated at rt and the residue was used in next step
immediately.
Step D. ((3aR,4R,6R,6aR)-6-(2-Chloro-4
((cyclopropylmethyl)amino)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-2,2-dimethylt-
etrahydrofuro[3,4-d][1,3]dioxol-4-yl)methyl benzoate (15d)
##STR00282##
[1372] To a suspension of
2-chloro-N-(cyclopropylmethyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine
(1.1 g, 4.9 mmol) in dry MeCN (30 mL) was added sodium hydride (60%
dispersion in mineral oil, 314 mg, 7.4 mmol) at rt. After the
reaction was stirred at rt for 30 min, a solution of 15c (6.8 mmol)
in dry MeCN (10 mL) was added. The mixture was stirred at rt
overnight and then poured into sat. NH.sub.4Cl. The solution was
extracted (EtOAc) and the organic layer was washed (brine), dried,
and concentrated. The residue was purified by flash column
chromatography (SiO.sub.2, 15% EtOAc/petroleum ether) to provide
the title compound (15d) (600 mg, 1.21 mmol, 30%), m/z (ESI, +ve
ion)=521 [M+Na].sup.+.
Step E. ((3aR,4R,6R,6aR)-6-(2-Chloro
4-((cyclopropylmethyl)amino)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-2,2-dimethy-
ltetrahydrofuro[3,4-d][1,3]diazol-4-yl)methanol (15e)
##STR00283##
[1374] To a solution of 15d (600 mg, 1.2 mmol) in methanol (17 mL)
was added K.sub.2CO.sub.3 (166 mg, 1.2 mmol) at rt. After the
mixture was stirred at 40.degree. C. for 0.5 h, it was concentrated
and the residue was purified by flash column chromatography
(SiO.sub.2, 33% EtOAc/petroleum ether) to provide the title
compound (15e) (400 mg, 1.01 mmol, 83%), m/z (ESI, +ve ion)=395.1
[M+H].sup.+.
Step F.
((((2R,3S,4R,5R)-5-(2-Chloro-4-((cyclopropylmethyl)amino)-7H-pyrro-
lo[2,3-d]pyrimidin-7-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)methyl)-
phosphonic Acid (15)
##STR00284##
[1376] The title compound was prepared from
((3aR,4R,6R,6aR)-2-chloro-4-((cyclopropylmethyl)amino)-7H-pyrrolo[2,3-d]p-
yrimidin-7-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methanol
(15e) by procedures similar to those described in Example 17, Steps
G and H. m/z (ESI, +ve ion)=448.8 [M+H].sup.+.
Example 16.
((((2R,3S,4R,5R)-5-(5-Chloro-7-((cyclopropylmethyl)amino)-3H-[1,2,3]triaz-
olo[4,5-d]pyrimidin-3-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)methyl-
)phosphonic Acid (16)
##STR00285##
[1377] Step A. 2,6-Dichloro-5-nitropyrimidin-4-amine (16a)
##STR00286##
[1379] To a solution of 2,4,6-trichloro-5-nitropyrimidine (9.0 g,
39.4 mmol) in THE (540 mL) was added an ammonia solution (10.8 mL,
10 N in EtOH, 78.8 mmol) dropwise at -70.degree. C. After the
reaction was stirred at -70.degree. C. for 30 min, it was acidified
with AcOH (pH 4-5) and concentrated. The residue was diluted with
EtOAc and the resulting mixture was stirred for 30 min and
filtered. The solids were washed with EtOAc and the organics were
combined and concentrated to afford the title compound (16a) (8.0
g, 97%), which was directly used for the next step without further
purification.
Step B. 2,6-Dichloropyrimidine-4,5-diamine (16b)
##STR00287##
[1381] A mixture of iron powder (10.7 g, 191 mmol), acetic acid (24
ml) and ethanol (30 mL) was heated at 55.degree. C. for 0.5 h. A
solution of 16a (8.0 g, 38.3 mmol) in ethanol (50 ml) was added
dropwise. After the mixture was stirred at 55.degree. C. for 20
min, it was cooled to rt and filtered. The filtrate was
concentrated, the residue was diluted with water and the solution
extracted with EtOAc. The combined organics were washed with water
and brine, dried and concentrated. The residue was purified by
column chromatography (petroleum ether/ethyl acetate: from 5:1 to
3:1) to give the title compound (161)) (4.4 g, 60.4%) as a white
solid.
Step C. 5,7-Dichloro-3H-[1,2,3]triazolo[4,5-d]pyrimidine (16c)
##STR00288##
[1383] A suspension of 2,6-dichloropyrimidine-4,5-diamine (16b)
(4.4 g, 24.58 mmol) in water (47 ml) was heated and the solid was
dissolved. The solution was cooled to 0.degree. C., and acetic acid
(94 ml) was added, followed by addition of a solution of sodium
nitrite (3.05 g, 44.3 mmol) in water (47 mL) during a period of 15
min. The reaction mixture was stirred at 0.degree. C. for another
20 min and then was extracted with EtOAc. The organics were
neutralized, dried and concentrated, the crude product was purified
by column chromatography (petroleum ether/ethyl acetate: from 3:1
to 2:1) to provide the title compound (16c) (3.4 g, 72.8%) as a
yellow solid.
Step D.
(2R,3R,4R,5R)-2-(Acetoxymethyl)-5-(5,7-dichloro-3H-[1,2,3]triazolo-
[4,5-d]pyrimidin-3-yl)tetrahydrofuran-3,4-diyl Diacetate (16d)
##STR00289##
[1385] .beta.-D-Ribofuranose 1,2,3,5-tetraacetate (5.73 g, 18.0
mmol) was heated at 90.degree. C.; for 10 min before 16c (3.4 g,
18.0 mmol) and SnCl.sub.4 (105 mg) were added. After the mixture
was heated at 130.degree. C. for 15 min, it was cooled to rt,
diluted with water, extracted with DCM. The combined organics were
washed with water and brine, dried and concentrated. The residue
was purified by column chromatography on silica gel (petroleum
ether/ethyl acetate: from 8:1 to 5:1) to afford crude product,
which was purified by Supercritical Fluid Chromatography (SFC) to
give the title compound (16d) (4.0 g. 51% yield) as a yellow
solid.
Step E.
((3aR,4R,6R,6aR)-6-(5-Chloro-7-((cyclopropylmethyl)amino)-3H-[1,2,-
3]triazolo[4,5-d]pyrimidin-3-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dio-
xol-4-yl)methanol (16e)
##STR00290##
[1387] The title compound was prepared from
(2R,3R,4R,5R)-2-(acetoxymethyl)-5-(5,7-dichloro-3H-[1,2,3]triazolo[4,5-d]-
pyrimidin-3 yl)tetrahydrofuran-3,4-diyl diacetate (16d) by
procedures similar to those described in Example 1. Steps B, C, and
D.
Step F.
((((2R,3S,4R,5R)-5-(5-Chloro-7-((cyclopropylmethyl)amino)-3H-[1,2,-
3]triazolo[4,5-d]pyrimidin-3-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy-
)methyl)phosphonic Acid (16)
##STR00291##
[1389] The title compound was prepared from
((3aR,4R,6R,6aR)-6-(5-chloro-7-((cyclopropylmethyl)amino)-3H-[1,2,3]triaz-
olo[4,5-d]pyrimidin-3-yl)-2,2-dimethyltetrahydrofuran[3,4-d][1,3]dioxol-4--
yl)methanol (16e) by procedures similar to those described in
Example 17, Steps G and H. .sup.1H NMR (400 MHz, D.sub.2O). .delta.
5.90 (s, 1H), 4.71 (s, 1H), 4.33 (t, J=4.8 Hz, 1H), 4.03 (d, J=2.4
Hz, 1H), 3.54 (d, J=2.4 Hz, 1H), 3.52 (m, 1H), 3.33 (d, J=8.4 Hz,
2H), 3.06 (m, 2H), 0.85 (m, 1H), 0.26 (m, 2H), 0.00 (m, 2H), m/z
(EST, +ve ion)=449.2 [M-H].sup.-.
Example 17.
((((2R,3S,4R,5R)-5-(4-((2-Chlorobenzyl)amino)-6-(hydroxymethyl)-1H-pyrazo-
lo[3,4-d]pyrimidin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)methyl)-
phosphonic Acid (17)
##STR00292##
[1390] Step A.
((3aR,4R,6R,6aR)-6-(6-Chloro-4-((2-chlorobenzyl)amino)-1H-pyrazolo[3,4-d]-
pyrimidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methyl
Benzoate (17a)
##STR00293##
[1392] To a solution of 2-chlorobenzyl analog of 1d (2.8 g, 6.0
mmol) in DCM (60 mL) was added Et.sub.2N (1.5 g, 15 mmol), DMAP (36
mg, 0.3 mmol), and BzCl (0.84 mL, 7.2 mmol) successively at rt.
After the mixture was stirred at rt overnight, it was washed
(water, saturated aqueous NaHCO.sub.3, and brine). The organic
phase was dried (Na.sub.2SO.sub.4) and concentrated under reduced
pressure. The residue was purified by column chromatography on
silica gel to give the title compound (17a) (2.4 g, 4.23 mmol,
71%). .sup.1H NMR (400 MHz, D.sub.2O) .delta. 6.28-5.90 (m, 1H),
4.71 (s, 1H), 4.32 (t, J=4.8 Hz, 1H), 4.04-4.03 (m, 1H), 3.55-3.52
(m, 1H), 3.46 (t, J=6.0 Hz; 1H), 3.33 (d, J=7.8 Hz, 2H), 3.05 (d,
J=7.2 Hz, 2H), 0.85-0.84 (m, 1H), 0.26-0.24 (m, 2H), 0.00 (m, 2H),
m/z (ESI, +ve ion)=569.1 [M+H].sup.+.
Step B.
((3aR,4R,6R,6aR)-6-(4-((2-Chlorobenzyl)amino-6-((E)-styryl)-1H-pyr-
azolo[3,4-d]pyrimidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-
-yl)methyl Benzoate (17b)
##STR00294##
[1394] 17a (2.2 g, 3.9 mmol), phenylvinylboronic acid (1.2 g, 7.8
mmol), and sodium carbonate (1.2 g, 11.7 mmol) were suspended in
THF/H.sub.2O (3:1, 40 mL). The mixture was degassed by N.sub.2
three times. Subsequently Ph(PPh.sub.3).sub.4 (0.48 g, 0.42 mmol)
was added and the mixture was degassed for another 5 min. After the
mixture was stirred at reflex for 20 h, it was cooled to rt and
filtered. The filtrate was extracted (EtOAc) and the organic layers
was washed (brine), dried (Na.sub.2SO.sub.4), and concentrated. The
residue was purified by column chromatography to afford the title
compound (17b) (1.8 g, 73%) as a yellow solid. m/z (ESI, +ve
ion)=637.2 [M+H].sup.+.
Step C.
((3aR,4R,6R,6aR)-6-(44(2-Chlorobenzyl)amino)-6-formyl-1H-pyrazolo[-
3,4-d]pyrimidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)me-
thyl Benzoate (17c)
##STR00295##
[1396] 17b (2.25 g, 3.5 mmol), NaIO.sub.4 (4.5 g, 21.0 mmol), and
2,6-lutidine (0.75 g, 7.0 mmol) were suspended in THE/H.sub.2O
(2:1, 60 mL). Subsequently potassium osmate dehydrate (33 mg, 0.09
mmol) was added. After the resulting mixture was stirred at rt for
20 h, it was quenched (water) and the solution was extracted
(EtOAc). The organic layers was washed (water and brine), dried
(Na.sub.2SO.sub.4) and concentrated under reduced pressure. The
residue was purified by column chromatography to afford the title
compound (17c) (1.4 g, 70%) as a yellow solid. m/z (ESI, +ve
ion)=563.2 [M+H].sup.+.
Step D.
((3aR,4R,6R,6aR)-6-(4-((2-Chlorobenzyl)amino)-6-(hydroxymethyl)-1H-
-pyrazolo[3,4-d]pyrimidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]diox-
ol-4-yl)methyl Benzoate (17d)
##STR00296##
[1398] To a solution of 17c (0.5 g, 0.9 mmol) in MeOH (10 mL) was
added NaBH.sub.4 (50 mg, 1.35 mmol). After the mixture was stirred
at rt for 1.5 h, it was quenched with water. The solution was
extracted (EtOAc). The organic layers were washed (brine), dried
(Na.sub.2SO.sub.4), and concentrated under reduced pressure. The
residue was purified by column chromatography to afford the title
compound (17d) (340 mg, 74%) as a white solid. m/z (ESI, +ve
ion)=565.2 [M+H].sup.+.
Step E.
((3aR,4R,6R,6aR)-6-(4-((2-Chlorobenzyl)amino)-6-(((tetrahydro-2H-p-
yran-2-yl)oxy)methyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-2,2-dimethyltetrah-
ydrofuro[3,4-d][1,3]diozol-4-yl)methyl Benzoate (17e)
##STR00297##
[1400] To a solution of 17d (400 mg, 0.7 mmol) in DCM (15 mL) was
added 3,4-dihydro-2H-pyran (1.78 g, 21 mmol) and PPTS (0.18 g, 0.7
mmol). The mixture was stirred at rt overnight and additional
3,4-dihydro-2H-pyran (1.78 g, 21 mmol) and PPTS (0.18 g, 0.7 mmol)
were added. After the mixture was stirred at rt for two days, it
was quenched (water) and extracted (DCM). The organic layers were
washed (brine), dried (Na.sub.2SO.sub.4) and concentrated under
reduced pressure to afford the title compound (17e) (0.5 g, 100%)
as a yellow solid. The crude product was used directly without
further purification. m/z (ESI, +ve ion)=649.2 [M+H].sup.+.
Step F.
((3aR,4R,6R,6aR)-6-(4-((2-Chlorobenzyl)amino)-6-(((tetrahydro-2H-p-
yran-2-yl)oxy)methyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-2,2-dimethyltetrah-
ydrofuro[3,4-d][1,3]diozol-4-yl)methanol (171)
##STR00298##
[1402] A mixture of 17e (340 mg, 0.5 mmol) and K.sub.2CO.sub.3 (217
mg, 2.1 mmol) in MeOH (8 mL) was stirred at rt for 30 min. AcOH
(190 mg 4.2 mmol) was added and the resulting mixture was
concentrated in vacuo and the residue was purified by column
chromatography to afford the title compound (17f) (260 mg, 91%) as
a white solid. m/z (ESI, +ve ion)=545.2 [M+H].sup.+.
Step G. Di-tert-utyl
((((3aR,4R,6R,6aR)-6-(4-((2-chlorobenzyl)amino)-6-(((tetrahydro-2H-pyran--
2-yl)oxy)methyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-2,2-dimethyltetrahydrof-
uro[3,4-d][1,3]dioxol-4-yl)methoxy)methyl)phosphonate (17 g)
##STR00299##
[1404] To a solution of 17f (260 mg, 0.5 mmol) in dry THF (10 mL)
was added sodium hydride (60% dispersion in mineral oil, 136 mg,
3.4 mmol) at -40.degree. C. The mixture was stirred at -40.degree.
C. for 30 min and then a solution of
(di-tert-butoxyphosphoryl)methyl trifluoromethanesulfonate (517 mg,
1.5 mmol) in THF (5 mL) was added dropwise. After the mixture was
stirred at rt for 1 h, AcOH (0.15 mL) was added. The mixture was
concentrated in vacuo to afford the title compound (17g) (360 mg,
100%) as a yellow solid. The crude was used directly without
further purification. m/z (ESI, +ve ion)=751.3 [M+H].sup.+.
Step H.
((((2R,3S,4R,5R)-5-(4-((2-Chlorobenzyl)amino)-6-(hydroxymethyl)-1H-
-pyrazolo[3,4-d]pyrimidin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)-
methyl)phosphonic Acid (17)
##STR00300##
[1406] To a solution of 17 g (360 mg, 0.5 mmol) in
1,1,1,3,3,3-hexafluoro-2-propano (10 mL) was added 6 N HCl (0.5
mL). The mixture was stirred at rt for 2 h and the neutralized by
ammonium hydroxide (pH=7). The mixture was concentrated and the
residue was purified by reverse preparative HPLC to afford the
title compound (17) (60 mg, 24% for the two steps) as a
trifluoroacetate. .sup.1H NMR (400 MHz, D.sub.2O) .delta. 8.38-8.07
(m, 1H), 7.38-7.33 (m, 2H), 7.30-7.19 (m, 2H), 6.25-6.21 (m, 1H),
4.24 (td, J=7.05, 1.97 Hz, 1H), 4.96 (s, 1H), 4.85 (s, 1H),
4.79-4.70 (m, 3H), 4.44-3.39 (m, 1H), 4.20-4.18 (m, 1H), 3.74-3.70
(m, 1H), 3.65-3.60 (m, 1H), 3.57-3.50 (m, 2H), m/z (ESI, +ve
ion)=515.1 [M+H].sup.30.
Example 18.
((((2R,3S,4R,5R)-5-(4-((3-Chlorobenzyl)amino)-6-cyano-1H-pyrazolo[3,4-d]p-
yrimidin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)methyl)phosphonic
Acid (18)
##STR00301##
[1407] Step A.
(2R,3R,4R,5R)-2-(Acetoxymethyl)-5-(4-((3-chlorobenzyl)amino)-6-cyano-1H-p-
yrazolo[3,4-d]pyrimidin-1-yl)tetrahydrofuran-3,4-diyl Diacetate
(18a)
##STR00302##
[1409] To a mixture of zinc cyanide (128 mg, 1.09 mmol) in dry DMF
(15 mL) was added 3-chlorobenzyl analog of 1b (1 g, 1.81 mmol),
tetrakis(triphenylphosphine)palladium (209 mg, 1.81 mmol), and TEA
(220 mg, 2.18 mmol). After the mixture was stirred at 100.degree.
C. under N.sub.2 for 6 h, it was cooled and diluted (EtOAc and
water). The organic layer was washed (brine), dried
(Na.sub.2SO.sub.4), and evaporated. The residue was purified by
flash column chromatography (SiO.sub.2, 33% EtOAc/petroleum ether)
to provide the title compound (18a) (500 mg, 51%), m/z (ESI, +ve
ion)=542.7 [M+H].sup.+.
Step B.
((((2R,3S,4R,5R)-5-(4-((3-Chlorobenzyl)amino)-6-cyano-1H-pyrazolo[-
3,4-d]pyrimidin-1
yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)methyl)phosphonic
Acid (18)
##STR00303##
[1411] The title compound was prepared from
(2R,3R,4R,5R)-2-(acetoxymethyl)-5-(4-(3-chlorobenzyl)amino)-6-cyano-1H-py-
razolo[3,4-d]pyrimidin-1-yl)tetrahydrofuran-3,4-diyl Diacetate
(18a) by procedures similar to those described in Example 1, Steps
C and D, followed by procedures in Example 17, Step G and H.
.sup.1H NMR (400 MHz, D.sub.2O) .delta. 8.12-7.91 (m, 1H),
7.24-7.17 (m, 4H), 6.10-6.25 (m, 1H), 4.66-4.58 (m, 2H), 4.33-4.31
(t, J=5.0 Hz, 1H), 4.16-4.14 (m, 1H), 3.68-3.56 (m, 2H), 3.41-3.28
(m, 3H), m/z (ESI, +ve ion)=511.2 [M+H].sup.+.
Example 19.
((((2R,3S,4R,5R)-5-(6-Chloro-4-((2-chlorobenzyl)amino)-1H-pyrazolo[3,4-d]-
pyrimidin-1-yl)-3,4-dihydroxy-3-methyltetrahydrofuran-2-yl)methoxy)methyl)-
phosphonic Acid (19)
##STR00304##
[1412] Step A.
((3aR,5R,6S,6aR)-6-Hydroxy-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-
-yl)methyl Benzoate (19a)
##STR00305##
[1414] BzCl (5.91 g, 42 mmol) was added slowly to a solution of
(3aR,5R,6S,6aR)-5-(hydroxymethyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]d-
ioxol-6-ol (8 g, 42 mmol) in pyridine (80 mL) at 0.degree. C. The
mixture was stirred at rt for 2 h, it was concentrated and the
residue was diluted with EtOAc and aq. citric acid. The organic
layer was washed (brine), dried and concentrated. The residue was
purified by flash column chromatography to provide the title
compound (19a) (11 g, 89%), m/z (ESI, +ve ion)=295.4
[M+H].sup.+.
Step B.
((3aR,5R,6aS)-2,2-Dimethyl-6-oxotetrahydrofuro[2,3-d][1,3]diozol-5-
-yl)methyl Benzoate (19b)
##STR00306##
[1416] To a solution of 19a (6.5 g, 22.1 mmol) in DCM (130 ml) was
added PDC (5 g, 13.3 mmol) and acetic anhydride (6.76 g, 66.3 mmol)
at rt. After the mixture was refluxed for 2 h, it was filtered and
the filtrate was concentrated in vacuo. The residue was purified by
flash column chromatography to provide the title compound (19b)
(4.2 g, 65% yield), m/z (ESI, +ve ion)=333.3 [M+MeCN].sup.+.
Step C.
((3aR,5R,6R,6aR)-6-Hydroxy-2,2,6-trimethyltetrahydrofuro[2,3-d][1,-
3]diozol-5-yl)methyl Benzoate (19c)
##STR00307##
[1418] To a solution of 19b (1 g, 3.4 mmol) in dry THF (20 ml) was
added dropwise MeMgBr (3 M in THF, 1.7 ml, 5.1 mmol) at 0.degree.
C. After the mixture was stirred for 0.5 h, it was quenched (aq.
NH.sub.4Cl) and extracted (EtOAc). The organic layer was dried and
concentrated to afford the title compound (19c) (1.2 g, 3.63 mmol).
The crude product was used in the next step without further
purification. m/z (ESI, +ve ion)=331.4 [M+H].sup.+.
Step D.
((2R,3S,4R,5S)-3,4,5-Trihydroxy-3-methyltetrahydrofuran-2-yl)methy-
l Benzoate (19d)
##STR00308##
[1420] A solution of 19c (1.2 g, 3.63 mmol) in TFA (90% in water,
10 ml) was stirred at rt for 0.5 h. The mixture was concentrated in
vacuo to dryness and the residue was used in the next step without
further purification. m/z (ESI, +ve ion)=291.4 [M+Na].sup.+.
Step E.
(3R,4R,5R)-5-((Benzoyloxy)methyl)-4-methyltetrahydrofuran-2,3,4-tr-
iyl Triacetate (19e)
##STR00309##
[1422] To a solution of crude 19d prepared from above step in
pyridine (20 ml) were added acetic anhydride (7 ml) and DMAP (20
mg). After the mixture was stirred at rt overnight, it was
concentrated in vacuo and the residue was diluted with EtOAc. The
solution was washed (water and brine) and the organic layer was
dried, concentrated. The residue was purified by flash column
chromatography to provide the title compound (19e) (430 mg, 32%),
m/z (ESI, +ve ion)=417.4.
Step F.
(2R,3R,4R,5R)-2-((Benzoylozy)methyl)-5-(4,6-dichloro-1H-pyrazolo[3-
,4-d]pyrimidin-1-yl)-3-methyltetrahydrofuran-3,4-diyl Diacetate
(19f)
##STR00310##
[1424] To a solution of 4,6-dichloro-1H-pyrazolo[3,4-d]pyrimidine
(206 mg, 1.09 mmol) and 19e (430 mg, 1.09 mmol) in MeCN (10 ml)
were added TMSOTf (969 mg, 4.36 mmol) and DBU (497 mg, 3.27 mmol)
successively. After the mixture was stirred at rt for 2 h, it was
diluted (EtOAc). The organic layer was washed (brine), dried, and
concentrated. The residue was purified by flash column
chromatography to provide the title compound (191) (375 mg, 66%),
m/z (EST, +ve ion)=545.4.
Step 1. ((((2R,3S,4R,5R)-5-(6-Chloro
4-((2-chlorobenzyl)amino)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-3,4-dihydroxy-
-3-methyltetrahydrofuran-2-yl)methoxy)methyl)phosphonic Acid
(19)
##STR00311##
[1426] The title compound was prepared
(2R,3R,4R,5R)-2-((benzoyloxy)methyl)-5-(4,6-dichloro-1H-pyrazolo[3,4-d]py-
rimidin-1-yl)-3-methyltetrahydrofuran-3,4-diyl diacetate (19f) by
procedures similar to those described in Example 1, Steps B. C, and
D, followed by procedure in Example 17, Step G and H. .sup.1H NMR
(400 MHz, D.sub.2O) .delta. 8.06-7.78 (m, 1H), 7.32-7.29 (m, 2H),
7.18-7.16 (m, 2H), 6.02-6.00 (d, J=7.6 Hz, 1H), 4.70-4.51 (m, 3H),
4.18-4.12 (m, 1H), 3.63-3.60 (m, 2H), 3.44-3.40 (m, 2H), 1.28 (s,
3H). m/z (ESI, +ve ion)=533.9 [M+H].sup.+.
Example 20.
(2-((((2R,3S,4R,5R)-5-(6-Chloro-4-((2-chlorobenzyl)amino)-1H-pyrazolo[3,4-
-d]pyrimidin-1-yl)
3,4-dihydroxytetrahydrofuran-2-yl)methyl)(isobutyl)amino)-2-oxoethyl)phos-
phonic Acid (20))
##STR00312##
[1427] Step A.
(3aS,4S,6R,6aR)-6-(6-Chloro-4-((2-chlorobenzyl)amino)-1H-pyrazolo[3,4-d]p-
yrimidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxole
4-carbaldehyde (20a)
##STR00313##
[1429] Dichloroacetic acid (82 mg, 0.641 mmol) was added dropwise
to a cooled solution of
((3aR,4R,6R,6aR)-6-(6-chloro-4-((2-chlorobenzyl)amino)-1H-pyrazolo[3,4-d]-
pyrimidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methanol
(1d) (600 mg, 129 mmol) and EDCl.HCl salt (850 mg) in DMSO (5 mL).
After the reaction mixture was stirred at rt for 3 h. it was
quenched by addition of water (15 mL) and EtOAc (15 mL). The
resultant phases were separated and the aqueous phase was extracted
(EtOAc) and the combined organic phases were washed (brine), dried,
and concentrated to afford a yellow solid which was used in next
step without purification.
Step B.
6-chloro-N-(2-Chlorobenzyl)-1-((3aR,4R,6R,6aR)-6-((isobutylamino)m-
ethyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-1H-pyrazolo[3,4--
d]pyrimidin-4-amine (20b)
##STR00314##
[1431] To a solution of 20a (600 mg, 1.3 mmol) in DCE (8 mL) was
added 2-methylpropan-1-amine (280 mg, 3.9 mmol) and acetic acid
(332 mg, 3.9 mmol). The mixture was stirred for 5 min before sodium
triacetoxyborohydride (822 mg, 3.9 mmol) was added. After the
mixture was stirred at rt for 1 h, it was quenched (sat.
NaHCO.sub.3) and the resulting solution was stirred for 30 min. The
solution was extracted (EtOAc) and the organic layer was dried
(MgSO.sub.4) and concentrated. The residue was purified by flash
column chromatography to provide the title compound (20b) (310 mg,
46%), m/z (ESI, +ve ion)=520.8 [M+H].sup.+.
Step C. Diethyl
(2-((((3aR,4R,6R,6aR)-6-(6-Chloro-4-((2-chlorobenzyl)amino)-1H-pyrazolo[3-
,4-d]pyrimidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)met-
hyl)(isobutyl)amino)-2-oxoethyl)phosphonate (20c)
##STR00315##
[1433] To a solution of 20b (300 mg, 0.6 mmol) and
2-(diethoxyphosphoryl) acetic acid (180 mg, 0.95 mmol) in DMF (8
ml) was added DIPEA (327 mg, 2.52 mmol) and HATU (362 mg, 0.95
mmol) at 0.degree. C. After the mixture was stirred at rt for 1 h,
it was poured into water and the solution was extracted (EtOAc).
The organic layer was dried, concentrated. The residue was purified
by flash column chromatography to provide the title compound (20c)
(350 mg, 87% yield), m/z (ESI, +ve ion)=699.6 [M+H].sup.+.
Step D.
(2-((((2R,3S,4R,5R)-5-(6-Chloro-4-((2-chlorbenzyl)amino)-1H-pyrazo-
lo[3,4-d]pyrimidin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl)(isobuty-
l)amino)-2-oxoethyl)phosphonic Acid (20)
##STR00316##
[1435] TMSBr (2.63 g. 17.2 mmol) and TEA (2.32 g, 22.9 mmol) were
added to a solution of 20c (350 mg. 0.5 mmol) in MeCN (20 ml) at
rt. After the mixture was stirred at rt overnight, it was
concentrated to dryness. The residue was treated with 50% aq. TFA
(10 ml) and the solution was stirred for 2 h. The solution was
purified by reverse preparative to provide the title compound (20)
(70 mg, 19.4% yield), m/z (ESI, +ve ion)=603.0 [M+H].sup.+.
Example 23.
((((1R,2R,3S,4R)-4-(5-Chloro-7-(((R)-2,3-dihydro-1H-inden-1-yl)amino)-3H--
[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)-2,3-dihydroxycyclopentyl)methoxy)met-
hyl)phosphonic Acid (23)
##STR00317##
[1436] Step A.
((3aR,4R,6R,6aS)-6-Amino-2,2-dimethyltetrahydro-3aH-cydopenta[d][1,3]diox-
ol-4-yl)methanol (23a)
##STR00318##
[1438] 2,2-Dimethoxypropane (4.5 g, 43.3 mol) and
para-toluenesulfonic acid (163 mg, 0.87 mmol) were added to a
solution of (1R,2S,3R,5R)-3-amino-5-(hydroxymethyl)
cyclopentane-1,2-diol hydrochloride (1.59 g, 8.66 mmo) in acetone
(16 ml) and the mixture was stirred at rt overnight. After
trimethylamine (2.5 ml) was added, the mixture was stirred another
5 min before the solvent was removed under reduced pressure. The
residue was diluted with brine and the solution was extracted with
EtOAc. The combined organics were dried, filtered, and concentrated
to afford the title compound (23a) (1.3 g, 80% yield).
Step B.
((3aR,4R,6R,6aS)-6-(2,6-Dichloro-5-nitropyrimidin-4-ylamino)-2,2-d-
imethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl)methanol
(23b)
##STR00319##
[1440] 2,4,6-Trichloro-5-nitropyrimidine (2.18 g, 9.6 mmol) and
triethylamine (970 mg, 9.6 mmol) were added to a solution of 23a
(1.8 g, 9.6 mmol) in THE (20 ml) successively. After the reaction
mixture was stirred at rt for 20 min, it was diluted with
EtOAc/Et.sub.2O (1:1) and washed with 10% citric acid, brine, dried
and concentrated. The residue was purified by column chromatography
(DCM/MeOH: from 30:1 to 10:1) to yield the title compound (23b)
(1.6 g, 43%).
Step C.
((3aR,4R,6R,6aS)-6-(5-Amino-2,6-dichloropyrimidin-1-ylamino)-2,2-d-
imethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl)methanol
(23c)
##STR00320##
[1442] Iron powder (1.08 g, 19.4 mmol) and acetic acid (1.16 g
19.36 mmol) were added to a solution of 23b (918 mg, 2.42 mmol) in
ethanol (13 ml) and water (10 ml). After the reaction mixture was
heated at 60.degree. C. for 15 min, it was filtrated and the solid
washed with EtOAc. The filtrate was washed with brine and the
combined organic phases were concentrated in vacuo to afford the
title compound (23c) (800 mg), which was used in the next step
without further purification.
Step D.
((3aR,4R,6R,6aS)-6-(5,7-Dichloro-3H-[1,2,3]triazolo[4,5-d]pyrimidi-
n-3-yl)-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl)methanol
(23d)
##STR00321##
[1444] J tert-Butyl nitrite (314 mg, 2.68 mmol) was added to a
solution of 23c (700 mg, 2.0 mmol) in anhydrous MeCN (20 ML) under
N.sub.2. The mixture was heated at 60.degree. C. for 2 h and then
cooled to rt, concentrated to dryness. The residue was purified by
column chromatography (DCM/MeOH: from 30:1 to 10:1) to give the
title compound (23d) (600 mg, 83%).
Step E.
((3aR,4R,6R,6aS)-6-(5-chloro-7-(((S)-2,3-dihydro-1H-inden-1-yl)ami-
no)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)-2,2-dimethyltetrahydro-4H-cyc-
lopenta[d][1,3]dioxol-4-yl)methanol (23e)
##STR00322##
[1446] A mixture of 23d (1.3 g, 3.62 mmol),
(S)-2,3-dihydro-1H-inden-1-amine HCl (614 mg, 3.62 mmol), and
Et.sub.3N (438 mg, 0.919 mmol) in ethanol (30 ml) was stirred at rt
overnight. The mixture was concentrated and the residue was
purified by column chromatography (petroleum ether/ethyl
acetate=10:1 to 2:1) to give the title compound (23e) (1.2 g, 76%),
m/z (ESI, +ve ion)=457.4[M-H].sup.+.
Step G:
((((1R,2R,3S,4R)-4-(5-chloro-7-(((R)-2,3-dihydro-1H-inden-1-yl)ami-
no)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)-2,3-dihydroxycyclopentyl)meth-
oxy)methyl)phosphonic Acid (23)
##STR00323##
[1448] The title compound was prepared from
((3aR,4R,6R,6aS)-6-(5-chloro-7-(((S)-2,3-dihydro-1H-inden-1-yl)amino)-3H--
[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)-2,2-dimethyltetrahydro-4H-cyclopenta-
[d][1,3]dioxol-4-yl)methanol (23e) by procedures similar to those
described in Example 7, Steps B and C. .sup.1H NMR (400 MHz,
D.sub.2O) .delta. 7.27-7.14 (m, 4H), 5.76-5.65 (m, 1H), 4.96-4.88
(m, 1H), 4.57-4.48 (m, 1H), 4.12-4.05 (m, 1H), 3.59-3.55 (m, 2H),
3.43-3.38 (m, 2H), 2.98-2.96 (m, 1H), 2.88-2.84 (m, 1H), 2.54-2.35
(m, 3H), 2.02-1.88 (m, 1H), 1.85-1.71 (m, 1H), m/z (ESI, +ve
ion)=510.8 [M+H].sup.+.
[1449] The following examples were made according to the procedures
described in Examples 1-8 and 13-23 using the appropriate starting
material.
TABLE-US-00003 Ex. LC-MS 24 520.1 [M + H].sup.+ 25 510 [M -
H].sup.- 26 527.2 [M + H].sup.+ 27 518 [M - H].sup.- 28 635.1 [M -
H].sup.- 29 501.9 [M - H].sup.- 30 520.8 [M + H].sup.+ 31 525.9 [M
+ H].sup.+ 32 553.9 [M + H].sup.+ 33 533.8 [M + H].sup.+ 34 533.8
[M + H].sup.+ 35 553.9 [M + H].sup.+ 36 547.9 [M + H].sup.+ 37
533.8 [M + H].sup.+ 38 449.9 [M + H].sup.+ 39 535.1 [M + H].sup.+
40 518.9 [M + H].sup.+ 41 499.9 [M + H].sup.+ 42 465.8 [M +
H].sup.+ 43 422.2 [M - H].sup.- 44 497.9 [M - H].sup.- 45 479.9 [M
+ H].sup.+ 46 508.8 [M - H].sup.- 47 552.8 [M - H].sup.- 48 540.2
[M + H].sup.+ 49 535.9 [M + H].sup.+ 50 532 [M - H].sup.- 51 536.81
[M + H].sup.+ 52 409.5 [M + H].sup.+ 53 477.6 [M + H].sup.+ 54
557.8 [M + H].sup.+ 55 555.1 [M + H].sup.+ 56 514.8 [M + H].sup.+
57 395.8 [M + H].sup.+ 58 535.7 [M - H].sup.- 59 534.9 [M +
H].sup.+ 60 531.7 [M - H].sup.- 61 568.0 [M + H].sup.+ 62 498.0 [M
+ H].sup.+ 63 452.3 [M + H].sup.+ 64 533.9 [M + H].sup.+ 65 521.0
[M + H].sup.+ 66 512.0 [M + H].sup.+ 67 555.5 [M - H].sup.- 68
461.8 [M - H].sup.- 69 480.1 [M + H].sup.+ 70 479.8 [M + H].sup.+
71 479.8 [M + H].sup.+ 72 463.9 [M + H].sup.+ 73 478 [M - H].sup.-
74 436 [M - H].sup.- 75 471.9 [M + H].sup.+ 76 436.1 [M + H].sup.+
77 580.0 [M + H].sup.+ 78 466.1 [M + H].sup.+ 79 448 [M - H].sup.-
80 466.3 [M + H].sup.+ 81 449.8 [M + H].sup.+ 82 444.1 [M -
H].sup.- 83 436.0 [M + H].sup.+ 84 512.0 [M + H].sup.+ 85 463.8 [M
+ H].sup.+ 86 500.4 [M + H].sup.+ 87 483.8 [M - H].sup.- 88 512.1
[M + H].sup.+ 89 494.2 [M + H].sup.+ 90 485.8 [M - H].sup.- 91
464.0 [M + H].sup.+ 92 464.3 [M + H].sup.+ 93 477.9 [M + H].sup.+
94 464.1 [M + H].sup.+ 95 463.2 [M - H].sup.- 96 461.8 [M -
H].sup.- 97 462.8 [M + H].sup.+
Example 98.
((N-(((2R,3S,4R,5R)-5-(6-Chloro-4-(cyclopentylamino)-1H-pyrazolo[3,4-d]py-
rimidin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl)-N-methylsulfamoyl)-
methyl)phosphonic Acid (98)
##STR00324##
[1450] Step A.
6-Chloro-N-cyclopentyl-1-(3aR,4R,6R,6aR)-2,2-dimethyl-6-((methylamino)met-
hyl)tetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-a-
mine (98a)
##STR00325##
[1452] The title compound was prepared from cyclopentane analog of
1d via Swern oxidation and reductive animation successively.
Step B.
N-(((3aR,4R,6R$6aR)-6-(6-Chloro-4-(cyclopentylamino)-1H-pyrazolo[3-
,4-d]pyrimidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]diozol-4-yl)met-
hyl)-N-methylmethanesulfonamide (98b)
##STR00326##
[1454] To an oven dried flask was added
1-[(3aR,4R,6R,6aR)-2,2-dimethyl-6-(methylaminomethyl)-3a,4,6,6a-tetrahydr-
ofuro[3,4-d][1,3]dioxol-4-yl]-6-chloro-N-cyclopentyl-pyrazolo[3,4-d]pyrimi-
din-4-amine (98a) (156 mg, 0.37 mmol) and DCM (1.7 mL). To this
solution was added triethylamine (0.15 mL, 1.1 mmol) and
methanesulfonyl chloride (0.03 mL, 0.44 mmd) at rt. The mixture was
allowed to stir at rt overnight. The mixture was concentrated and
the residue was purified by flash column chromatography (0-6%
MeOH/DCM) to afford the title compound (98b) (143 mg, 77% yield).
m/z (ESI, +ve ion)=501.1 [M+H].sup.+.
Step C. tert-Butyl
(6-chloro-1-(3aR,4R,6R,6aR)-2,2-dimethyl-6-((N-methylmethylsulfonamido)me-
thyl)tetrahydrofuro[3,4-d][1,3]diozol-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-4--
yl)(cyclopentyl)carbamate (98c)
##STR00327##
[1456] To an oven dried flask was added a solution of 98b (100 mg,
0.20 mmol) in MeCN (3 mL). To this solution was added triethylamine
(0.08 mL, 0.60 mmd) followed by addition of di-tert-butyl
dicarbonate (0.14 mL, 0.60 mmol) and 4-dimethylaminopyridine (2 mg,
0.02 mmol). The mixture was allowed to stir at rt overnight. The
mixture was concentrated and the residue was purified by flash
column chromatography (0-100% EtOAc/hexanes) to give title compound
(98c) (107 mg, 89% yield), m/z (ESI, +ve ion)=601.2
[M+H].sup.+.
Step D.
((N-(((2R,3S,4R,5R)-5-(6-Chloro-4-(cyclopentylamino)-1H-pyrazolo[3-
,4-d]pyrimidin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl)-N-methylsul-
famoyl)methyl)phosphonic Acid (98)
##STR00328##
[1458] The title compound was prepared from tert-butyl
(6-chloro-1-((3aR,4R,6R,6aR)-2,2-dimethyl-6-((N-methylmethylsulfonamido)m-
ethyl)tetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-
-yl)(cyclopentyl)carbamate (98c) by procedures similar to those
described in Example 3, Steps B and C. m/z (ESI, +ve ion)=541.1
[M+H].sup.+.
Example 99.
((((2R,3S,4R,5R)-5-(6-Chloro-4-(N-cyclopentylacetamido)-1H-pyrazolo[3,4-d-
]pyrimidin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)methyl)phosphon-
ic Acid (99)
##STR00329##
[1459] Step A. Di-tert-Butyl
((((3aR,4R,6R,6aR)-6-(6-chloro-4-(cyclopentylamino)-1H-pyrazolo[3,4-d]pyr-
imidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methoxyl)me-
thyl)phosphonate (99a)
##STR00330##
[1461] The title compound was prepared from cyclopentane analog of
1d by procedures similar to those described in Example 17, Step
G.
Step B. Di-tert-butyl ((((3aR,4R,6R,6aR)-6-(6-chloro-4
(N-cyclopentylacetamido)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-2,2-dimethylte-
trahydrofuro[3,4-d][1,3]dioxol-4-yl)methoxyl)methyl)phosphonate
(99b)
##STR00331##
[1463] Sodium hydride (60% in mineral oil, 323 mg, 8.0 mmol) was
added to a solution of 99a (2 g, 4.0 mmol) in dry DMF (40 ml) at
0.degree. C. followed by stirring for 10 min at the same
temperature. Acetic anhydride (2.06 g, 20 mmol) was added dropwise
over ten min. The mixture was allowed to warm to rt and stirred
overnight. The mixture was poured into sat.NH.sub.4Cl and extracted
with EA. The organic layer was washed with water, brine, dried and
concentrated in vacuo to afford the title compound (99b), which was
used directed for the next step without further purification. m/z
(ESI, +ve ion)=[M+Na].sup.+.
Step C.
((((2R,3S,4R,5R)-5-(6-Chloro-4-(N-cyclopentylacetamido)-1H-pyrazol-
o[3,4-d]pyrimidin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)methyl)p-
hosphonic Acid (99)
##STR00332##
[1465] The title compound was prepared from Di-tert-butyl
((((3aR,4R,6R,6aR)-6-(6-chloro-4-(N-cyclopentylacetamido)-1H-pyrazolo[3,4-
-d]pyrimidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)metho-
xy)methyl)phosphonate (99b)) by procedures similar to those
described in Example 17, Step H. m/z (ESI, +ve ion)=506.1
[M+H].sup.+.
Example 100.
((((2R,3S,4R,5R)-5-(6-chloro-4-(5-methylfuran-2-yl)-1H-pyrazolo[3,4-d]pyr-
imidin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)methyl)phosphonic
Acid (100)
##STR00333##
[1466] Step A.
(2R,3R,4R,5R)-2-(Acetoxymethyl)-5-(6-chloro-4-(5-methylfuran-2-yl)-1H-pyr-
azolo[3,4-d]pyrimidin-1-yl)tetrahydrofuran-3,4-diyl Diacetate
(100a)
##STR00334##
[1468] To a solution of 1a (6.7 g, 15 mmol) and
(5-methylfuran-2-yl)boronic acid (1.91 g, 15 mmol) in THE (85 ml)
were added sat. NaHCO.sub.3 (40 ml) and Pd(PPh.sub.3).sub.4 (875
mg, 0.75 mmol). The mixture was flushed with N.sub.2 and then
heated at reflux overnight. The mixture was cooled to rt and then
treated with water/EtOAc. The organic layer was washed with water,
brine, dried over Na.sub.2SO.sub.4 and concentrated in vacuo. The
residue was purified by flash column chromatography (PE/EA=3:1) to
afford the title compound (100a) (4.4 g, 60% yield). m/z (EST, +ve
ion)=493.1 [M+H].sup.+.
Step B.
((3aR,4R,6R,6aR)-6-(6-chloro-4-(5-methylfuran-2-yl)-1H-pyrazolo[3,-
4-d]pyrimidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)meth-
anol (100b)
##STR00335##
[1470] The title compound was prepared
(2R,3R,4R,5R)-2-(acetoxymethyl)-5-(6-chloro-4-(5-methylfuran-2-yl)-1H-pyr-
azolo[3,4-d]pyrimidin-1-yl)tetrahydrofuran-3,4-diyl diacetate
(100a)) by procedures similar to those described in Example 1,
Steps C and D.
Step C. ((((2R,3S,4R,5R)-5
(6-chloro-4-(5-methylfuran-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-3,4-di-
hydroxytetrahydrofuran-2-yl)methoxy)methyl)phosphonic Acid
(100)
##STR00336##
[1472] The title compound was prepared
((3aR,4R,6R,6aR)-6-(6-chloro-4-(5-methylfuran-2-yl)-1H-pyrazolo[3,4-d]pyr-
imidin-1-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methanol
(100b) by procedures similar to those described in Example 7, Steps
B and C. .sup.1H NMR (400 MHz, D.sub.2O) .delta. 800-7.95 (d,
J=17.2 Hz, 1H), 6.91-6.87 (d, J=16.0 Hz, 1H), 6.09-6.03 (m, 2H),
4.44-4.41 (t, J=4.80 Hz, 1H), 4.17 (m, 1H), 3.77-3.59 (m, 4H),
2.22-2.21 (d, J=4.8 Hz, 3H), m/z (ESI, +ve ion)=461.2
[M+H].sup.+.
Example 101.
(3-((2R,3S,4R,5R)-5-(6-Chloro-4-(cyclopentylamino)-1H-pyrazolo[3,4-d]pyri-
midin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)propyl)phosphonic
Acid (101)
##STR00337##
[1473] Step A. Diethyl
((E)-3-(3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]di-
oxol-4-yl)alkyl)phosphonate (101a)
##STR00338##
[1475] An oven dried 3-neck flask with reflux condenser was purged
with argon and added
benzylidene(dichloro)(1,3-dimesityl-2-imidazolidinylidene)ruthenium-tricy-
clohexylphosphine (1:1, 290 mg, 0.34 mmol) and DCM (8 mL). To the
mixture was added
(3aR,4R.sup.6R,6aR)-4-methoxy-2,2-dimethyl-6-vinyl-3a,4,6,6a-te-
trahydrofuro[3,4-d][1,3]dioxole (1.94 g, 9.69 mmol) in DCM (1 mL),
followed by addition of a solution of diethyl alkylphosphonate (2.5
g. 14.0 mmol) in DCM (1 mL) all at once. After the solution was
stirred at reflux for 18 h, it was concentrated and the residue was
purified by flash column chromatography (0-100% EtOAc/hexanes
followed by 0-10% MeOH/DCM) to give the title compound (101a) (1.81
g, 53% yield) as a yellow oil.
Step B
(3-((2R,3S,4R,5R)-5-(6-(Cloro-4-(cyclopentylamino)-1H-pyrazolo[3,4--
d]pyrimidin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)propyl)phosphonic
Acid (101)
##STR00339##
[1477] The title compound was prepared diethyl
((E)-3-((3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]d-
ioxol-4-yl)alkyl)phosphonate (101a) by procedures similar to those
described in Example 4, Steps C-H. NMR (400 MHz, 1320) S 8.15-7.99
(m, 1H), 6.01 (m, 1H), 5.17-4.96 (m, 3H), 4.32-4.18 (m, 2H),
4.12-3.98 (m, 1H), 2.08-1.88 (m, 2H), 1.64-1.29 (m, 10H), m/z (ESI,
+ve ion)=462.1 [M+H].sup.+.
[1478] The following examples were made according to the procedures
described in Examples 1-8, 13-23, 98-101 using the appropriate
starting material.
TABLE-US-00004 Ex. LC-MS 102 491.8 [M + H].sup.+ 103 491.9 [M +
H].sup.+ 104 477.7 [M + H].sup.+ 105 477.8 [M + H].sup.+ 106 543 [M
+ H].sup.+ 107 496.1 [M - H].sup.- 108 513.2 [M + H].sup.+ 109 505
[M + H].sup.+ 110 498.8 [M + H].sup.+ 111 512.4 [M + H].sup.+ 112
512 [M + H].sup.+ 113 513 [M + H].sup.+ 114 567.2 [M + H].sup.+ 115
506.2 [M + H].sup.+ 116 566.1 [M + H].sup.+ 117 552.1 [M + H].sup.+
118 566.9 [M - H].sup.- 119 553.2 [M + H].sup.+ 120 567.2 [M -
H].sup.- 121 561.2 [M + H].sup.+ 122 569.1 [M + H].sup.+ 123 558 [M
- H].sup.- 124 475.8 [M - H].sup.- 125 508.1 [M + H].sup.+ 126
560.3 [M + H].sup.+ 127 568.3 [M + H].sup.+ 128 526.2 [M + H].sup.+
129 582.2 [M + H].sup.+ 130 560.8 [M + H].sup.+ 131 662 [M +
H].sup.+ 132 487.8 [M + H].sup.+ 133 570 [M + H].sup.+ 134 524.1 [M
- H].sup.- 135 524.1 [M - H].sup.- 136 560.2 [M + H].sup.+ 137
462.9 [M + H].sup.+ 138 473.2 [M - H].sup.-
II. Biological Evaluation
Example A1: Biochemical Assay
Assay Reaction Conditions
[1479] Assay Volume: 70 .mu.l [1480] Reaction Volume: 50 .mu.l
[1481] CD73: 0.3208 nM [1482] AMP: 15 .mu.M [1483] Assay Buffer: 2
5 mM Tris-HCL, pH 7.4, 0.01% Brij-35, 0.01% BSA, 5 mM
MgCl.sub.2
Assay Procedure;
[1484] Used 384 clear plate.
[1485] Made dose titration of testing compounds in assay buffer, 10
points 1/2 log titrations in duplicates starting at 100 .mu.M.
[1486] Added 25 .mu.l of CD73 to each well for a final
concentration of 320 pM.
[1487] Incubated at RT for 15 min.
[1488] Added 25 .mu.l of AMP to each well for a final concentration
of 15 .mu.M.
[1489] Incubated at RT for 10 min.
[1490] Added 10 .mu.l of Malachite Green Reagent A, incubate at RT
for 10 min.
[1491] Added 10 .mu.l of Malachite Green Reagent B, incubate at RT
for 45 min.
[1492] Read the Absorbance on Envision plate reader using
excitation filter: Cy5 620 nM.
[1493] The ability of the compounds disclosed herein to inhibit
CD73 activity was quantified and the respective IC.sub.50 values
were determined. Table 1 provides the biochemical IC.sub.50 values
of compounds disclosed herein.
TABLE-US-00005 Ex. Biochemical IC.sub.50 Ex. Biochemical IC.sub.50
Ex Biochenlica IC.sub.50 1 A 48 A 93 A 2 C 49 A 94 A 3 A 50 C 95 A
4 C 51 A 96 A 5 C 52 A 97 C 6 C 53 A 98 A 7 A 54 C 99 A 8 B 55 C
100 A 9 A 56 C 101 B 10 A 57 B 102 A 11 C 58 A 103 A 12 A 59 A 104
A 13 A 60 C 105 A 14 A 61 A 106 A 15 A 62 A 107 A 16 A 63 A 108 A
17 A 64 B 109 A 18 A 65 C 110 A 19 B 66 A 111 A 20 C 67 C 112 A 23
A 68 A 113 A 24 A 69 A 114 A 25 A 70 p 115 B 26 B 71 p 116 A 27 A
72 A 117 A 28 C 73 A 118 A 29 A 74 A 119 A 30 A 75 A 120 A 31 A 76
A 121 A 32 A 77 A 122 A 33 A 78 A 123 A 34 A 79 A 124 A 35 A 80 A
125 A 36 C 81 A 126 A 37 A 82 B 127 A 38 A 83 A 128 A 39 A 84 A 129
A 40 A 85 C 130 A 41 A 86 A 132 C 42 A 87 A 133 A 43 A 88 C 134 A
44 C 89 A 135 A 45 A 90 B 136 A 46 A 91 A 137 A 47 A 92 A 138 A A:
IC.sub.50 .ltoreq. 500 nM; B: 500 nM < IC.sub.50 .ltoreq. 1
.mu.M C: 1 .mu.M < IC.sub.50
* * * * *