U.S. patent application number 14/662145 was filed with the patent office on 2015-12-03 for substituted heteroaryl aldehyde compounds and methods for their use in increasing tissue oxygenation.
This patent application is currently assigned to Global Blood Therapeutics, Inc.. The applicant listed for this patent is Cytokinetics, Inc., Global Blood Therapeutics, Inc., The Regents of the University of Califorina. Invention is credited to Chihyuan Chuang, Lan Hua, Matthew P. Jacobson, Brian Metcalf, Bradley Morgan, Kumar Paulvannan, Jeffrey Warrington.
Application Number | 20150344483 14/662145 |
Document ID | / |
Family ID | 48698670 |
Filed Date | 2015-12-03 |
United States Patent
Application |
20150344483 |
Kind Code |
A1 |
Metcalf; Brian ; et
al. |
December 3, 2015 |
SUBSTITUTED HETEROARYL ALDEHYDE COMPOUNDS AND METHODS FOR THEIR USE
IN INCREASING TISSUE OXYGENATION
Abstract
Provided are substituted heteroaryl aldehydes and derivatives
thereof that act as allosteric modulators of hemoglobin, methods
and intermediates for their preparation, pharmaceutical
compositions comprising the modulators, and methods for their use
in treating disorders mediate by hemoglobin and disorders that
would benefit from increased tissue oxygenation.
Inventors: |
Metcalf; Brian; (Moraga,
CA) ; Chuang; Chihyuan; (Millbrae, CA) ;
Warrington; Jeffrey; (San Mateo, CA) ; Paulvannan;
Kumar; (San Jose, CA) ; Jacobson; Matthew P.;
(San Francisco, CA) ; Hua; Lan; (Mountain View,
CA) ; Morgan; Bradley; (Moraga, CA) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Global Blood Therapeutics, Inc.
Cytokinetics, Inc.
The Regents of the University of Califorina |
South San Francisco
South San Francisco
Oakland |
CA
CA
CA |
US
US
US |
|
|
Assignee: |
Global Blood Therapeutics,
Inc.
The Regents of the University of Califorina
Cytokinetics, Inc.
|
Family ID: |
48698670 |
Appl. No.: |
14/662145 |
Filed: |
March 18, 2015 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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13730730 |
Dec 28, 2012 |
9012450 |
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14662145 |
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61661327 |
Jun 18, 2012 |
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61581063 |
Dec 28, 2011 |
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Current U.S.
Class: |
514/249 ;
514/253.09; 514/300; 514/303; 514/307; 514/314; 514/333; 514/335;
514/338; 514/340; 514/341; 514/350; 544/350; 544/353; 544/364;
546/119; 546/121; 546/122; 546/146; 546/174; 546/256; 546/261;
546/268.4; 546/271.4; 546/271.7; 546/272.4; 546/275.1; 546/275.4;
546/275.7; 546/298 |
Current CPC
Class: |
C07D 401/12 20130101;
C07D 405/14 20130101; C07D 413/12 20130101; C07D 213/69 20130101;
C07D 213/65 20130101; C07D 213/68 20130101; C07D 213/80 20130101;
C07D 487/04 20130101; C07D 401/14 20130101; C07D 471/04
20130101 |
International
Class: |
C07D 487/04 20060101
C07D487/04; C07D 471/04 20060101 C07D471/04; C07D 213/69 20060101
C07D213/69; C07D 213/65 20060101 C07D213/65; C07D 401/12 20060101
C07D401/12; C07D 401/14 20060101 C07D401/14; C07D 213/80 20060101
C07D213/80; C07D 405/14 20060101 C07D405/14; C07D 213/68 20060101
C07D213/68; C07D 413/12 20060101 C07D413/12 |
Claims
1. A compound of Formula (I): ##STR00384## or a tautomer or
pharmaceutically acceptable salt thereof, wherein Q is selected
from the group consisting of aryl, heteroaryl, and
heterocycloalkyl, each optionally substituted with one to three
R.sup.a; Y is O or CR.sup.1aR.sup.1b, where R.sup.1a is H or halo
and R.sup.1b is selected from the group consisting of H, halo, and
OH; X is selected from the group consisting of O,
>CH(CH.sub.2).sub.nR.sup.8, and C(R.sup.9).sub.2 where n is 0 or
1, R.sup.8 is OH, and R.sup.9 is independently H or halo; or Y--X
taken together is --NHC(O)-- or --C(O)NH--; R.sup.2, R.sup.3,
R.sup.4, and R.sup.5 are independently absent or selected from the
group consisting of hydrogen, halo, R.sup.b, OR.sup.d,
O(CH.sub.2).sub.zOR.sup.d, O(CH.sub.2)zNR.sup.dR.sup.d,
OC(O)R.sup.e, SR.sup.d, CN, NO.sub.2, CO.sub.2R.sup.d,
CONR.sup.dR.sup.d, C(O)R.sup.d, OC(O)NR.sup.dR.sup.d,
NR.sup.dR.sup.d, NR.sup.dC(O)R.sup.e, NR.sup.dC(O).sub.2R.sup.e,
NR.sup.dC(O)NR.sup.dR.sup.d, S(O)R.sup.e, S(O).sub.2R.sup.e,
NR.sup.dS(O).sub.2R.sup.e, S(O).sub.2NR.sup.dR.sup.d, and N.sub.3
where z is 1, 2, or 3; or R.sup.5 is --(CH.sub.2).sub.pR.sup.5a
where p is 0 or 1 and R.sup.5a is OH; R.sup.6 and R.sup.7 together
form oxo or an aldehyde protecting group, or R.sup.6 together with
R.sup.1b, R.sup.8, or R.sup.5 forms a cyclic ether where one of
R.sup.1b, R.sup.8, or R.sup.5a is O, R.sup.6 is a bond, and R.sup.7
is selected from the group consisting of OH, C.sub.1-8alkoxy, and
haloC.sub.1-8alkoxy; T.sup.1, T.sup.2, T.sup.3, and T.sup.4 are
independently C or N provided that at least one of T.sup.1,
T.sup.2, T.sup.3, and T.sup.4 is N and at least one of T.sup.1,
T.sup.2, T.sup.3, and T.sup.4 is C; each R.sup.a is independently
selected from the group consisting of halo, R.sup.b, OR.sup.d,
O(CH.sub.2).sub.uOR.sup.d, O(CH.sub.2).sub.uNR.sup.dR.sup.d,
O(CH.sub.2).sub.uNR.sup.dC(O)R.sup.e,
O(CH.sub.2).sub.uNR.sup.dC(O).sub.2R.sup.e,
O(CH.sub.2).sub.uNR.sup.dS(O).sub.2R.sup.e, NH.sub.2,
--(CH.sub.2).sub.kOC(O)R.sup.e, --(CH.sub.2).sub.kSR.sup.d, CN,
NO.sub.2, --(CH.sub.2).sub.kCO.sub.2(C.sub.1-8alkyl)OH,
--(CH.sub.2).sub.kCO.sub.2(C.sub.1-8alkyl)(heteroaryl)C(O)(C.sub.1-8alkyl-
), --(CH.sub.2).sub.kCO.sub.2R.sup.d,
--(CH.sub.2).sub.kCONR.sup.dR.sup.d,
--(CH.sub.2).sub.kNR.sup.dC(O)R.sup.e,
--(CH.sub.2).sub.kNR.sup.dC(O).sub.2R.sup.e,
--(CH.sub.2).sub.kC(O)R.sup.d,
--(CH.sub.2).sub.kOC(O)NR.sup.dR.sup.d,
--NR.sup.d(CH.sub.2).sub.uOR.sup.d,
--NR.sup.d(CH.sub.2).sub.uNR.sup.dR.sup.d,
--NR.sup.d(CH.sub.2).sub.uNR.sup.dC(O)R.sup.e,
--NR.sup.d(CH.sub.2).sub.uNR.sup.dC(O).sub.2R.sup.e,
--NR.sup.d(CH.sub.2).sub.uNR.sup.dS(O).sub.2R.sup.e,
--(CH.sub.2).sub.kNR.sup.dC(O)R.sup.e,
--(CH.sub.2).sub.kNR.sup.dC(O).sub.2R.sup.d,
--(CH.sub.2).sub.kNR.sup.dC(O)NR.sup.dR.sup.d,
--(CH.sub.2).sub.kS(O)R.sup.e, --(CH.sub.2).sub.kS(O).sub.2R.sup.e,
--(CH.sub.2).sub.kNR.sup.dS(O).sub.2R.sup.e,
--C(O)(CH.sub.2).sub.kNR.sup.dS(O).sub.2R.sup.e,
--(CH.sub.2).sub.kC(O)NR.sup.dS(O).sub.2R.sup.e,
--(CH.sub.2).sub.kS(O).sub.2NR.sup.dR.sup.d, N.sub.3,
--(CH.sub.2).sub.karyl optionally substituted with one to three
R.sup.c, --NR.sup.d(CH.sub.2).sub.karyl optionally substituted with
one to three R.sup.c, --(CH.sub.2).sub.kheteroaryl optionally
substituted with one to three R.sup.c,
--NR.sup.d(CH.sub.2).sub.kheteroaryl optionally substituted with
one to three R.sup.c, --(CH.sub.2).sub.kheterocycloalkyl optionally
substituted with one to three R.sup.c, and
--NR.sup.d(CH.sub.2).sub.kheterocycloalkyl optionally substituted
with one to three R.sup.c where k is 0, 1, 2, 3, 4, 5, or 6 and u
is 1, 2, 3, 4, 5, or 6; each R.sup.b is independently selected from
the group consisting of C.sub.1-8alkyl, C.sub.2-8alkenyl, and
C.sub.2-8alkynyl, each optionally independently substituted with
one to three halo, OR.sup.d, or NR.sup.dR.sup.d; each R.sup.c is
independently selected from the group consisting of halo,
C.sub.1-8alkyl, haloC.sub.1-8alkyl, C.sub.2-8alkenyl,
haloC.sub.2-8alkenyl, C.sub.2-8alkynyl, haloC.sub.2-8alkynyl,
(CH.sub.2).sub.mOR.sup.f, OC(O)R.sup.g, SR.sup.f, CN, NO.sub.2,
(CH.sub.2).sub.mCO.sub.2R.sup.f, CONR.sup.fR.sup.f, C(O)R.sup.f,
OC(O)NR.sup.fR.sup.f, (CH.sub.2).sub.mNR.sup.fR.sup.f,
NR.sup.fC(O)R.sup.g, NR.sup.fC(O).sub.2R.sup.g,
NR.sup.fC(O)NR.sup.fR.sup.f, S(O)R.sup.g, S(O).sub.2R.sup.g,
NR.sup.fS(O).sub.2R.sup.g, S(O).sub.2NR.sup.fR.sup.f, N.sub.3,
(R.sup.f).sub.mSiC.sub.1-8alkyl, heteroaryl optionally substituted
with one to three R.sup.h, cycloalkyl optionally substituted with
one to three R.sup.h, and heterocycloalkyl optionally substituted
with one to three R.sup.h where m is selected from the group
consisting of 0, 1, 2, 3, 4, 5, and 6; each R.sup.h is
independently selected from the group consisting of halo,
C.sub.1-8alkyl, haloC.sub.1-8alkyl, OR.sup.j, OC(O)R, SR.sup.j,
NO.sub.2, CO.sub.2R.sup.j, CONR.sup.jR.sup.j, C(O)R.sup.j,
OC(O)NR.sup.jR.sup.j, NR.sup.jR.sup.j, NR.sup.jC(O)R.sup.t,
NR.sup.jC(O).sub.2R.sup.t, NR.sup.jC(O)NR.sup.jR.sup.j,
S(O)R.sup.t, S(O).sub.2R.sup.t, NR.sup.jS(O).sub.2R.sup.t, and
S(O).sub.2NR.sup.jR.sup.j; R.sup.d, R.sup.f, and R.sup.jare each
independently selected from the group consisting of hydrogen,
C.sub.1-8 alkyl, haloC.sub.1-8alkyl, C.sub.2-8 alkenyl,
haloC.sub.2-8alkenyl, C.sub.2-8 alkynyl, and haloC.sub.2-8alkynyl;
and R.sup.e, R.sup.g, and R.sup.t are each independently selected
from the group consisting of C.sub.1-8alkyl, haloC.sub.1-8alkyl,
C.sub.2-8 alkenyl, haloC.sub.2-8alkenyl, C.sub.2-8 alkynyl, and
haloC.sub.2-8alkynyl; provided that X and Y are not both O;
provided that when X is O, R.sup.1b is not OH; and provided that
when Y is O, and n is 0, R.sup.8 is not OH.
2. A according to claim 1, or a tautomer or pharmaceutically
acceptable salt thereof, wherein: Y is CH.sub.2; X is O or
CH.sub.2; T.sup.1, T.sup.2, T.sup.3, and T.sup.4 are C or N,
provided that no more than one of T.sup.1, T.sup.2, T.sup.3, and
T.sup.4 is N; Q is selected from the group consisting of i)
heteroaryl optionally substituted with one to three R.sup.a;
wherein R.sup.2, R.sup.3, R.sup.4, and R.sup.5, are independently
absent or selected from the group consisting of hydrogen, halo,
R.sup.b, OR.sup.d, O(CH.sub.2).sub.zOR.sup.d,
O(CH.sub.2).sub.zNR.sup.dR.sup.d, OC(O)R.sup.e, SR.sup.d, CN,
NO.sub.2, CO.sub.2R.sup.d, CONR.sup.dR.sup.d, C(O)R.sup.d,
OC(O)NR.sup.dR.sup.d, NR.sup.dR.sup.d, NR.sup.dC(O)R.sup.e,
NR.sup.dC(O).sub.2R.sup.e, NR.sup.dC(O)NR.sup.dR.sup.d,
S(O)R.sup.e, S(O).sub.2R.sup.e, NR.sup.dS(O).sub.2R.sup.e,
S(O).sub.2NR.sup.dR.sup.d, and N.sub.3 where z is 1, 2, or 3; ii)
aryl substituted with one to three
--(CH.sub.2).sub.kCO.sub.2R.sup.d; wherein R.sup.2 and R.sup.5 are
independently absent or selected from the group consisting of
hydrogen, halo, OR.sup.d, O(CH.sub.2).sub.zOR.sup.d,
O(CH.sub.2).sub.zNR.sup.dR.sup.d, OC(O)R.sup.e, SR.sup.d, CN,
NO.sub.2, CO.sub.2R.sup.d, CONR.sup.dR.sup.d, C(O)R.sup.d,
OC(O)NR.sup.dR.sup.d, NR.sup.dR.sup.d, NR.sup.dC(O)R.sup.e,
NR.sup.dC(O).sub.2R.sup.e, NR.sup.dC(O)NR.sup.dR.sup.d,
S(O)R.sup.e, S(O).sub.2R.sup.e, NR.sup.dS(O).sub.2R.sup.e,
S(O).sub.2NR.sup.dR.sup.d, and N.sub.3 where z is 1, 2, or 3;
R.sup.3 and R.sup.4 are independently absent or selected from the
group consisting of hydrogen, halo, R.sup.b, OR.sup.d,
O(CH.sub.2).sub.zOR.sup.d, O(CH.sub.2).sub.zNR.sup.dR.sup.d,
OC(O)R.sup.e, SR.sup.d, CN, NO.sub.2, CO.sub.2R.sup.d,
CONR.sup.dR.sup.d, C(O)R.sup.d, OC(O)NR.sup.dR.sup.d,
NR.sup.dR.sup.d, NR.sup.dC(O)R.sup.e, NR.sup.dC(O).sub.2R.sup.e,
NR.sup.dC(O)NR.sup.dR.sup.d, S(O)R.sup.e, S(O).sub.2R.sup.e,
NR.sup.dS(O).sub.2R.sup.e, S(O).sub.2NR.sup.dR.sup.d, and N.sub.3
where z is 1, 2, or 3; iii) unsubstituted aryl, wherein R.sup.2,
R.sup.3, and R.sup.4, are independently absent or selected from the
group consisting of hydrogen, halo, R.sup.b, OR.sup.d,
O(CH.sub.2).sub.zOR.sup.d, O(CH.sub.2).sub.zNR.sup.dR.sup.d,
OC(O)R.sup.e, SR.sup.d, CN, NO.sub.2, CO.sub.2R.sup.d,
CONR.sup.dR.sup.d, C(O)R.sup.d, OC(O)NR.sup.dR.sup.d,
NR.sup.dR.sup.d, NR.sup.dC(O)R.sup.e, NR.sup.dC(O).sub.2R.sup.e,
NR.sup.dC(O)NR.sup.dR.sup.d, S(O)R.sup.e, S(O).sub.2R.sup.e,
NR.sup.dS(O).sub.2R.sup.e, S(O).sub.2NR.sup.dR.sup.d, and N.sub.3
where z is 1, 2, or 3; and R.sup.5 is absent or is OR.sup.2; and
iv) heterocycloalkyl, optionally substituted with one to three
R.sup.a; wherein R.sup.2, R.sup.3, R.sup.4, and R.sup.5, are
independently absent or selected from the group consisting of
hydrogen, R.sup.b, OR.sup.d, O(CH.sub.2).sub.zOR.sup.d,
O(CH.sub.2).sub.zNR.sup.dR.sup.d, OC(O)R.sup.e, SR.sup.d, CN,
NO.sub.2, CO.sub.2R.sup.d, CONR.sup.dR.sup.d, C(O)R.sup.d,
OC(O)NR.sup.dR.sup.d, NR.sup.dR.sup.d, NR.sup.dC(O)R.sup.e,
NR.sup.dC(O).sub.2R.sup.e, NR.sup.dC(O)NR.sup.dR.sup.d,
S(O)R.sup.e, S(O).sub.2R.sup.e, NR.sup.dS(O).sub.2R.sup.e,
S(O).sub.2NR.sup.dR.sup.d, and N.sub.3 where z is 1, 2, or 3;
R.sup.6 and R.sup.7 together form oxo or an aldehyde protecting
group; each R.sup.a is independently selected from the group
consisting of halo, R.sup.h, OR.sup.d, O(CH.sub.2).sub.uOR.sup.d,
O(CH.sub.2).sub.uNR.sup.dR.sup.d,
O(CH.sub.2).sub.uNR.sup.dC(O)R.sup.e,
O(CH.sub.2).sub.uNR.sup.dC(O).sub.2R.sup.e,
O(CH.sub.2).sub.uNR.sup.dS(O).sub.2R.sup.e, NH.sub.2,
--(CH.sub.2).sub.kOC(O)R.sup.e, --(CH.sub.2).sub.kSR.sup.d, CN,
NO.sub.2, --(CH.sub.2).sub.kCO.sub.2(C.sub.1-8alkyl)OH,
--(CH.sub.2).sub.kCO.sub.2(C.sub.1-8alkyl)(heteroaryl)C(O)(C.sub.1-8alkyl-
), --(CH.sub.2).sub.kCO.sub.2R.sup.d,
--(CH.sub.2).sub.kCONR.sup.dR.sup.d,
--(CH.sub.2).sub.kNR.sup.dC(O)R.sup.e,
--(CH.sub.2).sub.kNR.sup.dC(O).sub.2R.sup.e,
--(CH.sub.2).sub.kC(O)R.sup.d,
--(CH.sub.2).sub.kOC(O)NR.sup.dR.sup.d,
--NR.sup.d(CH.sub.2).sub.uOR.sup.d,
--NR.sup.d(CH.sub.2).sub.uNR.sup.dR.sup.d,
--NR.sup.d(CH.sub.2).sub.uNR.sup.dC(O)R.sup.e,
--NR.sup.d(CH.sub.2).sup.uNR.sup.dC(O).sub.2R.sup.e,
--NR.sup.d(CH.sub.2).sub.uNR.sup.dS(O).sub.2R.sup.e,
--(CH.sub.2).sub.kNR.sup.dC(O)R.sup.e,
--(CH.sub.2).sub.kNR.sup.dC(O).sub.2R.sup.d,
--(CH.sub.2).sub.kNR.sup.dC(O)NR.sup.dR.sup.d,
--(CH.sub.2).sub.kS(O)R.sup.e, --(CH.sub.2).sub.kS(O).sub.2R.sup.e,
--(CH.sub.2).sub.kNR.sup.dS(O).sub.2R.sup.e,
--C(O)(CH.sub.2).sub.kNR.sup.dS(O).sub.2R.sup.e,
--(CH.sub.2).sub.kC(O)NR.sup.dS(O).sub.2R.sup.e,
--(CH.sub.2).sub.kS(O).sub.2NR.sup.dR.sup.d, N.sub.3,
--(CH.sub.2).sub.karyl optionally substituted with one to three
R.sup.c, --NR.sup.d(CH.sub.2).sub.karyl optionally substituted with
one to three R.sup.c, --(CH.sub.2).sub.kheteroaryl optionally
substituted with one to three R.sup.c,
--NR.sup.d(CH.sub.2).sub.kheteroaryl optionally substituted with
one to three R.sup.c, --(CH.sub.2).sub.kheterocycloalkyl optionally
substituted with one to three R.sup.c, and
--NR.sup.d(CH.sub.2).sub.kheterocycloalkyl optionally substituted
with one to three R.sup.c where k is 0, 1, 2, 3, 4, 5, or 6 and u
is 1, 2, 3, 4, 5, or 6; each R.sup.b is independently selected from
the group consisting of C.sub.1-8alkyl, C.sub.2-8alkenyl, and
C.sub.2-8alkynyl, each optionally independently substituted with
one to three halo, OR.sup.d, or NR.sup.dR.sup.d; each R.sup.c is
independently selected from the group consisting of halo,
C.sub.1-8alkyl, haloC.sub.1-8alkyl, C.sub.2-8alkenyl,
haloC.sub.2-8alkenyl, C.sub.malkynyl, haloC.sub.2-8alkynyl,
(CH.sub.2).sub.mOR.sup.f, OC(O)R.sup.g, SR.sup.f, CN, NO.sub.2,
(CH.sub.2).sub.mCO.sub.2R.sup.f, CONR.sup.fR.sup.f, C(O)R.sup.f,
OC(O)NR.sup.fR.sup.f, (CH.sub.2).sub.mNR.sup.fR.sup.f,
NR.sup.fC(O)R.sup.g, NR.sup.fC(O).sub.2R.sup.g,
NR.sup.fC(O)NR.sup.fR.sup.f, S(O)R.sup.g, S(O).sub.2R.sup.g,
NR.sup.fS(O).sub.2R.sup.g, S(O).sub.2NR.sup.fR.sup.f, N.sub.3,
(R.sup.f).sub.mSiC.sub.1-8alkyl, heteroaryl optionally substituted
with one to three R.sup.h, cycloalkyl optionally substituted with
one to three R.sup.h, and heterocycloalkyl optionally substituted
with one to three R.sup.h where m is selected from the group
consisting of 0, 1, 2, 3, 4, 5, and 6; each R.sup.h is
independently selected from the group consisting of halo,
C.sub.1-8alkyl, haloC.sub.1-8alkyl, OR.sup.j, OC(O)R, SR.sup.j,
NO.sub.2, CO.sub.2R.sup.j, CONR.sup.jR.sup.j, C(O)R.sup.j,
OC(O)NR.sup.jR.sup.j, NR.sup.jR.sup.j, NR.sup.jC(O)R.sup.t,
NR.sup.jC(O).sub.2R.sup.t, NR.sup.jC(O)NR.sup.jR.sup.j,
S(O)R.sup.t, S(O).sub.2R.sup.t, NR.sup.jS(O).sub.2R.sup.t, and
S(O).sub.2NR.sup.jR.sup.j; R.sup.d, R.sup.f, and R.sup.j are each
independently selected from the group consisting of hydrogen,
C.sub.1-8 alkyl, haloC.sub.1-8alkyl, C.sub.2-8 alkenyl,
haloC.sub.2-8alkenyl, C.sub.2-8 alkynyl, and haloC.sub.2-8alkynyl;
and R.sup.e, R.sup.g, and R.sup.t are each independently selected
from the group consisting of C.sub.1-8alkyl, haloC.sub.1-8alkyl,
C.sub.2-8 alkenyl, haloC.sub.2-8alkenyl, C.sub.2-8 alkynyl, and
haloC.sub.2-8alkynyl.
3. A compound according to claim 2, or a tautomer or
pharmaceutically acceptable salt thereof, wherein R.sup.6 and
R.sup.7 together form oxo.
4. A compound according to claim 2 wherein R.sup.2 and R.sup.3 are
independently absent or selected from the group consisting of
hydrogen, R.sup.b, OR.sup.d, O(CH.sub.2).sub.zOR.sup.d,
O(CH.sub.2).sub.zNR.sup.dR.sup.d, OC(O)R.sup.e, CO.sub.2R.sup.d,
CONR.sup.dR.sup.d, and C(O)R.sup.d, where z is 1, 2, or 3.
5. A compound according to claim 2, wherein T.sup.2 is N; R.sup.2
and R.sup.5 are H; R.sup.3 is absent; and R.sup.4 is
C.sub.1-8alkoxy, haloC.sub.1-8alkoxy, and
O(CH.sub.2).sub.2C.sub.1-8alkyl.
6. A compound according to claim 2, wherein T.sup.2 is N; R.sup.2
and R.sup.4 are H; R.sup.3 is absent; and R.sup.5 is selected from
hydroxy and C.sub.1-8alkoxy.
7. A compound according to claim 2, wherein T.sup.4 is N; R.sup.2
and R.sup.3 are H; R.sup.5 is absent; and R.sup.4 is selected from
C.sub.1-8alkyl and C.sub.1-8alkoxy.
8. A compound according to any of claims 5-7, wherein Q is selected
from the group consisting of an imidazopyridinyl group, a
pyrrolopyridinyl group, a pyrazolopyridinyl group, a
triazolopyridinyl group, a pyrazolopyrazinyl group, a pyridinyl
group, a pyrazinyl group, an oxazolyl group, an imidazolyl group, a
triazolyl group, a tetrazolyl group, a pyrazolyl group, a
quinolinyl group, an isoquinolinyl group, an indazolyl group, a
benzooxazolyl group, a naphthyridinyl group, and a quinoxalinyl
group; and wherein Q is optionally substituted with one to three
R.sup.a.
9. A compound according to any of claims 5-7, wherein Q is selected
from the group consisting of: ##STR00385## ##STR00386## and wherein
Q is optionally substituted with one to three R.sup.a.
10. A compound according to claim 2, wherein T.sup.1 is N; R.sup.3,
R.sup.4, and R.sup.5 are H; and R.sup.2 is absent.
11. A compound according to claim 2, wherein T.sup.2 is N; R.sup.2,
R.sup.4, and R.sup.5 are H; and R.sup.3 is absent.
12. A compound according to claim 2, wherein T.sup.3 is N; R.sup.2,
R.sup.3, and R.sup.5 are H; and R.sup.4 is absent.
13. A compound according to claim 2, wherein T.sup.4 is N; R.sup.2,
R.sup.3, and R.sup.4 are H; and R.sup.5 is absent.
14. A compound according to any of claims 10-13, wherein Q is
selected from the group consisting of an imidazopyridinyl group, a
pyrrolopyridinyl group, a pyrazolopyridinyl group, a
triazolopyridinyl group, a pyrazolopyrazinyl group, a pyridinyl
group, a pyrazinyl group, an oxazolyl group, an imidazolyl group, a
triazolyl group, a tetrazolyl group, a pyrazolyl group, a
quinolinyl group, an isoquinolinyl group, an indazolyl group, a
benzooxazolyl group, a naphthyridinyl group, and a quinoxalinyl
group; and Q is optionally substituted with one to three
R.sup.a.
15. A compound according to any of claims 10-13, wherein Q is
selected from the group consisting of: ##STR00387## ##STR00388##
and wherein Q is optionally substituted with one to three
R.sup.a.
16. A compound of claim 2 selected from the group consisting of:
4-(pyridin-3-ylmethoxy)nicotinaldehyde,
3-(pyridin-3-ylmethoxy)isonicotinaldehyde,
2-(imidazo[1,2-a]pyridin-8-ylmethoxy)nicotinaldehyde,
3-(imidazo[1,2-a]pyridin-8-ylmethoxy)picolinaldehyde,
5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-methoxyisonicotinaldehyde,
3-(imidazo[1,2-a]pyridin-8-ylmethoxy)isonicotinaldehyde,
3-(imidazo[1,5-a]pyridin-8-ylmethoxy)isonicotinaldehyde,
2-methoxy-5-(pyrazolo[1,5-a]pyrazin-3-ylmethoxy)isonicotinaldehyde,
8-((3-formylpyridin-2-yloxy)methyl)imidazo[1,2-a]pyridine-6-carboxamide,
8((4-formyl-6-methoxypyridin-3-yloxy)methyl)imidazo[1,2-a]pyridine-6-carb-
oxamide,
5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-oxo-1,2-dihydropyridine-4-
-carbaldehyde,
2-(2-(imidazo[1,2-a]pyridin-8-yl)ethyl)nicotinaldehyde,
5-(2-(imidazo[1,2-a]pyridin-8-yl)ethyl)-2-methoxyisonicotinaldehyde,
5-((1H-pyrazolo[3,4-b]pyridin-4-yl)methoxy)-2-methoxyisonicotinaldehyde,
3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)pyrazolo[1,5-a]pyrazine-2-ca-
rboxamide,
5-((2-(1H-pyrazol-5-yl)pyrazolo[1,5-a]pyrazin-3-yl)methoxy)-2-m-
ethoxyisonicotinaldehyde,
2-(imidazo[1,2-a]pyridin-2-ylmethoxy)nicotinaldehyde,
2-methoxy-5-((4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazin-3-yl)methoxy)isoni-
cotinaldehyde,
2-(imidazo[1,2-a]pyridin-8-ylmethoxy)nicotinaldehyde,
5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-methylisonicotinaldehyde,
3-((1H-pyrrolo[2,3-b]pyridin-4-yl)methoxy)isonicotinaldehyde,
3-(imidazo[1,2-a]pyridin-8-ylmethoxy)isonicotinaldehyde,
3-(pyrrolo[1,2-a]pyrazin-6-ylmethoxy)isonicotinaldehyde,
6-((4-formylpyridin-3-yloxy)methyl)pyrrolo[1,2-a]pyrazine-7-carbonitrile,
6-((4-formylpyridin-3-yloxy)methyl)pyrrolo[1,2-a]pyrazine-7-carboxamide,
3-((1H-pyrazolo[3,4-b]pyridin-4-yl)methoxy)isonicotinaldehyde,
3-(pyrazolo[1,5-a]pyrazin-3-ylmethoxy)isonicotinaldehyde,
2-methoxy-5-((6-oxo-1,6-dihydropyridin-3-yl)methoxy)isonicotinaldehyde,
2-methoxy-5-((2-oxo-1,2-dihydropyridin-4-yl)methoxy)isonicotinaldehyde,
2-methoxy-5-(oxazol-5-ylmethoxy)isonicotinaldehyde,
5-((1H-imidazol-5-yl)methoxy)-2-methoxyisonicotinaldehyde,
5-((1H-imidazol-2-yl)methoxy)-2-methoxyisonicotinaldehyde,
5-((4H-1,2,4-triazol-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
5-((1H-tetrazol-5-yl)methoxy)-2-methoxyisonicotinaldehyde,
5-((1H-pyrazol-5-yl)methoxy)-2-methoxyisonicotinaldehyde,
5-((1H-pyrazol-4-yl)methoxy)-2-methoxyisonicotinaldehyde,
2-methoxy-5-(oxazol-4-ylmethoxy)isonicotinaldehyde,
2-methoxy-5-((2-methylpyridin-3-yl)methoxy)isonicotinaldehyde,
2-methoxy-5-((4-methylpyridin-3-yl)methoxy)isonicotinaldehyde,
2-methoxy-5-((6-(trifluoromethyl)pyridin-3-yl)methoxy)isonicotinaldehyde,
2-methoxy-5-((6-methylpyridin-3-yl)methoxy)isonicotinaldehyde,
2-methoxy-5-(pyridin-3-ylmethoxy)isonicotinaldehyde,
2-methoxy-5-((5-methylpyridin-3-yl)methoxy)isonicotinaldehyde,
5-(isoquinolin-1-ylmethoxy)-2-methoxyisonicotinaldehyde,
2-methoxy-5-(quinolin-2-ylmethoxy)isonicotinaldehyde,
2-methoxy-5-(pyridin-4-ylmethoxy)isonicotinaldehyde,
2-methoxy-5-((3-methylpyridin-4-yl)methoxy)isonicotinaldehyde,
5-((3-bromopyridin-4-yl)methoxy)-2-methoxyisonicotinaldehyde,
3-(imidazo[1,2-a]pyridin-8-ylmethoxy)-6-methylpicolinaldehyde,
(5-(imidazo[1,2-a]pyridin-5-ylmethoxy)-2-methoxypyridin-4-yl)(methoxy)met-
hanol,
N-(4-formylpyridin-3-yl)imidazo[1,2-a]pyridine-8-carboxamide,
2-methoxy-5-((6-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl)methoxy)isoni-
cotinaldehyde, methyl
2-((4-formyl-6-methoxypyridin-3-yloxy)methyl)imidazo[1,2-a]pyridine-8-car-
boxylate,
2-methoxy-5-((1-methyl-2-oxo-1,2-dihydropyridin-4-yl)methoxy)iso-
nicotinaldehyde,
5-((3-bromoimidazo[1,2-a]pyridin-2-yl)methoxy)-2-methoxyisonicotinaldehyd-
e,
5-((6-bromoimidazo[1,2-a]pyridin-2-yl)methoxy)-2-methoxyisonicotinaldeh-
yde,
5-((8-bromoimidazo[1,2-a]pyridin-2-yl)methoxy)-2-methoxyisonicotinald-
ehyde,
2-methoxy-5-((3-methyl-[1,2,4]triazolo[4,3-a]pyridin-8-yl)methoxy)i-
sonicotinaldehyde,
5-((3-(1H-pyrazol-5-yl)imidazo[1,2-a]pyridin-2-yl)methoxy)-2-methoxyisoni-
cotinaldehyde,
5-((6-(1H-pyrazol-3-yl)imidazo[1,2-a]pyridin-2-yl)methoxy)-2-methoxyisoni-
cotinaldehyde,
2-methoxy-5-((8-(1-methyl-1H-pyrazol-5-yl)imidazo[1,2-a]pyridin-2-yl)meth-
oxy)isonicotinaldehyde,
5-((4-formyl-6-methoxypyridin-3-yloxy)methyl)picolinonitrile,
5-((2-bromopyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)picolinonitrile,
5-((2-(1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
5-((5-bromopyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
methyl
2-((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yloxy)methyl)imidazo[1,2-a]p-
yridine-8-carboxylate,
2-((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yloxy)methyl)imidazo[1,2-a]p-
yridine-8-carboxamide,
2-((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yloxy)methyl)-N-methylimidaz-
o[1,2-a]pyridine-8-carboxamide,
5-((5-(1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
5-((4-(1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
2-((4-(dihydroxymethyl)-6-methoxypyridin-3-yloxy)methyl)-N-methylimidazo[-
1,2-a]pyridine-8-carboxamide,
2-((4-(dihydroxymethyl)-6-methoxypyridin-3-yloxy)methyl)imidazo[1,2-a]pyr-
idine-8-carboxamide,
2-methoxy-5-((5-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde,
2-methoxy-5-((5-(1-methyl-1H-pyrazol-3-yl)pyridin-3-yl)methoxy)i-
sonicotinaldehyde,
5-((5-(1H-pyrazol-4-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
2-methoxy-5-((5-(1-methyl-1H-pyrazol-4-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde, methyl
5-((4-formyl-6-methoxypyridin-3-yloxy)methyl)nicotinate,
5-((4-formyl-6-methoxypyridin-3-yloxy)methyl)nicotinic acid,
2-methoxy-5-(quinolin-3-ylmethoxy)isonicotinaldehyde,
6-methyl-3-(quinolin-3-ylmethoxy)picolinaldehyde,
5-(isoquinolin-7-ylmethoxy)-2-methoxyisonicotinaldehyde,
3-(isoquinolin-7-ylmethoxy)-6-methylpicolinaldehyde,
2-methoxy-5-((1-methyl-1H-indazol-4-yl)methoxy)isonicotinaldehyde,
6-methyl-3((1-methyl-1H-indazol-4-yl)methoxy)picolinaldehyde,
tert-butyl
4-((2-formyl-6-methylpyridin-3-yloxy)methyl)-1H-indazole-1-carboxylate,
5-((1H-indazol-4-yl)methoxy)-2-methoxyisonicotinaldehyde,
3-((1H-indazol-4-yl)methoxy)-6-methylpicolinaldehyde,
6-methoxy-3-((1-methyl-1H-indazol-6-yl)methoxy)picolinaldehyde,
2-methoxy-5-((1-methyl-1H-indazol-7-yl)methoxy)isonicotinaldehyde,
6-methoxy-3-((1-methyl-1H-indazol-6-yl)methoxy)picolinaldehyde,
6-methyl-3 ((1-methyl-1H-indazol-7-yl)methoxy)picolinaldehyde,
3-(isoquinolin-1-ylmethoxy)-6-methylpicolinaldehyde,
6-methyl-3-(quinolin-2-ylmethoxy)picolinaldehyde,
5-((4-(1H-pyrazol-4-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
5-((6-bromoimidazo[1,2-a]pyridin-8-yl)methoxy)-2-methoxyisonicotinaldehyd-
e,
8-((4-formyl-6-methoxypyridin-3-yloxy)methyl)imidazo[1,2-a]pyridine-6-c-
arbonitrile,
5-((4-formyl-6-methoxypyridin-3-yloxy)methyl)nicotinonitrile,
3-(benzo[d]oxazol-4-ylmethoxy)-6-methylpicolinaldehyde,
8-((4-formyl-6-methoxypyridin-3-yloxy)methyl)imidazo[1,2-a]pyridine-6-car-
boxamide,
5-((4-formyl-6-methoxypyridin-3-yloxy)methyl)nicotinamide,
5-((6-(1H-pyrazol-4-yl)imidazo[1,2-a]pyridin-8-yl)methoxy)-2-methoxyisoni-
cotinaldehyde,
5-(benzo[d]oxazol-4-ylmethoxy)-2-methoxyisonicotinaldehyde,
5-((6-(1H-pyrazol-5-yl)imidazo[1,2-a]pyridin-8-yl)methoxy)-2-methoxyisoni-
cotinaldehyde,
5-((1,5-naphthyridin-4-yl)methoxy)-2-methoxyisonicotinaldehyde,
3-((1,5-naphthyridin-4-yl)methoxy)-6-methylpicolinaldehyde,
5-((1H-indazol-5-yl)methoxy)-2-methoxyisonicotinaldehyde,
6-methyl-3-((1-methyl-1H-indazol-5-yl)methoxy)picolinaldehyde,
3-((3-chloro-1-methyl-1H-indazol-5-yl)methoxy)-6-methylpicolinaldehyde,
2-methoxy-5-((1-methyl-1H-indazol-5-yl)methoxy)isonicotinaldehyde,
5-((3-chloro-1-methyl-1H-indazol-5-yl)methoxy)-2-methoxyisonicotinaldehyd-
e,
N-(4-formyl-6-methoxypyridin-3-yl)imidazo[1,2-a]pyridine-8-carboxamide,
3-((1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-4-yl)methoxy)-6-methylpicolina-
ldehyde,
5-((1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-4-yl)methoxy)-2-methox-
yisonicotinaldehyde,
3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)picolinamide,
5-((2-chloroquinolin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
5-((2-(1H-pyrazol-5-yl)quinolin-3-yl)methoxy)-2-methoxyisonicotinaldehyde-
, 2-methoxy-5-(quinoxalin-2-ylmethoxy)isonicotinaldehyde,
6-methyl-3-(quinolin-5-ylmethoxy)picolinaldehyde,
2-methoxy-5-(quinolin-5-ylmethoxy)isonicotinaldehyde,
6-methyl-3-((1-methyl-1H-pyrazolo[3,4-b]pyridin-5-yl)methoxy)picolinaldeh-
yde,
2-methoxy-5-((1-methyl-1H-pyrazolo[3,4-b]pyridin-5-yl)methoxy)isonico-
tinaldehyde,
5-((7-(1H-pyrazol-3-yl)imidazo[1,5-a]pyridin-8-yl)methoxy)-2-methoxyisoni-
cotinaldehyde,
5-((5-(2H-tetrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde-
,
5-((6-(2H-tetrazol-5-yl)imidazo[1,2-a]pyridin-8-yl)methoxy)-2-methoxyiso-
nicotinaldehyde, ethyl
2-(5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-methoxypyridin-4-yl)thiazolidi-
ne-4-carboxylate,
2-methoxy-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde,
5-((2-(1H-pyrazol-4-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotin-
aldehyde,
2-methoxy-5-((2-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)i-
sonicotinaldehyde,
2-methoxy-5-((2-(1-methyl-1H-pyrazol-3-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde,
5-((2-(2H-tetrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonicoti-
naldehyde,
2-methoxy-5-((2-(4-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-
isonicotinaldehyde,
5-((3-(1H-pyrazol-5-yl)isoquinolin-4-yl)methoxy)-2-methoxyisonicotinaldeh-
yde,
5-((2-(1H-pyrazol-1-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldeh-
yde,
3-((2-(1H-pyrazol-1-yl)pyridin-3-yl)methoxy)-6-methylpicolinaldehyde,
6-methyl-3-(pyridin-3-ylmethoxy)picolinaldehyde, methyl
8-(((4-formyl-6-methoxypyridin-3-yl)oxy)methyl)imidazo[1,2-a]pyridine-6-c-
arboxylate, methyl
2-bromo-8-(((4-formyl-6-methoxypyridin-3-yl)oxy)methyl)imidazo[1,2-a]pyri-
dine-6-carboxylate,
3-(imidazo[1,5-a]pyridin-8-ylmethoxy)-6-methylpicolinaldehyde,
5-(imidazo[1,5-a]pyridin-8-ylmethoxy)-2-methoxyisonicotinaldehyde,
(5-(methoxycarbonyl)pyridin-3-yl)methyl
5-(((4-formyl-6-methoxypyridin-3-yl)oxy)methyl)nicotinate,
5-((2-(1,4-dimethyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonic-
otinaldehyde,
5-((2-(1,5-dimethyl-1H-pyrazol-4-yl)pyridin-3-yl)methoxy)-2-methoxyisonic-
otinaldehyde, 2-hydroxyethyl
5-(((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yl)oxy)methyl)nicotinate,
methyl
5-(((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yl)oxy)methyl)nicoti-
nate, methyl
5-(((4-(bis(2-hydroxyethoxy)methyl)-6-methoxypyridin-3-yl)oxy)methyl)nico-
tinate,
5-((2-(1,3-dimethyl-1H-pyrazol-4-yl)pyridin-3-yl)methoxy)-2-methox-
yisonicotinaldehyde,
5-((2-(1,3-dimethyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonic-
otinaldehyde,
5-((2-(1-ethyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotina-
ldehyde,
5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methox-
yisonicotinaldehyde,
2-methoxy-5-((2-(3-methyl-1H-pyrazol-1-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde,
5-(((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yl)oxy)methyl)nico-
tinic acid,
(E)-2-methoxy-5-((2-(4-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonic-
otinaldehyde oxime,
(E)-2-methoxy-5-(pyridin-3-ylmethoxy)isonicotinaldehyde oxime,
2-(5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-methoxypyridin-4-yl)thiazolidi-
ne,
1-(2-(5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-methoxypyridin-4-yl)thia-
zolidin-3-yl)ethanone,
5-((2-(4-(1H-pyrazol-3-yl)piperazin-1-yl)pyridin-3-yl)methoxy)-2-methoxyi-
sonicotinaldehyde,
2-(difluoromethoxy)-5-(imidazo[1,2-a]pyridin-8-ylmethoxy)isonicotinaldehy-
de, 2-methoxy-5-((2-phenylpyridin-3-yl)methoxy)isonicotinaldehyde,
5-((3-(1-isopropyl-1H-pyrazol-5-yl)pyridin-4-yl)methoxy)-2-methoxyisonico-
tinaldehyde,
5-([2,3'-bipyridin]-3-ylmethoxy)-2-methoxyisonicotinaldehyde,
2-methoxy-5-((2-(o-tolyl)pyridin-3-yl)methoxy)isonicotinaldehyde,
2-methoxy-5-((2'-methoxy-[2,3'-bipyridin]-3-yl)methoxy)isonicotinaldehyde-
, 4-(((2-formyl-6-methylpyridin-3-yl)oxy)methyl)benzoic acid,
4-(((2-formylpyridin-3-yl)oxy)methyl)benzoic acid, methyl
3-(((4-formylpyridin-3-yl)oxy)methyl)benzoate, methyl
3-(((2-formyl-6-methylpyridin-3-yl)oxy)methyl)benzoate,
3-(((4-formylpyridin-3-yl)oxy)methyl)benzoic acid,
3-(((2-formyl-6-methylpyridin-3-yl)oxy)methyl)benzoic acid,
3-(((2-formylpyridin-3-yl)oxy)methyl)benzoic acid,
2-methoxy-5-((2-(1-(2-methoxyethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-
isonicotinaldehyde,
2-methoxy-5-((2-(1-propyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde,
2-methoxy-5-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl)pyridi-
n-3-yl)methoxy)isonicotinaldehyde,
5-((2-(1-(2,2-difluoroethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-meth-
oxyisonicotinaldehyde,
3-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)picolinaldehyde,
3-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-6-methylpicolina-
ldehyde,
2-(difluoromethoxy)-5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3--
yl)methoxy)isonicotinaldehyde,
5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-(2-methoxyethoxyl)isonicotinaldeh-
yde,
5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-(2-methoxy-
ethoxy)isonicotinaldehyde,
5-((3-(1-isopropyl-1H-pyrazol-5-yl)pyrazin-2-yl)methoxy)-2-methoxyisonico-
tinaldehyde,
3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)picolinate,
5-((2-(2-hydroxypropan-2-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinalde-
hyde,
2-(2-methoxyethoxy)-5-((2-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)met-
hoxy)isonicotinaldehyde,
2-(2-methoxyethoxy)-5-((2-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-
nicotinaldehyde,
3-hydroxy-5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonico-
tinaldehyde, 3-(benzyloxy)-5-hydroxyisonicotinaldehyde,
3-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-5-methoxyisonico-
tinaldehyde,
5-((2-(2-isopropyl-2H-1,2,4-triazol-3-yl)pyridin-3-yl)methoxy)-2-methoxyi-
sonicotinaldehyde,
5-((2-(1-isopropyl-4-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-metho-
xyisonicotinaldehyde,
5-((2-(1-(2-hydroxyethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxy-
isonicotinaldehyde, 6-(((4-formylpyridin-3-yl)oxy)methyl)picolinic
acid, 2,2,2-trifluoroacetic
acid:6-(((4-formylpyridin-3-yl)oxy)methyl)picolinic acid (1:1),
2-methoxy-5-((2-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazol-5-yl)pyr-
idin-3-yl)methoxy)isonicotinaldehyde,
5-((2-(4-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-oxo-1,2-dihydropy-
ridine-4-carbaldehyde,
5-((2-(1-cyclobutyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonic-
otinaldehyde,
5-((2-(1-cyclohexyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonic-
otinaldehyde,
5-((2-(1-(cyclohexylmethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-metho-
xyisonicotinaldehyde,
5-((2-(1-cyclopentyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisoni-
cotinaldehyde,
2-(5-(3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)pyridin-2-yl)-1H-pyraz-
ol-1-yl)acetic acid, methyl
3-(5-(3-(((4-formyl-6-methoxypyridin-3-yl)oxy)methyl)pyridin-2-yl)-1H-pyr-
azol-1-yl)propanoate,
3-(3-(3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)pyridin-2-yl)-1H-pyraz-
ol-1-yl)propanoic acid,
3-(5-(3-(((4-formyl-6-methoxypyridin-3-yl)oxy)methyl)pyridin-2-yl)-1H-pyr-
azol-1-yl)propanoic acid,
3-(((4-formyl-6-methoxypyridin-3-yl)oxy)methyl)benzoic acid,
6-(((4-formylpyridin-3-yl)oxy)methyl)nicotinonitrile
2,2,2-trifluoroacetate,
6-(((4-formylpyridin-3-yl)oxy)methyl)nicotinic acid,
6-(((4-formylpyridin-3-yl)oxy)methyl)nicotinic acid hydrochloride,
6-(((4-formylpyridin-3-yl)oxy)methyl)-N-(methylsulfonyl)nicotinamide,
2,2,2-trifluoroacetic
acid:6-(((4-formylpyridin-3-yl)oxy)methyl)-N-(methylsulfonyl)nicotinamide
(2:1),
2-(2-methoxyethoxy)-5-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-y-
l)pyridin-3-yl)methoxy)isonicotinaldehyde,
2-methoxy-5-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyridin-3-yl)m-
ethoxy)isonicotinaldehyde,
2-(2-methoxyethoxy)-5-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyri-
din-3-yl)methoxy)isonicotinaldehyde,
2-methyl-5-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl)pyridin-3-yl)met-
hoxy)isonicotinaldehyde,
2-methyl-5-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyridin-3-yl)me-
thoxy)isonicotinaldehyde,
3-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)ison-
icotinaldehyde,
3-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)iso-
nicotinaldehyde,
3-chloro-5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonicot-
inaldehyde,
3-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-5-methylisonicot-
inaldehyde,
3-chloro-5-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyridin-3-yl)me-
thoxy)isonicotinaldehyde, and
3-methyl-5-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl)pyridin-3-yl)met-
hoxy)isonicotinaldehyde, or a tautomer or pharmaceutically
acceptable salt thereof.
17. A compound of claim 2 selected from the group consisting of:
5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-methoxyisonicotinaldehyde,
2-methoxy-5-((5-methylpyridin-3-yl)methoxy)isonicotinaldehyde,
5-(isoquinolin-1-ylmethoxy)-2-methoxyisonicotinaldehyde,
2-methoxy-5-(quinolin-2-ylmethoxy)isonicotinaldehyde,
2-methoxy-5-(pyridin-4-ylmethoxy)isonicotinaldehyde,
3-(imidazo[1,2-a]pyridin-8-ylmethoxy)-6-methylpicolinaldehyde,
methyl
2-((4-formyl-6-methoxypyridin-3-yloxy)methyl)imidazo[1,2-a]pyridine-8-car-
boxylate,
2-methoxy-5-((3-methyl-[1,2,4]triazolo[4,3-a]pyridin-8-yl)methox-
y)isonicotinaldehyde,
5-((2-bromopyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
5-((2-(1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
5-((5-bromopyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
2-methoxy-5-((5-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde, 5-((4-formyl-6-methoxypyridin-3-yloxy)methyl)nicotinic
acid, 2-methoxy-5-(quinolin-3-ylmethoxy)isonicotinaldehyde,
2-methoxy-5-((1-methyl-1H-indazol-4-yl)methoxy)isonicotinaldehyde,
tert-butyl
4-((2-formyl-6-methylpyridin-3-yloxy)methyl)-1H-indazole-1-carboxylate,
6-methyl-3-((1-methyl-1H-indazol-6-yl)methoxy)picolinaldehyde,
6-methyl-3-((1-methyl-1H-indazol-7-yl)methoxy)picolinaldehyde,
3-(isoquinolin-1-ylmethoxy)-6-methylpicolinaldehyde,
5-(benzo[d]oxazol-4-ylmethoxy)-2-methoxyisonicotinaldehyde,
3-((1,5-naphthyridin-4-yl)methoxy)-6-methylpicolinaldehyde,
6-methyl-3-((1-methyl-1H-indazol-5-yl)methoxy)picolinaldehyde,
6-methyl-3-(quinolin-5-ylmethoxy)picolinaldehyde,
2-methoxy-5-(quinolin-5-ylmethoxy)isonicotinaldehyde,
2-methoxy-5-((2-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde,
2-methoxy-5-((2-(1-methyl-1H-pyrazol-3-yl)pyridin-3-yl)methoxy)i-
sonicotinaldehyde,
5-((2-(2H-tetrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde-
,
2-methoxy-5-((2-(4-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonicoti-
naldehyde,
5-((3-(1H-pyrazol-5-yl)isoquinolin-4-yl)methoxy)-2-methoxyisoni-
cotinaldehyde,
5-((2-(1H-pyrazol-1-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
5-(imidazo[1,5-a]pyridin-8-ylmethoxy)-2-methoxyisonicotinaldehyde,
5-((2-(1,5-dimethyl-1H-pyrazol-4-yl)pyridin-3-yl)methoxy)-2-methoxyisonic-
otinaldehyde,
5-((2-(1-ethyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotina-
ldehyde,
5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methox-
yisonicotinaldehyde,
2-(difluoromethoxy)-5-(imidazo[1,2-a]pyridin-8-ylmethoxy)isonicotinaldehy-
de, 2-methoxy-5-((2-phenylpyridin-3-yl)methoxy)isonicotinaldehyde,
5-((3-(1-isopropyl-1H-pyrazol-5-yl)pyridin-4-yl)methoxy)-2-methoxyisonico-
tinaldehyde,
5-([2,3'-bipyridin]-3-ylmethoxy)-2-methoxyisonicotinaldehyde,
2-methoxy-5-((2-(o-tolyl)pyridin-3-yl)methoxy)isonicotinaldehyde,
2-methoxy-5-((2'-methoxy-[2,3'-bipyridin]-3-yl)methoxy)isonicotinaldehyde-
, 4-(((2-formyl-6-methylpyridin-3-yl)oxy)methyl)benzoic acid,
4-(((2-formylpyridin-3-yl)oxy)methyl)benzoic acid, methyl
3-(((4-formylpyridin-3-yl)oxy)methyl)benzoate, methyl
3-(((2-formyl-6-methylpyridin-3-yl)oxy)methyl)benzoate,
3-(((4-formylpyridin-3-yl)oxy)methyl)benzoic acid,
3-(((2-formyl-6-methylpyridin-3-yl)oxy)methyl)benzoic acid,
3-(((2-formylpyridin-3-yl)oxy)methyl)benzoic acid,
2-methoxy-5-((2-(1-(2-methoxyethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-
isonicotinaldehyde,
2-methoxy-5-((2-(1-propyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde,
2-methoxy-5-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl)pyridi-
n-3-yl)methoxy)isonicotinaldehyde,
5-((2-(1-(2,2-difluoroethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-meth-
oxyisonicotinaldehyde,
3-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)picolinaldehyde,
3-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-6-methylpicolina-
ldehyde,
2-(difluoromethoxy)-5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3--
yl)methoxy)isonicotinaldehyde,
5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-(2-methoxyethoxyl)isonicotinaldeh-
yde,
5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-(2-methoxy-
ethoxyl)isonicotinaldehyde,
5-((3-(1-isopropyl-1H-pyrazol-5-yl)pyrazin-2-yl)methoxy)-2-methoxyisonico-
tinaldehyde,
3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)picolinate,
5-((2-(2-hydroxypropan-2-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinalde-
hyde,
2-(2-methoxyethoxy)-5-((2-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)met-
hoxy)isonicotinaldehyde,
2-(2-methoxyethoxy)-5-((2-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-
nicotinaldehyde,
3-hydroxy-5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonico-
tinaldehyde, 3-(benzyloxy)-5-hydroxyisonicotinaldehyde,
3-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-5-methoxyisonico-
tinaldehyde,
5-((2-(2-isopropyl-2H-1,2,4-triazol-3-yl)pyridin-3-yl)methoxy)-2-methoxyi-
sonicotinaldehyde,
5-((2-(1-isopropyl-4-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-metho-
xyisonicotinaldehyde,
5-((2-(1-(2-hydroxyethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxy-
isonicotinaldehyde, 6-(((4-formylpyridin-3-yl)oxy)methyl)picolinic
acid 2,2,2-trifluoroacetic
acid:6-(((4-formylpyridin-3-yl)oxy)methyl)picolinic acid (1:1),
2-methoxy-5-((2-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazol-5-yl)pyr-
idin-3-yl)methoxy)isonicotinaldehyde,
5-((2-(4-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-oxo-1,2-dihydropy-
ridine-4-carbaldehyde,
5-((2-(1-cyclobutyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonic-
otinaldehyde,
5-((2-(1-cyclohexyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonic-
otinaldehyde,
5-((2-(1-(cyclohexylmethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-metho-
xyisonicotinaldehyde,
5-((2-(1-cyclopentyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisoni-
cotinaldehyde,
2-(5-(3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)pyridin-2-yl)-1H-pyraz-
ol-1-yl)acetic acid, methyl
3-(5-(3-(((4-formyl-6-methoxypyridin-3-yl)oxy)methyl)pyridin-2-yl)-1H-pyr-
azol-1-yl)propanoate,
3-(3-(3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)pyridin-2-yl)-1H-pyraz-
ol-1-yl)propanoic acid,
3-(5-(3-(((4-formyl-6-methoxypyridin-3-yl)oxy)methyl)pyridin-2-yl)-1H-pyr-
azol-1-yl)propanoic acid,
3-(((4-formyl-6-methoxypyridin-3-yl)oxy)methyl)benzoic acid,
6-(((4-formylpyridin-3-yl)oxy)methyl)nicotinonitrile
2,2,2-trifluoroacetate,
6-(((4-formylpyridin-3-yl)oxy)methyl)nicotinic acid,
6-(((4-formylpyridin-3-yl)oxy)methyl)nicotinic acid hydrochloride,
6-(((4-formylpyridin-3-yl)oxy)methyl)-N-(methylsulfonyl)nicotinamide,
2,2,2-trifluoroacetic
acid:6-(((4-formylpyridin-3-yl)oxy)methyl)-N-(methylsulfonyl)nicotinamide
(2:1),
2-(2-methoxyethoxy)-5-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-y-
l)pyridin-3-yl)methoxy)isonicotinaldehyde,
2-methoxy-5-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyridin-3-yl)m-
ethoxy)isonicotinaldehyde,
2-(2-methoxyethoxy)-5-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyri-
din-3-yl)methoxy)isonicotinaldehyde,
2-methyl-5-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl)pyridin-3-yl)met-
hoxy)isonicotinaldehyde,
2-methyl-5-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyridin-3-yl)me-
thoxy)isonicotinaldehyde,
3-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)ison-
icotinaldehyde,
3-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)iso-
nicotinaldehyde,
3-chloro-5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonicot-
inaldehyde,
3-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-5-methylisonicot-
inaldehyde,
3-chloro-5-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyridin-3-yl)me-
thoxy)isonicotinaldehyde, and
3-methyl-5-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl)pyridin-3-yl)met-
hoxy)isonicotinaldehyde, or a tautomer or pharmaceutically
acceptable salt thereof.
18. A pharmaceutical composition comprising a compound of any of
the preceding claims or a tautomer or pharmaceutically acceptable
salt thereof.
19. A method for increasing tissue oxygenation, the method
comprising administering to a subject in need thereof a
therapeutically effective amount of a compound of any of the
preceding claims or a tautomer or pharmaceutically acceptable salt
thereof.
20. A method for treating a condition associated with oxygen
deficiency, the method comprising administering to a subject in
need thereof a therapeutically effective amount of a compound of
any of the preceding claims or a tautomer or pharmaceutically
acceptable salt thereof.
21. The method of claim 20, wherein the condition is selected from
the group consisting of sickle cell disease, cancer, a pulmonary
disorder, stroke, high altitude sickness, an ulcer, a pressure
sore, Alzheimer's disease, acute respiratory disease syndrome, and
a wound.
22. The method according to any of claims 19-21 wherein the
compound is selected from the group consisting of:
4-(pyridin-3-ylmethoxy)nicotinaldehyde,
3-(pyridin-3-ylmethoxy)isonicotinaldehyde,
2-(imidazo[1,2-a]pyridin-8-ylmethoxy)nicotinaldehyde,
3-(imidazo[1,2-a]pyridin-8-ylmethoxy)picolinaldehyde,
5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-methoxyisonicotinaldehyde,
3-(imidazo[1,2-a]pyridin-8-ylmethoxy)isonicotinaldehyde,
3-(imidazo[1,5-a]pyridin-8-ylmethoxy)isonicotinaldehyde,
2-methoxy-5-(pyrazolo[1,5-a]pyrazin-3-ylmethoxy)isonicotinaldehyde,
8-((3-formylpyridin-2-yloxy)methyl)imidazo[1,2-a]pyridine-6-carboxamide,
8-((4-formyl-6-methoxypyridin-3-yloxy)methyl)imidazo[1,2-a]pyridine-6-car-
boxamide,
5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-oxo-1,2-dihydropyridine--
4-carbaldehyde,
2-(2-(imidazo[1,2-a]pyridin-8-yl)ethyl)nicotinaldehyde,
5-(2-(imidazo[1,2-a]pyridin-8-yl)ethyl)-2-methoxyisonicotinaldehyde,
5-((1H-pyrazolo[3,4-b]pyridin-4-yl)methoxy)-2-methoxyisonicotinaldehyde,
3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)pyrazolo[1,5-a]pyrazine-2-ca-
rboxamide,
5-((2-(1H-pyrazol-5-yl)pyrazolo[1,5-a]pyrazin-3-yl)methoxy)-2-m-
ethoxyisonicotinaldehyde,
2-(imidazo[1,2-a]pyridin-2-ylmethoxy)nicotinaldehyde,
2-methoxy-5-((4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazin-3-yl)methoxy)isoni-
cotinaldehyde,
2-(imidazo[1,2-a]pyridin-8-ylmethoxy)nicotinaldehyde,
5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-methylisonicotinaldehyde,
3-((1H-pyrrolo[2,3-b]pyridin-4-yl)methoxy)isonicotinaldehyde,
3-(imidazo[1,2-a]pyridin-8-ylmethoxy)isonicotinaldehyde,
3-(pyrrolo[1,2-a]pyrazin-6-ylmethoxy)isonicotinaldehyde,
6-(4-formylpyridin-3-yloxy)methyl)pyrrolo[1,2-a]pyrazine-7-carbonitrile,
6-((4-formylpyridin-3-yloxy)methyl)pyrrolo[1,2-a]pyrazine-7-carboxamide,
3-((1H-pyrazolo[3,4-b]pyridin-4-yl)methoxy)isonicotinaldehyde,
3-(pyrazolo[1,5-a]pyrazin-3-ylmethoxy)isonicotinaldehyde,
2-methoxy-5-((6-oxo-1,6-dihydropyridin-3-yl)methoxy)isonicotinaldehyde,
2-methoxy-5-((2-oxo-1,2-dihydropyridin-4-yl)methoxy)isonicotinaldehyde,
2-methoxy-5-(oxazol-5-ylmethoxy)isonicotinaldehyde,
5-((1H-imidazol-5-yl)methoxy)-2-methoxyisonicotinaldehyde,
5-((1H-imidazol-2-yl)methoxy)-2-methoxyisonicotinaldehyde,
5-((4H-1,2,4-triazol-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
5-((1H-tetrazol-5-yl)methoxy)-2-methoxyisonicotinaldehyde,
5-((1H-pyrazol-5-yl)methoxy)-2-methoxyisonicotinaldehyde,
5-((1H-pyrazol-4-yl)methoxy)-2-methoxyisonicotinaldehyde,
2-methoxy-5-(oxazol-4-ylmethoxy)isonicotinaldehyde,
2-methoxy-5-((2-methylpyridin-3-yl)methoxy)isonicotinaldehyde,
2-methoxy-5-((4-methylpyridin-3-yl)methoxy)isonicotinaldehyde,
2-methoxy-5-((6-(trifluoromethyl)pyridin-3-yl)methoxy)isonicotinaldehyde,
2-methoxy-5-((6-methylpyridin-3-yl)methoxy)isonicotinaldehyde,
2-methoxy-5-(pyridin-3-ylmethoxy)isonicotinaldehyde,
2-methoxy-5-((5-methylpyridin-3-yl)methoxy)isonicotinaldehyde,
5-(isoquinolin-1-ylmethoxy)-2-methoxyisonicotinaldehyde,
2-methoxy-5-(quinolin-2-ylmethoxy)isonicotinaldehyde,
2-methoxy-5-(pyridin-4-ylmethoxy)isonicotinaldehyde,
2-methoxy-5-((3-methylpyridin-4-yl)methoxy)isonicotinaldehyde,
5-((3-bromopyridin-4-yl)methoxy)-2-methoxyisonicotinaldehyde,
3-(imidazo[1,2-a]pyridin-8-ylmethoxy)-6-methylpicolinaldehyde,
(5-(imidazo[1,2-a]pyridin-5-ylmethoxy)-2-methoxypyridin-4-yl)(methoxy)met-
hanol,
N-(4-formylpyridin-3-yl)imidazo[1,2-a]pyridine-8-carboxamide,
2-methoxy-5-((6-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl)methoxy)isoni-
cotinaldehyde, methyl
2-((4-formyl-6-methoxypyridin-3-yloxy)methyl)imidazo[1,2-a]pyridine-8-car-
boxylate,
2-methoxy-5-((1-methyl-2-oxo-1,2-dihydropyridin-4-yl)methoxy)iso-
nicotinaldehyde,
5-((3-bromoimidazo[1,2-a]pyridin-2-yl)methoxy)-2-methoxyisonicotinaldehyd-
e,
5-((6-bromoimidazo[1,2-a]pyridin-2-yl)methoxy)-2-methoxyisonicotinaldeh-
yde,
5-((8-bromoimidazo[1,2-a]pyridin-2-yl)methoxy)-2-methoxyisonicotinald-
ehyde,
2-methoxy-5-((3-methyl-[1,2,4]triazolo[4,3-a]pyridin-8-yl)methoxy)i-
sonicotinaldehyde,
5-((3-(1H-pyrazol-5-yl)imidazo[1,2-a]pyridin-2-yl)methoxy)-2-methoxyisoni-
cotinaldehyde,
5-((6-(1H-pyrazol-3-yl)imidazo[1,2-a]pyridin-2-yl)methoxy)-2-methoxyisoni-
cotinaldehyde,
2-methoxy-5-((8-(1-methyl-1H-pyrazol-5-yl)imidazo[1,2-a]pyridin-2-yl)meth-
oxy)isonicotinaldehyde,
5((4-formyl-6-methoxypyridin-3-yloxy)methyl)picolinonitrile,
5-((2-bromopyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)picolinonitrile,
5-((2-(1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
5-((5-bromopyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
methyl
2-((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yloxy)methyl)imidazo[1,2-a]p-
yridine-8-carboxylate,
2-((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yloxy)methyl)imidazo[1,2-a]p-
yridine-8-carboxamide,
2-((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yloxy)methyl)-N-methylimidaz-
o[1,2-a]pyridine-8-carboxamide,
5-((5-(1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
5-((4-(1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
2-((4-(dihydroxymethyl)-6-methoxypyridin-3-yloxy)methyl)-N-methylimidazo[-
1,2-a]pyridine-8-carboxamide,
2-((4-(dihydroxymethyl)-6-methoxypyridin-3-yloxy)methyl)imidazo[1,2-a]pyr-
idine-8-carboxamide,
2-methoxy-5-((5-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde,
2-methoxy-5-((5-(1-methyl-1H-pyrazol-3-yl)pyridin-3-yl)methoxy)i-
sonicotinaldehyde,
5-((5-(1H-pyrazol-4-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
2-methoxy-5-((5-(1-methyl-1H-pyrazol-4-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde, methyl
5-((4-formyl-6-methoxypyridin-3-yloxy)methyl)nicotinate,
5-((4-formyl-6-methoxypyridin-3-yloxy)methyl)nicotinic acid,
2-methoxy-5-(quinolin-3-ylmethoxy)isonicotinaldehyde,
6-methyl-3-(quinolin-3-ylmethoxy)picolinaldehyde,
5-(isoquinolin-7-ylmethoxy)-2-methoxyisonicotinaldehyde,
3-(isoquinolin-7-ylmethoxy)-6-methylpicolinaldehyde,
2-methoxy-5-((1-methyl-1H-indazol-4-yl)methoxy)isonicotinaldehyde,
6-methyl-3-((1-methyl-1H-indazol-4-yl)methoxy)picolinaldehyde,
tert-butyl
4-((2-formyl-6-methylpyridin-3-yloxy)methyl)-1H-indazole-1-carboxylate,
5-((1H-indazol-4-yl)methoxy)-2-methoxyisonicotinaldehyde,
3-((1H-indazol-4-yl)methoxy)-6-methylpicolinaldehyde,
6-methoxy-3-((1-methyl-1H-indazol-6-yl)methoxy)picolinaldehyde,
2-methoxy-5-((1-methyl-1H-indazol-7-yl)methoxy)isonicotinaldehyde,
6-methoxy-3-((1-methyl-1H-indazol-6-yl)methoxy)picolinaldehyde,
6-methyl-3-((1-methyl-1H-indazol-7-yl)methoxy)picolinaldehyde,
3-(isoquinolin-1-ylmethoxy)-6-methylpicolinaldehyde,
6-methyl-3-(quinolin-2-ylmethoxy)picolinaldehyde,
5-((4-(1H-pyrazol-4-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
5-((6-bromoimidazo[1,2-a]pyridin-8-yl)methoxy)-2-methoxyisonicotinaldehyd-
e,
8-((4-formyl-6-methoxypyridin-3-yloxy)methyl)imidazo[1,2-a]pyridine-6-c-
arbonitrile,
5-((4-formyl-6-methoxypyridin-3-yloxy)methyl)nicotinonitrile,
3-(benzo[d]oxazol-4-ylmethoxy)-6-methylpicolinaldehyde,
8-((4-formyl-6-methoxypyridin-3-yloxy)methyl)imidazo[1,2-a]pyridine-6-car-
boxamide,
5-((4-formyl-6-methoxypyridin-3-yloxy)methyl)nicotinamide,
5-((6-(1H-pyrazol-4-yl)imidazo[1,2-a]pyridin-8-yl)methoxy)-2-methoxyisoni-
cotinaldehyde,
5-(benzo[d]oxazol-4-ylmethoxy)-2-methoxyisonicotinaldehyde,
5-((6-(1H-pyrazol-5-yl)imidazo[1,2-a]pyridin-8-yl)methoxy)-2-methoxyisoni-
cotinaldehyde,
5-((1,5-naphthyridin-4-yl)methoxy)-2-methoxyisonicotinaldehyde,
3-((1,5-naphthyridin-4-yl)methoxy)-6-methylpicolinaldehyde,
5-((1H-indazol-5-yl)methoxy)-2-methoxyisonicotinaldehyde,
6-methyl-3-((1-methyl-1H-indazol-5-yl)methoxy)picolinaldehyde,
3-((3-chloro-1-methyl-1H-indazol-5-yl)methoxy)-6-methylpicolinaldehyde,
2-methoxy-5-((1-methyl-1H-indazol-5-yl)methoxy)isonicotinaldehyde,
5-((3-chloro-1-methyl-1H-indazol-5-yl)methoxy)-2-methoxyisonicotinaldehyd-
e,
N-(4-formyl-6-methoxypyridin-3-yl)imidazo[1,2-a]pyridine-8-carboxamide,
3-((1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-4-yl)methoxy)-6-methylpicolina-
ldehyde,
5-((1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-4-yl)methoxy)-2-methox-
yisonicotinaldehyde,
3-(4-formyl-6-methoxypyridin-3-yloxy)methyl)picolinamide,
5-((2-chloroquinolin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
5-((2-(1H-pyrazol-5-yl)quinolin-3-yl)methoxy)-2-methoxyisonicotinaldehyde-
, 2-methoxy-5-(quinoxalin-2-ylmethoxy)isonicotinaldehyde,
6-methyl-3-(quinolin-5-ylmethoxy)picolinaldehyde,
2-methoxy-5-(quinolin-5-ylmethoxy)isonicotinaldehyde,
6-methyl-3-((1-methyl-1H-pyrazolo[3,4-b]pyridin-5-yl)methoxy)picolinaldeh-
yde,
2-methoxy-5-((1-methyl-1H-pyrazolo[3,4-b]pyridin-5-yl)methoxy)isonico-
tinaldehyde,
5-((7-(1H-pyrazol-3-yl)imidazo[1,5-a]pyridin-8-yl)methoxy)-2-methoxyisoni-
cotinaldehyde,
5-((5-(2H-tetrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde-
,
5-((6-(2H-tetrazol-5-yl)imidazo[1,2-a]pyridin-8-yl)methoxy)-2-methoxyiso-
nicotinaldehyde, ethyl
2-(5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-methoxypyridin-4-yl)thiazolidi-
ne-4-carboxylate,
2-methoxy-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde,
5-((2-(1H-pyrazol-4-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotin-
aldehyde,
2-methoxy-5-((2-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)i-
sonicotinaldehyde,
2-methoxy-5-((2-(1-methyl-1H-pyrazol-3-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde,
5-((2-(2H-tetrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonicoti-
naldehyde,
2-methoxy-5-((2-(4-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-
isonicotinaldehyde,
5-((3-(1H-pyrazol-5-yl)isoquinolin-4-yl)methoxy)-2-methoxyisonicotinaldeh-
yde,
5-((2-(1H-pyrazol-1-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldeh-
yde,
3-((2-(1H-pyrazol-1-yl)pyridin-3-yl)methoxy)-6-methylpicolinaldehyde,
6-methyl-3-(pyridin-3-ylmethoxy)picolinaldehyde, methyl
8-(((4-formyl-6-methoxypyridin-3-yl)oxy)methyl)imidazo[1,2-a]pyridine-6-c-
arboxylate, methyl
2-bromo-8-(((4-formyl-6-methoxypyridin-3-yl)oxy)methyl)imidazo[1,2-a]pyri-
dine-6-carboxylate,
3-(imidazo[1,5-a]pyridin-8-ylmethoxy)-6-methylpicolinaldehyde,
5-(imidazo[1,5-a]pyridin-8-ylmethoxy)-2-methoxyisonicotinaldehyde,
(5-(methoxycarbonyl)pyridin-3-yl)methyl
5-(((4-formyl-6-methoxypyridin-3-yl)oxy)methyl)nicotinate,
5-((2-(1,4-dimethyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonic-
otinaldehyde,
5-((2-(1,5-dimethyl-1H-pyrazol-4-yl)pyridin-3-yl)methoxy)-2-methoxyisonic-
otinaldehyde, 2-hydroxyethyl
5-(((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yl)oxy)methyl)nicotinate,
methyl
5-(((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yl)oxy)methyl)nicoti-
nate, methyl
5-(((4-(bis(2-hydroxyethoxy)methyl)-6-methoxypyridin-3-yl)oxy)methyl)nico-
tinate,
5-((2-(1,3-dimethyl-1H-pyrazol-4-yl)pyridin-3-yl)methoxy)-2-methox-
yisonicotinaldehyde,
5-((2-(1,3-dimethyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonic-
otinaldehyde,
5-((2-(1-ethyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotina-
ldehyde,
5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methox-
yisonicotinaldehyde,
2-methoxy-5-((2-(3-methyl-1H-pyrazol-1-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde,
5-(((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yl)oxy)methyl)nico-
tinic acid,
(E)-2-methoxy-5-((2-(4-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonic-
otinaldehyde oxime,
(E)-2-methoxy-5-(pyridin-3-ylmethoxy)isonicotinaldehyde oxime,
2-(5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-methoxypyridin-4-yl)thiazolidi-
ne,
1-(2-(5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-methoxypyridin-4-yl)thia-
zolidin-3-yl)ethanone,
5-((2-(4-(1H-pyrazol-3-yl)piperazin-1-yl)pyridin-3-yl)methoxy)-2-methoxyi-
sonicotinaldehyde,
2-(difluoromethoxy)-5-(imidazo[1,2-a]pyridin-8-ylmethoxy)isonicotinaldehy-
de, 2-methoxy-5-((2-phenylpyridin-3-yl)methoxy)isonicotinaldehyde,
5-((3-(1-isopropyl-1H-pyrazol-5-yl)pyridin-4-yl)methoxy)-2-methoxyisonico-
tinaldehyde,
5-([2,3'-bipyridin]-3-ylmethoxy)-2-methoxyisonicotinaldehyde,
2-methoxy-5-((2-(o-tolyl)pyridin-3-yl)methoxy)isonicotinaldehyde,
2-methoxy-5-((2'-methoxy-[2,3'-bipyridin]-3-yl)methoxy)isonicotinaldehyde-
, methyl 4-(((2-formylpyridin-3-yl)oxy)methyl)benzoate,
4-(((2-formyl-6-methylpyridin-3-yl)oxy)methyl)benzoic acid,
4-(((2-formylpyridin-3-yl)oxy)methyl)benzoic acid, methyl
3-(((4-formylpyridin-3-yl)oxy)methyl)benzoate, methyl
3-(((2-formyl-6-methylpyridin-3-yl)oxy)methyl)benzoate,
3-(((4-formylpyridin-3-yl)oxy)methyl)benzoic acid,
3-(((2-formyl-6-methylpyridin-3-yl)oxy)methyl)benzoic acid,
3-(((2-formylpyridin-3-yl)oxy)methyl)benzoic acid,
2-methoxy-5-((2-(1-(2-methoxyethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-
isonicotinaldehyde,
2-methoxy-5-((2-(1-propyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde,
2-methoxy-5-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl)pyridi-
n-3-yl)methoxy)isonicotinaldehyde,
5-((2-(1-(2,2-difluoroethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-meth-
oxyisonicotinaldehyde,
3-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)picolinaldehyde,
3-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-6-methylpicolina-
ldehyde,
2-(difluoromethoxy)-5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3--
yl)methoxy)isonicotinaldehyde,
5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-(2-methoxyethoxyl)isonicotinaldeh-
yde,
5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-(2-methoxy-
ethoxy)isonicotinaldehyde,
5-((3-(1-isopropyl-1H-pyrazol-5-yl)pyrazin-2-yl)methoxy)-2-methoxyisonico-
tinaldehyde,
3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)picolinate,
5-((2-(2-hydroxypropan-2-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinalde-
hyde,
2-(2-methoxyethoxy)-5-((2-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)met-
hoxy)isonicotinaldehyde,
2-(2-methoxyethoxy)-5-((2-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-
nicotinaldehyde,
3-hydroxy-5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonico-
tinaldehyde, 3-(benzyloxy)-5-hydroxyisonicotinaldehyde,
3-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-5-methoxyisonico-
tinaldehyde,
5-((2-(2-isopropyl-2H-1,2,4-triazol-3-yl)pyridin-3-yl)methoxy)-2-methoxyi-
sonicotinaldehyde,
5-((2-(1-isopropyl-4-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-258
methoxyisonicotinaldehyde,
5-((2-(1-(2-hydroxyethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxy-
isonicotinaldehyde, 6-(((4-formylpyridin-3-yl)oxy)methyl)picolinic
acid, 2,2,2-trifluoroacetic
acid:6-(((4-formylpyridin-3-yl)oxy)methyl)picolinic acid (1:1),
2-methoxy-5-((2-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazol-5-yl)pyr-
idin-3-yl)methoxy)isonicotinaldehyde,
5-((2-(4-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-oxo-1,2-dihydropy-
ridine-4-carbaldehyde,
5-((2-(1-cyclobutyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonic-
otinaldehyde,
5-((2-(1-cyclohexyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonic-
otinaldehyde,
5-((2-(1-(cyclohexylmethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-metho-
xyisonicotinaldehyde,
5-((2-(1-cyclopentyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisoni-
cotinaldehyde,
2-(5-(3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)pyridin-2-yl)-1H-pyraz-
ol-1-yl)acetic acid, methyl
3-(5-(3-(((4-formyl-6-methoxypyridin-3-yl)oxy)methyl)pyridin-2-yl)-1H-pyr-
azol-1-yl)propanoate,
3-(3-(3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)pyridin-2-yl)-1H-pyraz-
ol-1-yl)propanoic acid,
3-(5-(3-(((4-formyl-6-methoxypyridin-3-yl)oxy)methyl)pyridin-2-yl)-1H-pyr-
azol-1-yl)propanoic acid,
3-(((4-formyl-6-methoxypyridin-3-yl)oxy)methyl)benzoic acid,
6-(((4-formylpyridin-3-yl)oxy)methyl)nicotinonitrile
2,2,2-trifluoroacetate,
6-(((4-formylpyridin-3-yl)oxy)methyl)nicotinic acid,
6-(((4-formylpyridin-3-yl)oxy)methyl)nicotinic acid hydrochloride,
6-(((4-formylpyridin-3-yl)oxy)methyl)-N-(methylsulfonyl)nicotinamide,
2,2,2-trifluoroacetic
acid:6-(((4-formylpyridin-3-yl)oxy)methyl)-N-(methylsulfonyl)nicotinamide
(2:1),
2-(2-methoxyethoxy)-5-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-y-
l)pyridin-3-yl)methoxy)isonicotinaldehyde,
2-methoxy-5-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyridin-3-yl)m-
ethoxy)isonicotinaldehyde,
2-(2-methoxyethoxy)-5-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyri-
din-3-yl)methoxy)isonicotinaldehyde,
2-methyl-5-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl)pyridin-3-yl)met-
hoxy)isonicotinaldehyde,
2-methyl-5-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyridin-3-yl)me-
thoxy)isonicotinaldehyde,
3-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)ison-
icotinaldehyde,
3-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)iso-
nicotinaldehyde,
3-chloro-5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonicot-
inaldehyde,
3-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-5-methylisonicot-
inaldehyde,
3-chloro-5-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyridin-3-yl)me-
thoxy)isonicotinaldehyde, and
3-methyl-5-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl)pyridin-3-yl)met-
hoxy)isonicotinaldehyde, or a tautomer or pharmaceutically
acceptable salt thereof.
23. The method of claim 22, wherein the compound is selected from
the group consisting of:
5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-methoxyisonicotinaldehyde,
2-methoxy-5-((5-methylpyridin-3-yl)methoxy)isonicotinaldehyde,
5-(isoquinolin-1-ylmethoxy)-2-methoxyisonicotinaldehyde,
2-methoxy-5-(quinolin-2-ylmethoxy)isonicotinaldehyde,
2-methoxy-5-(pyridin-4-ylmethoxy)isonicotinaldehyde,
3-(imidazo[1,2-a]pyridin-8-ylmethoxy)-6-methylpicolinaldehyde,
methyl
2-((4-formyl-6-methoxypyridin-3-yloxy)methyl)imidazo[1,2-a]pyridine-8-car-
boxylate,
2-methoxy-5-((3-methyl-[1,2,4]triazolo[4,3-a]pyridin-8-yl)methox-
y)isonicotinaldehyde,
5-((2-bromopyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
5-((2-(1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
5-((5-bromopyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
2-methoxy-5-((5-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde, 5-((4-formyl-6-methoxypyridin-3-yloxy)methyl)nicotinic
acid, 2-methoxy-5-(quinolin-3-ylmethoxy)isonicotinaldehyde,
2-methoxy-5-((1-methyl-1H-indazol-4-yl)methoxy)isonicotinaldehyde,
tert-butyl
4-((2-formyl-6-methylpyridin-3-yloxy)methyl)-1H-indazole-1-carboxylate,
6-methyl-3-((1-methyl-1H-indazol-6-yl)methoxy)picolinaldehyde,
6-methyl-3-((1-methyl-1H-indazol-7-yl)methoxy)picolinaldehyde,
3-(isoquinolin-1-ylmethoxy)-6-methylpicolinaldehyde,
5-(benzo[d]oxazol-4-ylmethoxy)-2-methoxyisonicotinaldehyde,
3-((1,5-naphthyridin-4-yl)methoxy)-6-methylpicolinaldehyde,
6-methyl-3-((1-methyl-1H-indazol-5-yl)methoxy)picolinaldehyde,
6-methyl-3-(quinolin-5-ylmethoxy)picolinaldehyde,
2-methoxy-5-(quinolin-5-ylmethoxy)isonicotinaldehyde,
2-methoxy-5-((2-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde,
2-methoxy-5-((2-(1-methyl-1H-pyrazol-3-yl)pyridin-3-yl)methoxy)i-
sonicotinaldehyde,
5-((2-(2H-tetrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde-
,
2-methoxy-5-((2-(4-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonicoti-
naldehyde,
5-((3-(1H-pyrazol-5-yl)isoquinolin-4-yl)methoxy)-2-methoxyisoni-
cotinaldehyde,
5-((2-(1H-pyrazol-1-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
5-(imidazo[1,5-a]pyridin-8-ylmethoxy)-2-methoxyisonicotinaldehyde,
5-((2-(1,5-dimethyl-1H-pyrazol-4-yl)pyridin-3-yl)methoxy)-2-methoxyisonic-
otinaldehyde,
5-((2-(1-ethyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotina-
ldehyde,
5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methox-
yisonicotinaldehyde,
2-(difluoromethoxy)-5-(imidazo[1,2-a]pyridin-8-ylmethoxy)isonicotinaldehy-
de, 2-methoxy-5-((2-phenylpyridin-3-yl)methoxy)isonicotinaldehyde,
5-((3-(1-isopropyl-1H-pyrazol-5-yl)pyridin-4-yl)methoxy)-2-methoxyisonico-
tinaldehyde,
5-([2,3'-bipyridin]-3-ylmethoxy)-2-methoxyisonicotinaldehyde,
2-methoxy-5-((2-(o-tolyl)pyridin-3-yl)methoxy)isonicotinaldehyde,
2-methoxy-5-((2'-methoxy-[2,3'-bipyridin]-3-yl)methoxy)isonicotinaldehyde-
, methyl 4-(((2-formylpyridin-3-yl)oxy)methyl)benzoate,
4-(((2-formyl-6-methylpyridin-3-yl)oxy)methyl)benzoic acid,
4-(((2-formylpyridin-3-yl)oxy)methyl)benzoic acid, methyl
3-(((4-formylpyridin-3-yl)oxy)methyl)benzoate, methyl
3-(((2-formyl-6-methylpyridin-3-yl)oxy)methyl)benzoate,
3-(((4-formylpyridin-3-yl)oxy)methyl)benzoic acid,
3-(((2-formyl-6-methylpyridin-3-yl)oxy)methyl)benzoic acid,
3-(((2-formylpyridin-3-yl)oxy)methyl)benzoic acid,
2-methoxy-5-((2-(1-(2-methoxyethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-
isonicotinaldehyde,
2-methoxy-5-((2-(1-propyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde,
2-methoxy-5-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl)pyridi-
n-3-yl)methoxy)isonicotinaldehyde,
5-((2-(1-(2,2-difluoroethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-meth-
oxyisonicotinaldehyde,
3-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)picolinaldehyde,
3-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-6-methylpicolina-
ldehyde,
2-(difluoromethoxy)-5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3--
yl)methoxy)isonicotinaldehyde,
5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-(2-methoxyethoxyl)isonicotinaldeh-
yde,
5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-(2-methoxy-
ethoxyl)isonicotinaldehyde,
5-((3-(1-isopropyl-1H-pyrazol-5-yl)pyrazin-2-yl)methoxy)-2-methoxyisonico-
tinaldehyde,
3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)picolinate,
5-((2-(2-hydroxypropan-2-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinalde-
hyde,
2-(2-methoxyethoxy)-5-((2-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)met-
hoxy)isonicotinaldehyde,
2-(2-methoxyethoxy)-5-((2-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-
nicotinaldehyde,
3-hydroxy-5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonico-
tinaldehyde, 3-(benzyloxy)-5-hydroxyisonicotinaldehyde,
3-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-5-methoxyisonico-
tinaldehyde,
5-((2-(2-isopropyl-2H-1,2,4-triazol-3-yl)pyridin-3-yl)methoxy)-2-methoxyi-
sonicotinaldehyde,
5-((2-(1-isopropyl-4-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-metho-
xyisonicotinaldehyde,
5-((2-(1-(2-hydroxyethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxy-
isonicotinaldehyde, 6-(((4-formylpyridin-3-yl)oxy)methyl)picolinic
acid 2,2,2-trifluoroacetic
acid:6-(((4-formylpyridin-3-yl)oxy)methyl)picolinic acid (1:1),
2-methoxy-5-((2-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazol-5-yl)pyr-
idin-3-yl)methoxy)isonicotinaldehyde,
5-((2-(4-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-oxo-1,2-dihydropy-
ridine-4-carbaldehyde,
5-((2-(1-cyclobutyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonic-
otinaldehyde,
5-((2-(1-cyclohexyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonic-
otinaldehyde,
5-((2-(1-(cyclohexylmethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-metho-
xyisonicotinaldehyde,
5-((2-(1-cyclopentyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisoni-
cotinaldehyde,
2-(5-(3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)pyridin-2-yl)-1H-pyraz-
ol-1-yl)acetic acid, methyl
3-(5-(3-(((4-formyl-6-methoxypyridin-3-yl)oxy)methyl)pyridin-2-yl)-1H-pyr-
azol-1-yl)propanoate,
3-(3-(3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)pyridin-2-yl)-1H-pyraz-
ol-1-yl)propanoic acid,
3-(5-(3-(((4-formyl-6-methoxypyridin-3-yl)oxy)methyl)pyridin-2-yl)-1H-pyr-
azol-1-yl)propanoic acid,
3-(((4-formyl-6-methoxypyridin-3-yl)oxy)methyl)benzoic acid,
6-(((4-formylpyridin-3-yl)oxy)methyl)nicotinonitrile
2,2,2-trifluoroacetate,
6-(((4-formylpyridin-3-yl)oxy)methyl)nicotinic acid,
6-(((4-formylpyridin-3-yl)oxy)methyl)nicotinic acid hydrochloride,
6-(((4-formylpyridin-3-yl)oxy)methyl)-N-(methylsulfonyl)nicotinamide,
2,2,2-trifluoroacetic
acid:6-(((4-formylpyridin-3-yl)oxy)methyl)-N-(methylsulfonyl)nicotinamide
(2:1),
2-(2-methoxyethoxy)-5-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-y-
l)pyridin-3-yl)methoxy)isonicotinaldehyde,
2-methoxy-5-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyridin-3-yl)m-
ethoxy)isonicotinaldehyde,
2-(2-methoxyethoxy)-5-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyri-
din-3-yl)methoxy)isonicotinaldehyde,
2-methyl-5-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl)pyridin-3-yl)met-
hoxy)isonicotinaldehyde,
2-methyl-5-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyridin-3-yl)me-
thoxy)isonicotinaldehyde,
3-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)ison-
icotinaldehyde,
3-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)iso-
nicotinaldehyde,
3-chloro-5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonicot-
inaldehyde,
3-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-5-methylisonicot-
inaldehyde,
3-chloro-5-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyridin-3-yl)me-
thoxy)isonicotinaldehyde, and
3-methyl-5-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl)pyridin-3-yl)met-
hoxy)isonicotinaldehyde, or a tautomer or pharmaceutically
acceptable salt thereof.
Description
REFERENCES TO RELATED APPLICATIONS
[0001] This application is a continuation of U.S. patent
application Ser. No. 13/730,730 filed Dec. 28, 2012, which claims
the benefit under 35 U.S.C. .sctn.119(e) to U.S. Provisional Patent
Application Nos. 61/661,327 filed Jun. 18, 2012 and 61/581,063
filed Dec. 28, 2011, the disclosures of which are hereby
incorporated by reference in their entireties for all purpose.
FIELD OF THE INVENTION
[0002] The present invention generally relates to substituted
heteroaryl aldehydes and derivatives thereof that act as allosteric
modulators of hemoglobin, methods and intermediates for their
preparation, pharmaceutical compositions comprising the modulators,
and methods for their use in treating disorders mediate by
hemoglobin and disorders that would benefit from increased tissue
oxygenation.
BACKGROUND OF THE INVENTION
[0003] Hemoglobin (Hb) is a tetrameric protein in red blood cells
that transports up to four oxygen molecules from the lungs to
various tissues and organs throughout the body. Hemoglobin binds
and releases oxygen through conformational changes, and is in the
tense (T) state when it is unbound to oxygen and in the relaxed (R)
state when it is bound to oxygen. The equilibrium between the two
conformational states is under allosteric regulation. Natural
compounds such as 2,3-bisphosphoglycerate (2,3-BPG), protons, and
carbon dioxide stabilize hemoglobin in its de-oxygenated T state,
while oxygen stabilizes hemoglobin in its oxygenated R state. Other
relaxed R states have also been found, however their role in
allosteric regulation has not been fully elucidated.
[0004] Sickle cell disease is a prevalent disease particularly
among those of African and Mediterranean descent. Sickle hemoglobin
(HbS) contains a point mutation where glutamic acid is replaced
with valine, allowing the T state to become susceptible to
polymerization to give the HbS containing red blood cells their
characteristic sickle shape. The sickled cells are also more rigid
than normal red blood cells, and their lack of flexibility can lead
to blockage of blood vessels. Certain synthetic aldehydes have been
found to shift the equilibrium from the polymer forming T state to
the non-polymer forming R state (Nnamani et al. Chemistry &
Biodiversity Vol. 5, 2008 pp. 1762-1769) by acting as allosteric
modulators to stabilize the R state through formation of a Schiff
base with an amino group on hemoglobin.
[0005] U.S. Pat. No. 7,160,910 discloses 2-furfuraldehydes and
related compounds that are also allosteric modulators of
hemoglobin. One particular compound
5-hydroxymethyl-2-furfuraldehyde (5HMF) was found to be a potent
hemoglobin modulator both in vitro and in vivo. Transgenic mice
producing human HbS that were treated with 5HMF were found to have
significantly improved survival times when exposed to extreme
hypoxia (5% oxygen). Under these hypoxic conditions, the 5HMF
treated mice were also found to have reduced amounts of
hypoxia-induced sickled red blood cells as compared to the
non-treated mice.
[0006] A need exists for therapeutics that can shift the
equilibrium between the deoxygenated and oxygenated states of Hb to
treat disorders that are mediated by Hb or by abnormal Hb such as
HbS. A need also exists for therapeutics to treat disorders that
would benefit from having Hb in the R state with an increased
affinity for oxygen. Such therapeutics would have applications
ranging, for example, from sensitizing hypoxic tumor cells that are
resistant to standard radiotherapy or chemotherapy due to the low
levels of oxygen in the cell, to treating pulmonary and
hypertensive disorders, and to promoting wound healing.
BRIEF SUMMARY OF THE INVENTION
[0007] The present invention provides, in one aspect, allosteric
modulators of hemoglobin. In another aspect, provided are
pharmaceutical compositions comprising the allosteric modulators
disclosed herein. In other aspects, provided are methods for
treating disorders mediated by hemoglobin and methods for
increasing tissue oxygenation for treating disorders that would
benefit from increased oxygenation, such methods comprising
administering the allosteric modulators disclosed herein to a
subject in need thereof. In still other aspects, provided are
methods for preparing the allosteric modulators disclosed herein.
These and other embodiments of the invention are more fully
described in the description that follows.
DETAILED DESCRIPTION OF THE INVENTION
I. Definitions
[0008] As used herein, the below terms have the following meanings
unless specified otherwise.
[0009] The abbreviations used herein are conventional, unless
otherwise defined: aq=aqueous; Boc=t-butylcarboxy,
(Boc).sub.2O=di-tert-butyl dicarbonate, .degree. C.=degrees
celcius, mCPBA=m-chloroperoxybenzoic acid, DCM=dichloromethane
(CH.sub.2Cl.sub.2), DIBAL=diisobutylaluminum hydride,
DIEA=diisopropylethyl amine; DMF=dimethyl formamide, EtOAc=ethyl
acetate, EtOH=ethanol, g=gram, H.sub.2=hydrogen; H.sub.2O=water;
HBr=hydrogen bromide; HCl=hydrogen chloride, HPLC=high pressure
liquid chromatography, h=hour, LAH=lithium aluminum hydride
(LiAlH.sub.4); MeCN=acetonitrile; LRMS=Low Resolution Mass Spectrum
MS=Mass Spectrum, m/z=mass to charge ratio, MHz=Mega Hertz,
MeOH=methanol, .mu.M=micromolar, .mu.L=microliter, mg=milligram,
mM=millimolar, mmol=millimole, mL=milliliter, min=minute, M=molar,
Na.sub.2CO.sub.3=sodium carbonate, ng=nanogram, N=Normal,
NMR=nuclear magnetic resonance, Pd/C=palladium on carbon,
rp=reverse phase, sat=saturated, rt=room temperature,
SEM=(2-(trimethylsilyl)ethoxy)methyl, TEA=triethylamine,
THF=tetrahydrofuran, TFA=trifluoroacetic acid, TLC=thin layer
chromatography, and TMS=trimethylsilyl.
[0010] It is noted here that as used in this specification and the
appended claims, the singular forms "a," "an," and "the" include
plural reference unless the context clearly dictates otherwise.
[0011] "Alkoxy" refers to --O(alkyl) where alkyl as defined herein.
Representative examples of alkoxy groups include methoxy, ethoxy,
t-butoxy, and the like.
[0012] "Alkyl," by itself or as part of another substituent, means,
unless otherwise stated, a straight or branched chain, fully
saturated aliphatic hydrocarbon radical having the number of carbon
atoms designated. For example, "C.sub.1-8alkyl" refers to a
hydrocarbon radical straight or branched, containing from 1 to 8
carbon atoms that is derived by the removal of one hydrogen atom
from a single carbon atom of a parent alkane. Alkyl includes
branched chain isomers of straight chain alkyl groups such as
isopropyl, t-butyl, isobutyl, sec-butyl, and the like.
Representative alkyl groups include straight and branched chain
alkyl groups having 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12 carbon
atoms. Further representative alkyl groups include straight and
branched chain alkyl groups having 1, 2, 3, 4, 5, 6, 7 or 8 carbon
atoms.
[0013] "Alkenyl" refers to a linear monovalent hydrocarbon radical
or a branched monovalent hydrocarbon radical having the number of
carbon atoms indicated in the prefix and containing at least one
double bond, but no more than three double bonds. For example,
C.sub.2-8alkenyl is meant to include, ethenyl, propenyl,
1,3-butadienyl and the like.
[0014] "Alkynyl" means a linear monovalent hydrocarbon radical or a
branched monovalent hydrocarbon radical containing at least one
triple bond and having the number of carbon atoms indicated in the
prefix. The term "alkynyl" is also meant to include those alkyl
groups having one triple bond and one double bond. For example,
C.sub.2-8alkynyl is meant to include ethynyl, propynyl and the
like.
[0015] The term "allosteric modulators" refers to compounds that
bind to hemoglobin to modulate its affinity for oxygen. In one
group of embodiments, the allosteric modulators act to stabilize or
destabilize a particular hemoglobin conformation. In one group of
embodiments, the modulators stabilize the relaxed R state. In other
embodiments, the modulators destabilize the tense T state. In one
group of embodiments, the allosteric modulators can destabilize one
conformation while stabilizing another. In some such embodiments,
the modulators stabilize a relaxed R state and destabilize the
tense T state. The modulators, in addition to modulating the
affinity of hemoglobin for oxygen, may also confer additional
properties to hemoglobin such as increasing its solubility. The
present disclosure is not intended to be limited to the mechanism
by which the allosteric modulators interact with and regulate
hemoglobin. In one group of embodiments, the allosteric modulators
inhibit the polymerization of HbS and the sickling of red blood
cells. In one group of embodiments, the binding of the allosteric
modulators provided herein to hemoglobin can occur through covalent
or non-covalent interactions. In one embodiment, the allosteric
modulators react through its aldehyde substituent with an amine
group on a hemoglobin amino acid side chain to form a Schiff
base.
[0016] "Amino" refers to a monovalent radical --NH.sub.2.
[0017] "Aryl" by itself or as part of another substituent refers to
a polyunsaturated, aromatic, hydrocarbon group containing from 6 to
14 carbon atoms, which can be a single ring or multiple rings (up
to three rings) which are fused together or linked covalently. Thus
the phrase includes, but is not limited to, groups such as phenyl,
biphenyl, anthracenyl, naphthyl by way of example. Non-limiting
examples of aryl groups include phenyl, 1-naphthyl, 2-naphthyl and
4-biphenyl.
[0018] "Bond" when used as an element in a Markush group means that
the corresponding group does not exist, and the groups of both
sides are directly linked.
[0019] "Cycloalkyl" refers to a saturated or partially saturated
cyclic group of from 3 to 14 carbon atoms and no ring heteroatoms
and having a single ring or multiple rings including fused,
bridged, and spiro ring systems. The term "cycloalkyl" includes
cycloalkenyl groups, a partially saturated cycloalkyl ring having
at least one site of >C.dbd.C<ring unsaturation. Examples of
cycloalkyl groups include, for instance, adamantyl, cyclopropyl,
cyclobutyl, cyclopentyl, cyclooctyl, and cyclohexenyl. "C.sub.u'-v'
cycloalkyl" refers to cycloalkyl groups having u' to v' carbon
atoms as ring members. "C.sub.u'-v' cycloalkenyl" refers to
cycloalkenyl groups having u' to v' carbon atoms as ring
members.
[0020] The term "hemoglobin" as used herein refers to any
hemoglobin protein, including normal hemoglobin (Hb) and sickle
hemoglobin (HbS).
[0021] "Heteroaryl" refers to a cyclic or polycyclic radical having
at least one aromatic ring and from one to five ring heteroatom
selected from N, O, and S, and optionally one or more oxo (.dbd.O)
substituents attached to one or more carbon ring atoms, and wherein
the nitrogen and sulfur ring atoms are optionally oxidized. A
heteroaryl group can be attached to the remainder of the molecule
through a heteroatom or through a carbon atom and can contain 5 to
10 carbon atoms. Heteroaryl groups include polycyclic aromatic
ring(s) fused to non-aromatic cycloalkyl or heterocycloalkyl
groups, and where the point of attachment to the remainder of the
molecule can be through any suitable ring atom of any ring. In a
polycyclic heteroaryl group, the ring heteroatom(s) can be in
either an aromatic or non-aromatic ring or both. The term "aromatic
ring" include any ring having at least one planar resonance
structure where 2n+2 pi electrons are delocalized about the ring.
Examples of heteroaryl groups include, but are not limited to,
imidazopyridinyl groups, pyrrolopyridinyl groups, pyrazolopyridinyl
groups, triazolopyridinyl groups, pyrazolopyrazinyl groups,
pyridinyl groups, pyrazinyl groups, oxazolyl groups, imidazolyl
groups, triazolyl groups, tetrazolyl groups, pyrazolyl groups,
quinolinyl groups, isoquinolinyl groups, indazolyl groups,
benzooxazolyl groups, naphthyridinyl groups, and quinoxalinyl
groups. Other non-limiting examples of heteroaryl groups include
xanthine, hypoxanthine, 5-benzothiazolyl, purinyl,
2-benzimidazolyl, benzopyrazolyl, 5-indolyl, azaindole,
1-isoquinolyl, 5-isoquinolyl, 2-quinoxalinyl, 5-quinoxalinyl,
3-quinolyl, 6-quinolyl 1-pyrrolyl, 2-pyrrolyl, 3-pyrrolyl,
1-pyrazolyl, 3-pyrazolyl, 2-imidazolyl, 4-imidazolyl, pyrazinyl,
2-oxazolyl, 4-oxazolyl, 5-oxazolyl, 3-isoxazolyl, 4-isoxazolyl,
5-isoxazolyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, 2-furyl,
3-furyl, 2-thienyl, 3-thienyl, 2-pyridyl, 3-pyridyl, 4-pyridyl,
2-pyrimidyl and 4-pyrimidyl. "Bicyclic heteroaryl" refers to a
heteroaryl radical that contains two rings.
[0022] The term "heterocycloalkyl" refers to a cycloalkyl group
containing at least one ring heteroatom and optionally one or more
oxo substituents. As used herein, the term "heteroatom" is meant to
include oxygen (O), nitrogen (N), and sulfur (S), wherein the
heteroatoms are optionally oxidized, and the nitrogen atom(s) are
optionally quaternized. Each heterocycle can be attached at any
available ring carbon or heteroatom. Each heterocycle may have one
or more rings. When multiple rings are present, they can be fused
together. Each heterocycle typically contains 1, 2, 3, 4 or 5,
independently selected heteroatoms. Preferably, these groups
contain 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 carbon atoms, 0, 1, 2, 3, 4
or 5 nitrogen atoms, 0, 1 or 2 sulfur atoms and 0, 1 or 2 oxygen
atoms. More preferably, these groups contain 1, 2 or 3 nitrogen
atoms, 0-1 sulfur atoms and 0-1 oxygen atoms. Non-limiting examples
of heterocycle groups include morpholin-3-one, piperazine-2-one,
piperazin-1-oxide, piperidine, morpholine, piperazine, isoxazoline,
pyrazoline, imidazoline, pyrrolidine, and the like.
[0023] "Halo" or "halogen" by themselves or as part of another
substituent, mean, unless otherwise stated, a fluorine, chlorine,
bromine, or iodine atom. Additionally, terms such as "haloalkyl",
are meant to include alkyl in which one or more hydrogen is
substituted with halogen atoms which can be the same or different,
in a number ranging from one up to the maximum number of halogens
permitted e.g. for alkyl, (2m'+1), where m' is the total number of
carbon atoms in the alkyl group. For example, the term
"haloC.sub.1-8alkyl" is meant to include difluoromethyl,
trifluoromethyl, 2,2,2-trifluoroethyl, 4-chlorobutyl,
3-bromopropyl, and the like. The term "haloalkenyl", and
"haloalkynyl" refers to alkenyl and alkynyl radicals having one or
more halogen atoms. Additionally, term "haloalkoxy" refers to an
alkoxy radical substituted with one or more halogen atoms. In one
group of embodiments, the haloalkyl, haloalkenyl, haloalkynyl, and
haloalkoxy groups have from one to 5 or from one to 3 halo atoms.
Examples of haloalkoxy groups include difluoromethoxy and
trifluoromethoxy. In one group of embodiments, the halo atoms of
the haloalkenyl and haloalkynyl groups are attached to the
aliphatic portions of these groups.
[0024] The terms "optional" or "optionally" as used throughout the
specification means that the subsequently described event or
circumstance may but need not occur, and that the description
includes instances where the event or circumstance occurs and
instances in which it does not. For example, "heteroaryl group
optionally substituted with an alkyl group means that the alkyl may
but need not be present, and the description includes situations
where the heteroaryl group is substituted with an alkyl group and
situations where the heteroaryl group is not substituted with the
alkyl group.
[0025] "Oxo" refers to the divalent atom .dbd.O.
[0026] In each of the above embodiments designating a number of
atoms e.g. "C.sub.1-8" is meant to include all possible embodiments
that have one fewer atom. Non-limiting examples include C.sub.1-4,
C.sub.1-5, C.sub.1-6, C.sub.1-7, C.sub.2-8, C.sub.2-7, C.sub.3-8,
C.sub.3-7 and the like.
[0027] The term "pharmaceutically acceptable salts" is meant to
include salts of the active compounds which are prepared with
relatively nontoxic acids or bases, depending on the particular
substituents found on the compounds described herein. When
compounds of the present invention contain relatively acidic
functionalities, base addition salts can be obtained by contacting
the neutral form of such compounds with a sufficient amount of the
desired base, either neat or in a suitable inert solvent. Examples
of salts derived from pharmaceutically-acceptable inorganic bases
include aluminum, ammonium, calcium, copper, ferric, ferrous,
lithium, magnesium, manganic, manganous, potassium, sodium, zinc
and the like. Salts derived from pharmaceutically-acceptable
organic bases include salts of primary, secondary and tertiary
amines, including substituted amines, cyclic amines,
naturally-occurring amines and the like, such as arginine, betaine,
caffeine, choline, N,N'-dibenzylethylenediamine, diethylamine,
2-diethylaminoethanol, 2-dimethylaminoethanol, ethanolamine,
ethylenediamine, N-ethylmorpholine, N-ethylpiperidine, glucamine,
glucosamine, histidine, hydrabamine, isopropylamine, lysine,
methylglucamine, morpholine, piperazine, piperidine, polyamine
resins, procaine, purines, theobromine, triethylamine,
trimethylamine, tripropylamine, tromethamine and the like. When
compounds of the present invention contain relatively basic
functionalities, acid addition salts can be obtained by contacting
the neutral form of such compounds with a sufficient amount of the
desired acid, either neat or in a suitable inert solvent. Examples
of pharmaceutically acceptable acid addition salts include those
derived from inorganic acids like hydrochloric, hydrobromic,
nitric, carbonic, monohydrogencarbonic, phosphoric,
monohydrogenphosphoric, dihydrogenphosphoric, sulfuric,
monohydrogensulfuric, hydriodic, or phosphorous acids and the like,
as well as the salts derived from relatively nontoxic organic acids
like acetic, propionic, isobutyric, malonic, benzoic, succinic,
suberic, fumaric, mandelic, phthalic, benzenesulfonic,
p-tolylsulfonic, citric, tartaric, methanesulfonic, and the like.
Also included are salts of amino acids such as arginate and the
like, and salts of organic acids like glucuronic or galactunoric
acids and the like (see, e.g., Berge, S. M. et al., "Pharmaceutical
Salts," Journal of Pharmaceutical Science, 66:1-19, 1977). Certain
specific compounds of the present invention contain both basic and
acidic functionalities that allow the compounds to be converted
into either base or acid addition salts.
[0028] The neutral forms of the compounds may be regenerated by
contacting the salt with a base or acid and isolating the parent
compound in the conventional manner. The parent form of the
compound differs from the various salt forms in certain physical
properties, such as solubility in polar solvents, but otherwise the
salts are equivalent to the parent form of the compound for the
purposes of the present invention.
[0029] The term "pharmaceutically acceptable carrier or excipient"
means a carrier or excipient that is useful in preparing a
pharmaceutical composition that is generally safe, non-toxic and
neither biologically nor otherwise undesirable, and includes a
carrier or excipient that is acceptable for veterinary use as well
as human pharmaceutical use. A "pharmaceutically acceptable carrier
or excipient" as used in the specification and claims includes both
one and more than one such carrier or excipient.
[0030] The terms "pharmaceutically effective amount",
"therapeutically effective amount" or "therapeutically effective
dose" refers to the amount of the subject compound that will elicit
the biological or medical response of a tissue, system, animal or
human that is being sought by the researcher, veterinarian, medical
doctor or other clinician. The term "therapeutically effective
amount" includes that amount of a compound that, when administered,
is sufficient to prevent development of, or alleviate to some
extent, one or more of the symptoms of the condition or disorder
being treated. The therapeutically effective amount will vary
depending on the compound, the disorder or condition and its
severity and the age, weight, etc., of the mammal to be
treated.
[0031] "Protecting group" refers to a group of atoms that, when
attached to a reactive functional group in a molecule, mask, reduce
or prevent the reactivity of the functional group. Typically, a
protecting group may be selectively removed as desired during the
course of a synthesis. Examples of protecting groups can be found
in Greene and Wuts, Protective Groups in Organic Chemistry,
3.sup.rd Ed., 1999, John Wiley & Sons, NY and Harrison et al.,
Compendium of Synthetic Organic Methods, Vols. 1-8, 1971-1996, John
Wiley & Sons, NY. Representative amino protecting groups
include, but are not limited to, formyl, acetyl, trifluoroacetyl,
benzyl, benzyloxycarbonyl ("CBZ"), tert-butoxycarbonyl ("Boc"),
trimethylsilyl ("TMS"), 2-trimethylsilyl-ethanesulfonyl ("TES"),
trityl and substituted trityl groups, allyloxycarbonyl,
9-fluorenylmethyloxycarbonyl ("FMOC"), nitro-veratryloxycarbonyl
("NVOC") and the like. Representative hydroxy protecting groups
include, but are not limited to, those where the hydroxy group is
either acylated or alkylated such as benzyl and trityl ethers, as
well as alkyl ethers, tetrahydropyranyl ethers, trialkylsilyl
ethers (e.g., TMS or TIPPS groups) and allyl ethers.
[0032] The term "aldehyde protecting group" refers to any known
protecting group used to mask the aldehyde functionality. Aldehyde
protecting groups include acetals and hemiacetals. The acetals and
hemiacetals can be prepared from C.sub.1-8 alcohols or C.sub.2-8
diols. In one group of embodiments, the aldehyde protecting group
is a five or six membered cyclic acetal formed from condensation of
the aldehyde with ethylene or propylene glycol. In another group of
embodiments the aldehyde protecting group is an imine or
hydroxyimine. The aldehyde protecting groups of the present
disclosure also include prodrug groups that convert the aldehyde to
a prodrug, where the aldehyde is formed in vivo as the active agent
under physiological conditions upon administration of the prodrug.
The prodrug group can also serve to increase the bioavailability of
the aldehyde. In one group of embodiments, the prodrug group is
hydrolyzed in vivo to the aldehyde. In one group of embodiments,
the aldehyde protecting group is a thiazolidine or
N-acetylthiazolidine prodrug group. In one group of embodiments,
the aldehyde protecting group is a thiazolidine prodrug group
disclosed in U.S. Pat. No. 6,355,661. In one group of embodiments
the modulators provided herein are condensed with L-cysteine or a
L-cysteine derivative to form the corresponding thiazolidine
protected aldehyde prodrug. In one group of embodiments, the
thiazolidine has the formula
##STR00001##
wherein R.sup.11 is selected from the group consisting of OH,
alkoxy, substituted alkoxy, cycloalkoxy, substituted cycloalkoxy,
aryloxy, substituted aryloxy, heteroaryloxy, substituted
heteroaryloxy, N(R.sup.13).sub.2 where R.sup.13 is independently H,
alkyl, substituted alkyl, alkenyl, substituted alkenyl, aryl,
substituted aryl, heteroaryl, and substituted heteroaryl; R.sup.12
is H or -L-R.sup.14, where L is carbonyl or sulfonyl; R.sup.14 is
selected from the group consisting of alkyl, substituted alkyl,
aryl, substituted aryl, heteroaryl, and substituted heteroaryl; the
wavy line signifies the point of attachment to the phenyl ring of
the allosteric modulators disclosed herein; and the term
"substituted" refers to substitution by one or more substituents
selected from the group consisting of COOH, CHO, oxyacyl, acyloxy,
cycloacyloxy, phenol, phenoxy, pyridinyl, pyrrolidinyl, amino,
amido, hydroxy, alkoxy, cycloalkoxy, F, Cl, Br, NO.sub.2, cyano,
sulfuryl, and the like. In one group of embodiments, provided are
modulators having a thiazolidine protecting group where R.sup.11 is
alkoxy and R.sup.12 is H, or where R.sup.11 is OH and R.sup.12 is
--C(O)alkyl, or where R.sup.11 is NH (heteroaryl) and R.sup.12 is
--C(O)alkyl.
[0033] The term "sickle cell disease" refers to diseases mediated
by sickle hemoglobin (HbS) that results from a single point
mutation in the hemoglobin (Hb). Sickle cell diseases includes
sickle cell anemia, sickle-hemoglobin C disease (HbSC), sickle
beta-plus-thalassaemia (HbS/.beta..sup.+) and sickle
beta-zero-thalassaemia)(HbS/.beta..sup.0).
[0034] The "subject" is defined herein to include animals such as
mammals, including, but not limited to, primates (e.g., humans),
cows, sheep, goats, horses, dogs, cats, rabbits, rats, mice and the
like. In preferred embodiments, the subject is a human.
[0035] "Tautomer" refers to alternate forms of a molecule that
differ in the position of a proton, such as enol-keto and
imine-enamine tautomers, or the tautomeric forms of heteroaryl
groups containing a --N.dbd.C(H)--NH-- ring atom arrangement, such
as pyrazoles, imidazoles, benzimidazoles, triazoles, and
tetrazoles. A person of ordinary skill in the art would recognize
that other tautomeric ring atom arrangements are possible.
[0036] The terms "treat", "treating", "treatment" and grammatical
variations thereof as used herein, includes partially or completely
delaying, alleviating, mitigating or reducing the intensity,
progression, or worsening of one or more attendant symptoms of a
disorder or condition and/or alleviating, mitigating or impeding
one or more causes of a disorder or condition. Treatments according
to the invention may be applied preventively, prophylactically,
pallatively or remedially.
[0037] The symbol > when used in connection with a substituent
signifies that the substituent is a divalent substituent attached
to two different atoms through a single atom on the
substituent.
[0038] The term "wavy line" signifies the point of attachment of
the substituent to the remainder of the molecule. When the wavy
line is not depicted as being specifically appended to a specific
ring atom, the point of attachment can be to any suitable atom of
the substituent. For example, the wavy line in the following
structure:
##STR00002##
is intended to include, as the point of attachment, any of the six
substitutable carbon atoms.
[0039] Compounds that have the same molecular formula but differ in
the nature or sequence of bonding of their atoms or the arrangement
of their atoms in space are termed "isomers". Isomers that differ
in the arrangement of their atoms in space are termed
"stereoisomers". "Stereoisomer" and "stereoisomers" refer to
compounds that exist in different stereoisomeric forms if they
possess one or more asymmetric centers or a double bond with
asymmetric substitution and, therefore, can be produced as
individual stereoisomers or as mixtures. Stereoisomers include
enantiomers and diastereomers. Stereoisomers that are not mirror
images of one another are termed "diastereomers" and those that are
non-superimposable mirror images of each other are termed
"enantiomers". When a compound has an asymmetric center, for
example, it is bonded to four different groups, a pair of
enantiomers is possible. An enantiomer can be characterized by the
absolute configuration of its asymmetric center and is described by
the R- and S-sequencing rules of Cahn and Prelog, or by the manner
in which the molecule rotates the plane of polarized light and
designated as dextrorotatory or levorotatory (i.e., as (+) or
(-)-isomers respectively). A chiral compound can exist as either
individual enantiomer or as a mixture thereof. A mixture containing
equal proportions of the enantiomers is called a "racemic mixture".
Unless otherwise indicated, the description is intended to include
individual stereoisomers as well as mixtures. The methods for the
determination of stereochemistry and the separation of
stereoisomers are well-known in the art (see discussion in Chapter
4 of ADVANCED ORGANIC CHEMISTRY, 4th edition J. March, John Wiley
and Sons, New York, 1992) differ in the chirality of one or more
stereocenters.
[0040] The compounds of the present invention may also contain
unnatural proportions of atomic isotopes at one or more of the
atoms that constitute such compounds. For example, the compounds
may be radiolabeled with isotopes, such as for example deuterium
(.sup.2H), tritium (.sup.3H), iodine-125 (.sup.125I) or carbon-14
(.sup.14C). All isotopic variations of the compounds of the present
invention, whether radioactive or not, are intended to be
encompassed within the scope of the present invention.
[0041] Unless indicated otherwise, the nomenclature of substituents
that are not explicitly defined herein are arrived at by naming the
terminal portion of the functionality followed by the adjacent
functionality toward the point of attachment. For example, the
substituent "alkoxyalkyl" refers to an akyl group that is
substituted with alkoxy and "hydoxyalkyl" refers to an akyl group
that is substituted with hydroxy. For both of these substituents,
the point of attachment is at the alkyl group.
[0042] It is understood that the definitions and formulas provided
herein are not intended to include impermissible substitution
patterns (e.g., methyl substituted with 5 fluoro groups). Such
impermissible substitution patterns are well known to the skilled
artisan.
II. Hemoglobin Modulators
[0043] In one group of embodiments, provided is a compound of
Formula (I):
##STR00003##
or a tautomer or pharmaceutically acceptable salt thereof,
[0044] wherein Q is selected from the group consisting of aryl,
heteroaryl, and heterocycloalkyl, each optionally substituted with
one to three R.sup.a; [0045] Y is O or CR.sup.1aR.sup.1b, where
R.sup.1a is H or halo and R.sup.1b is selected from the group
consisting of H, halo, and OH;
[0046] X is selected from the group consisting of 0,
>CH(CH.sub.2).sub.nR.sup.8, and C(R.sup.9).sub.2 where n is 0 or
1, R.sup.8 is OH, and R.sup.9 is independently H or halo; or Y--X
taken together is --NHC(O)-- or --C(O)NH--;
[0047] R.sup.2, R.sup.3, R.sup.4, and R.sup.5 are independently
absent or selected from the group consisting of hydrogen, halo,
R.sup.b, OR.sup.d, O(CH.sub.2).sub.zOR.sup.d,
O(CH.sub.2).sub.zNR.sup.dR.sup.d, OC(O)R.sup.e, SR.sup.d, CN,
NO.sub.2, CO.sub.2R.sup.d, CONR.sup.dR.sup.d, C(O)R.sup.d,
OC(O)NR.sup.dR.sup.d, NR.sup.dR.sup.d, NR.sup.dC(O)R.sup.e,
NR.sup.dC(O).sub.2R.sup.e, NR.sup.dC(O)NR.sup.dR.sup.d,
S(O)R.sup.e, S(O).sub.2R.sup.e, NR.sup.dS(O).sub.2R.sup.e,
S(O).sub.2NR.sup.dR.sup.d, and N.sub.3 where z is 0, 1, 2, or 3; or
R.sup.5 is --(CH.sub.2).sub.pR.sup.5a where p is 0 or 1 and
R.sup.5a is OH;
[0048] R.sup.6 and R.sup.7 together form oxo or an aldehyde
protecting group, or R.sup.6 together with R.sup.1b, R.sup.8, or
R.sup.5 forms a cyclic ether where one of R.sup.1b, R.sup.8, or
R.sup.5a is O, R.sup.6 is a bond, and R.sup.7 is selected from the
group consisting of OH, C.sub.1-8alkoxy, and
haloC.sub.1-8alkoxy;
[0049] T.sup.1, T.sup.2, T.sup.3, and T.sup.4 are independently C
or N provided that at least one of T.sup.1, T.sup.2, T.sup.3, and
T.sup.4 is N and at least one of T.sup.1, T.sup.2, T.sup.3, and
T.sup.4 is C;
[0050] each R.sup.a is independently selected from the group
consisting of halo, R.sup.b, OR.sup.d, O(CH.sub.2).sub.u--OR.sup.d,
O(CH.sub.2).sub.uNR.sup.dR.sup.d,
O(CH.sub.2).sub.uNR.sup.dC(O)R.sup.e,
O(CH.sub.2).sub.uNR.sup.dC(O).sub.2R.sup.e,
O(CH.sub.2).sub.uNR.sup.dS(O).sub.2R.sup.e, NH.sub.2,
--(CH.sub.2).sub.kOC(O)R.sup.e, --(CH.sub.2).sub.kSR.sup.d, CN,
NO.sub.2, --(CH.sub.2).sub.kCO.sub.2(C.sub.1-8alkyl)OH,
--(CH.sub.2).sub.kCO.sub.2(C.sub.1-8alkyl)(heteroaryl)C(O)(C.sub.1-8alkyl-
), --(CH.sub.2).sub.kCO.sub.2R.sup.d,
--(CH.sub.2).sub.kCONR.sup.dR.sup.d,
--(CH.sub.2).sub.kNR.sup.dC(O)R.sup.e,
--(CH.sub.2).sub.kNR.sup.dC(O).sub.2R.sup.e,
--(CH.sub.2).sub.kC(O)R.sup.d,
--(CH.sub.2).sub.kOC(O)NR.sup.dR.sup.d,
--NR.sup.d(CH.sub.2).sub.uOR.sup.d,
--NR.sup.d(CH.sub.2).sub.uNR.sup.dR.sup.d,
--NR.sup.d(CH.sub.2).sub.uNR.sup.dC(O)R.sup.e,
--NR.sup.d(CH.sub.2).sub.uNR.sup.dC(O).sub.2R.sup.e,
--NR.sup.d(CH.sub.2).sub.uNR.sup.dS(O).sub.2R.sup.e,
--(CH.sub.2).sub.kNR.sup.dC(O)R.sup.e,
--(CH.sub.2).sub.kNR.sup.dC(O).sub.2R.sup.d,
--(CH.sub.2).sub.kNR.sup.dC(O)NR.sup.dR.sup.d,
--(CH.sub.2).sub.kS(O)R.sup.e, --(CH.sub.2).sub.kS(O).sub.2R.sup.e,
--(CH.sub.2).sub.kNR.sup.dS(O).sub.2R.sup.e,
--C(O)(CH.sub.2).sub.kNR.sup.dS(O).sub.2R.sup.e,
--(CH.sub.2).sub.kC(O)NR.sup.dS(O).sub.2R.sup.e,
--(CH.sub.2).sub.kS(O).sub.2NR.sup.dR.sup.d, N.sub.3,
--(CH.sub.2).sub.karyl optionally substituted with one to three
R.sup.c, --NR.sup.d(CH.sub.2).sub.karyl optionally substituted with
one to three R.sup.c, --(CH.sub.2).sub.kheteroaryl optionally
substituted with one to three R.sup.c,
--NR.sup.d(CH.sub.2).sub.kheteroaryl optionally substituted with
one to three R.sup.c, --(CH.sub.2).sub.kheterocycloalkyl optionally
substituted with one to three R.sup.c, and
--NR.sup.d(CH.sub.2).sub.kheterocycloalkyl optionally substituted
with one to three R.sup.c where k is 0, 1, 2, 3, 4, 5, or 6 and u
is 1, 2, 3, 4, 5, or 6;
[0051] each R.sup.b is independently selected from the group
consisting of C.sub.1-8alkyl, C.sub.2-8alkenyl, and
C.sub.2-8alkynyl, each optionally independently substituted with
one to three halo, OR.sup.d, or NR.sup.dR.sup.d;
[0052] each R.sup.c is independently selected from the group
consisting of halo, C.sub.1-8alkyl, haloC.sub.1-8alkyl,
C.sub.2-8alkenyl, haloC.sub.2-8alkenyl, C.sub.2-8alkynyl,
haloC.sub.2-8alkynyl, (CH.sub.2).sub.mOR.sup.f, OC(O)R.sup.g,
SR.sup.f, CN, NO.sub.2, (CH.sub.2).sub.mCO.sub.2R.sup.f,
CONR.sup.fR.sup.f, C(O)R.sup.f, OC(O)NR.sup.fR.sup.f,
(CH.sub.2).sub.mNR.sup.fR.sup.f, NR.sup.fC(O)R.sup.g,
NR.sup.fC(O).sub.2R.sup.g, NR.sup.fC(O)NR.sup.fR.sup.f,
S(O)R.sup.g, S(O).sub.2R.sup.g, NR.sup.fS(O).sub.2R.sup.g,
S(O).sub.2NR.sup.fR.sup.f, N.sub.3,
(R.sup.f).sub.mSiC.sub.1-8alkyl, heteroaryl optionally substituted
with one to three R.sup.h, cycloalkyl optionally substituted with
one to three R.sup.h, and heterocycloalkyl optionally substituted
with one to three R.sup.h where m is selected from the group
consisting of 0, 1, 2, 3, 4, 5, and 6;
[0053] each R.sup.h is independently selected from the group
consisting of halo, C.sub.1-8alkyl, haloC.sub.1-8alkyl, OR.sup.j,
OC(O)R, SR.sup.j, NO.sub.2, CONR.sup.jR.sup.j, C(O)R.sup.j,
OC(O)NR.sup.jR.sup.j, NR.sup.jR.sup.j, NR.sup.jC(O)R.sup.t,
NR.sup.jC(O).sub.2R.sup.t, NR.sup.jC(O)NR.sup.jR.sup.j,
S(O)R.sup.t, S(O).sub.2R.sup.t, NR.sup.jS(O).sub.2R.sup.t, and
S(O).sub.2NR.sup.jR.sup.j;
[0054] R.sup.d, R.sup.f, and R.sup.j are each independently
selected from the group consisting of hydrogen, C.sub.1-8 alkyl,
haloC.sub.1-8alkyl, C.sub.2-8 alkenyl, haloC.sub.2-8alkenyl,
C.sub.2-8 alkynyl, and haloC.sub.2-8alkynyl; and
[0055] R.sup.e, R.sup.g, and R.sup.t are each independently
selected from the group consisting of C.sub.1-8alkyl,
haloC.sub.1-8alkyl, C.sub.2-8 alkenyl, haloC.sub.2-8alkenyl,
C.sub.2-8 alkynyl, and haloC.sub.2-8alkynyl.
[0056] In one group of embodiments, X and Y are not both O.
[0057] In one group of embodiments, when X is O, R.sup.1b is not
OH.
[0058] In one group of embodiments, when Y is O, and n is 0,
R.sup.8 is not OH.
[0059] In one group of embodiments, z is 0. In another group of
embodiments, z is 1. In yet another group of embodiments, z is 2.
In still another group of embodiments, z is 3.
[0060] In one group of embodiments, when R.sup.6 and R.sup.7
together are oxo, Y is CH.sub.2, X is O or CH.sub.2, and R.sup.5 is
H, halo, OH, CHO, or OCH.sub.3, then Q is V or W.
[0061] In one group of embodiments, the compound is not
##STR00004## ##STR00005##
[0062] In one group of embodiments, provided is a compound of
Formula (Ia):
##STR00006##
or a tautomer or pharmaceutically acceptable salt thereof,
[0063] wherein Q is selected from the group consisting of aryl,
heteroaryl, and heterocycloalkyl, each optionally substituted with
one to three R.sup.a;
[0064] Y is O or CR.sup.1aR.sup.1b, where R.sup.1a is H or halo and
R.sup.1b is selected from the group consisting of H, halo, and
OH;
[0065] X is selected from the group consisting of O,
>CH(CH.sub.2).sub.nR.sup.8, and C(R.sup.9).sub.2 where n is 0 or
1, R.sup.8 is OH, and R.sup.9 is independently H or halo; or Y--X
taken together is --NHC(O)-- or --C(O)NH--;
[0066] R.sup.2, R.sup.3, R.sup.4, and R.sup.5 are independently
absent or selected from the group consisting of hydrogen, halo,
R.sup.b, OR.sup.d, OC(O)R.sup.e, SR.sup.d, CN, NO.sub.2,
CO.sub.2R.sup.d, CONR.sup.dR.sup.d, C(O)R.sup.d,
OC(O)NR.sup.dR.sup.d, NR.sup.dR.sup.d, NR.sup.dC(O)R.sup.e,
NR.sup.dC(O).sub.2R.sup.e, NR.sup.dC(O)NR.sup.dR.sup.d,
S(O)R.sup.e, S(O).sub.2R.sup.e, NR.sup.dS(O).sub.2R.sup.e,
S(O).sub.2NR.sup.dR.sup.d, and N.sub.3; or R.sup.5 is
--(CH.sub.2).sub.pR.sup.5a where p is 0 or 1 and R.sup.5a is
OH;
[0067] R.sup.6 and R.sup.7 together form oxo or an aldehyde
protecting group, or R.sup.6 together with R.sup.1b, R.sup.8, or
R.sup.5 forms a cyclic ether where one of R.sup.1b, R.sup.8, or
R.sup.5a is O, R.sup.6 is a bond, and R.sup.7 is selected from the
group consisting of OH, C.sub.1-8alkoxy, and
haloC.sub.1-8alkoxy;
[0068] T.sup.1, T.sup.2, T.sup.3, and T.sup.4 are independently C
or N provided that at least one of T.sup.1, T.sup.2, T.sup.3, and
T.sup.4 is N and at least one of T.sup.1, T.sup.2, T.sup.3, and
T.sup.4 is C;
[0069] each R.sup.a is independently selected from the group
consisting of halo, R.sup.b, OR.sup.d, OC(O)R.sup.e, SR.sup.d, CN,
NO.sub.2, CO.sub.2R.sup.d, CONR.sup.dR.sup.d, C(O)R.sup.d,
OC(O)NR.sup.dR.sup.d, NR.sup.dC(O)R.sup.e,
NR.sup.dC(O).sub.2R.sup.d, NR.sup.dC(O)NR.sup.dR.sup.d,
S(O)R.sup.e, S(O).sub.2R.sup.e, NR.sup.dS(O).sub.2R.sup.e,
S(O).sub.2NR.sup.dR.sup.d, N.sub.3, aryl optionally substituted
with one to three R.sup.c, heteroaryl optionally substituted with
one to three R.sup.c, and heterocycloalkyl optionally substituted
with one to three R.sup.c;
[0070] each R.sup.b is independently selected from the group
consisting of C.sub.1-8alkyl, C.sub.2-8alkenyl, and
C.sub.2-8alkynyl, each optionally independently substituted with
one to three halo, OR.sup.d, or NR.sup.dR.sup.d;
[0071] each R.sup.c is independently selected from the group
consisting of halo, C.sub.1-8alkyl, haloC.sub.1-8alkyl,
C.sub.2-8alkenyl, haloC.sub.2-8alkenyl, C.sub.2-8alkynyl,
haloC.sub.2-8alkynyl, (CH.sub.2).sub.mOR.sup.f, OC(O)R.sup.g,
SR.sup.f, CN, NO.sub.2, CO.sub.2R.sup.f, CONR.sup.fR.sup.f,
C(O)R.sup.f, OC(O)NR.sup.fR.sup.f, (CH.sub.2).sub.mNR.sup.fR.sup.f,
NR.sup.fC(O)R.sup.g, NR.sup.fC(O).sub.2R.sup.g,
NR.sup.fC(O)NR.sup.fR.sup.f, S(O)R.sup.g, S(O).sub.2R.sup.g,
NR.sup.fS(O).sub.2R.sup.g, S(O).sub.2NR.sup.fR.sup.f, and N.sub.3
where m is selected from the group consisting of 0, 1, 2, 3, 4, 5,
and 6;
[0072] each R.sup.d and R.sup.f is independently selected from the
group consisting of hydrogen, C.sub.1-8alkyl, haloC.sub.1-8alkyl,
C.sub.2-8alkenyl, haloC.sub.2-8alkenyl, C.sub.2-8alkynyl, and
haloC.sub.2-8alkynyl; and
[0073] each R.sup.e and R.sup.g is independently selected from the
group consisting of C.sub.1-8alkyl, haloC.sub.1-8alkyl, C.sub.2-8
alkenyl, haloC.sub.2-8alkenyl, C.sub.2-8 alkynyl, and
haloC.sub.2-8alkynyl;
[0074] provided that X and Y are not both O;
[0075] provided that when X is O, R.sup.1b is not OH;
[0076] provided that when Y is O, and n is 0, R.sup.8 is not
OH.
[0077] In one group of embodiments, the compound is not:
##STR00007## ##STR00008##
[0078] In one group of embodiments, provided is a compound having
Formula (Ia)
##STR00009##
or a tautomer or pharmaceutically acceptable salt thereof.
[0079] In one group of embodiments, provided is a compound having
Formula (Ib):
##STR00010##
or a tautomer or pharmaceutically acceptable salt thereof.
[0080] In one group of embodiments, provided is a compound having
Formula (Ic):
##STR00011##
or a tautomer or pharmaceutically acceptable salt thereof.
[0081] In one group of embodiments, provided is a compound having
Formula (Id):
##STR00012##
or a tautomer or pharmaceutically acceptable salt thereof.
[0082] In one group of embodiments, at least two of T.sup.1,
T.sup.2, T.sup.3, and T.sup.4 are N.
[0083] In one group of embodiments, provided is a compound having
Formula (Ie), (If), (Ig), or (Ih):
##STR00013##
or a tautomer or pharmaceutically acceptable salt thereof.
[0084] In one group of embodiments, provided is a compound having
Formula (If):
##STR00014##
or a tautomer or pharmaceutically acceptable salt thereof
[0085] In one group of embodiments, provided is a compound having
Formula (Ig):
##STR00015##
or a tautomer or pharmaceutically acceptable salt thereof.
[0086] In one group of embodiments, provided is a compound having
Formula (h):
##STR00016##
or a tautomer or pharmaceutically acceptable salt thereof.
[0087] In one group of embodiments, R.sup.6 and R.sup.7 together
form oxo.
[0088] In one group of embodiments, R.sup.6 and R.sup.7 together
form a thiazolidine.
[0089] In one group of embodiments, R.sup.6 together with R.sup.1b,
R.sup.8, or R.sup.5 forms a cyclic ether where one of R.sup.1b,
R.sup.8, or R.sup.5a is O, R.sup.6 is a bond, and R.sup.7 is
selected from the group consisting of OH, C.sub.1-8alkoxy, and
haloC.sub.1-8alkoxy.
[0090] In one group of embodiments, provided is a compound having
Formula (Ii):
##STR00017##
or a tautomer or pharmaceutically acceptable salt thereof, wherein
R.sup.10 is selected from the group consisting of H,
C.sub.1-8alkyl, and haloC.sub.1-8alkyl.
[0091] In one group of embodiments, provided is a compound having
Formula (Ij):
##STR00018##
or a tautomer or pharmaceutically acceptable salt thereof, wherein
R.sup.10 is selected from the group consisting of H,
C.sub.1-8alkyl, and haloC.sub.1-8alkyl.
[0092] In one group of embodiments, provided is a compound having
Formula (Ik):
##STR00019##
or a tautomer or pharmaceutically acceptable salt thereof, wherein
R.sup.10 is selected from the group consisting of H,
C.sub.1-8alkyl, and haloC.sub.1-8alkyl.
[0093] In one group of embodiments, provided is a compound having
Formula (II):
##STR00020##
or a tautomer or pharmaceutically acceptable salt thereof.
[0094] In one group of embodiments, provided is a compound having
Formula (Im):
##STR00021##
or a tautomer or pharmaceutically acceptable salt thereof.
[0095] In one group embodiments, at least one R.sup.a is heteroaryl
optionally substituted with one to three R.sup.c.
[0096] In one group of embodiments at least one R.sup.a is
heteroaryl attached to Q at the ring atom adjacent to ring atom
bearing Y.
[0097] In one group of embodiments at least one R.sup.a is
heteroaryl substituted with at least one C.sub.1-8alkyl. In one
group of embodiments at least one R.sup.a heteroaryl is substituted
with at least one methyl.
[0098] In one group of embodiments at least one R.sup.a is
pyrazolyl substituted with at least one C.sub.1-8alkyl. In one
group of embodiments at least one R.sup.a is pyrazoyl substituted
with at least one C.sub.1-8alkyl. In one group of embodiments, at
least one R.sup.a is pyrazol-5-yl. In one group of embodiments, at
least one R.sup.a is 4-methyl-pyrazol-5-yl.
[0099] In one group of embodiments, Q is a heteroaryl or
heterocycloalkyl group optionally substituted with one to three
R.sup.a.
[0100] In one group of embodiments, Q is a bicyclic heteroaryl or
heterocycloalkyl group optionally substituted with one to three
R.sup.a.
[0101] In one group of embodiments, Q is a bicyclic heteroaryl
group optionally substituted with one to three R.sup.a.
[0102] In one group of embodiments, Q is a bicyclic heteroaryl
group substituted with one to three R.sup.a. In one group of
embodiments, Q is isoquinolin-4-yl optionally substituted with one
to three R.sup.a wherein at least one R.sup.a is heteroaryl
optionally substituted with one to three R.sup.c. In one group of
embodiments at least one R.sup.a is heteroaryl attached to said Q
at the ring atom adjacent to ring atom bearing Y. In one group of
embodiments at least one R.sup.a is heteroaryl substituted with at
least one C.sub.1-8alkyl. In one group of embodiments at least one
R.sup.a heteroaryl is substituted with at least one methyl. In one
group of embodiments at least one R.sup.a is pyrazolyl substituted
with at least one C.sub.1-8alkyl. In one group of embodiments at
least one R.sup.a is pyrazoyl substituted with at least one methyl.
In one group of embodiments, R.sup.a is pyrazol-5-yl. In one group
of embodiments, R.sup.a is 4-methyl-pyrazol-5-yl.
[0103] In one group of embodiments, Q is selected from the group
consisting of
##STR00022## ##STR00023##
naphthalene containing two to four ring nitrogen atoms, each
optionally substituted with one to three R.sup.a and wherein the
wavy line signifies the point of attachment to Y.
[0104] In one group of embodiments, Q is selected from the group
consisting of
##STR00024##
wherein Q is optionally substituted with one to three R.sup.a.
[0105] In one group of embodiments, Q is selected from the group
consisting of
##STR00025##
[0106] In one group of embodiments, Q is substituted with
CONR.sup.dR.sup.d, NR.sup.dR.sup.d, or heteroaryl optionally
substituted with one to three R.sup.c. In one group of embodiments,
Q is substituted with heteroaryl having one to two nitrogen ring
atoms.
[0107] In one group of embodiments, Q is not unsubstituted
pyridin-2-yl, unsubstituted pyridin-3-yl, or unsubstituted
pyridine-4-yl. In one group of embodiments, Q is pyridin-2-yl,
pyridin-3-yl, or pyridine-4-yl, each of which is substituted with
one to three R.sup.c.
[0108] In one group of embodiments, Q is pyridin-2-yl,
pyridin-3-yl, or pyridine-4-yl, said Q is optionally substituted
with CN or CONR.sup.dR.sup.d.
[0109] In one group of embodiments, Q is pyridin-2-yl,
pyridin-3-yl, or pyridine-4-yl, said Q is optionally substituted
with one to three R.sup.a wherein at least one R.sup.a is
heteroaryl optionally substituted with one to three R.sup.c. In one
group of embodiments at least one R.sup.a is heteroaryl attached to
said Q at the ring atom adjacent to ring atom bearing Y. In one
group of embodiments at least one R.sup.a is heteroaryl substituted
with at least one C.sub.1-8alkyl. In one group of embodiments at
least one R.sup.a heteroaryl is substituted with at least one
methyl. In one group of embodiments at least one R.sup.a is
pyrazolyl substituted with at least one C.sub.1-8alkyl. In one
group of embodiments at least one R.sup.a is pyrazoyl substituted
with at least one methyl. In one group of embodiments, R.sup.a is
pyrazol-5-yl. In one group of embodiments, R.sup.a is
4-methyl-pyrazol-5-yl.
[0110] In one group of embodiments, Q is substituted with at least
one R.sup.a selected from the group consisting of
--(CH.sub.2).sub.kOH, --(CH.sub.2).sub.kNH.sub.2,
--(CH.sub.2).sub.kNH(C.sub.1-8alkyl),
--(CH.sub.2).sub.kN(C.sub.1-8alkyl)(C.sub.1-8alkyl),
--(CH.sub.2).sub.kNHC(O)(C.sub.1-8alkyl),
--(CH.sub.2).sub.kN(C.sub.1-8alkyl)C(O)(C.sub.1-8alkyl),
--(CH.sub.2).sub.kNHC(O).sub.2(C.sub.1-8alkyl),
--(CH.sub.2).sub.kN(C.sub.1-8alkyl)C(O).sub.2(C.sub.1-8alkyl),
--(CH.sub.2).sub.kNHS(O).sub.2(C.sub.1-8alkyl),
--(CH.sub.2).sub.kN(C.sub.1-8alkyl)S(O).sub.2(C.sub.1-8alkyl), and
--(CH.sub.2).sub.kheterocycloalkyl optionally substituted with one
to three R.sup.c where k is selected from the group consisting of
0, 1, 2, 3, 4, 5, and 6. In some embodiments the heterocycloalkyl
group is morpholino or piperazinyl optionally substituted with
alkyl, --C(O)C.sub.1-8alkyl, --C(O).sub.2C.sub.1-8alkyl, or
--S(O).sub.2C.sub.1-8alkyl.
[0111] In one group of embodiments, Q is substituted with at least
one R.sup.a selected from the group consisting of
--NR.sup.d(CH.sub.2).sub.kOH, --NR.sup.d(CH.sub.2).sub.kNH.sub.2,
--NR.sup.d(CH.sub.2).sub.kNH(C.sub.1-8alkyl),
--NR.sup.d(CH.sub.2).sub.kN(C.sub.1-8alkyl)(C.sub.1-8alkyl),
--NR.sup.d(CH.sub.2).sub.kNHC(O)(C.sub.1-8alkyl),
--NR.sup.d(CH.sub.2).sub.kN(C.sub.1-8alkyl)C(O)(C.sub.1-8alkyl),
--NR.sup.d(CH.sub.2).sub.kNHC(O).sub.2(C.sub.1-8alkyl),
--NR.sup.d(CH.sub.2).sub.kN(C.sub.1-8alkyl)C(O).sub.2(C.sub.1-8alkyl),
--NR.sup.d(CH.sub.2).sub.kNHS(O).sub.2(C.sub.1-8alkyl),
--NR.sup.d(CH.sub.2).sub.kN(C.sub.1-8alkyl)S(O).sub.2(C.sub.1-8alkyl),
and --NR.sup.d(CH.sub.2).sub.kheterocycloalkyl optionally
substituted with one to three R.sup.c where k is selected from the
group consisting of 0, 1, 2, 3, 4, 5, and 6. In some embodiments,
R.sup.d is H or C.sub.1-8alkyl. In some embodiments the
heterocycloalkyl group is morpholino or piperazinyl optionally
substituted with alkyl, --C(O)C.sub.1-8alkyl,
--C(O).sub.2C.sub.1-8alkyl, or --S(O).sub.2C.sub.1-8alkyl.
[0112] In one group of embodiments, Q is substituted with at least
one R.sup.a selected from the group consisting of
O(CH.sub.2).sub.kOH, O(CH.sub.2).sub.kNH.sub.2,
O(CH.sub.2).sub.kNH(C.sub.1-8alkyl),
O(CH.sub.2).sub.kN(C.sub.1-8alkyl)(C.sub.1-8alkyl),
O(CH.sub.2).sub.kNHC(O)(C.sub.1-8alkyl),
O(CH.sub.2).sub.kN(C.sub.1-8alkyl)C(O)(C.sub.1-8alkyl),
O(CH.sub.2).sub.kNHC(O).sub.2(C.sub.1-8alkyl),
O(CH.sub.2).sub.kN(C.sub.1-8alkyl)C(O).sub.2(C.sub.1-8alkyl),
O(CH.sub.2).sub.kNHS(O).sub.2(C.sub.1-8alkyl),
O(CH.sub.2).sub.kN(C.sub.1-8alkyl)S(O).sub.2(C.sub.1-8alkyl), and
O(CH.sub.2).sub.kheterocycloalkyl optionally substituted with one
to three R.sup.c where k is selected from the group consisting of
0, 1, 2, 3, 4, 5, and 6. In some embodiments the heterocycloalkyl
group is morpholino or piperazinyl optionally substituted with
alkyl, --C(O)C.sub.1-8alkyl, --C(O).sub.2C.sub.1-8alkyl, or
--S(O).sub.2C.sub.1-8alkyl.
[0113] In one group of embodiments, T.sup.1 is C and R.sup.2 is
H.
[0114] In one group of embodiments, T.sup.2 is C and R.sup.3 is
H.
[0115] In one group of embodiments, T.sup.4 is C and R.sup.5 is
H.
[0116] In one group of embodiments, T.sup.3 is C and R.sup.4 is
C.sub.1-8 alkoxy.
[0117] In one group of embodiments, R.sup.2, R.sup.3, R.sup.5 when
present are H and R.sup.4 is C.sub.1-8 alkoxy.
[0118] In one group of embodiments, R.sup.4 is methoxy.
[0119] In one group of embodiments, R.sup.4 is haloalkoxy. In one
group of embodiments, R.sup.4 is OCHF.sub.2. In one group of
embodiments, R.sup.4 is OCF.sub.3.
[0120] In one group of embodiments, R.sup.2, R.sup.3, R.sup.4, and
R.sup.5 when present are H.
[0121] In one group of embodiments, one of R.sup.2, R.sup.3,
R.sup.4, and R.sup.5 is selected from the group consisting of
--O(CH.sub.2).sub.zOH, --O(CH.sub.2).sub.zNH.sub.2,
--O(CH.sub.2).sub.zNH(C.sub.1-8alkyl), and
--O(CH.sub.2).sub.zN(C.sub.1-8alkyl)(C.sub.1-8alkyl) where z is
selected from the group consisting of 0, 1, 2, 3, 4, 5, and 6.
[0122] In one group of embodiments, X is O.
[0123] In one group of embodiments, CH.sub.2.
[0124] In one group of embodiments, X is C(R.sup.9).sub.2 and at
least one of R.sup.9 is F.
[0125] In one group of embodiments, Y is CH.sub.2.
[0126] In one group of embodiments, Y is CR.sup.1aR.sup.1b and at
least one of R.sup.1a or R.sup.1b is F.
[0127] In one group of embodiments, the compound is not:
##STR00026## ##STR00027## ##STR00028## ##STR00029##
[0128] In another group of embodiments, the invention provides
compounds of Formula (Ib):
##STR00030##
or a tautomer or pharmaceutically acceptable salt thereof,
wherein:
[0129] Q is selected from the group consisting of aryl, heteroaryl,
and heterocycloalkyl, each optionally substituted with one to three
Ra;
[0130] Y is O or CH.sub.2;
[0131] X is O or CH.sub.2;
[0132] R.sup.2 and R.sup.3 are independently absent or selected
from the group consisting of hydrogen, halo, R.sup.b, OR.sup.d,
O(CH.sub.2).sub.zOR.sup.d, O(CH.sub.2).sub.zNR.sup.dR.sup.d,
OC(O)R.sup.e, SR.sup.d, CN, NO.sub.2, CO.sub.2R.sup.d,
CONR.sup.dR.sup.d, C(O)R.sup.d, OC(O)NR.sup.dR.sup.d,
NR.sup.dR.sup.d, NR.sup.dC(O)R.sup.e, NR.sup.dC(O).sub.2R.sup.e,
NR.sup.dC(O)NR.sup.dR.sup.d, S(O)R.sup.e, S(O).sub.2R.sup.e,
NR.sup.dS(O).sub.2R.sup.e, S(O).sub.2NR.sup.dR.sup.d, and N.sub.3
where z is 0, 1, 2, or 3;
[0133] R.sup.4 is absent or selected from the group consisting of
hydrogen, R.sup.b, OR.sup.d, O(CH.sub.2).sub.zOR.sup.d, where z is
0, 1, 2, or 3;
[0134] R.sup.5 is absent or selected from the group consisting of
hydrogen, halo, R.sup.b, and OR.sup.d;
[0135] R.sup.6 and R.sup.7 together form oxo or an aldehyde
protecting group;
[0136] T.sup.1, T.sup.2, T.sup.3, and T.sup.4 are independently C
or N provided that at least one of T.sup.1, T.sup.2, T.sup.3, and
T.sup.4 is N and at least one of T.sup.1, T.sup.2, T.sup.3, and
T.sup.4 is C;
[0137] each R.sup.a is independently selected from the group
consisting of halo, oxo, R.sup.b, OR.sup.d,
O(CH.sub.2).sub.uOR.sup.d, O(CH.sub.2).sub.uNR.sup.dR.sup.d,
O(CH.sub.2).sub.uNR.sup.dC(O)R.sup.e,
O(CH.sub.2).sub.uNR.sup.dC(O).sub.2R.sup.e,
O(CH.sub.2).sub.uNR.sup.dS(O).sub.2R.sup.e, NH.sub.2,
--(CH.sub.2).sub.kOC(O)R.sup.e, --(CH.sub.2).sub.kSR.sup.d, CN,
NO.sub.2, --(CH.sub.2).sub.kCO.sub.2(C.sub.1-8alkyl)OH,
--(CH.sub.2).sub.kCO.sub.2(C.sub.1-8alkyl)(heteroaryl)C(O)(C.sub.1-8alkyl-
), --(CH.sub.2).sub.kCO.sub.2R.sup.d,
--(CH.sub.2).sub.kCONR.sup.dR.sup.d,
--(CH.sub.2).sub.kNR.sup.dC(O)R.sup.e,
--(CH.sub.2).sub.kNR.sup.dC(O).sub.2R.sup.e,
--(CH.sub.2).sub.kC(O)R.sup.d,
--(CH.sub.2).sub.kOC(O)NR.sup.dR.sup.d,
--NR.sup.d(CH.sub.2).sub.uOR.sup.d,
--NR.sup.d(CH.sub.2).sub.uNR.sup.dR.sup.d,
--NR.sup.d(CH.sub.2).sub.uNR.sup.dC(O)R.sup.e,
--NR.sup.d(CH.sub.2).sub.uNR.sup.dC(O).sub.2R.sup.e,
--NR.sup.d(CH.sub.2).sub.uNR.sup.dS(O).sub.2R.sup.e,
--(CH.sub.2).sub.kNR.sup.dC(O)R.sup.e,
--(CH.sub.2).sub.kNR.sup.dC(O).sub.2R.sup.d,
--(CH.sub.2).sub.kNR.sup.dC(O)NR.sup.dR.sup.d,
--(CH.sub.2).sub.kS(O)R.sup.e, --(CH.sub.2).sub.kS(O).sub.2R.sup.e,
--(CH.sub.2).sub.kNR.sup.dS(O).sub.2R.sup.e,
--C(O)(CH.sub.2).sub.kNR.sup.dS(O).sub.2R.sup.e,
--(CH.sub.2).sub.kC(O)NR.sup.dS(O).sub.2R.sup.e,
--(CH.sub.2).sub.kS(O).sub.2NR.sup.dR.sup.d, N.sub.3,
--(CH.sub.2).sub.karyl optionally substituted with one to three
R.sup.c, --NR.sup.d(CH.sub.2).sub.karyl optionally substituted with
one to three R.sup.c, --(CH.sub.2).sub.kheteroaryl optionally
substituted with one to three R.sup.c,
--NR.sup.d(CH.sub.2).sub.kheteroaryl optionally substituted with
one to three R.sup.c, --(CH.sub.2).sub.kheterocycloalkyl optionally
substituted with one to three R.sup.c, and
--NR.sup.d(CH.sub.2).sub.kheterocycloalkyl optionally substituted
with one to three R.sup.c where k is 0, 1, 2, 3, 4, 5, or 6 and u
is 1, 2, 3, 4, 5, or 6;
[0138] each R.sup.b is independently selected from the group
consisting of C.sub.1-8alkyl, C.sub.2-8alkenyl, and
C.sub.2-8alkynyl, each optionally independently substituted with
one to three halo, OR.sup.d, or NR.sup.dR.sup.d;
[0139] each R.sup.c is independently selected from the group
consisting of halo, C.sub.1-8alkyl, haloC.sub.1-8alkyl,
C.sub.2-8alkenyl, haloC.sub.2-8alkenyl, C.sub.2-8alkynyl,
haloC.sub.2-8alkynyl, (CH.sub.2).sub.mOR.sup.f, OC(O)R.sup.g,
SR.sup.f, CN, NO.sub.2, (CH.sub.2).sub.mCO.sub.2R.sup.f,
CONR.sup.fR.sup.f, C(O)R.sup.f, OC(O)NR.sup.fR.sup.f,
(CH.sub.2).sub.mNR.sup.fR.sup.f, NR.sup.fC(O)R.sup.g,
NR.sup.fC(O).sub.2R.sup.g, NR.sup.fC(O)NR.sup.fR.sup.f,
S(O)R.sup.g, S(O).sub.2R.sup.g, NR.sup.fS(O).sub.2R.sup.g,
S(O).sub.2NR.sup.fR.sup.f, N.sub.3,
(R.sup.f).sub.mSiC.sub.1-8alkyl, heteroaryl optionally substituted
with one to three R.sup.h, cycloalkyl optionally substituted with
one to three R.sup.h, and heterocycloalkyl optionally substituted
with one to three R.sup.h where m is selected from the group
consisting of 0, 1, 2, 3, 4, 5, and 6;
[0140] each R.sup.h is independently selected from the group
consisting of halo, C.sub.1-8alkyl, haloC.sub.1-8alkyl, OR.sup.j,
OC(O)R, SR.sup.j, NO.sub.2, CO.sub.2R.sup.j, CONR.sup.jR.sup.j,
C(O)R.sup.j, OC(O)NR.sup.jR.sup.j, NR.sup.jR.sup.j,
NR.sup.jC(O)R.sup.t, NR.sup.jC(O).sub.2R.sup.t,
NR.sup.jC(O)NR.sup.jR.sup.j, S(O)R.sup.t, S(O).sub.2R.sup.t,
NR.sup.jS(O).sub.2R.sup.t, and S(O).sub.2NR.sup.jR.sup.j;
[0141] R.sup.d, R.sup.f, and R.sup.j are each independently
selected from the group consisting of hydrogen, C.sub.1-8 alkyl,
haloC.sub.1-8alkyl, C.sub.2-8 alkenyl, haloC.sub.2-8alkenyl,
C.sub.2-8 alkynyl, and haloC.sub.2-8 alkynyl; and
[0142] R.sup.e, R.sup.g, and R.sup.t are each independently
selected from the group consisting of C.sub.1-8alkyl,
haloC.sub.1-8alkyl, C.sub.2-8 alkenyl, haloC.sub.2-8alkenyl,
C.sub.2-8 alkynyl, and haloC.sub.2-8alkynyl;
[0143] provided that X and Y are not both O;
[0144] provided that when Q is phenyl and R.sup.4 is C.sub.1-8alkyl
or C.sub.2-8alkenyl, Q is substituted with at least one
R.sup.a;
[0145] provided that when R.sup.5 is halo, Q is substituted with at
least 1 R.sup.a;
[0146] provided that when R.sup.5 is R.sup.b, Q is not phenyl;
and
[0147] provided that when R.sup.2, R.sup.3, R.sup.4, and R.sup.5
are H and Q is phenyl, Q is substituted with at least one R.sup.a
selected from 4-carboxy, 3-carboxy, and (C.sub.1-8 alkyl
3-carboxylate).
[0148] In one group of embodiments, the invention provides
compounds of Formula Ib wherein R.sup.2 and R.sup.3 are
independently absent or selected from the group consisting of
hydrogen, R.sup.b, OR.sup.d, O(CH.sub.2).sub.zOR.sup.d,
O(CH.sub.2).sub.zNR.sup.dR.sup.d, OC(O)R.sup.e, CO.sub.2R.sup.d,
CONR.sup.dR.sup.d, and C(O)R.sup.d, where z is 1, 2, or 3.
[0149] In one group of embodiments, the invention provides
compounds of Formula Ib wherein at least one z is 0. In another
group of embodiments, at least one z is 1. In yet another group of
embodiments, at least one z is 2. In still another group of
embodiments, at least one z is 3. In another group of embodiments,
no z is 0.
[0150] In one group of embodiments, the invention provides
compounds of Formula Ib wherein T.sup.2 is N; T.sup.1, T.sup.3, and
T.sup.4 are C; R.sup.2 and R.sup.5 are H; R.sup.3 is absent; and
R.sup.4 is C.sub.1-8alkoxy.
[0151] In one group of embodiments, the invention provides
compounds of Formula Ib wherein T.sup.2 is N; T.sup.1, T.sup.3, and
T.sup.4 are C; R.sup.2 and R.sup.5 are H; R.sup.3 is absent; and
R.sup.5 is selected from hydroxy and C.sub.1-8alkoxy.
[0152] In one group of embodiments, the invention provides
compounds of Formula Ib wherein T.sup.4 is N; T.sup.1, T.sup.2, and
T.sup.3 are C; R.sup.2 and R.sup.3 are H; R.sup.5 is absent; and
R.sup.4 is selected from C.sub.1-8alkyl and C.sub.1-8alkoxy.
[0153] In one group of embodiments, the invention provides
compounds of Formula Ib wherein T.sup.1 is N; T.sup.2, T.sup.3, and
T.sup.4 are C; R.sup.3, R.sup.4, and R.sup.5 are H; and R.sup.2 is
absent.
[0154] In one group of embodiments, the invention provides
compounds of Formula Ib wherein T.sup.2 is N; T.sup.1, T.sup.3, and
T.sup.4 are C; R.sup.2, R.sup.4, and R.sup.5 are H; and R.sup.3 is
absent.
[0155] In one group of embodiments, the invention provides
compounds of Formula Ib wherein T.sup.3 is N; T.sup.1, T.sup.2, and
T.sup.4 are C; R.sup.2, R.sup.3, and R.sup.5 are H; and R.sup.4 is
absent.
[0156] In one group of embodiments, the invention provides
compounds of Formula Ib wherein T.sup.4 is N; T.sup.1, T.sup.2, and
T.sup.3 are C; R.sup.2, R.sup.3, and R.sup.4 are H; and R.sup.5 is
absent.
[0157] In one group of embodiments, the invention provides
compounds of Formula Ib wherein Q is selected from an
imidazopyridinyl group, a pyrrolopyridinyl group, a
pyrazolopyridinyl group, a triazolopyridinyl group, a
pyrazolopyrazinyl group, a pyridinyl group, a pyrazinyl group, an
oxazolyl group, an imidazolyl group, a triazolyl group, a
tetrazolyl group, a pyrazolyl group, a quinolinyl group, an
isoquinolinyl group, an indazolyl group, a benzooxazolyl group, a
naphthyridinyl group, and a quinoxalinyl group; and wherein Q is
optionally substituted with one to three R.sup.a.
[0158] In another group of embodiments, the invention provides
compounds of Formula Ic:
##STR00031##
or a tautomer or pharmaceutically acceptable salt thereof,
wherein:
[0159] Y is CH.sub.2;
[0160] X is O or CH.sub.2;
[0161] T.sup.1, T.sup.2, T.sup.3, and T.sup.4 are C or N, provided
that no more than one of T.sup.1, T.sup.2, T.sup.3, and T.sup.4 is
N;
[0162] Q is selected from the group consisting of
[0163] i) heteroaryl optionally substituted with one to three
R.sup.a; wherein [0164] R.sup.2, R.sup.3, R.sup.4, and R.sup.5, are
independently absent or selected from the group consisting of
hydrogen, halo, R.sup.b, OR.sup.d, O(CH.sub.2).sub.zOR.sup.d,
O(CH.sub.2).sub.zNR.sup.dR.sup.d, OC(O)R.sup.e, SR.sup.d, CN,
NO.sub.2, CO.sub.2R.sup.d, CONR.sup.dR.sup.d, C(O)R.sup.d,
OC(O)NR.sup.dR.sup.d, NR.sup.dR.sup.d, NR.sup.dC(O)R.sup.e,
NR.sup.dC(O).sub.2R.sup.e, NR.sup.dC(O)NR.sup.dR.sup.d,
S(O)R.sup.e, S(O).sub.2R.sup.e, NR.sup.dS(O).sub.2R.sup.e,
S(O).sub.2NR.sup.dR.sup.d, and N.sub.3 where z is 0, 1, 2, or
3;
[0165] ii) aryl substituted with one to three
--(CH.sub.2).sub.kCO.sub.2R.sup.d; wherein [0166] R.sup.2 and
R.sup.5 are independently absent or selected from the group
consisting of hydrogen, halo, OR.sup.d, O(CH.sub.2).sub.zOR.sup.d,
O(CH.sub.2).sub.zNR.sup.dR.sup.d, OC(O)R.sup.e, SR.sup.d, CN,
NO.sub.2, CO.sub.2R.sup.d, CONR.sup.dR.sup.d, C(O)R.sup.d,
OC(O)NR.sup.dR.sup.d, NR.sup.dR.sup.d, NR.sup.dC(O)R.sup.e,
NR.sup.dC(O).sub.2R.sup.e, NR.sup.dC(O)NR.sup.dR.sup.d,
S(O)R.sup.e, S(O).sub.2R.sup.e, NR.sup.dS(O).sub.2R.sup.e,
S(O).sub.2NR.sup.dR.sup.d, and N.sub.3 where z is 0, 1, 2, or 3;
[0167] R.sup.3 and R.sup.4 are independently absent or selected
from the group consisting of hydrogen, halo, R.sup.b, OR.sup.d,
O(CH.sub.2).sub.zOR.sup.d, O(CH.sub.2).sub.zNR.sup.dR.sup.d,
OC(O)R.sup.e, SR.sup.d, CN, NO.sub.2, CO.sub.2R.sup.d,
CONR.sup.dR.sup.d, C(O)R.sup.d, OC(O)NR.sup.dR.sup.d,
NR.sup.dR.sup.d, NR.sup.dC(O)R.sup.e, NR.sup.dC(O).sub.2R.sup.e,
NR.sup.dC(O)NR.sup.dR.sup.d, S(O)R.sup.e, S(O).sub.2R.sup.e,
NR.sup.dS(O).sub.2R.sup.e, S(O).sub.2NR.sup.dR.sup.d, and N.sub.3
where z is 0, 1, 2, or 3;
[0168] iii) unsubstituted aryl, wherein [0169] R.sup.2, R.sup.3,
and R.sup.4, are independently absent or selected from the group
consisting of hydrogen, halo, R.sup.b, OR.sup.d,
O(CH.sub.2).sub.zOR.sup.d, O(CH.sub.2).sub.zNR.sup.dR.sup.d,
OC(O)R.sup.e, SR.sup.d, CN, NO.sub.2, CO.sub.2R.sup.d,
CONR.sup.dR.sup.d, C(O)R.sup.d, OC(O)NR.sup.dR.sup.d,
NR.sup.dR.sup.d, NR.sup.dC(O)R.sup.e, NR.sup.dC(O).sub.2R.sup.e,
NR.sup.dC(O)NR.sup.dR.sup.d, S(O)R.sup.e, S(O).sub.2R.sup.e,
NR.sup.dS(O).sub.2R.sup.e, S(O).sub.2NR.sup.dR.sup.d, and N.sub.3
where z is 0, 1, 2, or 3; and [0170] R.sup.5 is absent or is
OR.sup.d; and
[0171] iv) heterocycloalkyl, optionally substituted with one to
three R.sup.a; wherein [0172] R.sup.2, R.sup.3, R.sup.4, and
R.sup.5, are independently absent or selected from the group
consisting of hydrogen, R.sup.b, OR.sup.d,
O(CH.sub.2).sub.zOR.sup.d, O(CH.sub.2).sub.zNR.sup.dR.sup.d,
OC(O)R.sup.e, SR.sup.d, CN, NO.sub.2, CO.sub.2R.sup.d,
CONR.sup.dR.sup.d, C(O)R.sup.d, OC(O)NR.sup.dR.sup.d,
NR.sup.dR.sup.d, NR.sup.dC(O)R.sup.e, NR.sup.dC(O).sub.2R.sup.e,
NR.sup.dC(O)NR.sup.dR.sup.d, S(O)R.sup.e, S(O).sub.2R.sup.e,
NR.sup.dS(O).sub.2R.sup.e, S(O).sub.2NR.sup.dR.sup.d, and N.sub.3
where z is 0, 1, 2, or 3;
[0173] R.sup.6 and R.sup.7 together form oxo or an aldehyde
protecting group;
[0174] each R.sup.a is independently selected from the group
consisting of halo, oxo, R.sup.b, OR.sup.d,
O(CH.sub.2).sub.uOR.sup.d, O(CH.sub.2).sub.uNR.sup.dR.sup.d,
O(CH.sub.2).sub.uNR.sup.dC(O)R.sup.e,
O(CH.sub.2).sub.uNR.sup.dC(O).sub.2R.sup.e,
O(CH.sub.2).sub.uNR.sup.dS(O).sub.2R.sup.e, NH.sub.2,
--(CH.sub.2).sub.kOC(O)R.sup.e, --(CH.sub.2).sub.kSR.sup.d, CN,
NO.sub.2, --(CH.sub.2).sub.kCO.sub.2(C.sub.1-8alkyl)OH,
--(CH.sub.2).sub.kCO.sub.2(C.sub.1-8alkyl)(heteroaryl)C(O)(C.sub.1-8alkyl-
), --(CH.sub.2).sub.kCO.sub.2R.sup.d,
--(CH.sub.2).sub.kCONR.sup.dR.sup.d,
--(CH.sub.2).sub.kNR.sup.dC(O)R.sup.e,
--(CH.sub.2).sub.kNR.sup.dC(O).sub.2R.sup.e,
--(CH.sub.2).sub.kC(O)R.sup.d,
--(CH.sub.2).sub.kOC(O)NR.sup.dR.sup.d,
--NR.sup.d(CH.sub.2).sub.uOR.sup.d,
--NR.sup.d(CH.sub.2).sub.uNR.sup.dR.sup.d,
--NR.sup.d(CH.sub.2).sub.uNR.sup.dC(O)R.sup.e,
--NR.sup.d(CH.sub.2).sub.uNR.sup.dC(O).sub.2R.sup.e,
--NR.sup.d(CH.sub.2).sub.uNR.sup.dS(O).sub.2R.sup.e,
--(CH.sub.2).sub.kNR.sup.dC(O)R.sup.e,
--(CH.sub.2).sub.kNR.sup.dC(O).sub.2R.sup.d,
--(CH.sub.2).sub.kNR.sup.dC(O)NR.sup.dR.sup.d,
--(CH.sub.2).sub.kS(O)R.sup.e, --(CH.sub.2).sub.kS(O).sub.2R.sup.e,
--(CH.sub.2).sub.kNR.sup.dS(O).sub.2R.sup.e,
--C(O)(CH.sub.2).sub.kNR.sup.dS(O).sub.2R.sup.e,
--(CH.sub.2).sub.kC(O)NR.sup.dS(O).sub.2R.sup.e,
--(CH.sub.2).sub.kS(O).sub.2NR.sup.dR.sup.d, N.sub.3,
--(CH.sub.2).sub.karyl optionally substituted with one to three
R.sup.c, --NR.sup.d(CH.sub.2).sub.karyl optionally substituted with
one to three R.sup.c, --(CH.sub.2).sub.kheteroaryl optionally
substituted with one to three R.sup.c,
--NR.sup.d(CH.sub.2).sub.kheteroaryl optionally substituted with
one to three R.sup.c, --(CH.sub.2).sub.kheterocycloalkyl optionally
substituted with one to three R.sup.c, and
--NR.sup.d(CH.sub.2).sub.kheterocycloalkyl optionally substituted
with one to three R.sup.c where k is 0, 1, 2, 3, 4, 5, or 6 and u
is 1, 2, 3, 4, 5, or 6;
[0175] each R.sup.b is independently selected from the group
consisting of C.sub.1-8alkyl, C.sub.2-8alkenyl, and
C.sub.2-8alkynyl, each optionally independently substituted with
one to three halo, OR.sup.d, or NR.sup.dR.sup.d;
[0176] each R.sup.c is independently selected from the group
consisting of halo, C.sub.1-8alkyl, haloC.sub.1-8alkyl,
C.sub.2-8alkenyl, haloC.sub.2-8alkenyl, C.sub.2-8alkynyl,
haloC.sub.2-8alkynyl, (CH.sub.2).sub.mOR.sup.f, OC(O)R.sup.g,
SR.sup.f, CN, NO.sub.2, (CH.sub.2).sub.mCO.sub.2R.sup.f,
CONR.sup.fR.sup.f, C(O)R.sup.f, OC(O)NR.sup.fR.sup.f,
(CH.sub.2).sub.mNR.sup.fR.sup.f, NR.sup.fC(O)R.sup.g,
NR.sup.fC(O).sub.2R.sup.g, NR.sup.fC(O)NR.sup.fR.sup.f,
S(O)R.sup.g, S(O).sub.2R.sup.g, NR.sup.fS(O).sub.2R.sup.g,
S(O).sub.2NR.sup.fR.sup.f, N.sub.3,
(R.sup.f).sub.mSiC.sub.1-8alkyl, heteroaryl optionally substituted
with one to three R.sup.h, cycloalkyl optionally substituted with
one to three R.sup.h, and heterocycloalkyl optionally substituted
with one to three R.sup.h where m is selected from the group
consisting of 0, 1, 2, 3, 4, 5, and 6; [0177] each R.sup.h is
independently selected from the group consisting of halo,
C.sub.1-8alkyl, haloC.sub.1-8alkyl, OR.sup.j, OC(O)R, SR.sup.j,
NO.sub.2, CO.sub.2R.sup.j, CONR.sup.jR.sup.j, C(O)R.sup.j,
OC(O)NR.sup.jR.sup.j, NR.sup.jR.sup.j, NR.sup.jC(O)R.sup.t,
NR.sup.jC(O).sub.2R.sup.t, NR.sup.jC(O)NR.sup.jR.sup.j,
S(O)R.sup.t, S(O).sub.2R.sup.t, NR.sup.jS(O).sub.2R.sup.t, and
S(O).sub.2NR.sup.jR.sup.j;
[0178] R.sup.d, R.sup.f, and R.sup.j are each independently
selected from the group consisting of hydrogen, C.sub.1-8 alkyl,
haloC.sub.1-8alkyl, C.sub.2-8 alkenyl, haloC.sub.2-8alkenyl,
C.sub.2-8 alkynyl, and haloC.sub.2-8alkynyl; and
[0179] R.sup.e, R.sup.g, and R.sup.t are each independently
selected from the group consisting of C.sub.1-8alkyl,
haloC.sub.1-8alkyl, C.sub.2-8 alkenyl, haloC.sub.2-8alkenyl,
C.sub.2-8 alkynyl, and haloC.sub.2-8alkynyl.
[0180] In one group of embodiments, the invention provides
compounds of Formula Ic, wherein R.sup.6 and R.sup.7 together form
oxo.
[0181] In one group of embodiments, the invention provides
compounds of Formula Ic, wherein R.sup.2 and R.sup.3 are
independently absent or selected from the group consisting of
hydrogen, R.sup.b, OR.sup.d, O(CH.sub.2).sub.zOR.sup.d,
O(CH.sub.2).sub.zNR.sup.dR.sup.d, OC(O)R.sup.e, CO.sub.2R.sup.d,
CONR.sup.dR.sup.d, and C(O)R.sup.d, where z is 1, 2, or 3.
[0182] In one group of embodiments, the invention provides
compounds of Formula Ic, wherein T.sup.2 is N; R.sup.2 and R.sup.5
are H; R.sup.3 is absent; and R.sup.4 is C.sub.1-8alkoxy,
haloC.sub.1-8alkoxy, and O(CH.sub.2).sub.2C.sub.1-8alkyl.
[0183] In one group of embodiments, the invention provides
compounds of Formula Ic, wherein T.sup.2 is N; R.sup.2 and R.sup.4
are H; R.sup.3 is absent; and R.sup.5 is selected from hydroxy and
C.sub.1-8alkoxy.
[0184] In one group of embodiments, the invention provides
compounds of Formula Ic, wherein T.sup.4 is N; R.sup.2 and R.sup.3
are H; R.sup.5 is absent; and R.sup.4 is selected from
C.sub.1-8alkyl and C.sub.1-8alkoxy.
[0185] In one group of embodiments, the invention provides
compounds of Formula Ic, wherein T.sup.1 is N; R.sup.3, R.sup.4,
and R.sup.5 are H; and R.sup.2 is absent.
[0186] In one group of embodiments, the invention provides
compounds of Formula Ic, wherein T.sup.2 is N; R.sup.2, R.sup.4,
and R.sup.5 are H; and R.sup.3 is absent.
[0187] In one group of embodiments, the invention provides
compounds of Formula Ic, wherein T.sup.3 is N; R.sup.2, R.sup.3,
and R.sup.5 are H; and R.sup.4 is absent.
[0188] In one group of embodiments, the invention provides
compounds of Formula Ic, wherein T.sup.4 is N; R.sup.2, R.sup.3,
and R.sup.4 are H; and R.sup.5 is absent.
[0189] In one group of embodiments, the invention provides
compounds of Formula Ic, or another group of embodiments of Formula
Ic that is disclosed herein, wherein Q is selected from the group
consisting of an imidazopyridinyl group, a pyrrolopyridinyl group,
a pyrazolopyridinyl group, a triazolopyridinyl group, a
pyrazolopyrazinyl group, a pyridinyl group, a pyrazinyl group, an
oxazolyl group, an imidazolyl group, a triazolyl group, a
tetrazolyl group, a pyrazolyl group, a quinolinyl group, an
isoquinolinyl group, an indazolyl group, a benzooxazolyl group, a
naphthyridinyl group, and a quinoxalinyl group; and wherein Q is
optionally substituted with one to three R.sup.a.
[0190] In one group of embodiments, the invention provides
compounds of Formula Ic, or another group of embodiments of Formula
Ic that is disclosed herein, wherein Q is selected from the group
consisting of:
##STR00032## ##STR00033##
and wherein Q is optionally substituted with one to three
R.sup.a.
[0191] In one group of embodiments, the invention provides
compounds of Formula Ic wherein at least one z is 0. In another
group of embodiments, at least one z is 1. In yet another group of
embodiments, at least one z is 2. In still another group of
embodiments, at least one z is 3. In another group of embodiments,
no z is 0.
[0192] In certain embodiments, the compounds of Formula I, Ib and
Ic, or tautomers or pharmaceutically acceptable salts thereof, are
selected from Table 1 below.
TABLE-US-00001 TABLE 1 Compound Structure Name 1 ##STR00034##
4-(pyridin-3- ylmethoxy)nicotinaldehyde 2 ##STR00035##
3-(pyridin-3- ylmethoxy)isonicotinaldehyde 3 ##STR00036##
2-(imidazo[1,2-a]pyridin-8- ylmethoxy)nicotinaldehyde 4
##STR00037## 3-(imidazo[1,2-a]pyridin-8- ylmethoxy)picolinaldehyde
5 ##STR00038## 5-(imidazo[1,2-a]pyridin-8- ylmethoxy)-2-
methoxyisonicotinaldehyde 6 ##STR00039##
3-(imidazo[1,2-a]pyridin-8- ylmethoxy)isonicotinaldehyde 7
##STR00040## 3-(imidazo[1,5-a]pyridin-8-
ylmethoxy)isonicotinaldehyde 8 ##STR00041##
2-methoxy-5-(pyrazolo[1,5- a]pyrazin-3-
ylmethoxy)isonicotinaldehyde 9 ##STR00042## 8-((3-formylpyridin-2-
yloxy)methyl)imidazo[1,2- a]pyridine-6-carboxamide 10 ##STR00043##
8-((4-formyl-6-methoxypyridin-3- yloxy)methyl)imidazo[1,2-
a]pyridine-6-carboxamide 11 ##STR00044##
5-(imidazo[1,2-a]pyridin-8- ylmethoxy)-2-oxo-1,2-
dihydropyridine-4-carbaldehyde 12 ##STR00045##
2-(2-(imidazo[1,2-a]pyridin-8- yl)ethyl)nicotinaldehyde 13
##STR00046## 5-(2-(imidazo[1,2-a]pyridin-8- yl)ethyl)-2-
methoxyisonicotinaldehyde 14 ##STR00047##
5-((1H-pyrazolo[3,4-b]pyridin-4- yl)methoxy)-2-
methoxyisonicotinaldehyde 15 ##STR00048##
3-((4-formyl-6-methoxypyridin-3- yloxy)methyl)pyrazolo[1,5-
a]pyrazine-2-carboxamide 16 ##STR00049## 5-((2-(1H-pyrazol-5-
yl)pyrazolo[1,5-a]pyrazin-3- yl)methoxy)-2-
methoxyisonicotinaldehyde 17 ##STR00050##
2-(imidazo[1,2-a]pyridin-2- ylmethoxy)nicotinaldehyde 18
##STR00051## 2-methoxy-5-((4,5,6,7-
tetrahydropyrazolo[1,5-a]pyrazin- 3-yl)methoxy)isonicotinaldehyde
19 ##STR00052## 2-(imidazo[1,2-a]pyridin-8-
ylmethoxy)nicotinaldehyde 20 ##STR00053##
5-(imidazo[1,2-a]pyridin-8- ylmethoxy)-2- methylisonicotinaldehyde
21 ##STR00054## 3-((1H-pyrrolo[2,3-b]pyridin-4-
yl)methoxy)isonicotinaldehyde 22 ##STR00055##
3-(imidazo[1,2-a]pyridin-8- ylmethoxy)isonicotinaldehyde 23
##STR00056## 3-(pyrrolo[1,2-a]pyrazin-6-
ylmethoxy)isonicotinaldehyde 24 ##STR00057## 6-((4-formylpyridin-3-
yloxy)methyl)pyrrolo[1,2- a]pyrazine-7-carbonitrile 25 ##STR00058##
6-((4-formylpyridin-3- yloxy)methyl)pyrrolo[1,2-
a]pyrazine-7-carboxamide 26 ##STR00059##
3-((1H-pyrazolo[3,4-b]pyridin-4- yl)methoxy)isonicotinaldehyde 27
##STR00060## 3-(pyrazolo[1,5-a]pyrazin-3-
ylmethoxy)isonicotinaldehyde 28 ##STR00061##
2-methoxy-5-((6-oxo-1,6- dihydropyridin-3-
yl)methoxy)isonicotinaldehyde 29 ##STR00062##
2-methoxy-5-((2-oxo-1,2- dihydropyridin-4-
yl)methoxy)isonicotinaldehyde 30 ##STR00063##
2-methoxy-5-(oxazol-5- ylmethoxy)isonicotinaldehyde 31 ##STR00064##
5-((1H-imidazol-5-yl)methoxy)-2- methoxyisonicotinaldehyde 32
##STR00065## 5-((1H-imidazol-2-yl)methoxy)-2-
methoxyisonicotinaldehyde 33 ##STR00066## 5-((4H-1,2,4-triazol-3-
yl)methoxy)-2- methoxyisonicotinaldehyde 34 ##STR00067##
5-((1H-tetrazol-5-yl)methoxy)-2- methoxyisonicotinaldehyde 35
##STR00068## 5-((1H-pyrazol-5-yl)methoxy)-2-
methoxyisonicotinaldehyde 36 ##STR00069##
5-((1H-pyrazol-4-yl)methoxy)-2- methoxyisonicotinaldehyde 37
##STR00070## 2-methoxy-5-(oxazol-4- ylmethoxy)isonicotinaldehyde 38
##STR00071## 2-methoxy-5-((2-methylpyridin-3-
yl)methoxy)isonicotinaldehyde 39 ##STR00072##
2-methoxy-5-((4-methylpyridin-3- yl)methoxy)isonicotinaldehyde 40
##STR00073## 2-methoxy-5-((6- (trifluoromethyl)pyridin-3-
yl)methoxy)isonicotinaldehyde 41 ##STR00074##
2-methoxy-5-((6-methylpyridin-3- yl)methoxy)isonicotinaldehyde 42
##STR00075## 2-methoxy-5-(pyridin-3- ylmethoxy)isonicotinaldehyde
43 ##STR00076## 2-methoxy-5-((5-methylpyridin-3-
yl)methoxy)isonicotinaldehyde 44 ##STR00077##
5-(isoquinolin-1-ylmethoxy)-2- methoxyisonicotinaldehyde 45
##STR00078## 2-methoxy-5-(quinolin-2- ylmethoxy)isonicotinaldehyde
46 ##STR00079## 2-methoxy-5-(pyridin-4-
ylmethoxy)isonicotinaldehyde 47 ##STR00080##
2-methoxy-5-((3-methylpyridin-4- yl)methoxy)isonicotinaldehyde 48
##STR00081## 5-((3-bromopyridin-4- yl)methoxy)-2-
methoxyisonicotinaldehyde 49 ##STR00082##
3-(imidazo[1,2-a]pyridin-8- ylmethoxy)-6- methylpicolinaldehyde 50
##STR00083## (5-(imidazo[1,2-a]pyridin-5-
ylmethoxy)-2-methoxypyridin-4- yl)(methoxy)methanol 51 ##STR00084##
N-(4-formylpyridin-3- yl)imidazo[1,2-a]pyridine-8- carboxamide 52
##STR00085## 2-methoxy-5-((6- (trifluoromethyl)imidazo[1,2-
a]pyridin-2- yl)methoxy)isonicotinaldehyde 53 ##STR00086## methyl
2-((4-formyl-6- methoxypyridin-3- yloxy)methyl)imidazo[1,2-
a]pyridine-8-carboxylate 54 ##STR00087##
2-methoxy-5-((1-methyl-2-oxo- 1,2-dihydropyridin-4-
yl)methoxy)isonicotinaldehyde 55 ##STR00088##
5-((3-bromoimidazo[1,2-a]pyridin- 2-yl)methoxy)-2-
methoxyisonicotinaldehyde 56 ##STR00089##
5-((6-bromoimidazo[1,2-a]pyridin- 2-yl)methoxy)-2-
methoxyisonicotinaldehyde 57 ##STR00090##
5-((8-bromoimidazo[1,2-a]pyridin- 2-yl)methoxy)-2-
methoxyisonicotinaldehyde 58 ##STR00091## 2-methoxy-5-((3-methyl-
[1,2,4]triazolo[4,3-a]pyridin-8- yl)methoxy)isonicotinaldehyde 59
##STR00092## 5-((3-(1H-pyrazol-5- yl)imidazo[1,2-a]pyridin-2-
yl)methoxy)-2- methoxyisonicotinaldehyde 60 ##STR00093##
5-((6-(1H-pyrazol-3- yl)imidazo[1,2-a]pyridin-2- yl)methoxy)-2-
methoxyisonicotinaldehyde 61 ##STR00094##
2-methoxy-5-((8-(1-methyl-1H- pyrazol-5-yl)imidazo[1,2-
a]pyridin-2- yl)methoxy)isonicotinaldehyde 62 ##STR00095##
5-((4-formyl-6-methoxypyridin-3- yloxy)methyl)picolinonitrile 63
##STR00096## 5-((2-bromopyridin-3- yl)methoxy)-2-
methoxyisonicotinaldehyde 64 ##STR00097##
3-((4-formyl-6-methoxypyridin-3- yloxy)methyl)picolinonitrile 65
##STR00098## 5-((2-(1H-pyrazol-5-yl)pyridin-3- yl)methoxy)-2-
methoxyisonicotinaldehyde 66 ##STR00099## 5-((5-bromopyridin-3-
yl)methoxy)-2- methoxyisonicotinaldehyde 67 ##STR00100## methyl
2-((4-(1,3-dioxolan-2-yl)- 6-methoxypyridin-3-
yloxy)methyl)imidazo[1,2- a]pyridine-8-carboxylate 68 ##STR00101##
2-((4-(1,3-dioxolan-2-yl)-6- methoxypyridin-3-
yloxy)methyl)imidazo[1,2- a]pyridine-8-carboxamide 69 ##STR00102##
2-((4-(1,3-dioxolan-2-yl)-6- methoxypyridin-3-yloxy)methyl)-
N-methylimidazo[1,2-a]pyridine- 8-carboxamide 70 ##STR00103##
5-((5-(1H-pyrazol-5-yl)pyridin-3- yl)methoxy)-2-
methoxyisonicotinaldehyde 71 ##STR00104##
5-((4-(1H-pyrazol-5-yl)pyridin-3- yl)methoxy)-2-
methoxyisonicotinaldehyde 72 ##STR00105##
2-((4-(dihydroxymethyl)-6- methoxypyridin-3-yloxy)methyl)-
N-methylimidazo[1,2-a]pyridine- 8-carboxamide 73 ##STR00106##
2-((4-(dihydroxymethyl)-6- methoxypyridin-3-
yloxy)methyl)imidazo[1,2- a]pyridine-8-carboxamide 74 ##STR00107##
2-methoxy-5-((5-(1-methyl-1H- pyrazol-5-yl)pyridin-3-
yl)methoxy)isonicotinaldehyde 75 ##STR00108##
2-methoxy-5-((5-(1-methyl-1H- pyrazol-3-yl)pyridin-3-
yl)methoxy)isonicotinaldehyde 76 ##STR00109##
5-((5-(1H-pyrazol-4-yl)pyridin-3- yl)methoxy)-2-
methoxyisonicotinaldehyde 77 ##STR00110##
2-methoxy-5-((5-(1-methyl-1H- pyrazol-4-yl)pyridin-3-
yl)methoxy)isonicotinaldehyde 78 ##STR00111## methyl
5-((4-formyl-6- methoxypyridin-3- yloxy)methyl)nicotinate 79
##STR00112## 5-((4-formyl-6-methoxypyridin-3-
yloxy)methyl)nicotinic acid 80 ##STR00113##
2-methoxy-5-(quinolin-3- ylmethoxy)isonicotinaldehyde 81
##STR00114## 6-methyl-3-(quinolin-3- ylmethoxy)picolinaldehyde 82
##STR00115## 5-(isoquinolin-7-ylmethoxy)-2-
methoxyisonicotinaldehyde 83 ##STR00116##
3-(isoquinolin-7-ylmethoxy)-6- methylpicolinaldehyde 84
##STR00117## 2-methoxy-5-((1-methyl-1H- indazol-4-
yl)methoxy)isonicotinaldehyde 85 ##STR00118##
6-methyl-3-((1-methyl-1H- indazol-4- yl)methoxy)picolinaldehyde 86
##STR00119## tert-butyl 4-((2-formyl-6-
methylpyridin-3-yloxy)methyl)- 1H-indazole-1-carboxylate 87
##STR00120## 5-((1H-indazol-4-yl)methoxy)-2-
methoxyisonicotinaldehyde
88 ##STR00121## 3-((1H-indazol-4-yl)methoxy)-6-
methylpicolinaldehyde 89 ##STR00122## 6-methoxy-3-((1-methyl-1H-
indazol-6- yl)methoxy)picolinaldehyde 90 ##STR00123##
2-methoxy-5-((1-methyl-1H- indazol-7- yl)methoxy)isonicotinaldehyde
91 ##STR00124## 6-methyl-3-((1-methyl-1H- indazol-6-
yl)methoxy)picolinaldehyde 92 ##STR00125##
6-methyl-3-((1-methyl-1H- indazol-7- yl)methoxy)picolinaldehyde 93
##STR00126## 3-(isoquinolin-1-ylmethoxy)-6- methylpicolinaldehyde
94 ##STR00127## 6-methyl-3-(quinolin-2- ylmethoxy)picolinaldehyde
95 ##STR00128## 5-((4-(1H-pyrazol-4-yl)pyridin-3- yl)methoxy)-2-
methoxyisonicotinaldehyde 96 ##STR00129##
5-((6-bromoimidazo[1,2-a]pyridin- 8-yl)methoxy)-2-
methoxyisonicotinaldehyde 97 ##STR00130##
8-((4-formyl-6-methoxypyridin-3- yloxy)methyl)imidazo[1,2-
a]pyridine-6-carbonitrile 98 ##STR00131##
5-((4-formyl-6-methoxypyridin-3- yloxy)methyl)nicotinonitrile 99
##STR00132## 3-(benzo[d]oxazol-4-ylmethoxy)-
6-methylpicolinaldehyde 100 ##STR00133##
8-((4-formyl-6-methoxypyridin-3- yloxy)methyl)imidazo[1,2-
a]pyridine-6-carboxamide 101 ##STR00134##
5-((4-formyl-6-methoxypyridin-3- yloxy)methyl)nicotinamide 102
##STR00135## 5-((6-(1H-pyrazol-4- yl)imidazo[1,2-a]pyridin-8-
yl)methoxy)-2- methoxyisonicotinaldehyde 103 ##STR00136##
5-(benzo[d]oxazol-4-ylmethoxy)- 2-methoxyisonicotinaldehyde 104
##STR00137## 5-((6-(1H-pyrazol-5- yl)imidazo[1,2-a]pyridin-8-
yl)methoxy)-2- methoxyisonicotinaldehyde 105 ##STR00138##
5-((1,5-naphthyridin-4- yl)methoxy)-2- methoxyisonicotinaldehyde
106 ##STR00139## 3-((1,5-naphthyridin-4- yl)methoxy)-6-
methylpicolinaldehyde 107 ##STR00140##
5-((1H-indazol-5-yl)methoxy)-2- methoxyisonicotinaldehyde 108
##STR00141## 6-methyl-3-((1-methyl-1H- indazol-5-
yl)methoxy)picolinaldehyde 109 ##STR00142##
3-((3-chloro-1-methyl-1H-indazol- 5-yl)methoxy)-6-
methylpicolinaldehyde 110 ##STR00143## 2-methoxy-5-((1-methyl-1H-
indazol-5- yl)methoxy)isonicotinaldehyde 111 ##STR00144##
5-((3-chloro-1-methyl-1H-indazol- 5-yl)methoxy)-2-
methoxyisonicotinaldehyde 112 ##STR00145##
N-(4-formyl-6-methoxypyridin-3- yl)imidazo[1,2-a]pyridine-8-
carboxamide 113 ##STR00146## 3-((1,3-dimethyl-1H-pyrazolo[3,4-
b]pyridin-4-yl)methoxy)-6- methylpicolinaldehyde 114 ##STR00147##
5-((1,3-dimethyl-1H-pyrazolo[3,4- b]pyridin-4-yl)methoxy)-2-
methoxyisonicotinaldehyde 115 ##STR00148##
3-((4-formyl-6-methoxypyridin-3- yloxy)methyl)picolinamide 116
##STR00149## 5-((2-chloroquinolin-3- yl)methoxy)-2-
methoxyisonicotinaldehyde 117 ##STR00150##
5-((2-(1H-pyrazol-5-yl)quinolin-3- yl)methoxy)-2-
methoxyisonicotinaldehyde 118 ##STR00151##
2-methoxy-5-(quinoxalin-2- ylmethoxy)isonicotinaldehyde 119
##STR00152## 6-methyl-3-(quinolin-5- ylmethoxy)picolinaldehyde 120
##STR00153## 2-methoxy-5-(quinolin-5- ylmethoxy)isonicotinaldehyde
121 ##STR00154## 6-methyl-3-((1-methyl-1H-
pyrazolo[3,4-b]pyridin-5- yl)methoxy)picolinaldehyde 122
##STR00155## 2-methoxy-5-((1-methyl-1H- pyrazolo[3,4-b]pyridin-5-
yl)methoxy)isonicotinaldehyde 123 ##STR00156## 5-((7-(1H-pyrazol-3-
yl)imidazo[1,5-a]pyridin-8- yl)methoxy)-2-
methoxyisonicotinaldehyde 124 ##STR00157##
5-((5-(2H-tetrazol-5-yl)pyridin-3- yl)methoxy)-2-
methoxyisonicotinaldehyde 125 ##STR00158## 5-((6-(2H-tetrazol-5-
yl)imidazo[1,2-a]pyridin-8- yl)methoxy)-2-
methoxyisonicotinaldehyde 126 ##STR00159## ethyl
2-(5-(imidazo[1,2-a]pyridin- 8-ylmethoxy)-2-methoxypyridin-
4-yl)thiazolidine-4-carboxylate 127 ##STR00160##
2-methoxy-5-((2-(1-methyl-1H- pyrazol-4-yl)pyridin-3-
yl)methoxy)isonicotinaldehyde 128 ##STR00161##
5-((2-(1H-pyrazol-4-yl)pyridin-3- yl)methoxy)-2-
methoxyisonicotinaldehyde 129 ##STR00162##
2-methoxy-5-((2-(1-methyl-1H- pyrazol-5-yl)pyridin-3-
yl)methoxy)isonicotinaldehyde 130 ##STR00163##
2-methoxy-5-((2-(1-methyl-1H- pyrazol-3-yl)pyridin-3-
yl)methoxy)isonicotinaldehyde 131 ##STR00164##
5-((2-(2H-tetrazol-5-yl)pyridin-3- yl)methoxy)-2-
methoxyisonicotinaldehyde 132 ##STR00165##
2-methoxy-5-((2-(4-methyl-1H- pyrazol-5-yl)pyridin-3-
yl)methoxy)isonicotinaldehyde 133 ##STR00166## 5-((3-(1H-pyrazol-5-
yl)isoquinolin-4-yl)methoxy)-2- methoxyisonicotinaldehyde 134
##STR00167## 5-((2-(1H-pyrazol-1-yl)pyridin-3- yl)methoxy)-2-
methoxyisonicotinaldehyde 135 ##STR00168##
3-((2-(1H-pyrazol-1-yl)pyridin-3- yl)methoxy)-6-
methylpicolinaldehyde 136 ##STR00169## 6-methyl-3-(pyridin-3-
ylmethoxy)picolinaldehyde 137 ##STR00170## methyl 8-(((4-formyl-6-
methoxypyridin-3- yl)oxy)methyl)imidazo[1,2-
a]pyridine-6-carboxylate 138 ##STR00171## methyl
2-bromo-8-(((4-formyl-6- methoxypyridin-3-
yl)oxy)methyl)imidazo[1,2- a]pyridine-6-carboxylate 139
##STR00172## 3-(imidazo[1,5-a]pyridin-8- ylmethoxy)-6-
methylpicolinaldehyde 140 ##STR00173## 5-(imidazo[1,5-a]pyridin-8-
ylmethoxy)-2- methoxyisonicotinaldehyde 141 ##STR00174##
(5-(methoxycarbonyl)pyridin-3- yl)methyl 5-(((4-formyl-6-
methoxypyridin-3- yl)oxy)methyl)nicotinate 142 ##STR00175##
5-((2-(1,4-dimethyl-1H-pyrazol-5- yl)pyridin-3-yl)methoxy)-2-
methoxyisonicotinaldehyde 143 ##STR00176##
5-((2-(1,5-dimethyl-1H-pyrazol-4- yl)pyridin-3-yl)methoxy)-2-
methoxyisonicotinaldehyde 144 ##STR00177## 2-hydroxyethyl
5-(((4-(1,3- dioxolan-2-yl)-6-methoxypyridin-
3-yl)oxy)methyl)nicotinate 145 ##STR00178## methyl
5-(((4-(1,3-dioxolan-2-yl)- 6-methoxypyridin-3-
yl)oxy)methyl)nicotinate 146 ##STR00179## methyl 5-(((4-(bis(2-
hydroxyethoxy)methyl)-6- methoxypyridin-3- yl)oxy)methyl)nicotinate
147 ##STR00180## 5-((2-(1,3-dimethyl-1H-pyrazol-4-
yl)pyridin-3-yl)methoxy)-2- methoxyisonicotinaldehyde 148
##STR00181## 5-((2-(1,3-dimethyl-1H-pyrazol-5-
yl)pyridin-3-yl)methoxy)-2- methoxyisonicotinaldehyde 149
##STR00182## 5-((2-(1-ethyl-1H-pyrazol-5-
yl)pyridin-3-yl)methoxy)-2- methoxyisonicotinaldehyde 150
##STR00183## 5-((2-(1-isopropyl-1H-pyrazol-5-
yl)pyridin-3-yl)methoxy)-2- methoxyisonicotinaldehyde 151
##STR00184## 2-methoxy-5-((2-(3-methyl-1H- pyrazol-1-yl)pyridin-3-
yl)methoxy)isonicotinaldehyde 152 ##STR00185##
5-(((4-(1,3-dioxolan-2-yl)-6- methoxypyridin-3-
yl)oxy)methyl)nicotinic acid 153 ##STR00186##
(E)-2-methoxy-5-((2-(4-methyl- 1H-pyrazol-5-yl)pyridin-3-
yl)methoxy)isonicotinaldehyde oxime 154 ##STR00187##
(E)-2-methoxy-5-(pyridin-3- ylmethoxy)isonicotinaldehyde oxime 155
##STR00188## 2-(5-(imidazo[1,2-a]pyridin-8-
ylmethoxy)-2-methoxypyridin-4- yl)thiazolidine 156 ##STR00189##
1-(2-(5-(imidazo[1,2-a]pyridin-8- ylmethoxy)-2-methoxypyridin-4-
yl)thiazolidin-3-yl)ethanone 157 ##STR00190##
5-((2-(4-(1H-pyrazol-3- yl)piperazin-1-yl)pyridin-3- yl)methoxy)-2-
methoxyisonicotinaldehyde 158 ##STR00191## 2-(difluoromethoxy)-5-
(imidazo[1,2-a]pyridin-8- ylmethoxy)isonicotinaldehyde 159
##STR00192## 2-methoxy-5-((2-phenylpyridin-3-
yl)methoxy)isonicotinaldehyde 160 ##STR00193##
5-((3-(1-isopropyl-1H-pyrazol-5- yl)pyridin-4-yl)methoxy)-2-
methoxyisonicotinaldehyde 161 ##STR00194##
5-([2,3'-bipyridin]-3-ylmethoxy)- 2-methoxyisonicotinaldehyde 162
##STR00195## 2-methoxy-5-((2-(o-tolyl)pyridin-
3-yl)methoxy)isonicotinaldehyde 163 ##STR00196##
2-methoxy-5-((2'-methoxy-[2,3'- bipyridin]-3-
yl)methoxy)isonicotinaldehyde 164 ##STR00197## methyl
4-(((2-formylpyridin-3- yl)oxy)methyl)benzoate 165 ##STR00198##
4-(((2-formyl-6-methylpyridin-3- yl)oxy)methyl)benzoic acid 166
##STR00199## 4-(((2-formylpyridin-3- yl)oxy)methyl)benzoic acid 167
##STR00200## methyl 3-(((4-formylpyridin-3- yl)oxy)methyl)benzoate
168 ##STR00201## methyl 3-(((2-formyl-6- methylpyridin-3-
yl)oxy)methyl)benzoate 169 ##STR00202## 3-(((4-formylpyridin-3-
yl)oxy)methyl)benzoic acid 170 ##STR00203##
3-(((2-formyl-6-methylpyridin-3- yl)oxy)methyl)benzoic acid 171
##STR00204## 3-(((2-formylpyridin-3- yl)oxy)methyl)benzoic acid 172
##STR00205## 2-methoxy-5-((2-(1-(2- methoxyethyl)-1H-pyrazol-5-
yl)pyridin-3- yl)methoxy)isonicotinaldehyde 173 ##STR00206##
2-methoxy-5-((2-(1-propyl-1H- pyrazol-5-yl)pyridin-3-
yl)methoxy)isonicotinaldehyde 174 ##STR00207##
2-methoxy-5-((2-(1-(2,2,2- trifluoroethyl)-1H-pyrazol-5-
yl)pyridin-3- yl)methoxy)isonicotinaldehyde
175 ##STR00208## 5-((2-(1-(2,2-difluoroethyl)-1H-
pyrazol-5-yl)pyridin-3- yl)methoxy)-2- methoxyisonicotinaldehyde
176 ##STR00209## 3-((2-(1-isopropyl-1H-pyrazol-5- yl)pyridin-3-
yl)methoxy)picolinaldehyde 177 ##STR00210##
3-((2-(1-isopropyl-1H-pyrazol-5- yl)pyridin-3-yl)methoxy)-6-
methylpicolinaldehyde 178 ##STR00211##
2-(difluoromethoxy)-5-((2-(1- isopropyl-1H-pyrazol-5- yl)pyridin-3-
yl)methoxy)isonicotinaldehyde 179 ##STR00212##
5-(imidazo[1,2-a]pyridin-8- ylmethoxy)-2-(2-
methoxyethoxy)isonicotinaldehyde 180 ##STR00213##
5-((2-(1-isopropyl-1H-pyrazol-5- yl)pyridin-3-yl)methoxy)-2-(2-
methoxyethoxy)isonicotinaldehyde 181 ##STR00214##
5-((3-(1-isopropyl-1H-pyrazol-5- yl)pyrazin-2-yl)methoxy)-2-
methoxyisonicotinaldehyde 182 ##STR00215##
3-((4-formyl-6-methoxypyridin-3- yloxy)methyl)picolinate 183
##STR00216## 5-((2-(2-hydroxypropan-2- yl)pyridin-3-yl)methoxy)-2-
methoxyisonicotinaldehyde 184 ##STR00217##
2-(2-methoxyethoxy)-5-((2-(1- methyl-1H-pyrazol-5-yl)pyridin-3-
yl)methoxy)isonicotinaldehyde 185 ##STR00218##
2-(2-methoxyethoxy)-5-((2-(1- methyl-1H-pyrazol-5-yl)pyridin-3-
yl)methoxy)nicotinaldehyde 186 ##STR00219##
3-hydroxy-5-((2-(1-isopropyl-1H- pyrazol-5-yl)pyridin-3-
yl)methoxy)isonicotinaldehyde 187 ##STR00220## 3-(benzyloxy)-5-
hydroxyisonicotinaldehyde 188 ##STR00221##
3-((2-(1-isopropyl-1H-pyrazol-5- yl)pyridin-3-yl)methoxy)-5-
methoxyisonicotinaldehyde 189 ##STR00222##
5-((2-(2-isopropyl-2H-1,2,4- triazol-3-yl)pyridin-3- yl)methoxy)-2-
methoxyisonicotinaldehyde 190 ##STR00223##
5-((2-(1-isopropyl-4-methyl-1H- pyrazol-5-yl)pyridin-3-
yl)methoxy)-2- methoxyisonicotinaldehyde 191 ##STR00224##
5-((2-(1-(2-hydroxyethyl)-1H- pyrazol-5-yl)pyridin-3-
yl)methoxy)-2- methoxyisonicotinaldehyde 192 ##STR00225##
2,2,2-trifluoroacetic acid:6-(((4- formylpyridin-3-
yl)oxy)methyl)picolinic acid (1:1) 193 ##STR00226##
2-methoxy-5-((2-(1-((2- (trimethylsilyl)ethoxy)methyl)-1H-
pyrazol-5-yl)pyridin-3- yl)methoxy)isonicotinaldehyde 194
##STR00227## 5-((2-(4-methyl-1H-pyrazol-5-
yl)pyridin-3-yl)methoxy)-2-oxo- 1,2-dihydropyridine-4- carbaldehyde
195 ##STR00228## 5-((2-(1-cyclobutyl-1H-pyrazol-5-
yl)pyridin-3-yl)methoxy)-2- methoxyisonicotinaldehyde 196
##STR00229## 5-((2-(1-cyclohexyl-1H-pyrazol-5-
yl)pyridin-3-yl)methoxy)-2- methoxyisonicotinaldehyde 197
##STR00230## 5-((2-(1-(cyclohexylmethyl)-1H-
pyrazol-5-yl)pyridin-3- yl)methoxy)-2- methoxyisonicotinaldehyde
198 ##STR00231## 5-((2-(1-cyclopentyl-1H-pyrazol-
5-yl)pyridin-3-yl)methoxy)-2- methoxyisonicotinaldehyde 199
##STR00232## 2-(5-(3-((4-formyl-6- methoxypyridin-3-
yloxy)methyl)pyridin-2-yl)-1H- pyrazol-1-yl)acetic acid 200
##STR00233## methyl 3-(5-(3-(((4-formyl-6- methoxypyridin-3-
yl)oxy)methyl)pyridin-2-yl)-1H- pyrazol-1-yl)propanoate 201
##STR00234## 3-(3-(3-((4-formyl-6- methoxypyridin-3-
yloxy)methyl)pyridin-2-yl)-1H- pyrazol-1-yl)propanoic acid 202
##STR00235## 3-(5-(3-(((4-formyl-6- methoxypyridin-3-
yl)oxy)methyl)pyridin-2-yl)-1H- pyrazol-1-yl)propanoic acid 203
##STR00236## 3-(((4-formyl-6-methoxypyridin-3-
yl)oxy)methyl)benzoic acid 204 ##STR00237## 6-(((4-formylpyridin-3-
yl)oxy)methyl)nicotinonitrile 2,2,2-trifluoroacetate 205
##STR00238## 6-(((4-formylpyridin-3- yl)oxy)methyl)nicotinic acid
hydrochloride 206 ##STR00239## 2,2,2-trifluoroacetic acid:6-(((4-
formylpyridin-3-yl)oxy)methyl)- N-(methylsulfonyl)nicotinamide
(2:1) 207 ##STR00240## 2-(2-methoxyethoxy)-5-((2-(1-
(2,2,2-trifluoroethyl)-1H-pyrazol- 5-yl)pyridin-3-
yl)methoxy)isonicotinaldehyde 208 ##STR00241##
2-methoxy-5-((2-(1-(3,3,3- trifluoropropyl)-1H-pyrazol-5-
yl)pyridin-3- yl)methoxy)isonicotinaldehyde 209 ##STR00242##
2-(2-methoxyethoxy)-5-((2-(1- (3,3,3-trifluoropropyl)-1H-
pyrazol-5-yl)pyridin-3- yl)methoxy)isonicotinaldehyde 210
##STR00243## 2-methyl-5-((2-(1-(2,2,2-
trifluoroethyl)-1H-pyrazol-5- yl)pyridin-3-
yl)methoxy)isonicotinaldehyde 211 ##STR00244##
2-methyl-5-((2-(1-(3,3,3- trifluoropropyl)-1H-pyrazol-5-
yl)pyridin-3- yl)methoxy)isonicotinaldehyde 212 ##STR00245##
3-((2-(1-(2,2,2-trifluoroethyl)-1H- pyrazol-5-yl)pyridin-3-
yl)methoxy)isonicotinaldehyde 213 ##STR00246##
3-((2-(1-(3,3,3-trifluoropropyl)- 1H-pyrazol-5-yl)pyridin-3-
yl)methoxy)isonicotinaldehyde 214 ##STR00247##
3-chloro-5-((2-(1-isopropyl-1H- pyrazol-5-yl)pyridin-3-
yl)methoxy)isonicotinaldehyde 215 ##STR00248##
3-((2-(1-isopropyl-1H-pyrazol-5- yl)pyridin-3-yl)methoxy)-5-
methylisonicotinaldehyde 216 ##STR00249## 3-chloro-5-((2-(1-(3,3,3-
trifluoropropyl)-1H-pyrazol-5- yl)pyridin-3-
yl)methoxy)isonicotinaldehyde 217 ##STR00250##
3-methyl-5-((2-(1-(2,2,2- trifluoroethyl)-1H-pyrazol-5-
yl)pyridin-3- yl)methoxy)isonicotinaldehyde
[0193] In one group of embodiments, the compound is selected from
5-hydroxy-2-(2-methoxyethoxyl)isonicotinaldehyde (Compound 218),
5-hydroxy-2-(2-methoxyethoxy)nicotinaldehyde (Compound 219),
5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-oxo-1,2-dihydr-
opyridine-4-carbaldehyde (Compound 220),
5-((2-(4-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-oxo-1,2-dihydropy-
ridine-4-carbaldehyde (Compound 221), or a tautomer or
pharmaceutically acceptable salt thereof.
[0194] In one group of embodiments, the compound is selected from:
[0195]
5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-methoxy)isonicotinaldehyde,
[0196]
2-methoxy-5-((5-methylpyridin-3-yl)methoxy)isonicotinaldehyde,
[0197] 5-(isoquinolin-1-ylmethoxy)-2-methoxyisonicotinaldehyde,
[0198] 2-methoxy-5-(quinolin-2-ylmethoxy)isonicotinaldehyde, [0199]
2-methoxy-5-(pyridin-4-ylmethoxy)isonicotinaldehyde, [0200]
3-(imidazo[1,2-a]pyridin-8-ylmethoxy)-6-methylpicolinaldehyde,
[0201] methyl
2-((4-formyl-6-methoxypyridin-3-yloxy)methyl)imidazo[1,2-a]pyridin-
e-8-carboxylate, [0202]
2-methoxy-5((3-methyl-[1,2,4]triazolo[4,3-a]pyridin-8-yl)methoxy)isonicot-
inaldehyde, [0203]
5-((2-bromopyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
[0204]
5-((2-(1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
[0205]
5-((5-bromopyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
[0206]
2-methoxy-5-((5-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)iso-
nicotinaldehyde, [0207]
5-((4-formyl-6-methoxypyridin-3-yloxy)methyl)nicotinic acid, [0208]
2-methoxy-5-(quinolin-3-ylmethoxy)isonicotinaldehyde, [0209]
2-methoxy-5-((1-methyl-1H-indazol-4-yl)methoxy)isonicotinaldehyde,
[0210] tert-butyl
4-((2-formyl-6-methylpyridin-3-yloxy)methyl)-1H-indazole-1-carboxylate,
[0211]
6-methyl-3-((1-methyl-1H-indazol-6-yl)methoxy)picolinaldehyde,
[0212]
6-methyl-3-((1-methyl-1H-indazol-7-yl)methoxy)picolinaldehyde,
[0213] 3-(isoquinolin-1-ylmethoxy)-6-methylpicolinaldehyde, [0214]
5-(benzo[d]oxazol-4-ylmethoxy)-2-methoxyisonicotinaldehyde, [0215]
3-((1,5-naphthyridin-4-yl)methoxy)-6-methylpicolinaldehyde, [0216]
6-methyl-3-((1-methyl-1H-indazol-5-yl)methoxy)picolinaldehyde,
[0217] 6-methyl-3-(quinolin-5-ylmethoxy)picolinaldehyde, [0218]
2-methoxy-5-(quinolin-5-ylmethoxy)isonicotinaldehyde, [0219]
2-methoxy-5-((2-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde, [0220]
2-methoxy-5-((2-(1-methyl-1H-pyrazol-3-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde, [0221]
5-((2-(2H-tetrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde-
, [0222]
2-methoxy-5-((2-(4-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)is-
onicotinaldehyde, [0223]
5-((3-(1H-pyrazol-5-yl)isoquinolin-4-yl)methoxy)-2-methoxyisonicotinaldeh-
yde, [0224]
5-((2-(1H-pyrazol-1-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde,
[0225]
5-(imidazo[1,5-a]pyridin-8-ylmethoxy)-2-methoxyisonicotinaldehyde,
[0226]
5-((2-(1,5-dimethyl-1H-pyrazol-4-yl)pyridin-3-yl)methoxy)-2-methox-
yisonicotinaldehyde, [0227]
5-((2-(1-ethyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotina-
ldehyde, [0228]
5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonico-
tinaldehyde, [0229]
2-(difluoromethoxy)-5-(imidazo[1,2-a]pyridin-8-ylmethoxy)isonicotinaldehy-
de, [0230]
2-methoxy-5-((2-phenylpyridin-3-yl)methoxy)isonicotinaldehyde,
[0231]
5-((3-(1-isopropyl-1H-pyrazol-5-yl)pyridin-4-yl)methoxy)-2-methoxy-
isonicotinaldehyde, [0232]
5-([2,3'-bipyridin]-3-ylmethoxy)-2-methoxyisonicotinaldehyde,
[0233]
2-methoxy-5-((2-(o-tolyl)pyridin-3-yl)methoxy)isonicotinaldehyde,
[0234]
2-methoxy-5-((2'-methoxy-[2,3'-bipyridin]-3-yl)methoxy)isonicotinaldehyde-
, [0235] 4-(((2-formyl-6-methylpyridin-3-yl)oxy)methyl)benzoic
acid, [0236] 4-(((2-formylpyridin-3-yl)oxy)methyl)benzoic acid,
[0237] methyl 3-(((4-formylpyridin-3-yl)oxy)methyl)benzoate, [0238]
methyl 3-(((2-formyl-6-methylpyridin-3-yl)oxy)methyl)benzoate,
[0239] 3-(((4-formylpyridin-3-yl)oxy)methyl)benzoic acid, [0240]
3-(((2-formyl-6-methylpyridin-3-yl)oxy)methyl)benzoic acid, [0241]
3-(((2-formylpyridin-3-yl)oxy)methyl)benzoic acid, [0242]
2-methoxy-5-((2-(1-(2-methoxyethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-
isonicotinaldehyde, [0243]
2-methoxy-5-((2-(1-propyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde, [0244]
2-methoxy-5-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl)pyridin-3-yl)me-
thoxy)isonicotinaldehyde, [0245]
5-((2-(1-(2,2-difluoroethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-meth-
oxyisonicotinaldehyde, [0246]
3-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)picolinaldehyde,
[0247]
3-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-6-methylp-
icolinaldehyde, [0248]
2-(difluoromethoxy)-5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)metho-
xy)isonicotinaldehyde, [0249]
5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-(2-methoxyethoxyl)isonicotinaldeh-
yde, [0250]
5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-(2-methoxyetho-
xyl)isonicotinaldehyde, [0251]
5-((3-(1-isopropyl-1H-pyrazol-5-yl)pyrazin-2-yl)methoxy)-2-methoxyisonico-
tinaldehyde, [0252]
3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)picolinate, [0253]
5-((2-(2-hydroxypropan-2-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinalde-
hyde, [0254]
2-(2-methoxyethoxy)-5-((2-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-
isonicotinaldehyde, [0255]
2-(2-methoxyethoxy)-5-((2-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-
nicotinaldehyde, [0256]
3-hydroxy-5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonico-
tinaldehyde, [0257] 3-(benzyloxy)-5-hydroxyisonicotinaldehyde,
[0258]
3-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-5-methoxyisonico-
tinaldehyde, [0259]
5-((2-(2-isopropyl-2H-1,2,4-triazol-3-yl)pyridin-3-yl)methoxy)-2-methoxyi-
sonicotinaldehyde, [0260]
5-((2-(1-isopropyl-4-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-metho-
xyisonicotinaldehyde, [0261]
5-((2-(1-(2-hydroxyethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxy-
isonicotinaldehyde, [0262]
6-(((4-formylpyridin-3-yl)oxy)methyl)picolinic acid, [0263]
2,2,2-trifluoroacetic
acid:6-(((4-formylpyridin-3-yl)oxy)methyl)picolinic acid (1:1),
[0264]
2-methoxy-5-((2-(1((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazol-5-yl)pyri-
din-3-yl)methoxy)isonicotinaldehyde, [0265]
5-((2-(4-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-oxo-1,2-dihydropy-
ridine-4-carbaldehyde, [0266]
5-((2-(1-cyclobutyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonic-
otinaldehyde, [0267]
5-((2-(1-cyclohexyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonic-
otinaldehyde, [0268]
5-((2-(1-(cyclohexylmethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-metho-
xyisonicotinaldehyde, [0269]
5-((2-(1-cyclopentyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisoni-
cotinaldehyde, [0270]
2-(5-(3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)pyridin-2-yl)-1H-pyraz-
ol-1-yl)acetic acid, [0271] methyl
3-(5-(3-(((4-formyl-6-methoxypyridin-3-yl)oxy)methyl)pyridin-2-yl)-1H-pyr-
azol-1-yl)propanoate, [0272]
3-(3-(3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)pyridin-2-yl)-1H-pyraz-
ol-1-yl)propanoic acid, [0273]
3-(5-(3-(((4-formyl-6-methoxypyridin-3-yl)oxy)methyl)pyridin-2-yl)-1H-pyr-
azol-1-yl)propanoic acid, [0274]
3-(((4-formyl-6-methoxypyridin-3-yl)oxy)methyl)benzoic acid, [0275]
6-(((4-formylpyridin-3-yl)oxy)methyl)nicotinonitrile
2,2,2-trifluoroacetate, [0276]
6-(((4-formylpyridin-3-yl)oxy)methyl)nicotinic acid, [0277]
6-(((4-formylpyridin-3-yl)oxy)methyl)nicotinic acid hydrochloride,
[0278]
6-(((4-formylpyridin-3-yl)oxy)methyl)-N-(methylsulfonyl)nicotinamide,
[0279] 2,2,2-trifluoroacetic
acid:6-(((4-formylpyridin-3-yl)oxy)methyl)-N-(methylsulfonyl)nicotinamide
(2:1),
2-(2-methoxyethoxy)-5-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-y-
l)pyridin-3-yl)methoxy)isonicotinaldehyde, [0280]
2-methoxy-5-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyridin-3-yl)m-
ethoxy)isonicotinaldehyde, [0281]
2-(2-methoxyethoxy)-5-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyri-
din-3-yl)methoxy)isonicotinaldehyde, [0282]
2-methyl-5-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl)pyridin-3-yl)met-
hoxy)isonicotinaldehyde, [0283]
2-methyl-5-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyridin-3-yl)me-
thoxy)isonicotinaldehyde, [0284]
3-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)ison-
icotinaldehyde, [0285]
3-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)iso-
nicotinaldehyde, [0286]
3-chloro-5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonicot-
inaldehyde, [0287]
3-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-5-methylisonicot-
inaldehyde, [0288]
3-chloro-5-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyridin-3-yl)me-
thoxy)isonicotinaldehyde, and [0289]
3-methyl-5-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl)pyridin-3-yl)met-
hoxy)isonicotinaldehyde, or a tautomer or pharmaceutically
acceptable salt thereof
[0290] In one group of embodiments, provided is a pharmaceutical
composition comprising a compound of any of the above embodiments
or a tautomer or pharmaceutically acceptable salt thereof.
[0291] In one group of embodiments, provided is a compound in any
of the Examples or Tables. In another group of embodiments,
provided are any combinations of subembodiments as disclosed herein
including any combination of elements disclosed herein including
the a selection of any single elements.
[0292] The compounds of the present invention may be prepared by
known organic synthesis techniques, including the methods described
in more detail in the Examples.
[0293] In one group of embodiments, provided is an intermediate
compound used in the preparation of the compounds disclosed
herein.
[0294] In one group of embodiments, provided are methods for
preparing the compounds disclosed herein.
[0295] For example, Scheme I shows a synthetic route for the
synthesis of the compounds of Formula (I) where X is O and Y is
CH.sub.2. Phenol 1.1 is contacted with intermediate 1.2 in the
presence of base under ether forming conditions to give ether 1.3,
where Lg represents a leaving group such as a halogen leaving
group. Conversely, when X is O and Y is CH.sub.2, the compounds of
Formula (I) can be prepared using the appropriate starting
materials where the OH moiety of intermediate 1.1 is replaced with
a leaving group and the Lg group of intermediate 1.2 is replaced
with an OH group.
##STR00251##
[0296] Scheme II shows an example of a synthetic route for the
synthesis of the compounds of
[0297] Formula (I) where X and Y are CH.sub.2. Alkene 2.1 is
contacted with alkene 2.2 under metathesis forming conditions in
the presence of an appropriate transition metal catalyst. Suitable
catalysts include ruthenium catalysts such as Grubbs' catalyst.
Product 2.3 is then hydrogenated to give compound 2.4.
##STR00252##
[0298] Scheme III shows an example of a synthetic route for the
synthesis of the compounds of Formula (I) where R.sup.6 together
with R.sup.1b form a cyclic ether. Compound 3.1, is reacted with
diethylphosphite and a base such as sodium methoxide to give
intermediate 3.2, that is then condensed with aldehyde 3.3 to give
alkene 3.4. Treatment of the alkene with H.sub.2 under
hydrogenation conditions gives lactone 3.4, which is then reduced
with a suitable reducing agent such as LiBHEt.sub.3 to give cyclic
hemiacetal 3.5.
##STR00253##
[0299] Scheme IV shows an example of synthesis of the compounds of
Formula (I) where Q is pyridine-3-yl and R.sup.a heteroaryl. Acid
4.1 is reduced to alcohol 4.2 using known methods such as by
forming the anhydride (e.g. treatment with triethylamine and
i-butyl chloroformate) followed by reduction with NaBH.sub.4.
Alcohol 4.2 is converted to chloride 4.3 such as by treatment with
thionyl chloride. Coupling of the halide with alcohol 4.4 under
ether forming conditions gives the precursor 4.5 that can be
functionalized with a variety to heteroaryl R.sup.a groups. For
example, 4.5 can be coupled with pyrazole 4.6 under known
organometallic coupling conditions (e.g. Pd(PPh.sub.3).sub.4) to
give 4.7, where PG is a nitrogen protecting group such as a silyl
protecting group that can be removed to give the product 4.8.
##STR00254##
[0300] One skilled in the art will recognize that in certain
embodiments it may be advantageous to use a protecting group
strategy. The protecting group can be removed using methods known
to those skilled in the art.
[0301] The compounds of the present invention may generally be
utilized as the free base. Alternatively, the compounds of this
invention may be used in the form of acid addition salts.
[0302] It is understood that in another group of embodiments, any
of the above embodiments may also be combined with other
embodiments listed herein, to form other embodiments of the
invention. Similarly, it is understood that in other embodiments,
listing of groups includes embodiments wherein one or more of the
elements of those groups is not included.
III. Compositions and Methods of Administration
[0303] Depending on the intended mode of administration, the
pharmaceutical compositions may be in the form of solid, semi-solid
or liquid dosage forms, preferably in unit dosage form suitable for
single administration of a precise dosage. In addition to an
effective amount of the active compound(s), the compositions may
contain suitable pharmaceutically-acceptable excipients, including
adjuvants which facilitate processing of the active compounds into
preparations which can be used pharmaceutically. "Pharmaceutically
acceptable excipient" refers to an excipient or mixture of
excipients which does not interfere with the effectiveness of the
biological activity of the active compound(s) and which is not
toxic or otherwise undesirable to the subject to which it is
administered.
[0304] For solid compositions, conventional excipients include, for
example, pharmaceutical grades of mannitol, lactose, starch,
magnesium stearate, sodium saccharin, talc, cellulose, glucose,
sucrose, magnesium carbonate, and the like. Liquid
pharmacologically administrable compositions can, for example, be
prepared by dissolving, dispersing, etc., an active compound as
described herein and optional pharmaceutical adjuvants in water or
an aqueous excipient, such as, for example, water, saline, aqueous
dextrose, and the like, to form a solution or suspension. If
desired, the pharmaceutical composition to be administered may also
contain minor amounts of nontoxic auxiliary excipients such as
wetting or emulsifying agents, pH buffering agents and the like,
for example, sodium acetate, sorbitan monolaurate, triethanolamine
sodium acetate, triethanolamine oleate, etc.
[0305] For oral administration, the composition will generally take
the form of a tablet or capsule, or it may be an aqueous or
nonaqueous solution, suspension or syrup. Tablets and capsules are
preferred oral administration forms. Tablets and capsules for oral
use will generally include one or more commonly used excipients
such as lactose and corn starch. Lubricating agents, such as
magnesium stearate, are also typically added. When liquid
suspensions are used, the active agent may be combined with
emulsifying and suspending excipients. If desired, flavoring,
coloring and/or sweetening agents may be added as well. Other
optional excipients for incorporation into an oral formulation
include preservatives, suspending agents, thickening agents, and
the like.
[0306] Injectable formulations can be prepared in conventional
forms, either as liquid solutions or suspensions, solid forms
suitable for solubilization or suspension in liquid prior to
injection, or as emulsions or liposomal formulations. The sterile
injectable formulation may also be a sterile injectable solution or
a suspension in a nontoxic parenterally acceptable diluent or
solvent. Among the acceptable vehicles and solvents that may be
employed are water, Ringer's solution and isotonic sodium chloride
solution. In addition, sterile, fixed oils, fatty esters or polyols
are conventionally employed as solvents or suspending media.
[0307] The pharmaceutical compositions of this invention may also
be formulated in lyophilized form for parenteral administration.
Lyophilized formulations may be reconstituted by addition of water
or other aqueous medium and then further diluted with a suitable
diluent prior to use. The liquid formulation is generally a
buffered, isotonic, aqueous solution. Examples of suitable diluents
are isotonic saline solution, 5% dextrose in water, and buffered
sodium or ammonium acetate solution. Pharmaceutically acceptable
solid or liquid excipients may be added to enhance or stabilize the
composition, or to facilitate preparation of the composition.
[0308] Typically, a pharmaceutical composition of the present
invention is packaged in a container with a label, or instructions,
or both, indicating use of the pharmaceutical composition in the
treatment of the indicated disease.
[0309] The pharmaceutical composition may additionally contain one
or more other pharmacologically active agents in addition to a
compound of this invention.
[0310] Dosage forms containing effective amounts of the modulators
are within the bounds of routine experimentation and within the
scope of the invention. A therapeutically effective dose may vary
depending upon the route of administration and dosage form. The
representative compound or compounds of the invention is a
formulation that exhibits a high therapeutic index. The therapeutic
index is the dose ratio between toxic and therapeutic effects which
can be expressed as the ratio between LD.sub.50 and ED.sub.50. The
LD.sub.50 is the dose lethal to 50% of the population and the
ED.sub.50 is the dose therapeutically effective in 50% of the
population. The LD.sub.50 and ED.sub.50 are determined by standard
pharmaceutical procedures in animal cell cultures or experimental
animals. It should be understood that a specific dosage and
treatment regimen for any particular patient will depend upon a
variety of factors, including the activity of the specific compound
employed, the age, body weight, general health, sex and diet of the
patient, and the time of administration, rate of excretion, drug
combination, judgment of the treating physician and severity of the
particular disease being treated. The amount of active
ingredient(s) will also depend upon the particular compound and
other therapeutic agent, if present, in the composition.
IV. Methods
[0311] In one group of embodiments, provided is a method for
increasing tissue oxygenation, the method comprising administering
to a subject in need thereof a therapeutically effective amount of
a compound of any of the above embodiments or a tautomer or
pharmaceutically acceptable salt thereof.
[0312] In one group of embodiments, provided is a method for
treating a condition associated with oxygen deficiency, the method
comprising administering to a subject in need thereof a
therapeutically effective amount of a compound of any of the above
embodiments or a tautomer or pharmaceutically acceptable salt
thereof.
[0313] In one group of embodiments, provided is a method for
treating sickle cell disease, cancer, a pulmonary disorder, stroke,
high altitude sickness, an ulcer, a pressure sore, Alzheimer's
disease, acute respiratory disease syndrome, and a wound, the
method comprising administering to a subject in need thereof a
therapeutically effective amount of a compound of any of the above
embodiments or a tautomer or pharmaceutically acceptable salt
thereof.
[0314] In one group of embodiments, provided is a method for
increasing tissue oxygenation or for treating a condition
associated with oxygen deficiency, said method comprising
administering to a subject in need thereof a therapeutically
effective amount of a compound Formula (II):
##STR00255##
or a tautomer or pharmaceutically acceptable salt thereof,
[0315] wherein Q is selected from the group consisting of aryl,
heteroaryl, and heterocycloalkyl, each optionally substituted with
one to three R.sup.a;
[0316] Y is 0 or CR.sup.1aR.sup.1b, where R.sup.1a is H or halo and
R.sup.1b is selected from the group consisting of H, halo, and
OH;
[0317] X is selected from the group consisting of O,
>CH(CH.sub.2).sub.nR.sup.8, and C(R.sup.9).sub.2 where n is 0 or
1, R.sup.8 is OH, and R.sup.9 is independently H or halo; or Y--X
taken together is --NHC(O)-- or --C(O)NH--;
[0318] R.sup.2, R.sup.3, R.sup.4, and R.sup.5 are independently
absent or selected from the group consisting of hydrogen, halo,
R.sup.b, OR.sup.d, O(CH.sub.2).sub.zOR.sup.d,
O(CH.sub.2).sub.zNR.sup.dR.sup.d, OC(O)R.sup.e, SR.sup.d, CN,
NO.sub.2, CO.sub.2R.sup.d, CONR.sup.dR.sup.d, C(O)R.sup.d,
OC(O)NR.sup.dR.sup.d, NR.sup.dR.sup.d, NR.sup.dC(O)R.sup.e,
NR.sup.dC(O).sub.2R.sup.e, NR.sup.dC(O)NR.sup.dR.sup.d,
S(O)R.sup.e, S(O).sub.2R.sup.e, NR.sup.dS(O).sub.2R.sup.e,
S(O).sub.2NR.sup.dR.sup.d, and N.sub.3 where z is 0, 1, 2, or 3; or
R.sup.5 is --(CH.sub.2).sub.pR.sup.5a where p is 0 or 1 and
R.sup.5a is OH;
[0319] R.sup.6 and R.sup.7 together form oxo or an aldehyde
protecting group, or R.sup.6 together with R.sup.1b, R.sup.8, or
R.sup.5 forms a cyclic ether where one of R.sup.1b, R.sup.8, or
R.sup.5a is O, R.sup.6 is a bond, and R.sup.7 is selected from the
group consisting of OH, C.sub.1-8alkoxy, and
haloC.sub.1-8alkoxy;
[0320] T.sup.1, T.sup.2, T.sup.3, and T.sup.4 are independently C
or N provided that at least one of T.sup.1, T.sup.2, T.sup.3, and
T.sup.4 is N and at least one of T.sup.1, T.sup.2, T.sup.3, and
T.sup.4 is C;
[0321] each R.sup.a is independently selected from the group
consisting of halo, le, OR.sup.d, O(CH.sub.2).sub.uOR.sup.d,
O(CH.sub.2).sub.uNR.sup.dR.sup.d,
O(CH.sub.2).sub.uNR.sup.dC(O)R.sup.e,
O(CH.sub.2).sub.uNR.sup.dC(O).sub.2R.sup.e,
O(CH.sub.2).sub.uNR.sup.dS(O).sub.2R.sup.e, NH.sub.2,
--(CH.sub.2).sub.kOC(O)R.sup.e, --(CH.sub.2).sub.kSR.sup.d, CN,
NO.sub.2, --(CH.sub.2).sub.kCO.sub.2(C.sub.1-8alkyl)OH,
--(CH.sub.2).sub.kCO.sub.2(C.sub.1-8alkyl)(heteroaryl)C(O)(C.sub.1-8alkyl-
), --(CH.sub.2).sub.kCO.sub.2R.sup.d,
--(CH.sub.2).sub.kCONR.sup.dR.sup.d,
--(CH.sub.2).sub.kNR.sup.dC(O)R.sup.e,
--(CH.sub.2).sub.kNR.sup.dC(O).sub.2R.sup.e,
--(CH.sub.2).sub.kC(O)R.sup.d,
--(CH.sub.2).sub.kOC(O)NR.sup.dR.sup.d,
--NR.sup.d(CH.sub.2).sub.uOR.sup.d,
--NR.sup.d(CH.sub.2).sub.uNR.sup.dR.sup.d,
--NR.sup.d(CH.sub.2).sub.uNR.sup.dC(O)R.sup.e,
--NR.sup.d(CH.sub.2).sub.uNR.sup.dC(O).sub.2R.sup.e,
--NR.sup.d(CH.sub.2).sub.uNR.sup.dS(O).sub.2R.sup.e,
--(CH.sub.2).sub.kNR.sup.dC(O)R.sup.e,
--(CH.sub.2).sub.kNR.sup.dC(O).sub.2R.sup.d,
--(CH.sub.2).sub.kNR.sup.dC(O)NR.sup.dR.sup.d,
--(CH.sub.2).sub.kS(O)R.sup.e, --(CH.sub.2).sub.kS(O).sub.2R.sup.e,
--(CH.sub.2).sub.kNR.sup.dS(O).sub.2R.sup.e,
--C(O)(CH.sub.2).sub.kNR.sup.dS(O).sub.2R.sup.e,
--(CH.sub.2).sub.kC(O)NR.sup.dS(O).sub.2R.sup.e,
--(CH.sub.2).sub.kS(O).sub.2NR.sup.dR.sup.d, N.sub.3,
--(CH.sub.2).sub.karyl optionally substituted with one to three
R.sup.c, --NR.sup.d(CH.sub.2).sub.karyl optionally substituted with
one to three R.sup.c, --(CH.sub.2).sub.kheteroaryl optionally
substituted with one to three R.sup.c,
--NR.sup.d(CH.sub.2).sub.kheteroaryl optionally substituted with
one to three R.sup.c, --(CH.sub.2).sub.kheterocycloalkyl optionally
substituted with one to three R.sup.c, and
--NR.sup.d(CH.sub.2).sub.kheterocycloalkyl optionally substituted
with one to three R.sup.c where k is 0, 1, 2, 3, 4, 5, or 6 and u
is 1, 2, 3, 4, 5, or 6;
[0322] each R.sup.b is independently selected from the group
consisting of C.sub.1-8alkyl, C.sub.2-8alkenyl, and
C.sub.2-8alkynyl, each optionally independently substituted with
one to three halo, OR.sup.d, or NR.sup.dR.sup.d;
[0323] each R.sup.c is independently selected from the group
consisting of halo, C.sub.1-8alkyl, haloC.sub.1-8alkyl,
C.sub.2-8alkenyl, haloC.sub.2-8alkenyl, C.sub.2-8alkynyl,
haloC.sub.2-8alkynyl, (CH.sub.2).sub.mOR.sup.f, OC(O)R.sup.g,
SR.sup.f, CN, NO.sub.2, (CH.sub.2).sub.mCO.sub.2R.sup.f,
CONR.sup.fR.sup.f, C(O)R.sup.f, OC(O)NR.sup.fR.sup.f,
(CH.sub.2).sub.mNR.sup.fR.sup.f, NR.sup.fC(O)R.sup.g,
NR.sup.fC(O).sub.2R.sup.g, NR.sup.fC(O)NR.sup.fR.sup.f,
S(O)R.sup.g, S(O).sub.2R.sup.g, NR.sup.fS(O).sub.2R.sup.g,
S(O).sub.2NR.sup.fR.sup.f, N.sub.3,
(R.sup.f).sub.mSiC.sub.1-8alkyl, heteroaryl optionally substituted
with one to three R.sup.h, cycloalkyl optionally substituted with
one to three R.sup.h, and heterocycloalkyl optionally substituted
with one to three R.sup.h where m is selected from the group
consisting of 0, 1, 2, 3, 4, 5, and 6;
[0324] each R.sup.h is independently selected from the group
consisting of halo, C.sub.1-8alkyl, haloC.sub.1-8alkyl, OR.sup.j,
OC(O)R, SR.sup.j, NO.sub.2, CO.sub.2R.sup.j, CONR.sup.jR.sup.j,
C(O)R.sup.j, OC(O)NR.sup.jR.sup.j, NR.sup.jC(O)R.sup.t,
NR.sup.jC(O).sub.2R.sup.t, NR.sup.jC(O)NR.sup.jR.sup.j,
S(O)R.sup.t, S(O).sub.2R.sup.t, NR.sup.jS(O).sub.2R.sup.t, and
S(O).sub.2NR.sup.jR.sup.j;
[0325] R.sup.d, R.sup.f, and R.sup.j are each independently
selected from the group consisting of hydrogen, C.sub.1-8 alkyl,
haloC.sub.1-8alkyl, C.sub.2-8 alkenyl, haloC.sub.2-8alkenyl,
C.sub.2-8 alkynyl, and haloC.sub.2-8alkynyl; and
[0326] R.sup.e, R.sup.g, and R.sup.t are each independently
selected from the group consisting of C.sub.1-8alkyl,
haloC.sub.1-8alkyl, C.sub.2-8 alkenyl, haloC.sub.2-8alkenyl,
C.sub.2-8 alkynyl, and haloC.sub.2-8alkynyl;
[0327] provided that X and Y are not both O;
[0328] provided that when X is O, R.sup.1b is not OH; and
[0329] provided that when Y is O, and n is 0, R.sup.8 is not
OH.
[0330] In one group of embodiments, provided is a method of any of
the groups of embodiments disclosed herein, wherein at least one z
is 0. In another group of embodiments, at least one z is 1. In yet
another group of embodiments, at least one z is 2. In still another
group of embodiments, at least one z is 3. In another group of
embodiments, no z is 0.
V. Examples
[0331] The following examples are offered to illustrate, but not to
limit, the claimed invention.
Preparative Examples
[0332] The starting materials and reagents used in preparing these
compounds generally are either available from commercial suppliers,
such as Aldrich Chemical Co., or are prepared by methods known to
those skilled in the art following procedures set forth in
references such as Fieser and Fieser's Reagents for Organic
Synthesis; Wiley & Sons: New York, 1967-2004, Volumes 1-22;
Rodd's Chemistry of Carbon Compounds, Elsevier Science Publishers,
1989, Volumes 1-5 and Supplementals; and Organic Reactions, Wiley
& Sons: New York, 2005, Volumes 1-65.
[0333] The starting materials and the intermediates of the
synthetic reaction schemes can be isolated and purified if desired
using conventional techniques, including but not limited to,
filtration, distillation, crystallization, chromatography, and the
like. Such materials can be characterized using conventional means,
including physical constants and spectral data.
[0334] Unless specified to the contrary, the reactions described
herein preferably are conducted under an inert atmosphere at
atmospheric pressure at a reaction temperature range of from about
-78.degree. C. to about 150.degree. C., more preferably from about
0.degree. C. to about 125.degree. C., and most preferably and
conveniently at about room (or ambient) temperature, e.g., about
20.degree. C. to about 75.degree. C.
[0335] Referring to the examples that follow, compounds of the
present invention were synthesized using the methods described
herein, or other methods known in the art.
Example 1
Preparation of 3-(pyridin-3-ylmethoxy)isonicotinaldehyde
##STR00256##
[0336] Step 1:
##STR00257##
[0338] Acetyl chloride (20 mL) was added dropwise to methanol (200
mL) at 0.degree. C. After the addition, the reaction mixture was
stirred at this temp for 15 min and then 4.0 g of the acid was
added. The reaction mixture was heated at reflux for 12 h. Methanol
was removed to give a residue, which was then carefully neutralized
with aq. sat. NaHCO.sub.3 and then extracted with EtOAc (3.times.).
The organic layers were combined, dried and evaporated to give the
ester as a yellow solid, which was used in the next step without
further purification.
Step 2:
##STR00258##
[0340] A mixture of chloride (300 mg, 1.5 mmol, 1.0 eq),
hydroxypyridne (230 mg, 1.5 mmol, 1.0 eq) and potassium carbonate
(621 mg, 4.5 mmol, 3.0 eq) were taken in DMF (10 mL) and the
reaction mixture was heated at 80.degree. C. for 4 h. Solvent was
removed and the crude was purified by column chromatography
(Hexane/EtOAc to EtOAc/MeOH) to provide the coupled product.
Step 3:
##STR00259##
[0342] To an ice cold solution of ester (1.5 mmol, 1.0 eq) in THF
(15 mL) was slowly added LAH solution (1.5 mL, 2M solution in THF)
and the reaction mixture was stirred at this temp for 30 min. Then
excess ethyl acetate was added slowly to quench excess LAH. Then
water (1 mL), 15% NaOH (1 mL) and water (3 mL) were added and
stirred at rt for 30 min. The clear solution was filtered and the
solid was washed with ethyl acetate (3.times.). The organic layers
were combined, dried and evaporated to give the crude alcohol,
which was used in the next step without further purification.
Step 4:
##STR00260##
[0344] To a solution of the above alcohol (1.5 mmol, 1.0 eq) in DCM
(15 mL) was added Dess-Martin reagent (2.25 mmol, 454 mg, 1.5 eq)
and the reaction mixture was stirred at rt for 1 h. Solution was
diluted with 25 mL DCM and then a 1:1 mixture of sat. NaHCO.sub.3
and sat. Na.sub.2S.sub.2O.sub.3 was added and stirred for 30 min to
get two clear layers. Aqueous layer was separated and washed with
DCM (3x). Organic layer was dried and evaporated to give a crude
product, which was purified by column chromatography (EtOAc/MeOH).
NMR (400 MHz, CDCl.sub.3): .delta. 5.35 (s, 2H), 7.49 (m, 1H), 7.60
(d, 1H), 8.02 (m, 1H), 8.25 (m, 1H), 8.38 (s, 1H), 8.53 (m, 1H),
8.70 (m, 1H) 10.58 (s, 1H); MS: exact mass calculated for
C.sub.12H.sub.10N.sub.2O.sub.2, 214.07; m/z found, 215
[M+H].sup.+.
Example 2
Preparation of
3-(imidazo[1,2-a]pyridin-8-ylmethoxy)isonicotinaldehyde
##STR00261##
[0345] Step 1:
##STR00262##
[0347] To a DMF (15 mL) solution of the chloride (300 mg, 1.5 mmol,
1.0 eq) and phenol (230 mg, 1.5 mmol, 1.0 eq) was added
K.sub.2CO.sub.3 (621 mg, 4.5 mmol, 3.0 eq) and the reaction mixture
was heated at 80-90.degree. C. for 5 h. Solvent was removed and the
residue was purified by column chromatography (EtOAc/MeOH) to give
the alkylation product. MS: exact mass calculated for
C.sub.15H.sub.13N.sub.3O.sub.3, 283.10; m/z found, 284
[M+H].sup.+.
Step 2:
##STR00263##
[0349] To a cooled solution of the ester (1.5 mmol, 1.0 eq) in THF
(15 mL) was slowly added LAH in THF (1.5 mL, 2.0 M solution in THF,
2.0 eq) and the reaction mixture was stirred at this temperature
for 30 min. Excess ethyl acetate was added very slowly followed by
water (1.0 mL), 15% NaOH (1.0 mL) and water (3.0 mL) and the
mixture was stirred at rt for 30 min. The solution was filtered and
the solid was washed with ethyl acetate (3x). Combined organic
layers were dried and evaporated to provide the alcohol, which was
used in the next step without further purification. MS: exact mass
calculated for C.sub.14H.sub.13N.sub.3O.sub.2, 255.10; m/z found,
256 [M+H].sup.+.
Step 3:
##STR00264##
[0351] To a solution of the above alcohol (1.5 mmol, 1.0 eq) in DCM
(15 mL) was added Dess-Martin reagent (2.25 mmol, 954 mg, 1.5 eq)
and the reaction mixture was stirred at rt for 1 h. The reaction
was then diluted with 25 mL DCM and then a 1:1 mixture of sat.
NaHCO.sub.3 and sat. Na.sub.2S.sub.2O.sub.3 was added and stirred
for 30 min to get two clear layers. The aqueous layer was separated
and washed with DCM (3.times.). The organic layer was dried and
evaporated to give a crude product which was purified by column
chromatography (EtOAc/MeOH). MS: exact mass calculated for
Ca.sub.14H.sub.11N.sub.3O.sub.2, 253.09; m/z found, 254
[M+H].sup.+.
Example 3
Preparation of
3-(imidazo[1,5-a]pyridin-8-ylmethoxy)isonicotinaldehyde
##STR00265##
[0352] Step 1:
##STR00266##
[0354] To a solution of chloride (200 mg, 1.0 mmol, 1.0 eq), and
phenol (153 mg, 1.0 mmol, 1.0 eq) in DMF (15 mL) was added
K.sub.2CO.sub.3 (414 mg, 3.0 mmol, 3.0 eq) and the reaction mixture
was heated at 80-90.degree. C. for 5 h. Solvent was removed and the
residue was purified by column chromatography (EtOAc/MeOH) to give
the alkylation product. MS: exact mass calculated for
C.sub.15H.sub.13N.sub.3O.sub.3, 283.10; m/z found, 284
[M+H].sup.+.
Step 2:
##STR00267##
[0356] To a cooled solution of the ester (1.0 mmol, 1.0 eq) in THF
(15 mL) was slowly added LAH in THF (4 mmol, 2.0 mL, 2.0 M solution
in THF, 4.0 eq) and the reaction mixture was stirred at this
temperature for 30 min. Excess ethyl acetate was added very slowly
followed by water (1.0 mL), 15% NaOH (1.0 mL) and water (3.0 mL)
and the mixture was stirred at rt for 30 min. Filtered and the
solid was washed with ethyl acetate (3.times.). Combined organic
layers were dried and evaporated to provide the alcohol, which was
used in the next step without further purification. MS: exact mass
calculated for C.sub.14H.sub.13N.sub.3O.sub.2, 255.10; m/z found,
286 [M+H].sup.+.
Step 3:
##STR00268##
[0358] To a cooled solution of the ester (1.0 mmol, 1.0 eq) in THF
(15 mL) was slowly added LAH in THF (4 mmol, 2.0 mL, 2.0 M solution
in THF, 4.0 eq) and the reaction mixture was stirred at this
temperature for 30 min. Excess ethyl acetate was added very slowly
followed by water (1.0 mL), 15% NaOH (1.0 mL) and water (3.0 mL)
and the mixture was stirred at rt for 30 min. Reaction was filtered
and the solid was washed with ethyl acetate (3.times.). Combined
organic layers were dried and evaporated to provide the alcohol,
which was used in the next step without further purification. MS:
exact mass calculated for C.sub.14H.sub.13N.sub.3O.sub.2, 255.10;
m/z found, 286 [M+H].sup.+.
Example 4
Preparation of 4-(pyridin-3-ylmethoxy)nicotinaldehyde
##STR00269##
[0360] 4-chloro-3-pyridine aldehyde (1.0 g, 7 mmol, 1.0 eq),
3-hydroxymethyl pyridine (5.4 g, 49.45 mmol, 7 eq) and
p-tolunesulfonic acid mon hydrate (1.3 g, 7.0 mmol, 1.0 eq) in
benzene (30 mL) were heated using a Dean-Stark trap for 24 h.
Solvent was removed and purified by column chromatography to
provide the alkylation product. MS: exact mass calculated for
C.sub.12H.sub.10N.sub.2O.sub.2, 214.22; m/z found, 215
[M+H].sup.+.
Example 5
Preparation of
5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-methoxyisonicotinaldehyde
(Compound 5)
##STR00270##
[0361] Step 1:
##STR00271##
[0363] To a mixture of 6-methoxypyridin-3-ol (25 g, 0.2 mol) and
K.sub.2CO.sub.3 (82.8 g, 0.6 mol) in DMF (250 mL) was added
bromomethyl methyl ether (30 g, 0.24 mmol) slowly at rt for a
period of 1 h. The reaction mixture was filtered and the filtrate
was concentrated. The residue was purified on silica gel with 25%
EtOAc/hexanesas eluent to give 2-methoxy-5-(methoxymethoxy)pyridine
(20 g, 59%) as a colorless oil. LRMS (M+H.sup.+) m/z 170.1
Step 2:
##STR00272##
[0365] To a solution of 2-methoxy-5-(methoxymethoxy)pyridine (20 g,
0.12 mol) in THF was added diisopropylamine (0.24 g, 2.4 mmol). The
solution was cooled to -40.degree. C. followed by addition of MeLi
(3M/THF, 72 mL, 0.216 mol) slowly. The resulting mixture was warmed
to 0.degree. C., stirred at 0.degree. C. for 3 h, cooled back down
to -40.degree. C. and added N-formylpiperidine (24 mL, 0.216 mol).
After stirring at -40.degree. C. for 2 h, the mixture was quenched
with a mixed solution of HCl (37%, 120 mL) and THF (250 mL). The
temperature was then raised to rt and diluted with water (200 mL)
and EtOAc (200 mL). The pH of the mixture was adjusted to 8-9 with
solid K.sub.2CO.sub.3 and extracted with EtOAc (300 mL) twice. The
organic layer was combined, dried over Na.sub.2SO.sub.4, and
concentrated. The residue was purified on silica gel with 25%
EtOAc/hexanes as eluent to give
2-methoxy-5-(methoxymethoxy)isonicotinaldehyde (10 g, 42%) as a
pale yellow oil. .sup.1H NMR (400 MHz; CD.sub.3OD) 7.90 (s, 1H),
6.92 (s, 1H), 5.64 (s, 1H), 5.20 (s, 2H), 3.84 (s, 3H), 3.48 (s,
3H).
Step 3:
##STR00273##
[0367] To a solution of
2-methoxy-5-(methoxymethoxy)isonicotinaldehyde (10 g, 0.05 mol) in
THF (100 mL) was added 3 N HCl (150 mL). The reaction was stirred
at 50.degree. C. for 30 min, cooled to rt, and diluted with water
(100 mL). The mixture was neutralized to pH 7-8 and extracted with
EtOAc (200 mL) three times. The organic layer was dried over
Na.sub.2SO.sub.4 and concentrated to give
5-hydroxy-2-methoxyisonicotinaldehyde (4.2 g, 55%) as a yellow
solid. .sup.1H NMR (400 MHz; DMSO) .delta.=10.31 (s, 1H), 8.03 (s,
1H), 6.89 (s, 1H), 3.80 (s, 3H).
Step 4:
##STR00274##
[0369] A mixture of 5-hydroxy-2-methoxyisonicotinaldehyde (723.6
mg, 4.7 mmol), 8-(chloromethyl)-imidazol[1,2-a]pyridine (785 mg,
4.7 mmol), and K.sub.2CO.sub.3 (1.9 g, 14.1 mmol) in DMF (20 mL)
was heated at microwave reactor at 125.degree. C. for 15 min. The
mixture was filtered and concentrated. The residue was purified on
silica gel (50-100% EtOAc in hexanes) to give
5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-methoxyisonicotinaldehyde
(500 mg, 38%) as an off-white solid. .sup.1H NMR (400 MHz; DMSO)
6=10.37 (s, 1H), 8.58 (d, 1H), 8.39 (s, 1H), 8.02 (s, 1H), 7.61 (s,
1H), 7.44 (d, 1H), 6.98 (s, 1H), 6.93 (t, 1H), 5.61 (s, 2H), 3.84
(s, 3H). LRMS (M+H.sup.+) m/z 284.0.
[0370] Examples 6-13 were synthesized according to Example 5.
Example 6
Preparation of
2-methoxy-5((5-methylpyridin-3-yl)methoxy)isonicotinaldehyde
(Compound 43)
[0371] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.43 (s, 1H), 8.69 (s,
1H), 8.56 (s, 1H), 8.09 (s, 1H), 7.94 (s, 1H), 7.15-7.09 (m, 1H),
5.29 (s, 2H), 3.94 (s, 3H), 2.51 (s, 3H). 1H NMR (400 MHz, CDCl3)
.delta. 10.43 (s, 1H), 8.69 (s, 1H), 8.56 (s, 1H), 8.09 (s, 1H),
7.94 (s, 1H), 7.15-7.09 (m, 1H), 5.29 (s, 2H), 3.94 (s, 3H), 2.51
(s, 3H).
Example 7
Preparation of
5-(isoquinolin-1-ylmethoxy)-2-methoxyisonicotinaldehyde (Compound
44)
[0372] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.40 (s, 1H), 8.54 (d,
J=5.7 Hz, 1H), 8.30 (s, 1H), 8.31 (d, J=8.6 Hz, 1H), 7.90 (d, J=8.4
Hz, 1H), 7.78-7.63 (m, 3H), 7.07 (d, J=0.5 Hz, 1H), 5.82 (s, 2H),
3.91 (s, 3H).
Example 8
Preparation of 2-methoxy-5-(quinolin-2-ylmethoxy)isonicotinaldehyde
(Compound 45)
[0373] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.61 (s, 1H), 8.26 (d,
J=8.5 Hz, 1H), 8.12 (s, 1H), 8.10 (d, J=8.5 Hz, 1H), 7.87 (dd,
J=8.2, 1.1 Hz, 1H), 7.78 (ddd, J=8.4, 6.9, 1.4 Hz, 1H), 7.67 (d,
J=8.5 Hz, 1H), 7.60 (ddd, J=8.1, 7.0, 1.1 Hz, 1H), 7.13 (s, 1H),
5.52 (s, 2H), 3.91 (s, 3H).
Example 9
Preparation of 2-methoxy-5-(pyridin-4-ylmethoxy)isonicotinaldehyde
(Compound 46)
[0374] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.44 (s, 1H), 8.59 (d,
J=6.0 Hz, 2H), 7.92 (s, 1H), 7.30 (d, J=6.0 Hz, 2H), 7.06 (s, 1H),
5.16 (s, 2H), 3.84 (s, 3H).
Example 10
3-(imidazo[1,2-a]pyridin-8-ylmethoxy)-6-methylpicolinaldehyde
(Compound 49)
[0375] .sup.1H NMR (400 MHz, DMSO) .delta. 10.22 (s, 1H), 8.56 (d,
J=6.7 Hz, 1H), 8.02 (s, 1H), 7.82 (d, J=8.7 Hz, 1H), 7.60 (s, 1H),
7.53 (d, J=8.7 Hz, 1H), 7.47 (d, J=6.7 Hz, 1H), 6.96 (t, J=6.9 Hz,
1H), 5.59 (s, 2H), 2.49 (s, 3H).
Example 11
Preparation of methyl
2-((4-formyl-6-methoxypyridin-3-yloxy)methyl)imidazo[1,2-a]pyridine-8-car-
boxylate (Compound 53)
[0376] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.52 (s, 1H), 8.32
(dd, J=6.7, 1.3 Hz, 1H), 8.17 (s, 1H), 8.03 (dd, J=7.2, 1.3 Hz,
1H), 7.76 (s, 1H), 7.11 (s, 1H), 6.94 (t, J=7.0 Hz, 1H), 5.53 (s,
2H), 4.06 (s, 3H), 3.93 (s, 3H).
Example 12
Preparation of
2-methoxy-5-((3-methyl-[1,2,4]triazolo[4,3-a]pyridin-8-yl)methoxy)isonico-
tinaldehyde (Compound 58)
[0377] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.53 (s, 1H), 8.14 (s,
1H), 7.89 (d, J=6.9 Hz, 1H), 7.44 (dd, J=6.8, 1.1 Hz, 1H), 7.11 (s,
1H), 6.94 (t, J=6.9 Hz, 1H), 5.67 (s, 2H), 3.92 (s, 3H), 2.80 (s,
3H).
Example 13
Preparation of
5-((2-(1H-pyrazol-1-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde
(Compound 134)
[0378] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.47 (s, 1H), 8.53 (d,
J=2.1 Hz, 1H), 8.48 (d, J=4.7 Hz, 1H), 8.19 (d, J=7.8 Hz, 1H), 8.10
(s, 1H), 7.75 (s, 1H), 7.35 (dd, J=7.7, 4.7 Hz, 1H), 7.12 (s, 1H),
6.51 (dd, J=2.5, 1.8 Hz, 1H), 5.75 (s, 2H), 3.93 (s, 3H).
Example 14
Preparation of
5-((2-(1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde
(Compound 65)
Step 1:
##STR00275##
[0380] To a solution of 2-bromonicotinic acid (4.0 g, 20 mmol) and
triethylamine (3.34 mL, 24 mmol, 1.2 eq.) in THF (100 mL) was added
i-butyl chloroformate (3.12 mL, 24 mmol, 1.2 eq.) at 0.degree. C.
The mixture was stirred at 0.degree. C. for 10 min and filtered. To
this filtrate was added a suspension of NaBH.sub.4 (1.52 g, 40
mmol, 2 eq.) in water (1.0 mL) at 0.degree. C. The mixture was
stirred for 30 min, added water (3 mL), continued to stir for 2 h,
and concentrated to dryness. The crude was purified on silica gel
using a mixture of ethylacetate and hexanes as eluent to give
(2-bromopyridin-3-yl)methanol (3.4 g, 90%) as a white solid. LRMS
(M+H.sup.+) m/z 188.0.
Step 2:
##STR00276##
[0382] To (2-bromopyridin-3-yl)methanol (380 mg, 2 mmol) in DCM (5
mL) was added SOCl.sub.2 (1 mL) at rt. The reaction mixture was
stirred at rt for 4 h and concentrated to dryness. The crude solid
was suspended in toluene and concentrated to dryness. The process
was repeated three times and dried under vacuum to give an
off-white solid (480 mg), which was used for next step without
further purification.
Step 3:
##STR00277##
[0384] A mixture of 5-hydroxy-2-methoxyisonicotinaldehyde (306 mg,
2 mmol, 1 eq.), 2-bromo-3-(chloromethyl)pyridine (crude above, 2
mmol), and K.sub.2CO.sub.3 (828 mg, 6 mmol, 3 eq.) in DMF (1.0 mL)
was heated at 50.degree. C. for 2 h. The mixture was cooled and
added to water (50 mL) dropwise. The precipitate was filtered,
washed with water, dried under high vacuo to give
5-((2-bromopyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde (350
mg, 85%) as an yellow solid. .sup.1H NMR (400 MHz; CDCl.sub.3)
.delta.=10.51 (s, 1H), 8.42 (dd, 1H), 8.09 (s, 1H) 7.91 (d, 1H),
7.40 (dd, 1H), 7.15 (s, 1H), 5.27 (s, 2H), 3.95 (s, 3H). LRMS
(M+H.sup.+) m/z 323.0.
Step 4:
##STR00278##
[0386] 5-((2-bromopyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde
(258 mg, 0.8 mmol, 1 equiv),
1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazol-5-ylboronic acid
(233 mg, 0.96 mmol, 1.2 equiv), Pd(PPh.sub.3).sub.4 (92 mg, 0.08
mmol, 0.1 equiv), K.sub.2CO.sub.3 (331 mg, 2.4 mmol, 3 equiv) in a
round bottom flask were added dioxane (8 mL) and water (2 mL). The
mixture was heated 2 h at 90.degree. C., cooled, filtered, and
concentrated. The crude was purified on silica gel using a mixture
of EtOAc and hexanes as eluent to give
2-methoxy-5-((2-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazol-5-yl)pyr-
idin-3-yl)methoxy)isonicotinaldehyde (208 mg, 79%) as a white
solid. .sup.1H NMR (400 MHz; CDCl.sub.3) .delta.=10.54 (s, 1H),
8.85 (d, 1H), 8.18 (d, 1H) 8.03 (s, 1H), 7.73 (d, 1H), 7.56 (dd,
1H), 7.21 (s, 1H), 6.60 (d, 1H), 5.79 (s, 2H), 5.27 (s, 2H), 4.01
(s, 3H), 3.65 (t, 2H), 0.88 (t, 2H), 0.05 (s, 9H). LRMS (M+H.sup.+)
m/z 441.2.
Step 5:
##STR00279##
[0388] To
2-methoxy-5-((2-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazol-
-5-yl)pyridin-3-yl)methoxy)isonicotinaldehyde (120 mg, 0.27 mmol, 1
equiv) suspended in EtOH (1 mL) was added HCl (1.0 mL, 3 N). The
solution turned homogeneous and the mixture was stirred at rt
overnight. The EtOH was partially removed by blowing in N.sub.2 gas
and the precipitate was collected. The solid was washed with
acetonitrile and EtOAc and dried under high vacuo to give
5-((2-(1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde
dihydrochloride (100 mg, 96%) as a white solid. .sup.1H NMR (400
MHz; DMSO, 80.degree. C.) .delta.=10.27 (s, 1H), 8.68 (br, 1H),
8.32 (br, 1H), 8.22 (s, 1H), 7.82 (br, 1H), 7.57 (br, 1H), 7.00
(br, 2H), 5.75 (s, 2H), 3.89 (s, 3H). LRMS (M+H.sup.+) m/z
311.1.
[0389] Examples 15-22 were synthesized according to Example 14.
Example 15
Preparation of
5((2-bromopyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde
(Compound 63)
[0390] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.51 (s, 1H), 8.41
(dd, J=4.7, 1.8 Hz, 1H), 8.09 (s, 1H), 7.91 (dd, J=7.6, 1.6 Hz,
1H), 7.39 (dd, J=7.6, 4.8 Hz, 1H), 7.15 (s, 1H), 5.27 (s, 2H), 3.95
(s, 3H).
Example 16
Preparation of
5-((5-bromopyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde
(Compound 66)
[0391] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.47 (s, 1H), 8.73 (s,
1H), 8.65 (s, 1H), 8.07 (s, 1H), 7.99 (s, 1H), 7.15 (s, 1H), 5.22
(s, 2H), 3.95 (d, J=0.8 Hz, 3H).
Example 17
Preparation of
2-methoxy-5-((5-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde (Compound 74)
[0392] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.44 (s, 1H), 8.75
(dd, J=9.0, 2.1 Hz, 2H), 8.11 (s, 1H), 7.88 (t, J=2.1 Hz, 1H), 7.58
(d, J=1.9 Hz, 1H), 7.13 (s, 1H), 6.43 (d, J=1.9 Hz, 1H), 5.30 (s,
2H), 3.95 (s, 3H), 3.94 (s, 3H).
Example 18
Preparation of
5-((2-(1,5-dimethyl-1H-pyrazol-4-yl)pyridin-3-yl)methoxy)-2-methoxyisonic-
otinaldehyde (Compound 143)
[0393] .sup.1H NMR (400 MHz, CDCl.sub.3) .delta. 10.40 (s, 1H),
8.69 (dd, J=4.8, 1.7 Hz, 1H), 7.94 (s, 1H), 7.92 (dd, J=7.8, 1.7
Hz, 1H), 7.57 (s, 1H), 7.29 (dd, J=7.8, 4.8 Hz, 2H), 7.10 (s, 1H),
5.24 (s, 2H), 3.92 (s, 3H), 3.88 (s, 3H), 2.42 (s, 3H).
Example 19
Preparation of
5-((2-(1-ethyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotina-
ldehyde (Compound 149)
[0394] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.32 (s, 1H), 8.68
(dd, J=4.8, 1.6 Hz, 1H), 7.95 (dd, J=7.9, 1.6 Hz, 1H), 7.84 (s,
1H), 7.50 (d, J=1.9 Hz, 1H), 7.36 (dd, J=7.9, 4.8 Hz, 1H), 7.03 (s,
1H), 6.32 (d, J=1.9 Hz, 1H), 5.09 (s, 2H), 4.21 (q, J=7.2 Hz, 2H),
3.83 (s, 3H), 1.32 (t, J=7.2 Hz, 3H).
Example 20
Preparation of
2-methoxy-5-((2-phenylpyridin-3-yl)methoxy)isonicotinaldehyde
(Compound 159)
[0395] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.26 (s, 1H), 8.63
(dd, J=4.8, 1.6 Hz, 1H), 7.88 (dd, J=7.8, 1.6 Hz, 1H), 7.78 (s,
1H), 7.48-7.44 (m, 2H), 7.41-7.34 (m, 3H), 7.28 (dd, J=7.8, 4.8 Hz,
1H), 6.99 (s, 1H), 5.12 (s, 2H), 3.80 (s, 3H).
Example 21
Preparation of
2-methoxy-5-((2-(o-tolyl)pyridin-3-yl)methoxy)isonicotinaldehyde
(Compound 162)
[0396] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.36 (s, 1H), 8.71
(dd, J=4.8, 1.6 Hz, 1H), 7.99 (dd, J=7.8, 1.6 Hz, 1H), 7.80 (s,
1H), 7.40 (dd, J=7.8, 4.8 Hz, 1H), 7.36-7.29 (m, 2H), 7.28-7.23 (m,
1H), 7.23-7.18 (m, 1H), 7.06 (s, 1H), 4.98 (s, 2H), 3.89 (s, 3H),
2.13 (s, 3H).
Example 22
Preparation of
2-methoxy-5-((2'-methoxy-[2,3'-bipyridin]-3-yl)methoxy)isonicotinaldehyde
(Compound 163)
[0397] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.31 (s, 1H), 8.71
(dd, J=4.8, 1.4 Hz, 1H), 8.28 (dd, J=5.0, 1.9 Hz, 1H), 7.96 (dd,
J=7.8, 0.9 Hz, 1H), 7.82 (s, 1H), 7.74 (dd, J=7.3, 1.9 Hz, 1H),
7.41 (dd, J=7.8, 4.8 Hz, 1H), 7.09-7.03 (m, 2H), 5.14 (s, 2H), 3.96
(s, 3H), 3.89 (s, 3H).
Example 23
Preparation of
2-methoxy-5-((2-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazol-5-yl)pyr-
idin-3-yl)methoxy)isonicotinaldehyde (Compound 193)
[0398] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.54 (s, 1H), 8.84
(dd, J=4.8, 1.6 Hz, 1H), 8.14 (dd, J=7.9, 1.6 Hz, 1H), 8.03 (s,
1H), 7.72 (d, J=1.7 Hz, 1H), 7.55 (dd, J=7.9, 4.8 Hz, 1H), 7.21 (s,
1H), 6.60 (d, J=1.8 Hz, 1H), 5.79 (s, 2H), 5.27 (s, 2H), 4.01 (s,
3H), 3.66-3.59 (m, 2H), 0.92-0.80 (m, 2H), 0.00 (s, 9H).
Example 24
Preparation of 2-methoxy-5-(quinolin-3-ylmethoxy)isonicotinaldehyde
(Compound 80)
[0399] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.50 (s, 1H), 9.03 (d,
J=2.2 Hz, 1H), 8.27 (d, J=1.3 Hz, 1H), 8.17 (d, J=8.5 Hz, 1H), 8.15
(s, 1H), 7.89 (d, J=8.1 Hz, 1H), 7.79 (ddd, J=8.4, 6.9, 1.4 Hz,
1H), 7.63 (ddd, J=8.1, 7.0, 1.2 Hz, 1H), 7.14 (s, 1H), 5.42 (s,
2H), 3.94 (s, 3H).
Example 25
Preparation of
5-((4-formyl-6-methoxypyridin-3-yloxy)methyl)nicotinic acid
(Compound 79)
Step 1
##STR00280##
[0401] A mixture of 5-hydroxy-2-methoxyisonicotinaldehyde (352 mg,
2.29 mmol, 1 eq.), methyl 5-(chloromethyl)nicotinate hydrochloride
(506 mg, 2.29 mmol, 1 eq.), and K.sub.2CO.sub.3 (1.26 g, 9.16 mmol,
4 eq.) in DMF (8.0 mL) was heated at 60.degree. C. for 3 h. The
mixture was cooled and added into water (50 mL) dropwise. The
precipitate was filtered, washed with water, and dried to give
methyl 5-((4-formyl-6-methoxypyridin-3-yloxy)methyl)nicotinate (350
mg, 85%) as a yellow solid. .sup.1H NMR (400 MHz, CDCl.sub.3)
.delta. 10.47 (s, 1H), 9.26 (d, J=2.0 Hz, 1H), 8.90 (d, J=2.2 Hz,
1H), 8.42 (t, J=2.1 Hz, 1H), 8.09 (s, 1H), 7.15 (s, 1H), 5.29 (s,
2H), 4.01 (s, 3H), 3.95 (s, 3H). LRMS (M+H.sup.+) m/z 303.1.
Step 2
##STR00281##
[0403] To 5-((4-formyl-6-methoxypyridin-3-yloxy)methyl)nicotinate
(96 mg, 0.32 mmol, 1 eq.) in a mixture of MeOH/THF (1/3, 8.0 mL)
was added NaOH (3 N, 1.7 mL, 5.1 mmol, 16 eq.). The mixture was
stirred at rt for 2 h, acidified to pH 3, extracted with EtOAc
(3.times.20 mL). The combined organic layers were dried over
Na.sub.2SO.sub.4 and concentrated to give
5-((4-formyl-6-methoxypyridin-3-yloxy)methyl)nicotinic acid (86 mg,
93%) as a white solid. .sup.1H NMR (400 MHz, DMSO) .delta. 13.55
(s, 1H), 10.34 (s, 1H), 9.06 (d, J=1.9 Hz, 1H), 8.96 (d, J=2.0 Hz,
1H), 8.42 (t, J=2.0 Hz, 1H), 8.34 (s, 1H), 7.02 (s, 1H), 5.44 (s,
2H), 3.86 (s, 3H). LRMS (M+H.sup.+) m/z 289.1.
[0404] Examples 26-35 were synthesized according to the procedure
in Example 25.
Example 26
Preparation of methyl 4-(((3-formylpyridin-3-yl)oxy)methyl)benzoate
(Compound 164)
[0405] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.44 (s, 1H), 8.46
(dd, J=4.3, 0.6 Hz, 1H), 8.11 (d, J=8.1 Hz, 2H), 7.58 (d, J=8.0 Hz,
2H), 7.50-7.40 (m, 2H), 5.33 (s, 2H), 3.95 (s, 3H).
Example 27
Preparation of
4-(((2-formyl-6-methylpyridin-3-yl)oxy)methyl)benzoic acid
(Compound 165)
[0406] .sup.1H NMR (400 MHz, CDCl.sub.3) .delta. 10.42 (s, 1H),
8.16 (d, J=8.2 Hz, 2H), 7.61 (d, J=8.1 Hz, 2H), 7.33 (d, J=1.8 Hz,
2H), 5.32 (s, 2H), 2.61 (s, 3H).
Example 28
Preparation of 4-(((2-formylpyridin-3-yl)oxy)methyl)benzoic acid
(Compound 166)
[0407] .sup.1H NMR (400 MHz, CDCl.sub.3) .delta. 10.35 (s, 1H),
8.38 (dd, J=4.3, 1.2 Hz, 1H), 8.08 (d, J 8.3 Hz, 2H), 7.54 (d,
J=8.2 Hz, 2H), 7.42-7.32 (m, 2H), 5.26 (s, 2H).
Example 29
Preparation of methyl 3-(((4-formylpyridin-3-yl)oxy)methyl)benzoate
(Compound 167)
[0408] .sup.1H NMR (400 MHz, CDCl.sub.3) .delta. 10.60 (s, 1H),
8.64 (s, 1H), 8.46 (d, J=4.7 Hz, 1H), 8.16 (s, 1H), 8.08 (d, J=7.8
Hz, 1H), 7.71-7.61 (m, 2H), 7.54 (t, J=7.7 Hz, 1H), 5.38 (s, 2H),
3.96 (s, 3H).
Example 30
Preparation of methyl
3-(((2-formyl-6-methylpyridin-3-yl)oxy)methyl)benzoate (Compound
168)
[0409] .sup.1H NMR (400 MHz, CDCl.sub.3) .delta. 10.40 (s, 1H),
8.11 (s, 1H), 8.02 (d, J=7.8 Hz, 1H), 7.70 (d, J=7.8 Hz, 1H), 7.50
(t, J=7.7 Hz, 1H), 7.35 (d, J=8.7 Hz, 1H), 7.29 (d, J=8.7 Hz, 1H),
5.26 (s, 2H), 3.93 (s, 3H).
Example 31
Preparation of 3-(((4-formylpyridin-3-yl)oxy)methyl)benzoic acid
(Compound 169)
[0410] .sup.1H NMR (400 MHz, DMSO) .delta. 13.21-12.87 (br, 1H),
10.45 (s, 1H), 8.82 (s, 1H), 8.43 (d, J=4.8 Hz, 1H), 8.11 (s, 1H),
7.94 (d, J=7.6 Hz, 1H), 7.81 (d, J=7.1 Hz, 1H), 7.63-7.46 (m, 2H),
5.52 (s, 2H).
Example 32
Preparation of
3-(((2-formyl-6-methylpyridin-3-yl)oxy)methyl)benzoic acid
(Compound 170)
[0411] .sup.1H NMR (400 MHz, DMSO) .delta. 12.83 (s, 1H), 9.99 (s,
1H), 7.87 (s, 1H), 7.71 (d, J=7.8 Hz, 1H), 7.60-7.50 (m 2H),
7.38-7.30 (m, 2H), 5.16 (s, 2H).
Example 33
Preparation of 3-((2-formylpyridin-3-yl)oxy)methyl)benzoic acid
(Compound 171)
[0412] .sup.1H NMR (400 MHz, DMSO) .delta. 13.04 (s, 1H), 10.23 (s,
1H), 8.40 (d, J=4.4 Hz, 1H), 8.10 (s, 1H), 7.93 (d, J=7.7 Hz, 1H),
7.84 (d, J=8.5 Hz, 1H), 7.80 (d, J=7.7 Hz, 1H), 7.68 (dd, J=8.6,
4.4 Hz, 1H), 7.57 (t, J=7.7 Hz, 1H), 5.41 (s, 2H).
Example 34
Preparation of
3-(((4-formyl-6-methoxypyridin-3-yl)oxy)methyl)benzoic acid
(Compound 203)
[0413] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.27 (s, 1H), 7.97 (s,
1H), 7.89 (d, J=7.8 Hz, 1H), 7.85 (s, 1H), 7.48 (d, J=7.7 Hz, 1H),
7.32 (t, J=7.7 Hz, 1H), 6.89 (s, 1H), 5.05 (s, 2H), 3.69 (s,
3H).
Example 35
Preparation of tert-butyl
4-(2-formyl-6-methylpyridin-3-yloxy)methyl)-1H-indazole-1-carboxylate
(Compound 86)
[0414] The title compound was prepared as for Example 34 above.
[0415] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.35 (s, 1H), 8.40 (s,
1H), 8.23 (d, J=8.6 Hz, 1H), 7.57 (dd, J=8.4, 7.3 Hz, 1H), 7.43 (d,
J=7.2 Hz, 1H), 7.37 (d, J=8.6 Hz, 1H), 7.30 (d, J=8.6, 1H), 5.58
(s, 2H), 2.58 (s, 3H), 1.75 (s, 9H).
Example 36
Preparation of
5-methoxy-2-((1-methyl-1H-indazol-4-yl)methoxy)isonicatinaldehyde
(Compound 115)
Step 1
##STR00282##
[0417] To a mixture of 1-methyl-1H-indazole-4-carbaldehyde (180 mg,
1.12 mol) in THF (10 mL) was added NaBH.sub.4 (85 mg, 2.24 mmol) at
r.t. The reaction mixture was stirred at r.t. for 1 h, acidified to
pH 3, and extracted with EtOAc. The combined organic layer was
washed with saturated sodium bicarbonate solution and brine, dried
over Na.sub.2SO.sub.4, filtered, and concentrated to give a crude
solid (191 mg), which was used for next step without further
purification.
Step 2
##STR00283##
[0419] To (1-methyl-1H-indazol-4-yl)methanol (191 mg) in DCM (5 mL)
was added SOCl.sub.2 (2 mL) at rt. The reaction mixture was stirred
at rt for 4 h and concentrated to dryness. The crude solid was
suspended in toluene and concentrated to dryness. The process was
repeated three times and dried under vacuum to give an off-white
solid (210 mg), which was used for next step without further
purification.
Step 3
##STR00284##
[0421] A mixture of 2-hydroxy-5-methoxyisonicatinaldehyde (170 mg,
1.12 mmol), 4-(chloromethyl)-1-methyl-1H-indazole (1.12 mmol), and
K.sub.2CO.sub.3 (618 mg, 4.48 mmol) is refluxed in CH.sub.3CN (20
mL) for 2 h. The mixture is filtered and the solid is washed with
DCM. The filtrate is concentrated and purified on silica gel using
a mixture of EtOAc and MeOH as eluent to give
5-methoxy-2-((1-methyl-1H-indazol-4-yl)methoxy)isonicatinaldehyde
as a white solid.
[0422] Examples 37-45 were prepared according to Example 36.
Example 37
Preparation of
2-methoxy-5-(1-methyl-1H-indazol-4-yl)methoxy)isonicotinaldehyde
(Compound 84)
[0423] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.46 (s, 1H), 8.13 (s,
1H), 8.09 (s, 1H), 7.48-7.38 (m, 2H), 7.22 (dd, J=6.0, 0.8 Hz, 1H),
7.10 (s, 1H), 5.55 (s, 2H), 4.13 (s, 3H), 3.91 (s, 3H).
Example 38
Preparation of
6-methyl-3-((1-methyl-1H-indazol-6-yl)methoxy)picolinaldehyde
(Compound 91)
[0424] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.43 (s, 1H), 7.98 (d,
J=0.9 Hz, 1H), 7.75 (dd, J=8.3, 0.8 Hz, 1H), 7.60 (d, J=0.8 Hz,
1H), 7.39 (d, J=8.9 Hz, 1H), 7.30 (d, J=9.0 Hz, 1H), 7.18 (dd,
J=8.3, 1.3 Hz, 1H), 5.37 (s, 2H), 4.10 (s, 3H), 2.58 (s, 3H).
Example 39
Preparation of
6-methyl-3-((1-methyl-1H-indazol-7-yl)methoxy)picolinaldehyde
(Compound 92)
[0425] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.28 (s, 1H), 8.02 (s,
1H), 7.77 (dd, J=8.1, 1.0 Hz, 1H), 7.49 (d, J=8.6 Hz, 1H), 7.38
(dd, J=7.0, 1.0 Hz, 1H), 7.34 (d, J=8.6 Hz, 1H), 7.12 (dd, J=8.1,
7.0 Hz, 1H), 5.56 (s, 2H), 4.35 (s, 3H), 2.60 (s, 3H).
Example 40
Preparation of 3-(isoquinolin-1-ylmethoxy)-6-methylpicolinaldehyde
(Compound 93)
[0426] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.36 (s, 1H), 8.52 (d,
J=5.7 Hz, 1H), 8.48 (d, J=9.2 Hz, 1H), 7.88 (d, J=7.5 Hz, 1H),
7.77-7.66 (m, 4H), 7.27 (d, J=8.9 Hz, 1H), 5.86 (s, 2H), 2.55 (s,
3H).
Example 41
Preparation of
5-(benzo[d]oxazol-4-ylmethoxy)-2-methoxyisonicotinaldehyde
(Compound 103)
[0427] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.51 (s, 1H), 8.18 (d,
J=7.3 Hz, 2H), 7.63 (dd, J=8.1, 1.0 Hz, 1H), 7.52 (d, J=7.1 Hz,
1H), 7.46 (t, J=7.8 Hz, 1H), 7.11 (d, J=0.5 Hz, 1H), 5.65 (s, 2H),
3.92 (s, 3H).
Example 42
Preparation of
3-((1,5-naphthyridin-4-yl)methoxy)-6-methylpicolinaldehyde
(Compound 106)
[0428] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.41 (s, 1H), 9.15 (d,
J=2.1 Hz, 1H), 9.05 (dd, J=4.2, 1.6 Hz, 1H), 8.52 (d, J=1.1 Hz,
1H), 8.47 (d, J=8.5 Hz, 1H), 7.71 (dd, J=8.5, 4.2 Hz, 1H), 7.44 (d,
J=8.6 Hz, 1H), 7.35 (d, J=8.6 Hz, 1H), 5.50 (s, 2H), 2.62 (s,
3H).
Example 43
Preparation of
6-methyl-3-((1-methyl-1H-indazol-5-yl)methoxy)picolinaldehyde
(Compound 108)
[0429] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.43 (s, 1H), 8.01 (s,
1H), 7.81 (s, 1H), 7.50 (d, J=8.7 Hz, 1H), 7.45 (d, J=8.7 Hz, 1H),
7.42 (d, J=8.6 Hz, 1H), 7.30 (d, J=8.6 Hz, 1H), 5.34 (s, 2H), 4.11
(d, J=0.5 Hz, 3H), 2.59 (s, 3H).
Example 44
Preparation of 6-methyl-3-(quinolin-5-ylmethoxy)picolinaldehyde
(Compound 119)
[0430] .sup.1H NMR (400 MHz, DMSO) .delta. 10.13 (s, 1H), 8.96 (dd,
J=4.2, 1.6 Hz, 1H), 8.64 (d, J=8.4 Hz, 1H), 8.04 (d, J=8.4 Hz, 1H),
7.97 (d, J=8.7 Hz, 1H), 7.91 (d, J=7.2 Hz, 1H), 7.80 (dd, J=8.4,
7.1 Hz, 1H), 7.61 (dd, J=8.6, 4.2 Hz, 1H), 7.58 (d, J=8.8 Hz, 1H),
5.78 (s, 2H), 2.49 (s, 3H).
Example 45
Preparation of 2-methoxy-5-(quinolin-5-ylmethoxy)isonicotinaldehyde
(Compound 120)
[0431] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.23 (s, 1H), 8.94
(dd, J=4.3, 1.5 Hz, 1H), 8.43 (d, J=8.5 Hz, 1H), 8.16 (d, J=14.1
Hz, 1H), 8.13 (s, 2H), 7.68 (dd, J=8.3, 7.2 Hz, 1H), 7.61 (d, J=6.7
Hz, 1H), 7.47 (dd, J=8.6, 4.3 Hz, 1H), 7.02 (s, 1H), 5.56 (s, 2H),
3.84 (s, 3H).
Example 46
Preparation of
2-methoxy-5-((2-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde (Compound 129)
Step 1
##STR00285##
[0433] To a mixture of (2-bromopyridin-3-yl)methanol (20.0 g, 106.4
mmol, 1 eq.; refer to example 14) and imidazole (14.5 g, 212.8
mmol, 2 eq.) in DMF (50.0 mL) was added TBSCl (19.2 g, 150.7 mmol,
1.2 eq.) at rt. The mixture was stirred at rt for 1 h and diluted
with a mixture of water (100 mL) and EtOAc (300 mL). The organic
layer was washed with NH.sub.4Cl.sub.(sat.) solution and brine,
dried over Na.sub.2SO.sub.4, concentrated, and purified on silica
gel using 10% EtOAc/hexanes as eluent to give
2-bromo-3-((tert-butyldimethylsilyloxy)methyl)pyridine (30.1 g,
94%) as a colorless oil. LRMS (M+H.sup.+) m/z 302.0.
Step 2
##STR00286##
[0435] A mixture of
2-bromo-3-((tert-butyldimethylsilyloxy)methyl)pyridine (30.1 g,
100.0 mmol, 1 eq.) and Zn(CN).sub.2 (23.5 g, 200.0 mmol, 2.0 eq.)
in DMF (100.0 mL) was purged with N.sub.2 for 5 min and added
Pd(PPh.sub.3).sub.4 (5.78 g, 5.0 mmol, 0.05 eq.). The mixture was
heated at 120.degree. C. for 2 h under N.sub.2, cooled, filtered,
concentrated, and purified on silica gel using a mixture of EtOAc
and hexanes as eluent to give
3-((tert-butyldimethylsilyloxy)methyl)picolinonitrile (20.4 g, 82%)
as a colorless oil. LRMS (M+H.sup.+) m/z 249.1.
Step 3:
##STR00287##
[0437] Methylmagnesium bromide (3M/ether, 41.0 mL, 123.4 mmol) was
added to a stirred solution of
3-((tert-butyldimethylsilyloxy)methyl)picolinonitrile (20.4 g,
82.25 mmol) in THF (100.0 mL) at -78.degree. C. The reaction
mixture was warm to rt, quenched with aqueous citric acid solution,
and extracted with EtOAc (50 mL) twice. The combined organic layers
were washed with NaHCO.sub.3 (sat) solution and brine, dried over
Na.sub.2SO.sub.4, concentrated, and purified on silica gel using a
mixture of EtOAc/hexanes as eluent to give
1-(3-((tert-butyldimethylsilyloxy)methyl)pyridin-2-yl)ethanone
(12.9 g, 59%) as a colorless oil. LRMS (M+H.sup.+) m/z 266.2.
Step 4:
##STR00288##
[0439]
1-(3-((tert-butyldimethylsilyloxy)methyl)pyridin-2-yl)ethanone
(10.8 g, 40.75 mmol) in dimethoxy-N,N-dimethylmethanamine (15.0 mL)
was heated to reflux for 3 days. The mixture was concentrated and
used for next step without further purification. LRMS (M+H.sup.+)
m/z 321.1.
Step 5
##STR00289##
[0441] To
(E)-1-(3-((tert-butyldimethylsilyloxy)methyl)pyridin-2-yl)-3-(di-
methylamino)prop-2-en-1-one (crude above, 966.4 mg, 3.02 mmol, 1
eq.) in EtOH (10 mL) was added methylhydrazine (1.0 mL) at rt. The
mixture was heated at 80.degree. C. for 2 h, concentrated, and
purified on silica gel using a mixture of EtOAc and hexanes as
eluent to give a mixture of regio-isomers (420 mg; 46% for 2
steps). LRMS (M+H.sup.+) m/z 304.2.
Step 6
##STR00290##
[0443] To a mixture of
3-((tert-butyldimethylsilyloxy)methyl)-2-(1-methyl-1H-pyrazol-5-yl)pyridi-
ne and
3-((tert-butyldimethylsilyloxy)methyl)-2-(1-methyl-1H-pyrazol-3-yl)-
pyridine (420 mg, 1.38 mmol) in MeOH (20 mL) was added HCl (4 N,
2.0 mL). The mixture was stirred at rt for 1 h, concentrated, and
diluted with EtOAc (50 mL) and NaHCO.sub.3(sat) solution (10 mL).
The layers were separated and aqueous layer was extracted with
EtOAc three times. The combined organic layers were dried over
Na.sub.2SO.sub.4, concentrated, and purified on silica gel using
EtOAc as eluent to give
(2-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methanol (187 mg, 72%)
and (2-(1-methyl-1H-pyrazol-3-yl)pyridin-5-yl)methanol (55 mg, 21%)
as white solids. Data for
2-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methanol: .sup.1H NMR (400
MHz; CDCl.sub.3) 8.58 (d, 1H), 7.91 (d, 1H), 7.46 (s, 1H), 7.30
(dd, 1H), 6.36 (s, 1H), 4.62 (d, 2H), 3.83 (s, 3H), 2.1 (t, 1H).
LRMS (M+H.sup.+) m/z 190.1; data for
(2-(1-methyl-1H-pyrazol-3-yl)pyridin-5-yl)methanol: .sup.1H NMR
(400 MHz; CDCl.sub.3) 8.60 (d, 1H), 7.70 (d, 1H), 7.47 (s, 1H),
7.22 (dd, 1H), 6.99 (s, 1H), 5.91 (t, 1H), 4.68 (d, 2H), 4.01 (s,
3H). LRMS (M+H.sup.+) m/z 190.1
Step 7
##STR00291##
[0445] To (2-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methanol (182
mg, 0.96 mmol) in DCM (5 mL) was added SOCl.sub.2 (1.5 mL) at rt.
The reaction mixture was stirred at rt for 4 h and concentrated to
dryness. The crude solid was suspended in toluene and concentrated
to dryness. The process was repeated three times and dried under
vacuum to give
3-(chloromethyl)-2-(1-methyl-1H-pyrazol-5-yl)pyridine (236 mg) as
an off-white solid, which was used for next step without further
purification.
Step 8
##STR00292##
[0447] A mixture of 5-hydroxy-2-methoxyisonicotinaldehyde (147 mg,
0.96 mmol, 1 eq.),
3-(chloromethyl)-2-(1-methyl-1H-pyrazol-5-yl)pyridine hydrochloride
(236 mg, 0.96 mmol, 1 eq.), and K.sub.2CO.sub.3 (532 mg, 3.85 mmol,
3 eq.) in DMF (3.0 mL) was heated at 70.degree. C. for 2 h. The
mixture was cooled, filtered, concentrated, and purified on silica
gel using a mixture of EtOAc and hexanes as eluent to give
2-methoxy-5-((2-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde (232.5 mg, 75%) as an off-white solid. .sup.1H NMR (400
MHz, CDCl.sub.3) .delta. 10.40 (s, 1H), 8.77 (dd, J=4.7, 1.7 Hz,
1H), 8.03 (dd, J=7.9, 1.7 Hz, 1H), 7.93 (s, 1H), 7.55 (d, J=1.9 Hz,
1H), 7.44 (dd, J=7.9, 4.8 Hz, 1H), 7.11 (d, J=0.4 Hz, 1H), 6.43 (d,
J=1.9 Hz, 1H), 5.20 (s, 2H), 3.97 (s, 3H), 3.92 (s, 3H). LRMS
(M+H.sup.+) m/z 325.1.
[0448] 1H NMR (400 MHz, CDCl3) .delta. 10.40 (s, 1H), 8.77 (dd,
J=4.7, 1.7 Hz, 1H), 8.03 (dd, J=7.9, 1.7 Hz, 1H), 7.93 (s, 1H),
7.55 (d, J=1.9 Hz, 1H), 7.44 (dd, J=7.9, 4.8 Hz, 1H), 7.11 (d,
J=0.4 Hz, 1H), 6.43 (d, J=1.9 Hz, 1H), 5.20 (s, 2H), 3.97 (s, 3H),
3.92 (s, 3H).
Example 47
Preparation of
2-methoxy-5-((2-(1-methyl-1H-pyrazol-3-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde (Compound 130)
[0449] The title compound was prepared according to the procedure
in Example 46.
[0450] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.49 (s, 1H), 8.66
(dd, J=4.7, 1.3 Hz, 1H), 8.11 (s, 1H), 8.03 (dd, J=7.8, 1.0 Hz,
1H), 7.45 (d, J=2.3 Hz, 1H), 7.31 (dd, J=7.9, 4.8 Hz, 1H), 7.13 (s,
1H), 6.97 (d, J=2.0 Hz, 1H), 5.73 (s, 2H), 3.95 (s, 3H), 3.93 (s,
3H).
Example 48
Preparation of
5-((2-(2H-tetrazol-S-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde
(Compound 131)
Step 1:
##STR00293##
[0452] To a mixture of
5-((2-bromopyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde (100
mg, 0.31 mmol, 1 equiv), Zn (CN).sub.2 (71 mg, 0.62 mmol, 2.0
equiv), Pd(PPh.sub.3).sub.4 (72 mg, 0.06 mmol, 0.2 equiv) in a 5 mL
microwave tube was added DMF (2 mL). The mixture was heated 15 min
at 125.degree. C. in a microwave reactor. The solid was filtered
off and the filtrate was concentrated to dryness. The crude was
purified on silica gel using a mixture of EtOAc and hexanes as
eluent to give
3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)picolinonitrile (71
mg, 84%) as a white solid. .sup.1H NMR (400 MHz; CDCl.sub.3)
.delta.=10.54 (s, 1H), 8.86 (d, 1H), 8.22 (s, 1H), 8.20 (d, 1H),
7.74 (dd, 1H), 6.37 (s, 1H) 5.52 (s, 2H), 4.04 (s, 3H). LRMS
(M+H.sup.+) m/z 270.1.
Step 2:
##STR00294##
[0454] To TEA hydrochloride salt (123 mg, 0.89 mmol, 4 equiv.) and
3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)picolinonitrile (70
mg, 0.26 mmol, 1 equiv.) in chlorobenzene (5.0 mL) was added
NaN.sub.3 (48 mg, 0.89 mmol, 4 equiv.) at rt. The mixture was
heated to 110.degree. C. for 2 h, cooled to rt, and added water
(5.0 mL). The precipitate was filtered and washed with EtOAc and
water and dried under high vacuo to give
5-((2-(2H-tetrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde
as a white solid. .sup.1H NMR (400 MHz; DMSO) .delta.=10.23 (s,
1H), 8.61 (d, 1H), 8.16 (s, 1H), 8.10 (d, 1H), 7.38 (dd, 1H), 6.96
(s, 1H) 5.73 (s, 2H), 3.83 (s, 3H). LRMS (M+H.sup.+) m/z 313.0.
Example 49
Preparation of
2-methoxy-5-((2-(4-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde (Compound 132)
Step 1:
##STR00295##
[0456] To a mixture of
5-((2-bromopyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde (100
mg, 0.31 mmol, 1 equiv),
4-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazol-5-ylboronic acid
(98 mg, 0.47 mmol, 1.5 equiv), Pd(PPh.sub.3).sub.4 (70 mg, 0.06
mmol, 0.2 equiv), K.sub.2CO.sub.3 (171 mg, 1.24 mmol, 4 equiv) in a
5 mL microwave tube was added DMF (2 mL). The mixture was heated 30
min at 125.degree. C. in a microwave reactor. The solid was
filtered off and the filtrate was concentrated to dryness. The
crude was purified on silica gel using a mixture of EtOAc and
hexanes as eluent to give
2-methoxy-5-((2-(4-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazol-5-yl)py-
ridin-3-yl)methoxy)isonicotinaldehyde (110 mg, 87%) as a colorless
oil. LRMS (M+H.sup.+) m/z 409.2.
Step 2:
##STR00296##
[0458] To
2-methoxy-5-((2-(4-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazo-
l-5-yl)pyridin-3-yl)methoxy)isonicotinaldehyde (110 mg, 0.27 mmol,
1 equiv) suspended in EtOH (1 mL) was added HCl (1.0 mL, 3 N). The
solution turned homogeneous and the mixture was stirred at rt
overnight. The EtOH was partially removed by blowing in N.sub.2 gas
and basified to pH 9. The aqueous solution was extracted with EtOAc
three times. The organic layer was dried over Na.sub.2SO.sub.4 and
concentrated. The crude was purified on silica gel using a mixture
of MeOH and DCM as eluent to give
2-methoxy-5-((2-(4-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde (40 mg, 46%) as a white solid. .sup.1H NMR (400 MHz;
CDCl.sub.3) .delta.=10.45 (s, 1H), 8.76 (d, 1H), 8.07 (br, 1H),
8.05 (s, 1H), 7.53 (s, 1H), 7.40 (dd, 1H), 7.13 (s, 1H), 5.52 (br,
2H), 3.98 (s, 3H). LRMS (M+H.sup.+) m/z 325.1.
Example 50
Preparation of
5-((3-(1H-pyrazol-5-yl)isoquinolin-4-yl)methoxy)-2-methoxyisonicotinaldeh-
yde (Compound 133)
Step 1:
##STR00297##
[0460] To a mixture of POCl.sub.3 (0.73 mL, 7.85 mmol, 3.8 eqiv.)
and DMF (0.6 g, 8.16 mmol, 4.0 equiv.) in THF was added
1,2-dihydroisoquinolin-3(4H)-one at 0.degree. C. in portions for 5
min. The mixture was continued to stir at 0.degree. C. for 1 h and
poured into a mixture of 2 N NaOH (20 mL), ice (20 g), and toluene
(20 mL). The organic phase was separated and the aqueous layer was
extracted with toluene one more time. The combined organic layer
was washed with water, dried over Na.sub.2SO.sub.4, and
concentrated to half of its volume at low temperature in vacuo. To
this mixture was added 2 N H.sub.2SO.sub.4 (20 mL) under vigorous
stirring followed by ground KMnO.sub.4 in portions. The mixture was
continued to stir for another 4 h. The organic phase was separated,
dried over Na.sub.2SO.sub.4, and concentrated to give
3-chloroisoquinoline-4-carbaldehyde (220 mg, 50% pure) as a oil,
which was used for next step without further purification. LRMS
(M+H.sup.+) m/z 192.0.
Step 2:
##STR00298##
[0462] To 3-chloroisoquinoline-4-carbaldehyde (220 mg, crude) in
THF (10 mL) was added
[0463] NaBH.sub.4 (155 mg, 4.08 mmol) at 0.degree. C. The reaction
mixture was stirred at 0.degree. C. for 1 h, acidified to pH 3, and
extracted with EtOAc. The combined organic layers were washed with
saturated sodium bicarbonate solution and brine, dried over
Na.sub.2SO.sub.4, filtered, and concentrated to give a crude solid.
The crude was purified on silica gel using a mixture of EtOAc and
hexanes as eluent to give (3-chloroisoquinolin-4-yl)methanol (92
mg, 24% for three steps). LRMS (M+H.sup.+) m/z 194.0.
Step 3:
##STR00299##
[0465] To (3-chloroisoquinolin-4-yl)methanol (92 mg, 0.48 mmol) in
DCM (5 mL) was added SOCl.sub.2 (mL) at rt The reaction mixture was
stirred at rt for 4 h and concentrated to dryness. The crude solid
was suspended in toluene and concentrated to dryness. The process
was repeated three times and dried under vacuum to give an
off-white solid (120 mg), which was used for next step without
further purification.
Step 4:
##STR00300##
[0467] A mixture of 5-hydroxy-2-methoxyisonicotinaldehyde (73 mg,
0.48 mmol, 1 eq.), 3-chloro-4-(chloromethyl)isoquinoline (crude
above, 0.48 mmol), and K.sub.2CO.sub.3 (265 mg, 1.92 mmol, 4 eq.)
in DMF (2.0 mL) was heated at 60.degree. C. for 1 h. The mixture
was cooled, filtered, concentrated to dryness. The crude was
purified on silica gel using a mixture of EtOAc and hexanes to give
5-((3-chloroisoquinolin-4-yl)methoxy)-2-methoxyisonicotinaldehyde
(22 mg, 14%) as an yellow solid. .sup.1H NMR (400 MHz; CDCl.sub.3)
.delta.=10.19 (s, 1H), 9.05 (s, 1H), 8.23 (s, 1H) 8.06 (d, 1H),
7.98 (d, 1H), 7.76 (t, 1H), 7.63 (t, 1H), 7.01 (s, 1H), 5.72 (s,
2H), 3.87 (s, 3H). LRMS (M+H.sup.+) m/z 329.1.
Step 5:
##STR00301##
[0469] To a mixture of
5-((3-chloroisoquinolin-4-yl)methoxy)-2-methoxyisonicotinaldehyde
(18 mg, 0.05 mmol, 1 equiv),
1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazol-5-ylboronic acid
(20 mg, 0.08 mmol, 1.5 equiv), Pd(PPh.sub.3).sub.4 (12 mg, 0.01
mmol, 0.2 equiv), K.sub.2CO.sub.3 (30 mg, 0.22 mmol, 4 equiv) in a
5 mL microwave tube were added DMF (2 mL). The mixture was heated
30 min at 125.degree. C. in a microwave reactor. The solid was
filtered off and the filtrate was concentrated to dryness. The
crude was purified on silica gel using a mixture of EtOAc and
hexanes as eluent to give
2-methoxy-5-((3-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazol-5-yl)iso-
quinolin-4-yl)methoxy)isonicotinaldehyde (10 mg, 38%) as a white
solid. LRMS (M+H.sup.+) m/z 491.1.
Step 6:
##STR00302##
[0471] To
2-methoxy-5-((3-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazol-
-5-yl)isoquinolin-4-yl)methoxy)isonicotinaldehyde (10 mg, 0.02
mmol, 1 equiv) suspended in EtOH (1 mL) was added HCl (0.1 mL, 3
N). The solution turned homogeneous and the mixture was stirred at
rt overnight. The EtOH was partially removed by blowing in N.sub.2
gas and basified to pH 9. The aqueous solution was extracted with
EtOAc three times. The organic layer was dried over
Na.sub.2SO.sub.4 and concentrated. The crude was purified on silica
gel using MeOH and DCM as eluent to give
5-((3-(1H-pyrazol-5-yl)isoquinolin-4-yl)methoxy)-2-methoxyisonicotinaldeh-
yde (6.0 mg, 83%) as a white solid. .sup.1H NMR (400 MHz;
CDCl.sub.3) .delta.=10.17 (s, 1H), 9.25 (s, 1H), 8.18 (s, 1H), 8.05
(d, 1H), 7.99 (d, 1H), 7.73 (t, 1H), 7.60-7.68 (m, 2H), 7.03 (s,
1H), 6.70 (d, 1H), 5.85 (s, 2H), 3.85 (s, 3H). LRMS (M+H.sup.+) m/z
361.1.
Example 51
Preparation of
2-(imidazo[1,5-a]pyridin-8-ylmethoxy)-5-methoxyisonicotinaldehyde
Step 1:
##STR00303##
[0473] To a cold solution of 3-ethoxycarbonylpyridine (25 g, 165.4
mmol, 1 eq) in DCM was slowly added mCPBA (70% wt, 198.5 mmol) and
the reaction mixture was stirred at rt overnight. Reaction was
cooled and diluted with DCM and then neutralized with slow addition
of sat. NaHCO.sub.3. Aqueous layer was washed with DCM (3.times.)
and the combined organic layer was dried and evaporated to give a
residue, which was purified by column chromatography (EtOAc/MeOH)
to give 3-ethoxycarbonylpyridine N-oxide (13.6 g). MS: exact mass
calculated for C.sub.8H.sub.9NO.sub.3, 167.06; m/z found, 168
[M+H].sup.+.
Step 2:
##STR00304##
[0475] To a solution of 3-ethoxycarbonylpyridine N-oxide in 330 mL
of DCM were added trimethylsilyl cyanide (TMSCN) (11.0 g, 65.9
mmol, 1.0 eq) and dimethylcarbamoyl chloride (7.1 g, 65.9 mmol, 1.0
eq) and the reaction mixture was stirred at rt for 2 days. Then 10%
K.sub.2CO.sub.3 was slowly added to make the reaction mixture
basic. Organic layer was separated, dried and evaporated to provide
the crude, which was purified by column chromatography to provide
compounds A (5.7 g) and B (3.5 g).
Steps 3 and 4:
##STR00305##
[0477] To a solution of ethyl 2-cyano-3-pyridinecarboxylate (2.5 g)
and conc. HCl (5 mL) in 150 mL ethanol was added 10% Pd/C (wet, 250
mg) and the reaction mixture was hydrogenated using a hydrogen
balloon and stirred for 12 h. The reaction was filtered through
celite and ethanol was evaporated to give ethyl
2-(aminomethyl)-3-pyridinecarboxylate HCl as a white solid which
was used in the next step without further purification.
[0478] A mixture of 44.8 mL of acetic anhydride and 19.2 mL of
formic acid was heated in a 50-60.degree. C. oil bath temperature
for 3 h and then cooled to rt to give formic-acetic anhydride,
which was then slowly added to the solid ethyl
2-(aminomethyl)-3-pyridinecarboxylate HCl and then stirred at rt
for 8 h. Excess reagent was evaporated to give a residue, which was
neutralized by very slow addition of sat. NaHCO.sub.3 solution.
Solution was extracted with DCM, dried and evaporated to provide
ethyl imidazo[1,5-a]pyridine-8-carboxylate as a yellow solid (crude
weight 2.7 g). MS: exact mass calculated for
C.sub.10H.sub.10N.sub.2O.sub.2, 190.07; m/z found, 191
[M+H].sup.+.
Steps 5 and 6:
##STR00306##
[0480] To a cold solution of lithium aluminum hydride (1.62 g, 42.4
mmol, 4.0 eq) in THF (50 mL) was added the crude ethyl
imidazo[1,5-a]pyridine-8-carboxylate (2.7 g, 14.2 mmol, 1.0 eq) and
the reaction mixture was heated at reflux for 2 h. The reaction was
cooled and water (1.7 mL), 15% NaOH (1.7 mL) and water (5.1 mL)
were slowly added. Solution was diluted with excess EtOAc and
stirred at rt for 30 min. The solution was filtered and the solid
was washed with ethyl acetate. Organic layers were combined, dried
and solvent was removed to give crude
imidazo[1,5-a]pyridine-8-methanol, which was purified by column
chromatography (EtOAc/Hexane). MS: exact mass calculated for
C.sub.8H.sub.8N.sub.2O, 148.06; m/z found, 149 [M+H].sup.+.
[0481] To a solution of imidazo[1,5-a]pyridine-8-methanol (800 mg)
in chloroform (50 mL) was slowly added thionyl chloride (10 mL) and
the reaction mixture was stirred at rt for 8 h. Chloroform was
removed and the residue was then taken in toluene and toluene was
evaporated (3x) to give a solid, which was used in the next step
without further purification. MS: exact mass calculated for
C.sub.8H.sub.7ClN.sub.2, 166.03; m/z found, 167 [M+H].sup.+.
Step 7:
##STR00307##
[0483] To a solution of chloride (1.25 mmol, 1.0 eq), and
hydroxynicotinaldehyde (1.25 mmol, 1.0 eq) in DMF (10 mL) is added
K.sub.2CO.sub.3 (3.0 eq) and the reaction mixture was heated at
80-90.degree. C. for 5 h. Solvent is removed and the residue is
purified by column chromatography (EtOAc/MeOH).
Example 52
Preparation of
5-(imidazo[1,5-a]pyridin-8-ylmethoxy)-2-methoxyisonicotinaldehyde
(Compound 140)
[0484] The title compound was prepared according to the procedure
in Example 51.
[0485] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.47 (s, 1H), 8.21 (s,
1H), 8.11 (s, 1H), 7.97 (d, J=7.0 Hz, 1H), 7.52 (s, 1H), 7.12 (s,
1H), 6.87 (t, J=8.1 Hz, 1H), 6.62 (t, J=6.8 Hz, 1H), 5.37 (s, 2H),
3.92 (s, 3H).
Example 53
Preparation of
2-(5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-methoxypyridin-4-yl)thiazolidi-
ne (Compound 155)
##STR00308##
[0487] To a solution of aldehyde (0.326 g, 1.15 mmol, 1 eq) and
DIEA (0.15 g1.15 mmol, 1.0 eq) in EtOH (4 mL) was added
cysteamine.HCl (135 mg, 1.15 mmol, 1.0 eq) and the reaction mixture
was stirred at rt for 24 h. The reaction mixture was diluted with
water and the solid was filtered, washed (water) and dried. The
crude was purified by column chromatography (DCM/MeOH) to give the
pure material. MS: exact mass calculated for
C.sub.17H.sub.18N.sub.4O.sub.2S, 342.12; m/z found, 343
[M+H].sup.+.
Example 54
Preparation of
1-(2-(5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-methoxypyridin-4-yl)thiazol-
idin-3-yl)ethanone (Compound 156)
##STR00309##
[0489] To a solution of aldehyde (0.900 g, 3.18 mmol, 1 eq) and
DIEA) (0.45 g, 3.5 mmol, 1.1 eq) in EtOH (11 mL) was added
cysteamine.HCl (0.398 g, 3.5 mmol, 1.1 eq) and the reaction mixture
was stirred at rt for 24 h. Solvent was removed and the crude was
directly used in the next step. To a solution of crude thiazoline
(3.18 mmol) and DIEA (1.5 eq) in DCM (25 mL) at 0.degree. C. was
added acetyl chloride (1.2 eq) drop wise and the reaction mixture
was stirred at room temperature for 24 h. The reaction mix was
diluted with DCM and washed with saturated aq. NaHCO3. The organic
layer was dried and solvent was removed to give the crude amide,
which was purified by column chromatography (EtOAc/MeOH) to give
the amide. MS: exact mass calculated for C19H20N4O3S, 384.13; m/z
found, 385 [M+H]+.
Example 55
Preparation of 5-hydroxy-2-methoxyisonicotinaldehyde
Step 1
##STR00310##
[0491] To a solution of 6-methoxypyridin-3-ol (20 g, 0.16 mol, 1
eq.) in DMF (200 mL) was added NaH (60% in mineral oil; 9.6 g, 0.24
mol, 1.5 eq.) at 0-5.degree. C. portion-wise. Upon the completion
of addition, the mixture was continued to stir at 0-5.degree. C.
for 15 min, added chloromethyl methyl ether (15.5 g, 0.19 mol, 1.2
eq.), stirred at 0-5.degree. C. for another 20 min, and quenched
with NH.sub.4Cl.sub.(sat) solution. The aqueous layer was extracted
with EtOAc (3.times.100 mL) and the combined organic layers were
washed with water and brine, dried over Na.sub.2SO.sub.4,
concentrated, and purified on silica gel using 25% EtOAc/hexanes as
eluent to give 2-methoxy-5-(methoxymethoxy)pyridine (24.1 g, 89.3%)
as a colorless oil. .sup.1H NMR (400 MHz; CDCl.sub.3) 7.97 (d, 1H),
7.35 (dd, 1H), 6.70 (d, 1H), 5.12 (s, 2H), 3.91 (s, 3H), 3.51 (s,
3H). LRMS (M+H.sup.+) m/z 170.1
Step 2
##STR00311##
[0493] To a mixture of 2-methoxy-5-(methoxymethoxy)pyridine (30 g,
0.178 mol, 1 eq.) and diisopropylamine (507 uL, 3.6 mmol, 0.02 eq.)
in THF (500 mL) was added methyl lithium (1.6 M/THF, 200 mL, 0.32
mol, 1.8 eq.) at -40.degree. C. Upon the completion of addition,
the mixture was warmed to 0.degree. C., continued to stir at
0.degree. C. for 3 h, cooled back down to -40.degree. C. and added
DMF (24.7 mL, 0.32 mol, 1.8 eq.) slowly. The mixture was then
stirred at -40.degree. C. for 1 h, quenched with a mixture of HCl
(12 N, 120 mL) and THF (280 mL), warmed to rt, and added water (200
mL). The pH of the mixture was adjusted to pH 8-9 with solid
K.sub.2CO.sub.3. The aqueous layer was extracted with EtOAc (300
mL) twice. The combined organic layers were dried over
Na.sub.2SO.sub.4 and concentrated to give
2-methoxy-5-(methoxymethoxy)isonicotinaldehyde (33.5 g, 95.7%) as a
brown solid, which was used for next step without further
purification. .sup.1H NMR (400 MHz; CD.sub.3OD) 7.90 (s, 1H), 6.92
(s, 1H), 5.64 (s, 1H), 5.20 (s, 2H), 3.84 (s, 3H), 3.48 (s, 3H).
LRMS (M+H.sup.+) m/z 198.1
Step 3
##STR00312##
[0495] To a solution of
2-methoxy-5-(methoxymethoxy)isonicotinaldehyde (33.5 g, 0.17 mol, 1
eq.) in THF (150 mL) was added HCl (3 N, 250 mL, 4.4 eq.). The
reaction was stirred at 50.degree. C. for 1 h, cooled to rt, and
diluted with water (500 mL). The mixture was neutralized to pH 7-8
with solid K.sub.2CO.sub.3. The pale yellow solid was collected,
washed with water, and dried to give
5-hydroxy-2-methoxyisonicotinaldehyde (17.9 g, 74.6%) as a pale
yellow solid. .sup.1H NMR (400 MHz; DMSO) .delta.=10.31 (s, 1H),
8.03 (s, 1H), 6.89 (s, 1H), 3.80 (s, 3H). LRMS (M+H.sup.+) m/z
154.0.
Example 56
Preparation of
5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonico-
tinaldehyde (Compound 150)
Step 1:
##STR00313##
[0497] To
(E)-1-(3-((tert-butyldimethylsilyloxy)methyl)pyridin-2-yl)-3-(di-
methylamino)prop-2-en-1-one (crude, 1.03 g, 3.22 mmol, 1 eq.; refer
to Example 46) in EtOH (10 mL) was added isopropylhydrazine
hydrochloride (430 mg, 3.86 mmol, 1.2 eq.). The mixture was heated
at 80.degree. C. for 2 h, cooled, added HCl (6 N, 0.5 mL), and
stirred O/N. The mixture was concentrated and diluted with EtOAc
(80 mL) and NaHCO.sub.3(sat) (10 mL) solution. The layers were
separated and the aqueous layer was extracted with EtOAc three
times. The combined organic layers were dried over
Na.sub.2SO.sub.4, concentrated, and purified on silica gel using
EtOAc as eluent to give
(2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methanol (500 mg, 71%)
and (2-(1-isopropyl-1H-pyrazol-3-yl)pyridin-5-yl)methanol (55 mg,
25%) as pale yellow oils. Data for
2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methanol: .sup.1H NMR
(400 MHz, CDCl.sub.3) .delta. 8.67 (dd, J=4.7, 1.5 Hz, 1H), 8.0 (d,
J=7.8 Hz, 1H), 7.61 (d, J=1.8 Hz, 1H), 7.39 (dd, J=7.8, 4.8 Hz,
1H), 6.37 (d, J=1.8 Hz, 1H), 4.67 (s, 2H), 4.55 (sep, J=6.6 Hz 1H),
1.98-2.05 (br, 1H), 1.47 (d, J=6.6 Hz, 6H). LRMS (M+H.sup.+) m/z
218.1 Data for
(2-(1-isopropyl-1H-pyrazol-3-yl)pyridin-5-yl)methanol: .sup.1H NMR
(400 MHz, CDCl.sub.3) .delta. 8.62 (dd, J=4.8, 1.6 Hz, 1H), 7.72
(d, J=7.6 Hz, 1H), 7.55 (d, J=2.4 Hz, 1H), 7.23 (dd, J=7.6, 4.8 Hz,
1H), 6.99 (dd, J=8.0, 6.5 Hz, 1H), 6.07 (t, J=7.6 Hz, 1H), 4.67 (d,
J=7.6 Hz, 2H), 4.58 (sep, J=6.7 Hz, 1H), 1.60 (d, J=6.7 Hz, 1H).
LRMS (M+H.sup.+) m/z 218.1
Step 2:
##STR00314##
[0499] To (2-(1-iospropyl-1H-pyrazol-5-yl)pyridin-3-yl)methanol
(560 mg, 2.58 mmol) in DCM (10 mL) was added SOCl.sub.2 (3.0 mL) at
rt. The reaction mixture was stirred at rt for 4 h and concentrated
to dryness. The crude solid was suspended in toluene and
concentrated to dryness. The process was repeated three times and
dried under vacuum to give
3-(chloromethyl)-2-(1-isopropyl-1H-pyrazol-5-yl)pyridine
hydrochloride (700 mg) as an off-white solid, which was used for
next step without further purification.
Step 3:
##STR00315##
[0501] A mixture of 5-hydroxy-2-methoxyisonicotinaldehyde (395 mg,
2.58 mmol, 1 eq.),
3-(chloromethyl)-2-(1-isopropyl-1H-pyrazol-5-yl)pyridine
hydrochloride (700 mg, 2.58 mmol, 1 eq.), and K.sub.2CO.sub.3 (1.4
g, 10.32 mmol, 4 eq.) in DMF (10.0 mL) was heated at 70.degree. C.
for 2 h. The mixture was cooled, filtered, concentrated, and
purified on silica gel using a mixture of EtOAc and hexanes as
eluent to give
5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonico-
tinaldehyde (590 mg, 65%) as an off-white solid. .sup.1H NMR (400
MHz, CDCl.sub.3) .delta. 10.41 (s, 1H), 8.76 (dd, J=4.7, 1.6 Hz,
1H), 8.04 (dd, J=7.9, 1.6 Hz, 1H), 7.90 (s, 1H), 7.61 (d, J=1.8 Hz,
1H), 7.44 (dd, J=7.9, 4.8 Hz, 1H), 7.10 (s, 1H), 6.37 (d, J=1.8 Hz,
1H), 5.14 (s, 2H), 4.65 (sep, J=6.6 Hz, 1H), 3.91 (s, 3H), 1.49 (d,
J=6.6 Hz, 6H). LRMS (M+H.sup.+) m/z 353.1.
Step 4:
##STR00316##
[0503]
5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyi-
sonicotinaldehyde (980 mg, 2.78 mmol, 1 eq.) in HCl (6 N, 9.2 mL,
20 eq.) solution was freeze at -78.degree. C. The mixture was
lyophilized O/N to give
54(2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyiso-
nicotinaldehyde bis-hydrochloride as a yellow solid. .sup.1H NMR
(400 MHz, D.sub.2O) .delta. 8.85 (dd, J=5.7, 1.3 Hz, 1H), 8.78 (d,
J=8.2 Hz, 1H), 8.12 (dd, J=8.1, 5.7 Hz, 1H), 7.76 (s, 1H), 7.72 (d,
J=2.0 Hz, 1H), 7.46 (s, 1H), 6.65 (d, J=2.1 Hz, 1H), 6.09 (s, 1H),
5.09 (s, 2H), 4.24 (sep, J=6.6 Hz, 1H), 4.04 (s, 3H), 1.26 (d,
J=6.6 Hz, 7H). LRMS (M+H.sup.+) m/z 353.1.
[0504] .sup.1H NMR (400 MHz, CDCl.sub.3) .delta. 10.41 (s, 1H),
8.76 (dd, J=4.7, 1.6 Hz, 1H), 8.04 (dd, J=7.9, 1.6 Hz, 1H), 7.90
(s, 1H), 7.61 (d, J=1.8 Hz, 1H), 7.44 (dd, J=7.9, 4.8 Hz, 1H), 7.10
(s, 1H), 6.37 (d, J=1.8 Hz, 1H), 5.14 (s, 2H), 4.65 (hept, J=6.6
Hz, 1H), 3.91 (s, 3H), 1.49 (d, J=6.6 Hz, 6H).
Examples 57-62 were prepared according to the procedure in Example
55
Example 57
Preparation of
2-methoxy-5-((2-(1-(2-methoxyethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-
isonicotinaldehyde (Compound 172)
[0505] .sup.1H NMR (400 MHz, DMSO) .delta. 13.04 (s, 1H), 10.23 (s,
1H), 8.40 (d, J=4.4 Hz, 1H), 8.10 (s, 1H), 7.93 (d, J=7.7 Hz, 1H),
7.84 (d, J=8.5 Hz, 1H), 7.80 (d, J=7.7 Hz, 1H), 7.68 (dd, J=8.6,
4.4 Hz, 1H), 7.57 (t, J=7.7 Hz, 1H), 5.41 (s, 2H).
Example 58
Preparation of
2-methoxy-5-((2-(1-propyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonicotin-
aldehyde (Compound 173)
[0506] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.41 (s, 1H), 8.76
(dd, J=4.7, 1.6 Hz, 1H), 8.04 (dd, J=7.9, 1.3 Hz, 1H), 7.93 (s,
1H), 7.57 (d, J=1.8 Hz, 1H), 7.44 (dd, J=7.9, 4.8 Hz, 1H), 7.11 (s,
1H), 6.41 (d, J=1.9 Hz, 1H), 5.17 (s, 2H), 4.23 (t, J=7.4 Hz, 2H),
3.92 (s, 3H), 1.80 (sex, J=7.4 Hz, 2H), 0.81 (t, J=7.4 Hz, 3H).
Example 59
Preparation of
2-methoxy-5-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl)pyridin-3-yl)me-
thoxy)isonicotinaldehyde (Compound 174)
[0507] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.33 (s, 1H), 8.67
(dd, J=4.8, 1.6 Hz, 1H), 7.97 (dd, J=7.9, 1.4 Hz, 1H), 7.91 (s,
1H), 7.59 (d, J=1.9 Hz, 1H), 7.38 (dd, J=7.9, 4.8 Hz, 1H), 7.05 (s,
1H), 6.47 (d, J=1.9 Hz, 1H), 5.17 (q, J=8.6 Hz, 2H), 5.11 (s, 2H),
3.85 (s, 3H).
Example 60
Preparation of
5-((2-(1-(2,2-difluoroethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-meth-
oxyisonicotinaldehyde (Compound 175)
[0508] .sup.1H NMR (400 MHz, CDCl.sub.3) .delta. 10.31 (s, 1H),
8.66 (dd, J=4.8, 1.6 Hz, 1H), 7.96 (dd, J=7.9, 1.4 Hz, 1H), 7.87
(s, 1H), 7.55 (d, J=1.9 Hz, 1H), 7.36 (dd, J=7.9, 4.8 Hz, 1H), 7.02
(s, 1H), 6.42 (d, J=1.9 Hz, 1H), 6.11 (tt, J=56.0, 4.4 Hz, 1H),
5.11 (s, 2H), 4.67 (td, J=13.4, 4.4 Hz, 2H), 3.83 (s, 3H).
Example 61
Preparation of
3-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)picolinaldehyde
(Compound 176)
[0509] .sup.1H NMR (400 MHz, CDCl.sub.3) .delta. 10.34 (s, 1H),
8.76 (dd, J=4.7, 1.6 Hz, 1H), 8.47 (dd, J=4.4, 1.0 Hz, 1H), 8.32
(dd, J=7.9, 1.5 Hz, 1H), 7.64 (d, J=1.8 Hz, 1H), 7.49 (td, J=8.3,
4.6 Hz, 2H), 7.31 (d, J=8.5 Hz, 1H), 6.39 (d, J=1.8 Hz, 1H), 5.15
(s, 2H), 4.65 (sep, J=6.6 Hz, 1H), 1.49 (d, J=6.6 Hz, 6H).
Example 62
Preparation of
3-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-6-methylpicolina-
ldehyde (Compound 177)
[0510] .sup.1H NMR (400 MHz, CDCl.sub.3) .delta. 10.31 (s, 1H),
8.75 (dd, J=4.7, 1.3 Hz, 1H), 8.29 (d, J=7.9 Hz, 1H), 7.64 (d,
J=1.7 Hz, 1H), 7.48 (dd, J=7.9, 4.8 Hz, 1H), 7.31 (d, J=8.6 Hz,
1H), 7.20 (d, J=8.6 Hz, 1H), 6.38 (d, J=1.7 Hz, 1H), 5.11 (s, 2H),
4.64 (sep, J=6.6 Hz, 1H), 2.61 (s, 3H), 1.49 (d, J=6.6 Hz, 6H).
Example 63
Preparation of
5-((2-(1-cyclobutyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonic-
otinaldehyde (Compound 195)
[0511] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.31 (s, 1H), 8.68
(dd, J=4.8, 1.6 Hz, 1H), 7.94 (dd, J=7.9, 1.6 Hz, 1H), 7.79 (s,
1H), 7.54 (d, J=1.8 Hz, 1H), 7.36 (dd, J=7.9, 4.8 Hz, 1H), 7.01 (s,
1H), 6.30 (d, J=1.8 Hz, 1H), 5.05 (s, 2H), 4.77 (quin, J=8.4 Hz,
1H), 3.82 (s, 3H), 2.74-2.56 (m, 2H), 2.32-2.15 (m, 2H), 1.87-1.73
(m, 1H), 1.72-1.59 (m, 1H).
Example 64
Preparation of
5-((2-(1-cyclohexyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisonic-
otinaldehyde (Compound 196)
[0512] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.33 (s, 1H), 8.68
(dd, J=4.7, 1.5 Hz, 1H), 7.96 (dd, J=7.9, 1.2 Hz, 1H), 7.81 (s,
1H), 7.51 (d, J=1.8 Hz, 1H), 7.36 (dd, J=7.9, 4.8 Hz, 1H), 7.02 (s,
1H), 6.28 (d, J=1.8 Hz, 1H), 5.05 (s, 2H), 4.10 (quin, J=7.6 Hz,
1H), 3.83 (s, 3H), 1.96-1.83 (m, J=2.9 Hz, 4H), 1.83-1.68 (m, 2H),
1.68-1.45 (m, 2H), 1.33-1.06 (m, 2H).
Example 65
Preparation of
5-((2-(1-(cyclohexylmethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-metho-
xyisonicotinaldehyde (Compound 197)
[0513] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.43 (s, 1H), 8.76
(dd, J=4.7, 1.4 Hz, 1H), 8.04 (dd, J=7.9, 1.0 Hz, 1H), 7.93 (s,
1H), 7.58 (d, J=1.7 Hz, 1H), 7.45 (dd, J=7.9, 4.8 Hz, 1H), 7.11 (s,
1H), 6.40 (d, J=1.8 Hz, 1H), 5.16 (s, 2H), 4.13 (d, J=7.3 Hz, 2H),
3.92 (s, 3H), 1.92-1.74 (m, 1H), 1.60 (dd, J=8.2, 4.5 Hz, 3H), 1.47
(d, J=11.4 Hz, 2H), 1.21-0.98 (m, 3H), 0.91-0.71 (m, 2H).
Example 66
Preparation of
5-((2-(1-cyclopentyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxyisoni-
cotinaldehyde (Compound 198)
[0514] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.42 (s, 1H), 8.77
(dd, J=4.7, 1.5 Hz, 1H), 8.04 (dd, J=7.9, 1.2 Hz, 1H), 7.90 (s,
1H), 7.60 (d, J=1.8 Hz, 1H), 7.45 (dd, J=7.9, 4.8 Hz, 1H), 7.11 (s,
1H), 6.38 (d, J=1.9 Hz, 1H), 5.15 (s, 2H), 4.74 (quin, J=7.5 Hz,
1H), 3.92 (s, 3H), 2.23-1.85 (m, 6H), 1.63-1.51 (m, 2H).
Example 67
Preparation of
2-(difluoromethoxy)-5-(imidazo[1,2-a]pyridin-8-ylmethoxy)isonicotinaldehy-
de (Compound 158)
Step 1:
##STR00317##
[0516] To
5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-methoxyisonicotinaldehyd- e
(300 mg, 0.84 mmol, 1 equiv) in a vial was added HCl (6 N, 1 mL, 6
mmol). The mixture was concentrated, dried under vacuum at
60.degree. C. O/N, cooled to rt, and dissolved in NaOH (3 N, 5 mL),
filtered, and washed with EtOAc twice. The pH of the aqueous layer
was adjust to pH 6-7, filtered, and purified by RP-HPLC (Gemini
21.2.times.150 mm) with a mixture of CH.sub.3CN and water (0.1%
HCOOH) as eluent to give
5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-oxo-1,2-dihydropyridine-4-carbald-
ehyde formate (82.5 mg, 31%) as an yellow solid. .sup.1H NMR (400
MHz, D.sub.2O) .delta. 8.56 (d, J=7.1 Hz, 1H), 8.32 (s, 1H), 8.01
(d, J=2.1 Hz, 1H), 7.83 (d, J=7.2 Hz, 1H), 7.81 (t, J=2.1 Hz, 1H),
7.31 (t, J=7.2 Hz, 1H), 7.27 (s, 1H), 6.68 (s, 1H), 5.94 (s, 1H),
5.32 (s, 2H). LRMS (M+H.sup.+) m/z 270.1.
Step 2:
##STR00318##
[0518] To
5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-oxo-1,2-dihydropyridine--
4-carbaldehyde (100 mg, 0.37 mmol, 1 equiv) in CH.sub.3CN (10 mL)
was added sodium 2-chloro-2,2-difluoroacetate (84.5 mg, 0.56 mmol,
1.5 eq.). The mixture was stirred at rt O/N and concentrated. The
crude was purified on silica gel using 10% MeOH/DCM as eluent to
give
2-(difluoromethoxy)-5-(imidazo[1,2-a]pyridin-8-ylmethoxy)isonicotinaldehy-
de (6.0 mg, 5%) as a yellow solid. .sup.1H NMR (400 MHz,
CDCl.sub.3) .delta. 10.46 (s, 1H), 8.14 (s, 1H), 8.10 (d, J=7.0 Hz,
1H), 7.61 (s, 2H), 0.7.44 (t, J=60.0 Hz, 1H), 7.24-7.27 (m, 2H),
6.79 (t, J=7.0 Hz, 1H), 5.63 (s, 2H). LRMS (M+H.sup.+) m/z
320.0.
Example 68
Preparation of
2-(difluoromethoxy)-5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)metho-
xy)isonicotinaldehyde (Compound 178)
[0519] The title compound was prepared according to the procedure
in Example 67.
[0520] .sup.1H NMR (400 MHz, CDCl.sub.3) .delta. 10.44 (s, 1H),
8.80 (d, J=3.7 Hz, 1H), 8.03 (d, J=8.0 Hz, 1H), 7.95 (s, 1H), 7.63
(d, J=1.6 Hz, 1H), 7.47 (dd, J=7.9, 4.8 Hz, 1H), 7.33 (t, J=72.8
Hz, 1H), 6.37 (d, J=1.7 Hz, 1H), 5.21 (s, 2H), 4.67 (sep, J=6.6 Hz,
1H), 1.50 (d, J=6.6 Hz, 6H).
Example 69
Preparation of
5-((3-(1-isopropyl-1H-pyrazol-5-yl)pyridin-4-yl)methoxy)-2-methoxyisonico-
tinaldehyde (Compound 160)
##STR00319##
[0521] Step 1:
##STR00320##
[0523] To a mixture of 3-bromoisonicotinic acid (2.5 g, 12.37 mmol,
1 eq.) and TEA (3.44 mL, 24.75 mmol, 2.0 eq.) in THF (100 mL) was
added methyl chloroformate (1.2 mL, 14.85 mmol, 1.2 eq.) at
0.degree. C. The mixture was stirred at 0.degree. C. for 10 min and
filtered. To this filtrate was added a suspension of NaBH.sub.4
(0.95 g, 24.75 mmol, 2 eq.) in water (1.0 mL) at 0.degree. C. The
mixture was stirred at 0.degree. C. for 1 h, quenched with
NH.sub.4Cl.sub.(aq) solution, extracted with EtOAc twice. The
combined organic layers were dried over Na.sub.2SO.sub.4,
concentrated, and purified on silica gel using a mixture of EtOAc
and hexanes as eluent to give (3-bromopyridin-4-yl)methanol (1.2 g,
52%) as a white solid. .sup.1H NMR (400 MHz, CDCl.sub.3) .delta.
8.48 (s, 1H), 8.37 (d, J=4.9 Hz, 1H), 7.37 (d, J=4.9 Hz, 1H), 4.61
(d, J=5.5 Hz, 2H), 2.3 (t, J=5.5 Hz, 1H). LRMS (M+H.sup.+) m/z
188.0.
Step 2:
##STR00321##
[0525] To a mixture of (3-bromopyridin-4-yl)methanol (150 mg, 0.8
mmol, 1 eq.),
1-isopropyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyra-
zole (226 mg, 0.96 mmol, 1.2 eq.), Pd(dppf)Cl.sub.2 (58 mg, 0.08
mmol, 0.1 eq.), and K.sub.2CO.sub.3 (331 mg, 3.0 mmol, 3 eq.) in a
RB flask were added dioxane (6 mL) and water (2 mL). The mixture
was heated at 100.degree. C. for 2 h, cooled, filtered, and
concentrated. The crude was purified on silica gel using a mixture
of EtOAc and hexanes as eluent to give
(3-(1-isopropyl-1H-pyrazol-5-yl)pyridin-4-yl)methanol (75 mg, 43%)
as a yellow oil. LRMS (M+H.sup.+) m/z 218.1.
Step 3:
##STR00322##
[0527] (3-(1-isopropyl-1H-pyrazol-5-yl)pyridin-4-yl)methanol (75
mg, 0.35 mmol) in SOCl.sub.2 (5 mL) was heated at 60.degree. C. for
30 min and concentrated. The crude solid was suspended in toluene
and concentrated to dryness. The process was repeated three times
and dried under vacuum to give a brown solid (95 mg), which was
used for next step without further purification.
Step 4:
##STR00323##
[0529] A mixture of 5-hydroxy-2-methoxyisonicotinaldehyde (79 mg,
0.52 mmol, 1.5 eq.),
4-(chloromethyl)-3-(1-isopropyl-1H-pyrazol-5-yl)pyridine
hydrochloride (crude above, 0.35 mmol), and K.sub.2CO.sub.3 (145
mg, 1.05 mmol, 3 eq.) in DMF (10.0 mL) was heated at 100.degree. C.
for 2 h. The mixture was cooled, filtered, concentrated, and
purified on RP-HPLC (Gemini 21.2.times.150 mm) twice using a
mixture of CH.sub.3CN/water (0.1% HCOOH) as eluent to give
5-((3-(1-isopropyl-1H-pyrazol-5-yl)pyridin-4-yl)methoxy)-2-methoxyisonico-
tinaldehyde (6.0 mg, 5%) as an off-white solid. .sup.1H NMR (400
MHz, CDCl.sub.3) .delta. 10.29 (s, 1H), 8.63 (s, 1H), 8.42 (s, 1H),
7.67 (s, 1H), 7.54 (s, 1H), 7.52 (d, J=1.7 Hz, 1H), 6.96 (s, 1H),
6.15 (d, J=1.8 Hz, 1H), 4.87 (s, 2H), 4.06 (sep, J=6.6 Hz, 1H),
3.75 (s, 3H), 1.31 (d, J=6.6 Hz, 6H). LRMS (M+H.sup.+) m/z
353.1.
Example 70
Preparation of
5-([2,3'-bipyridin]-3-ylmethoxy)-2-methoxyisonicotinaldehyde
(Compound 161)
[0530] The title compound was prepared according to the procedure
in Example 69.
[0531] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.36 (s, 1H), 8.85 (d,
J=1.7 Hz, 1H), 8.78 (dd, J=4.8, 1.6 Hz, 1H), 8.71 (dd, J=4.8, 1.5
Hz, 1H), 8.02 (dd, J=7.8, 1.5 Hz, 1H), 7.96 (dt, J=7.9, 1.9 Hz,
1H), 7.90 (s, 1H), 7.49-7.42 (m, 2H), 7.10 (s, 1H), 5.21 (s, 2H),
3.91 (s, 3H).
Example 71
Preparation of
5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-(2-methoxyethoxyl)isonicotinaldeh-
yde (Compound 179)
##STR00324##
[0533] To a mixture of
5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-oxo-1,2-dihydropyridine-4-carbald-
ehyde (100 mg, 0.37 mmol, 1 equiv) and K.sub.2CO.sub.3 (153.2 mg,
1.11, 3.0 eq.) in DMF (5 mL) was added 1-bromo-2-methoxyethane
(154.3 mg, 1.11 mmol, 3.0 eq.). The mixture was stirred at rt O/N,
filtered, concentrated, and purified on silica gel using 10%
MeOH/DCM as eluent to give
5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-(2-methoxyethoxyl)isonicotin-
aldehyde (6.0 mg, 5%) as an yellow solid. .sup.1H NMR (400 MHz,
CDCl.sub.3) .delta. 10.45 (s, 1H), 8.08 (d, J=6.8 Hz, 1H), 8.06 (s,
1H), 7.60 (dd, J=6.8, 1.2 Hz, 2H), 7.27 (dd, J=6.9, 1.0 Hz, 1H),
7.09 (s, 1H), 6.78 (t, J=6.9 Hz, 1H), 5.58 (s, 2H), 4.35 (dd,
J=5.4, 3.9 Hz, 2H), 3.66 (dd, J=5.4, 3.9 Hz, 2H), 3.36 (s, 3H).
LRMS (M+H.sup.+) m/z 328.1.
Example 72
Preparation of
5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-(2-methoxyetho-
xyl)isonicotinaldehyde (Compound 180)
[0534] The title compound was prepared according to the procedure
in Example 71.
[0535] .sup.1H NMR (400 MHz, CDCl.sub.3) .delta. 10.40 (s, 1H),
8.76 (dd, J=4.7, 1.5 Hz, 1H), 8.04 (dd, J=7.9, 1.2 Hz, 1H), 7.87
(s, 1H), 7.61 (d, J=1.8 Hz, 1H), 7.44 (dd, J=7.9, 4.8 Hz, 1H), 7.16
(s, 1H), 6.37 (d, J=1.8 Hz, 1H), 5.14 (s, 2H), 4.65 (sep, J=6.6 Hz,
1H), 4.42 (t, J=4.8 Hz, 2H), 3.74 (t, J=4.8 Hz, 2H), 3.44 (s, 3H),
1.49 (d, J=6.6 Hz, 6H).
Example 73
Preparation of
5-((3-(1-isopropyl-1H-pyrazol-5-yl)pyrazin-2-yl)methoxy)-2-methoxyisonico-
tinaldehyde (Compound 181)
Step 1:
##STR00325##
[0537] To a solution of 3-chloropyrazine-2-carboxylic acid (2.0 g,
12.70 mmol, 1.0 eq.) and TEA (3.50 mL, 25.40 mmol, 2.0 eq.) in THF
(50 mL) was added methyl chloroformate (1.2 mL, 15.20 mmol, 1.2
eq.) at 0.degree. C. The mixture was stirred at 0.degree. C. for 10
min and filtered. To this filtrate was added a suspension of
NaBH.sub.4 (0.97 g, 25.40 mmol, 2 eq.) in water (1.0 mL) at
0.degree. C. The mixture was stirred at 0.degree. C. for 1 h,
quenched with NH.sub.4Cl.sub.(aq) solution, and extracted with
EtOAc twice. The combined organic layers were dried over
Na.sub.2SO.sub.4, concentrated, and purified on silica gel using a
mixture of EtOAc and hexanes as eluent to give
(3-chloropyrazin-2-yl)methanol (400 mg, 22%) as a white solid.
.sup.1H NMR (400 MHz, MeOD) .delta. 8.58 (d, J=2.5 Hz, 1H), 8.38
(d, J=2.5 Hz, 1H), 4.84 (s, 2H). LRMS (M+H.sup.+) m/z 145.1.
Step 2:
##STR00326##
[0539] To a mixture of (3-chloropyrazin-2-yl)methanol (200 mg, 1.4
mmol, 1 eq.),
1-isopropyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyra-
zole (393 mg, 1.67 mmol, 1.2 eq.), Pd(dppf)Cl.sub.2 (102 mg, 0.14
mmol, 0.1 eq.), and K.sub.2CO.sub.3 (580 mg, 4.2 mmol, 3 eq.) in a
RB flask were added dioxane (6 mL) and water (2 mL). The mixture
was heated at 100.degree. C. for 1 h, cooled to rt, filtered,
concentrated, and purified on silica gel using a mixture of EtOAc
and hexanes as eluent to give
(3-(1-isopropyl-1H-pyrazol-5-yl)pyrazin-2-yl)methanol (110 mg, 36%)
as a yellow oil. LRMS (M+H.sup.+) m/z 219.1.
Step 3:
##STR00327##
[0541] 3-(1-isopropyl-1H-pyrazol-5-yl)pyrazin-2-yl)methanol (75 mg,
0.35 mmol) in SOCl.sub.2 (5 mL) was heated at 60.degree. C. for 30
min and concentrated. The crude solid was suspended in toluene and
concentrated to dryness. The process was repeated three times and
dried under vacuum to give a brown solid (95 mg), which was used
for next step without further purification.
Step 4:
##STR00328##
[0543] A mixture of 5-hydroxy-2-methoxyisonicotinaldehyde (110 mg,
0.60 mmol, 1.2 eq.),
2-(chloromethyl)-3-(1-isopropyl-1H-pyrazol-5-yl)pyrazine
hydrochloride (crude above, 0.5 mmol, 1 eq.), and K.sub.2CO.sub.3
(207 mg, 1.50 mmol, 3 eq.) in DMF (15.0 mL) was heated at
100.degree. C. for 30 min. The mixture was cooled, filtered,
concentrated, and purified on silica gel using a mixture of EtOAc
and hexanes as eluent to give
5-((3-(1-isopropyl-1H-pyrazol-5-yl)pyrazin-2-yl)methoxy)-2-methoxyisonico-
tinaldehyde (12.0 mg, 68%) as an off-white solid. .sup.1H NMR (400
MHz, CDCl.sub.3) .delta. 10.31 (s, 1H), 8.73 (d, J=2.4 Hz, 1H),
8.65 (d, J=2.4 Hz, 1H), 8.05 (s, 1H), 7.61 (d, J=1.9 Hz, 1H), 7.06
(s, 1H), 6.49 (d, J=1.9 Hz, 1H), 5.32 (s, 2H), 4.68 (sep, J=6.6 Hz,
1H), 3.89 (s, 2H), 1.48 (d, J=6.6 Hz, 6H). LRMS (M+H.sup.+) m/z
354.1.
Example 74
Preparation of methyl
3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)picolinate (Compound
182)
##STR00329##
[0545] To
3-((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yloxy)methyl)picoli-
nic acid (55 mg, 0.17 mmol, 1 equiv) in MeOH (15 mL) was added
SOCl.sub.2 (5.0 mL). The mixture was heated to reflux O/N,
concentrated, and neutralized to pH 8-9 with NaHCO.sub.3(sat.)
solution. The aqueous layer was extracted with EtOAc three times.
The combined organic layers were dried over Na.sub.2SO.sub.4,
concentrated, and purified on silica gel using a mixture of EtOAc
and hexanes as eluent to give methyl
3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)picolinate (51.5 mg,
quantitative yield) as a white solid. .sup.1H NMR (400 MHz,
CDCl.sub.3) .delta. 10.44 (s, 1H), 8.67 (dd, J=4.6, 1.5 Hz, 1H),
8.14 (dd, J=8.0, 1.5 Hz, 1H), 8.03 (s, 1H), 7.51 (dd, J=8.0, 4.6
Hz, 1H), 7.06 (s, 1H), 5.60 (s, 2H), 3.95 (s, 3H), 3.85 (s, 3H).
LRMS (M+H.sup.+) m/z 303.1.
Example 75
Preparation of
5-((2-(2-hydroxypropan-2-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinalde-
hyde (Compound 183)
Step 1:
##STR00330##
[0547] Methylmagnesium bromide (3M/ether, 2.0 mL, 5.65 mmol, 1.5
eq.) was added to a stirred solution of
3-((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yloxy)methyl)picolinonitrile
(1180 mg, 3.76 mmol, 1 eq.) in THF (10.0 mL) at -78.degree. C.
After addition, the reaction mixture was allowed to warm to rt and
quenched with aqueous citric acid solution. The aqueous layer was
extracted with EtOAc (30 mL) twice. The combined organic layers
were washed with NaHCO.sub.3(sat) solution and brine, dried over
Na.sub.2SO.sub.4, concentrated, and purified on silica gel using a
mixture of EtOAc and hexanes as eluent to give
1-(3-((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yloxy)methyl)pyridin-2-yl-
)ethanone (776 mg, 63%) as a colorless oil. .sup.1H NMR (400 MHz,
CDCl.sub.3) .delta. 8.66 (d, J=4.0 Hz, 1H), 8.26 (d, J=7.9 Hz, 1H),
7.82 (s, 1H), 7.54 (dd, J=8.0, 4.0 Hz, 1H), 6.95 (s, 1H), 6.23 (s,
1H), 5.59 (s, 2H), 4.22-4.04 (m, 4H), 3.90 (s, 3H), 2.79 (s, 3H).
LRMS (M+H.sup.+) m/z 331.1.
Step 2:
##STR00331##
[0549] Methylmagnesium bromide (3M/ether, 0.25 mL, 0.75 mmol, 3.0
eq.) was added to a stirred solution of
1-(3-((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yloxy)methyl)pyridin-2-yl-
)propan-1-one (82 mg, 0.25 mmol, 1 eq.) in THF (5.0 mL) at
-78.degree. C. After addition, the reaction mixture was warm to rt
and quenched with aqueous citric acid solution. The aqueous layer
was extracted with EtOAc (20 mL) twice. The combined organic layers
were washed with NaHCO.sub.3(sat) solution and brine, dried over
Na.sub.2SO.sub.4, concentrated, and purified on silica gel using a
mixture of EtOAc and hexanes as eluent to give
2-(3-((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yloxy)methyl)pyridin-2-yl-
)propan-2-ol (38 mg, 44%) as a colorless oil. .sup.1H NMR (400 MHz,
CDCl.sub.3) .delta. 8.43 (dd, J=7.7, 1.6 Hz, 1H), 7.84 (dd, J=7.7,
1.5 Hz, 1H), 7.74 (s, 1H), 7.18 (dd, J=7.7, 4.7 Hz, 1H), 6.84 (s,
1H), 6.01 (s, 1H), 5.27 (s, 2H), 4.07-3.88 (m, 4H), 3.82 (s, 3H),
1.55 (s, 6H). LRMS (M+H.sup.+) m/z 347.1.
Step 3:
##STR00332##
[0551] To
2-(3-((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yloxy)methyl)pyr-
idin-2-yl)propan-2-ol (30 mg, 0.087 mmol, 1 eq.) in a RB flask was
added HCl (6 N, 3.0 mL). The mixture was warmed to 40.degree. C.
O/N, cooled to rt, neutralized to pH 7-8 with NaHCO.sub.3(sat)
solution, and extracted with EtOAc twice. The combined organic
layers were washed with brine, dried over Na.sub.2SO.sub.4,
concentrated, and purified on silica gel using a mixture of EtOAc
and hexanes as eluent to give
5-((2-(2-hydroxypropan-2-yl)pyridin-3-yl)methoxy)-2-methoxyisonicotinalde-
hyde (10.2 mg, 99%) as a pale-yellow oil. .sup.1H NMR (400 MHz,
CDCl.sub.3) .delta. 10.36 (s, 1H), 8.46 (dd, J=4.7, 1.6 Hz, 1H),
7.99 (s, 1H), 7.86 (dd, J=7.8, 1.5 Hz, 1H), 7.24 (dd, J=7.8, 4.7
Hz, 1H), 7.05 (s, 1H), 5.37 (s, 2H), 3.85 (s, 3H), 1.57 (s, 6H).
LRMS (M+H.sup.+) m/z 303.1.
Example 76
Preparation of 5-hydroxy-2-(2-methoxyethoxy)isonicotinaldehyde and
5-hydroxy-2-(2-methoxyethoxyl)nicotinaldehyde
Step 1
##STR00333##
[0553] To a solution of 6-(benzyloxy)pyridin-3-ol (2.0 g, 10 mmol,
1 eq.) in DMF (20 mL) was added NaH (60% in mineral oil; 0.6 g, 15
mmol, 1.5 eq.) at 0-5.degree. C. portion-wise. Upon the completion
of addition, the mixture was continued to stir at 0-5.degree. C.
for 15 min, added chloromethyl methyl ether (0.88 g, 11 mmol, 1.1
eq.), stirred at 0-5.degree. C. for another 20 min, and quenched
with NH.sub.4Cl.sub.(sat) solution. The aqueous layer was extracted
with EtOAc (3.times.20 mL) and the combined organic layers were
washed with water and brine, dried over Na.sub.2SO.sub.4,
concentrated, and purified on silica gel using 25% EtOAc/hexanes as
eluent to give 2-(benzyloxy)-5-(methoxymethoxy)pyridine (2.1 g,
87%) as a colorless oil. LRMS (M+H.sup.+) m/z 246.1
Step 2
##STR00334##
[0555] To 2-(benzyloxy)-5-(methoxymethoxy)pyridine (1.8 g, 8.71
mol) in EtOH was added Pd/C (1.0 g). The mixture was charged with
H.sub.2 (15 psi), stirred at rt for 45 min, filtered, and
concentrated to give 5-(methoxymethoxy)pyridin-2-ol (1.35 g,
quantitative yield) as a pale yellow solid. LRMS (M+H.sup.+) m/z
156.1
Step 3
##STR00335##
[0557] To a mixture of 5-(methoxymethoxy)pyridin-2-ol (1.35 g, 8.71
mmol, 1 eq.) and K.sub.2CO.sub.3 (6.01 g, 43.6 mmol, 5.0 eq.) in
DMF (30.0 mL) was added 1-bromo-2-methoxyethane (3.61 g, 26.1 mmol,
3 eq.). The mixture was heated at 60.degree. C. for 2 h, cooled,
filtered, concentrated, and purified on silica gel using a mixture
of EtOAc and hexanes as eluent to give
2-(2-methoxyethoxy)-5-(methoxymethoxy)pyridine (500 mg, 27%) as a
colorless oil. .sup.1H NMR (400 MHz, CDCl.sub.3) .delta. 7.94 (d,
J=3.0 Hz, 1H), 7.35 (ddd, J=8.9, 3.0, 1.0 Hz, 1H), 6.76 (dd, J=8.9,
1.0 Hz, 1H), 5.11 (s, 2H), 4.48-4.40 (m, 2H), 3.79-3.71 (m, 2H),
3.50 (s, 3H), 3.45 (s, 3H). LRMS (M+H.sup.+) m/z 214.1.
Step 4
##STR00336##
[0559] To a mixture of
2-(2-methoxyethoxy)-5-(methoxymethoxy)pyridine (1.34 g, 6.3 mol, 1
eq.) and diisopropylamine (17.5 uL, 0.13 mmol, 0.02 eq.) in THF (50
mL) was added methyl lithium (1.6 M/THF, 7 mL, 11.3 mol, 1.8 eq.)
at -40.degree. C. Upon the completion of addition, the mixture was
warmed to 0.degree. C., continued to stir at 0.degree. C. for 3 h,
cooled back down to -40.degree. C., and added DMF (0.83 mL, 11.3
mol, 1.8 eq.) slowly. The mixture was then stirred at -40.degree.
C. for 1 h, quenched with a mixture of HCl (12 N, 12 mL) and THF
(28 mL), warmed to rt, and added water (20 mL). The pH of the
mixture was adjusted to pH 8-9 with solid K.sub.2CO.sub.3. The
aqueous layer was extracted with EtOAc (30 mL) twice. The combined
organic layers were dried over Na.sub.2SO.sub.4, concentrated, and
purified on silica gel using a mixture of EtOAc and hexanes as
eluent to give a mixture of
2-(2-methoxyethoxy)-5-(methoxymethoxy)isonicotinaldehyde and
2-(2-methoxyethoxy)-5-(methoxymethoxy)nicotinaldehyde (5/1, 1.27 g,
83.6%) as a pale yellow oil. .sup.1H NMR (400 MHz, CDCl.sub.3)
.delta. 10.45 (s, 1H), 8.23 (s, 1H), 7.16 (s, 1H), 5.27 (s, 2H),
4.46 (dd, J=5.4, 3.9 Hz, 2H), 4.14 (q, J=7.1 Hz, 1H), 3.77-3.71 (m,
2H), 3.56 (s, 3H), 3.46 (s, 3H) and .sup.1H NMR (400 MHz,
CDCl.sub.3) .delta. 10.41 (s, 1H), 8.18 (d, J=3.2 Hz, 1H), 7.85 (d,
J=3.1 Hz, 1H), 5.16 (s, 2H), 4.64-4.57 (m, 2H), 3.85-3.79 (m,
J=5.4, 4.0 Hz, 2H), 3.50 (s, 3H), 3.46 (s, 3H); LRMS (M+H.sup.+)
m/z 242.1.1
Step 5
##STR00337##
[0561] To a solution of
2-methoxy-5-(methoxymethoxy)isonicotinaldehyde (1.27 g, 5.29 mol)
in THF (5 mL) was added HCl (3 N, 4 mL). The reaction was stirred
at 50.degree. C. for 1 h, cooled to rt, and diluted with water (5
mL). The mixture was neutralized to pH 7-8 with solid
K.sub.2CO.sub.3 and the aqueous layer was extracted with EtOAc (100
mL) twice. The combined organic layers were dried over
Na.sub.2SO.sub.4, concentrated, and purified on silica gel using a
mixture of EtOAc and hexanes to give
5-hydroxy-2-(2-methoxyethoxyl)isonicotinaldehyde (630 mg, 60%) and
5-hydroxy-2-(2-methoxyethoxyl)nicotinaldehyde (120 mg, 11%). Data
for 5-hydroxy-2-(2-methoxyethoxyl)isonicotinaldehyde: .sup.1H NMR
(400 MHz, CDCl.sub.3) .delta. 9.98 (s, 1H), 9.50 (s, 1H), 8.07 (s,
1H), 7.02 (s, 1H), 4.51-4.39 (m, 2H), 3.81-3.72 (m, 2H), 3.47 (s,
3H). LRMS (M+H.sup.+) m/z 198.1. Data for and
5-hydroxy-2-(2-methoxyethoxyl)nicotinaldehyde: .sup.1H NMR (400
MHz, CDCl.sub.3) .delta. 10.3 (s, 1H), 7.99 (d, J=3.2 Hz, 1H), 7.58
(d, J=3.2 Hz, 1H), 7.18-7.07 (br, 1H), 4.54 (dd, J=5.4, 3.7 Hz,
2H), 3.84 (dd, J=5.4, 3.7 Hz, 2H), 3.49 (s, 3H). LRMS (M+H.sup.+)
m/z 198.1
Example 77
Preparation of
2-(2-methoxyethoxy)-5-((2-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-
isonicotinaldehyde (Compound 184)
##STR00338##
[0563] A mixture of
5-hydroxy-2-(2-methoxyethoxyl)isonicotinaldehyde (125 mg, 0.63
mmol, 1 eq.), 3-(chloromethyl)-2-(1-methyl-1H-pyrazol-5-yl)pyridine
hydrochloride salt (120 mg, 0.63 mmol, 1 eq.), and Cs.sub.2CO.sub.3
(410 mg, 1.26 mmol, 2 eq.) in DMF (3.0 mL) was heated at 60.degree.
C. for 2 h. The mixture was cooled, filtered, concentrated, and
purified on silica gel using a mixture of EtOAc and hexanes as
eluent to give
2-(2-methoxyethoxy)-5-((2-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-
isonicotinaldehyde (59 mg, 25%) as a yellow oil. .sup.1H NMR (400
MHz, CDCl.sub.3) .delta. 10.22 (s, 1H), 8.59 (dd, J=4.7, 1.6 Hz,
1H), 7.87 (dd, J=7.9, 1.3 Hz, 1H), 7.73 (s, 1H), 7.38 (d, J=1.9 Hz,
1H), 7.27 (dd, J=7.9, 4.8 Hz, 1H), 7.00 (s, 1H), 6.25 (d, J=1.9 Hz,
1H), 5.02 (s, 2H), 4.26 (dd, J=5.4, 3.9 Hz, 2H), 3.80 (s, 3H), 3.57
(dd, J=5.4, 3.9 Hz, 2H), 3.28 (s, 3H). LRMS (M+H.sup.+) m/z
387.1.
Example 78
Preparation of
2-(2-methoxyethoxy)-5-((2-(1-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-
nicotinaldehyde (Compound 185)
[0564] The title compound was prepared according to the procedure
in Example 77.
[0565] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.38 (s, 1H), 8.74
(dd, J=4.7, 1.5 Hz, 1H), 8.07 (d, J=3.3 Hz, 1H), 7.98 (dd, J=7.9,
1.2 Hz, 1H), 7.64 (d, J=3.3 Hz, 1H), 7.53 (d, J=1.9 Hz, 1H), 7.41
(dd, J=7.9, 4.8 Hz, 1H), 6.41 (d, J=1.9 Hz, 1H), 5.04 (s, 2H),
4.62-4.51 (m, 2H), 3.96 (s, 3H), 3.82-3.76 (m, 2H), 3.45 (s,
3H).
Example 79
Preparation of
3-hydroxy-5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)isonico-
tinaldehyde (Compound 186)
Step 1:
##STR00339##
[0567] To a mixture of NaH (60% in mineral oil) (2.77 g, 69.25
mmol, 2.5 eq.) in DMF (40.0 mL) was added benzyl alcohol (6.6 g,
61.0 mmol, 2.2 eq.) at 0.degree. C. The mixture was stirred at
0.degree. C. for 10 min, added 3,5-dichloroisonicotinonitrile (4.8
g, 27.7 mmol, 1 eq.), continued to stir at 0.degree. C. for 30 min,
gradually warm to rt, stirred at rt O/N, and quenched with
NH.sub.4Cl.sub.(sat.) solution. The aqueous layer was extracted
with EtOAc three times. The combined organic layers were washed
with brine, dried over Na.sub.2SO.sub.4, concentrated, and purified
on silica gel using a mixture of EtOAc and hexanes as eluent to
give 3,5-bis(benzyloxy)isonicotinonitrile (4.94 g, 56%) as an
off-white solid. .sup.1H NMR (400 MHz, CDCl.sub.3) .delta. 8.14 (s,
2H), 7.58-7.30 (m, 10H), 5.33 (s, 4H). LRMS (M+H.sup.+) m/z
317.1
Step 2:
##STR00340##
[0569] To a mixture of 3,5-bis(benzyloxy)isonicotinonitrile (2.5 g,
7.9 mmol, 1 eq.) and K.sub.2CO.sub.3 (4.37 g, 31.6 mmol, 4 eq.) in
DMSO (10 mL) was added H.sub.2O.sub.2 (30% in water, 2.0 mL) at rt.
The mixture was stirred at rt O/N and added water (50 mL). The
solid was collected and dried to give
3,5-bis(benzyloxy)isonicotinamide (2.2 g, 83%) as a white solid.
.sup.1H NMR (400 MHz, CDCl.sub.3) .delta. 8.13 (s, 2H), 7.59-7.33
(m, 10H), 5.83 (s, 2H), 5.25 (s, 4H), 4.81 (s, 2H). LRMS
(M+H.sup.+) m/z 335.1
Step 3:
##STR00341##
[0571] To 3,5-bis(benzyloxy)isonicotinamide (1.6 g, 4.79 mmol) in
THF (30 mL) was added Cp2ZrCl (3.7 g, 14.4 mmol, 3 eq.) at rt. The
mixture was stirred at rt for 2 h, concentrated, and purified on
silica gel using a mixture of EtOAc and hexanes as eluent to give
3,5-bis(benzyloxy)isonicotinaldehyde (580 mg, 38%) and
(3,5-bis(benzyloxy)pyridin-4-yl)methanol (710 mg, 46%) as white
solids. Data for aldehyde .sup.1H NMR (400 MHz, CDCl.sub.3) .delta.
10.53 (s, 1H), 8.13 (s, 2H), 7.51-7.22 (m, 10H), 5.21 (s, 4H); LRMS
(M+H.sup.+) m/z 320.1. Data for alcohol .sup.1H NMR (400 MHz,
CDCl.sub.3) .delta. 8.12 (s, 2H), 7.58-7.34 (m, 10H), 5.22 (s, 4H),
4.87 (s, 1H).; LRMS (M+H) m/z 322.1.
Step 4:
##STR00342##
[0573] To a solution of (3,5-bis(benzyloxy)pyridin-4-yl)methanol
(910 mg, 2.83 mmol) and imidazole (385 mg, 5.66 mmol) in DMF (10.0
mL) was added TBSCl (513 mg, 3.4 mmol) at rt. The mixture was
stirred at rt for 1 h and diluted with a mixture of water (10 mL)
and EtOAc (40 mL). The organic layer was washed with
NH.sub.4Cl.sub.(sat) solution and brine, dried over
Na.sub.2SO.sub.4, concentrated, and purified on silica gel using
10% EtOAc/hexanes as eluent to give
3,5-bis(benzyloxy)-4-((tert-butyldimethylsilyloxy)methyl)pyridine
(728 mg, 59%) as an off-white solid. LRMS (M+H.sup.+) m/z
436.3.
Step 5:
##STR00343##
[0575] To
3,5-bis(benzyloxy)-4-((tert-butyldimethylsilyloxy)methyl)pyridin- e
(720 mg, 1.66 mmol, 1 eq.) in a mixture of EtOAc/EtOH (5/2, 28 mL)
was added Pd/C (400.0 mg). The mixture was charged with H.sub.2 (60
psi), stirred at rt for 2 h, filtered, and concentrated to give
4-((tert-butyldimethylsilyloxy)methyl)pyridine-3,5-diol as a yellow
solid. .sup.1H NMR (400 MHz, CDCl.sub.3) .delta. 7.54 (s, 2H), 4.91
(s, 2H), 0.73 (s, 9H), -0.00 (s, 6H). LRMS (M+H) m/z 256.1.
Step 6:
##STR00344##
[0577] A mixture of
4-((tert-butyldimethylsilyloxy)methyl)pyridine-3,5-diol (100 mg,
0.39 mmol, 2 eq.) and Cs.sub.2CO.sub.3 (381 mg, 1.17 mmol, 3 eq.)
in DMF (15 mL) was stirred at rt for 30 min. To this mixture was
added 3-(chloromethyl)-2-(1-isopropyl-1H-pyrazol-5-yl)pyridine
hydrochloride (53 mg, 0.39 mmol, 1 eq.) at rt. The mixture was
continued to stir at rt O/N, filtered, concentrated, and purified
on silica gel using a mixture of EtOAc and hexanes as eluent to
give
4-(hydroxymethyl)-5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy-
)pyridin-3-ol (36 mg, 27%) as a pale yellow oil. .sup.1H NMR (400
MHz, CDCl.sub.3) .delta. 8.51 (dt, J=33.0, 16.5 Hz, 1H), 7.72 (d,
J=1.6 Hz, 1H), 7.69 (s, 1H), 7.47 (s, 1H), 7.33 (s, 1H), 7.21 (dd,
J=7.8, 4.8 Hz, 1H), 6.10 (d, J=1.8 Hz, 1H), 4.84 (s, 2H), 4.68 (s,
1H), 4.44 (sep, 6.6 Hz, 1H), 1.24 (d, J=6.6 Hz, 6H). LRMS
(M+H.sup.+) m/z 341.1
Step 7:
##STR00345##
[0579] To
4-(hydroxymethyl)-5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-y-
l)methoxy)pyridin-3-ol (26 mg, 0.076 mmol, 1 eq.) in CH.sub.3CN (10
mL) was added MnO.sub.2 (66 mg, 0.76 mmol, 10 eq.). The mixture was
heated to 46.degree. C. with stirring O/N, cooled to rt, filtered,
and concentrated to give
3-hydroxy-5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy-
)isonicotinaldehyde as a pale yellow oil. .sup.1H NMR (400 MHz,
CDCl.sub.3) .delta. 11.06 (s, 1H), 10.35 (s, 1H), 8.70 (dd, J=4.7,
1.5 Hz, 1H), 8.11 (s, 1H), 7.89 (dd, J=7.9, 1.1 Hz, 1H), 7.80 (s,
1H), 7.53 (d, J=1.8 Hz, 1H), 7.36 (dd, J=7.9, 4.8 Hz, 1H), 6.27 (d,
J=1.8 Hz, 1H), 5.14 (s, 2H), 4.61 (sep, J=6.6 Hz, 1H), 1.41 (d,
J=6.6 Hz, 6H). LRMS (M+H.sup.+) m/z 339.1
Example 80
Preparation of 3-(benzyloxy)-5-hydroxyisonicotinaldehyde (Compound
187)
[0580] The title compound was prepared according to the procedure
in Example 79.
[0581] .sup.1H NMR (400 MHz, CDCl.sub.3) .delta. 11.08 (s, 1H),
10.41 (s, 1H), 8.08 (s, 1H), 7.99 (s, 1H), 7.39-7.28 (m, 5H), 5.18
(s, 2H).
Example 81
Preparation of
3-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-5-methoxyisonico-
tinaldehyde (Compound 188)
Step 1:
##STR00346##
[0583] To a solution of 3,5-difluoropyridine (5.4 g, 46.8 mmol, 1
eq.) in MeOH (45 mL) was added NaOMe (7.5 g, 140.4 mmol). The
mixture was divided into three microwave tubes and individually
heated at 135.degree. C. for 1 h in a microwave reactor. The three
tubes were combined, concentrated, and diluted with a mixture EtOAc
(100 mL) and brine (30 mL). The organic layer was dried over
Na.sub.2SO.sub.4 and concentrated. The crude was re-dissolved in
MeOH (45 mL) and added NaOMe (7.5 g, 140.4 mmol). The mixture was
again divided into three microwave tubes and individually heated at
135.degree. C. for 1 h in a microwave reactor. The three tubes were
combined and concentrated. The crude was dissolved in a mixture of
EtOAc (200 mL) and brine (30 mL). The organic layer was dried over
Na.sub.2SO.sub.4, concentrated, and purified on silica gel using a
mixture of EtOAc and hexanes as eluent to give
3,5-dimethoxypyridine (3.73 g, 57%) as an off-white solid. .sup.1H
NMR (400 MHz, CDCl.sub.3) .delta. 7.98 (d, J=2.4 Hz, 2H), 6.76 (t,
J=2.4 Hz, 1H), 3.88 (s, 6H). LRMS (M+H.sup.+) m/z 140.1.
Step 2:
##STR00347##
[0585] To a solution of 3,5-dimethoxypyridine (3.6 g, 25.90 mmol, 1
eq.) in THF (80 mL) was added BuLi (3M/hexanes, 13.0 mL, 38.85
mmol, 1.5 eq.) at -20.degree. C. The mixture was warmed to
0.degree. C., stirred at 0.degree. C. for 30 min, cooled back down
to -78.degree. C., and added DMF (3.8 g, 51.8 mmol, 2 eq.). The
mixture was gradually warmed to 0.degree. C., quenched with
NH.sub.4Cl.sub.(sat.) solution, and diluted with EtOAc. The aqueous
layer was extracted with EtOAc twice. The combined organic layers
were washed with brine, dried over Na.sub.2SO.sub.4, concentrated,
and purified on silica gel using a mixture of EtOAc and hexanes as
eluent to give 3,5-dimethoxyisonicotinaldehyde (2.7 g, 62%) as a
yellow solid. LRMS (M+H.sup.+) m/z 168.1.
Step 3:
##STR00348##
[0587] To a solution of 3,5-dimethoxyisonicotinaldehyde (2.7 g,
16.16 mmol, 1 eq.) in DCM (100 mL) was added AlCl.sub.3 (4.31 g,
32.32 mmol, 2.0 eq.) at rt. The mixture was reflux O/N, cooled to
rt, and added into ice (200 g). The aqueous layer was extracted
with DCM three times. The combined organic layers were dried over
Na.sub.2SO.sub.4, concentrated, and purified on silica gel using a
mixture of EtOAc and hexanes as eluent to give
3-hydroxy-5-methoxyisonicotinaldehyde (420 mg, 17%) as an off-white
solid. .sup.1H NMR (400 MHz, CDCl.sub.3) .delta. 10.96 (s, 1H),
10.26 (s, 1H), 7.96 (s, 1H), 7.80 (s, 1H), 3.84 (s, 3H). LRMS
(M+H.sup.+) m/z 154.1.
Step 4:
##STR00349##
[0589] A mixture of 3-hydroxy-5-methoxyisonicotinaldehyde (30 mg,
0.20 mmol, 1 eq.),
3-(chloromethyl)-2-(1-isopropyl-1H-pyrazol-5-yl)pyridine
hydrochloride (54 mg, 0.20 mmol, 1 eq.), and K.sub.2CO.sub.3 (110
mg, 0.80 mmol, 4 eq.) in DMF (2.0 mL) was heated at 70.degree. C.
for 2 h. The mixture was cooled, filtered, concentrated, and
purified on silica gel using a mixture of EtOAc and hexanes to give
34(2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-5-methoxyisonicot-
inaldehyde (30 mg, 43%) as an off-white solid. .sup.1H NMR (400
MHz, CDCl.sub.3) .delta. 10.46 (s, 1H), 8.65 (dd, J=4.7, 1.1 Hz,
1H), 8.13 (s, 1H), 8.11 (dd, J=7.9, 1.1 Hz, 1H), 7.96 (s, 1H), 7.54
(d, J=1.7 Hz, 1H), 7.37 (dd, J=7.9, 4.8 Hz, 1H), 6.29 (d, J=1.7 Hz,
1H), 5.11 (s, 2H), 4.55 (sep, J=6.6 Hz, 1H), 3.95 (s, 3H), 1.40 (d,
J=6.6 Hz, 6H). LRMS (M+H.sup.+) m/z 353.1.
Example 82
Preparation of
5-((2-(2-isopropyl-2H-1,2,4-triazol-3-yl)pyridin-3-yl)methoxy)-2-methoxyi-
sonicotinaldehyde (Compound 189)
Step 1:
##STR00350##
[0591] To 5-hydroxy-2-methoxyisonicotinaldehyde (1.0 g, 6.54 mmol,
1.0 eq.) in toluene (50.0 mL) were added ethane-1,2-diol (10.0 mL)
and PTSA (248 mg, 1.31 mmol, 0.2 eq.). The mixture was heated to
reflux O/N, cooled to rt, neutralized to pH 8, and extracted with
EtOAc three times. The combined organic layers were washed with
brine, dried over Na.sub.2SO.sub.4, and concentrated to give
4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-ol (980 mg, 76%) as an
off-white solid. LRMS (M+H.sup.+) m/z 198.1.
Step 2:
##STR00351##
[0593] A mixture of 4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-ol
(980 mg, 4.97 mmol, 1 eq.), 2-bromo-3-(chloromethyl)pyridine
hydrochloride (1.2 g, 4.93 mmol, 1 eq.) and K.sub.2CO.sub.3 (2.7 g,
19.88 mmol, 4 eq.) in DMF (10.0 mL) was heated at 70.degree. C. for
2 h. The mixture was cooled, filtered, concentrated, and purified
on silica gel using a mixture of EtOAc and hexanes as eluent to
give
5-((2-bromopyridin-3-yl)methoxy)-4-(1,3-dioxolan-2-yl)-2-methoxypyridine
(1.21 g, 66%) as a white solid. .sup.1H NMR (400 MHz, CDCl.sub.3)
.delta. 8.26 (dd, J=4.7, 1.9 Hz, 1H), 7.83 (dd, J=7.6, 1.9 Hz, 1H),
7.74 (s, 1H), 7.25 (dd, J=7.6, 4.8 Hz, 1H), 6.86 (s, 1H), 6.10 (s,
1H), 5.09 (s, 2H), 4.07-3.93 (m, 4H), 3.82 (s, 3H). LRMS
(M+H.sup.+) m/z 367.0.
Step 3:
##STR00352##
[0595] A mixture of
5-((2-bromopyridin-3-yl)methoxy)-4-(1,3-dioxolan-2-yl)-2-methoxypyridine
(1.1 g, 3.0 mmol, 1 eq.), Zn (CN).sub.2 (704 mg, 6.0 mmol, 2.0
eq.), and Pd(PPh.sub.3).sub.4 (346 mg, 0.3 mmol, 0.2 eq.) in DMF
(10 mL) was heated at 125.degree. C. for 2 h under N.sub.2. The
mixture was cooled, filtered, concentrated, and purified on silica
gel using a mixture of EtOAc and hexanes as eluent to give
3-((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yloxy)methyl)picolinonitrile
(820 mg, 84%) as a white solid. .sup.1H NMR (400 MHz, CDCl.sub.3)
.delta. 8.71 (d, J=4.6 Hz, 1H), 8.12 (dd, J=8.0, 0.7 Hz, 1H), 7.88
(s, 1H), 7.60 (dd, J=8.0, 4.7 Hz, 1H), 6.95 (s, 1H), 6.16 (s, 1H),
5.37 (s, 2H), 4.18-4.00 (m, 4H), 3.92 (s, 3H). LRMS (M+H.sup.+) m/z
314.1.
Step 4:
##STR00353##
[0597] To
3-((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yloxy)methyl)picoli-
nonitrile (150 mg, 0.48 mmol, 1 eq.) in a mixture of EtOH/water
(5/1, 12 mL) was added NaOH (192 mg, 4.8 mmol, 10 eq.). The mixture
was heated to reflux O/N, partially concentrated, added ice, and
acidified to pH 3 with HCl.sub.(conc.). The solid was collected and
dried to give
3-((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yloxy)methyl)picolinic
acid (145 mg, 91%) as a white solid. .sup.1H NMR (400 MHz, MeOD)
.delta. 8.38-8.48 (br, 1H), 8.28-8.35 (br, 1H), 7.76 (s, 1H),
7.50-7.70 (br, 1H), 6.81 (s, 1H), 6.04 (s, 1H), 5.50-5.64 (br, 2H),
4.03-3.87 (m, 3H), 3.75 (s, 3H). LRMS (M+H.sup.+) m/z 333.0.
Step 5:
##STR00354##
[0599] To a mixture of
3-((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yloxy)methyl)picolinic
acid (145 mg, 0.44 mmol, 1 eq.) and EDCI.HCl (169 mg, 0.88 mmol, 2
eq.) in DMF (3.0 mL) was added DIEA (146 uL, 0.88 mmol, 2 eq.). The
mixture was stirred at rt for 1 h and purified by RP-HPLC (Gemini
21.2.times.150 mm) using a mixture of CH.sub.3CN and water to
isolate the urea intermediate. The fractions were concentrated and
dissolved in EtOH (5.0 mL). To this mixture was added hydrazine
(0.5 mL) at rt. The mixture was stirred at rt for 1 h, partially
concentrated, and diluted with water (10 mL). The solid was
collected, washed with water, and dried to give
3-((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yloxy)methyl)picolinohydrazi-
de (97 mg, 64% for two steps) as a white solid. .sup.1H NMR (400
MHz, CDCl.sub.3) .delta. 9.13 (s, 1H), 8.51 (d, J=4.6 Hz, 1H), 8.24
(d, J=7.9 Hz, 1H), 7.85 (s, 1H), 7.51 (dd, J=8.0, 4.6 Hz, 1H), 6.95
(s, 1H), 6.24 (s, 1H), 5.80 (s, 2H), 4.20-4.06 (m, 4H), 3.90 (s,
3H). LRMS (M+H.sup.+) m/z 347.1.
Step 6:
##STR00355##
[0601] To a mixture of
3-((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yloxy)methyl)picolinohydrazi-
de (90 mg, 0.26 mmol, 1 eq.) and AcOH (0.4 mL) in dioxane (2.0 mL)
was added CH(OMe).sub.3 (0.4 mL). The mixture was sealed and heated
at 110.degree. C. for 1 h, cooled to rt, and added isopropyl amine
(0.4 mL). The mixture was re-sealed, heated at 110.degree. C. O/N,
concentrated, and purified on RP-HPLC (Gemini 21.2.times.150 mm)
using a mixture of CH.sub.3CN and water as eluent to give
4-(1,3-dioxolan-2-yl)-5-((2-(2-isopropyl-2H-1,2,4-triazol-3-yl)pyridin-3--
yl)methoxy)-2-methoxypyridine (68 mg, 66%) as a white solid.
.sup.1H NMR (400 MHz, CDCl.sub.3) .delta. 8.66 (dd, J=4.7, 1.2 Hz,
1H), 8.41 (s, 1H), 8.24 (dd, J=8.0, 1.2 Hz, 1H), 7.76 (s, 1H), 7.45
(dd, J=8.0, 4.7 Hz, 1H), 6.90 (s, 1H), 6.17 (s, 1H), 5.61 (s, 2H),
5.30 (sep, J=6.7 Hz, 1H), 4.17-4.02 (m, 4H), 3.88 (s, 3H), 1.55 (d,
J=6.7 Hz, 6H). LRMS (M+H.sup.+) m/z 398.2.
Step 7:
##STR00356##
[0603] To
4-(1,3-dioxolan-2-yl)-5-((2-(2-isopropyl-2H-1,2,4-triazol-3-yl)p-
yridin-3-yl)methoxy)-2-methoxypyridine (60 mg, 0.15 mmol, 1 eq.) in
a RB flask was added HCl (6 N, 2.0 mL). The mixture was warmed to
40.degree. C. O/N, cooled to rt, neutralized to pH 7-8 with
NaHCO.sub.3(sat) solution, and extracted with EtOAc three times.
The combined organic layers were washed with brine, dried over
Na.sub.2SO.sub.4, and concentrated to give
5-((2-(2-isopropyl-2H-1,2,4-triazol-3-yl)pyridin-3-yl)methoxy)-2-methoxyi-
sonicotinaldehyde (52.2 mg, 99%) as a yellow solid. .sup.1H NMR
(400 MHz, CDCl.sub.3) .delta. 10.35 (s, 1H), 8.62 (dd, J=4.6, 1.2
Hz, 1H), 8.33 (s, 1H), 8.11 (dd, J=8.0, 1.2 Hz, 1H), 7.98 (s, 1H),
7.40 (dd, J=8.0, 4.7 Hz, 1H), 6.99 (s, 1H), 5.62 (s, 2H), 5.28
(sep, J=6.7 Hz, 1H), 3.82 (s, 3H), 1.46 (d, J=6.7 Hz, 6H). LRMS
(M+H.sup.+) m/z 354.1.
Example 83
Preparation of
5-((2-(1-isopropyl-4-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-metho-
xyisonicotinaldehyde (Compound 190)
Step 1:
##STR00357##
[0605] Ethylmagnesium bromide (3M/ether, 1.53 mL, 4.60 mmol, 1.5
eq.) was added to a stirred solution of
3-((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yloxy)methyl)picolinonitrile
(960 mg, 3.07 mmol, 1 eq.) in THF (15.0 mL) at -78.degree. C. After
addition, the reaction mixture was allowed to warm to rt and
quenched with aqueous citric acid solution. The aqueous layer was
extracted with EtOAc (2.times.30 mL). The combined organic layers
were washed with NaHCO.sub.3 (sat) solution and brine, dried over
Na.sub.2SO.sub.4, concentrated, and purified on silica gel using a
mixture of EtOAc and hexanes as eluent to give
1-(3-((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yloxy)methyl)pyridin-2-yl-
)propan-1-one (611 mg, 58%) as a colorless oil. LRMS (M+H.sup.+)
m/z 345.1.
Step 2:
##STR00358##
[0607]
1-(3-((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yloxy)methyl)pyridi-
n-2-yl)propan-1-one (600 mg, 1.74 mmol) in
dimethoxy-N,N-dimethylmethanamine (10.0 mL) was heated to reflux
O/N. The mixture was concentrated to give
(E)-1-(3-((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yloxy)methyl)pyridin--
2-yl)-3-(dimethylamino)-2-methylprop-2-en-1-one, which was used for
next step without further purification. LRMS (M+H.sup.+) m/z
400.2.
Step 3:
##STR00359##
[0609] To
(E)-1-(3-((4-(1,3-dioxolan-2-yl)-6-methoxypyridin-3-yloxy)methyl-
)pyridin-2-yl)-3-(dimethylamino)-2-methylprop-2-en-1-one (crude,
230 mg, 0.58 mmol, 1 eq.) in EtOH (5 mL) was added
isopropylhydrazine hydrochloride (128 mg, 1.16 mmol, 2 eq.) at rt.
The mixture was heated at 80.degree. C. for 2 h, cooled to rt,
concentrated, and diluted with a mixture of EtOAc (50 mL) and
NaHCO.sub.3 (sat) (10.0 mL) solution. The layers were separated and
aqueous layer was extracted with EtOAc three times. The combined
organic layers were dried over Na.sub.2SO.sub.4, concentrated, and
purified on silica gel using a mixture of EtOAc and hexanes as
eluent to give
4-(1,3-dioxolan-2-yl)-5-((2-(1-isopropyl-4-methyl-1H-pyrazol-5-yl)pyridin-
-3-yl)methoxy)-2-methoxypyridine (48 mg, 20% for two steps).
.sup.1H NMR (400 MHz, CDCl.sub.3) .delta. 8.75 (dd, J=4.7, 1.4 Hz,
1H), 8.12 (d, J=8.1 Hz, 1H), 7.62 (s, 1H), 7.49-7.44 (m, 2H), 6.91
(s, 1H), 6.11 (s, 1H), 4.85-5.01 (m, 2H), 4.30-3.98 (m, 5H), 3.88
(s, 3H), 1.94 (s, 3H), 1.50 (d, J=6.7 Hz, 3H), 1.39 (d, J=6.7 Hz,
3H). LRMS (M+H.sup.+) m/z 411.2.
Step 4:
##STR00360##
[0611] To
4-(1,3-dioxolan-2-yl)-5-((2-(1-isopropyl-4-methyl-1H-pyrazol-5-y-
l)pyridin-3-yl)methoxy)-2-methoxypyridine (41 mg, 0.1 mmol, 1 eq.)
in a RB flask was added HCl (6 N, 2.0 mL). The mixture was warmed
to 40.degree. C. O/N, cooled to rt, neutralized to pH 7-8 with
NaHCO.sub.3(sat) solution, and extracted with EtOAc three times.
The combined organic layers were washed with brine, dried over
Na.sub.2SO.sub.4, concentrated, and purified on silica gel using a
mixture of EtOAc and hexanes as eluent to give
5-((2-(1-isopropyl-4-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-
-2-methoxyisonicotinaldehyde (33.3 mg, 99%) as an pale-yellow oil.
.sup.1H NMR (400 MHz, CDCl.sub.3) .delta. 10.32 (s, 1H), 8.71 (dd,
J=4.7, 1.6 Hz, 1H), 7.99 (dd, J=7.9, 1.5 Hz, 1H), 7.76 (s, 1H),
7.40 (dd, J=7.1, 4.7 Hz, 1H), 7.39 (s, 1H), 7.01 (s, 1H), 4.86-4.99
(m, 2H), 4.12 (sep, J=6.7, 1H), 3.82 (s, 3H), 1.86 (s, 3H), 1.40
(d, J=767 Hz, 3H), 1.29 (d, J=6.7 Hz, 3H). LRMS (M+H.sup.+) m/z
367.1.
Example 84
Preparation of
5-((2-(1-(2-hydroxyethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-methoxy-
isonicotinaldehyde (Compound 191)
[0612] The title compound was prepared according to the procedure
in Example 83.
[0613] .sup.1H NMR (400 MHz, CDCl.sub.3) .delta. 10.18 (s, 1H),
8.50 (dd, J=4.8, 1.6 Hz, 1H), 7.89 (dd, J=7.9, 1.5 Hz, 1H), 7.72
(s, 1H), 7.42 (d, J=1.9 Hz, 1H), 7.27 (dd, J=7.9, 4.9 Hz, 1H), 6.90
(s, 1H), 6.26 (d, J=1.9 Hz, 1H), 5.34 (s, 1H), 5.04 (s, 2H),
4.24-4.16 (m, 2H), 3.94-3.85 (m, 2H), 3.70 (s, 3H).
Example 85
Synthesis of 2,2,2-trifluoroacetic
acid:6-(((4-formylpyridin-3-yl)oxy)methyl)picolinic acid (1:1)
(Compound 192)
Step 1:
##STR00361##
[0615] Into a 25-mL round-bottom flask, was placed a solution of
pyridine-2,6-dicarboxylic acid (1 g, 5.98 mmol, 1.00 equiv) in
methanol (12.5 mL). Sulfuric acid (2.5 mL) was added to the
reaction mixture. The resulting solution was stirred overnight at
70.degree. C., and then it was quenched by the addition of 10 mL of
water. The pH value of the solution was adjusted to 7 with sodium
carbonate. The resulting solution was extracted with 2.times.25 mL
of dichloromethane, and the combined organic layers were dried over
anhydrous sodium sulfate and concentrated under vacuum. This
resulted in 0.95 g (81%) of 2,6-dimethyl pyridine-2,6-dicarboxylate
as a white solid
Step 2:
##STR00362##
[0617] Into a 100-mL round-bottom flask, was placed a solution of
2,6-dimethyl pyridine-2,6-dicarboxylate (950 mg, 4.87 mmol, 1.00
equiv) in a solvent mixture of methanol (33.2 mL) and
dichloromethane (14.2 mL). NaBH.sub.4 (185 mg, 5.02 mmol, 1.00
equiv) was added to the reaction mixture in several batches at
0.degree. C. The resulting solution was stirred overnight at room
temperature, and then it was quenched by the addition of 50 mL of
NH.sub.4Cl (aq.). The resulting solution was extracted with
2.times.50 mL of dichloromethane and the combined organic layers
were dried over anhydrous sodium sulfate and concentrated under
vacuum. The residue was applied onto a silica gel column with ethyl
acetate/petroleum ether (1:1-2:1) as eluent to yield 750 mg (92%)
of methyl 6-(hydroxymethyl)pyridine-2-carboxylate as a white
solid.
Step 3:
##STR00363##
[0619] Into a 50-mL round-bottom flask, which was purged and
maintained with an inert atmosphere of nitrogen, was placed a
solution of methyl 6-(hydroxymethyl)pyridine-2-carboxylate (300 mg,
1.79 mmol, 1.00 equiv) in tetrahydrofuran (15 mL).
4-(Dimethoxymethyl)pyridin-3-ol (304.2 mg, 1.80 mmol, 1.00 equiv),
and triphenylphosphane (615 mg, 2.34 mmol, 1.30 equiv) was added to
the reaction mixture. This was followed by the addition of DIAD
(473.1 mg, 2.34 mmol, 1.30 equiv) dropwise at 0.degree. C. The
resulting solution was stirred overnight at room temperature, and
then it was quenched by the addition of 10 mL of water. The
resulting solution was extracted with 2.times.50 mL of ethyl
acetate and the combined organic layers were dried over anhydrous
sodium sulfate and concentrated under vacuum. The residue was
applied onto a silica gel column with ethyl acetate/petroleum ether
(1:5-1:1) as eluent to yield 340 mg (60%) of methyl
6-([[4-(dimethoxymethyl)pyridin-3-yl]oxy]methyl)pyridine-2-carboxylate
as a white solid.
Step 4:
##STR00364##
[0621] Into a 100-mL round-bottom flask, was placed methyl
6-([[4-(dimethoxymethyl)pyridin-3-yl]oxy]methyl)pyridine-2-carboxylate
(310 mg, 0.97 mmol, 1.00 equiv) and sodium hydroxide (117 mg, 2.93
mmol, 3.00 equiv) in a solvent mixture of methanol (10 mL), water
(10 mL) and tetrahydrofuran (10 mL). The resulting solution was
stirred overnight at room temperature. The pH value of the solution
was adjusted to 4-5 with hydrogen chloride (1 mol/L). The resulting
solution was extracted with 3.times.20 mL of isopropal/DCM(1/3) and
the organic layers combined and dried over anhydrous sodium sulfate
and concentrated under vacuum. This resulted in 230 mg (78%) of
6-([[4-(dimethoxymethyl)pyridin-3-yl]oxy]methyl)pyridine-2-carboxylic
acid as a white solid.
Step 5:
##STR00365##
[0623] Into an 8-mL sealed tube, was placed a solution of
6-([[4-(dimethoxymethyl)pyridin-3-yl]oxy]methyl)pyridine-2-carboxylic
acid (150 mg, 0.49 mmol, 1.00 equiv) in dichloromethane (4 mL) and
trifluoroacetic acid (2 mL). The resulting solution was stirred for
3.5 h at 45.degree. C. in an oil bath. The resulting mixture was
concentrated under vacuum. The crude product (100 mg) was purified
by Prep-HPLC with the following conditions
(2#-AnalyseHPLC-SHIMADZU(HPLC-10)): Column, SunFire Prep C18 OBD
Column, 5 um, 19*150 mm, mobile phase, water with 0.05% TFA and
MeCN (10% MeCN up to 35% in 4 min, up to 100% in 1 min, down to 10%
in 1 min); Detector, Waters 2545 UvDector 254&220 nm. This
resulted in 49 mg (38%) of
6-[[(4-formylpyridin-3-yl)oxy]methyl]pyridine-2-carboxylic acid as
a light yellow solid. LC-MS-PH-GBT-ZL-HS-19-0 (ES, m/z): 259
[M+1].sup.+ H-NMR-PH-GBT-ZL-HS-19-0 (300 MHz, DMSO, ppm): 10.52 (s,
1H), 8.92 (s, 1H), 8.52 (d, J=4.8 Hz, 1H), 8.09 (m, 2H), 7.95 (m,
1H), 7.76 (d, J=4.8 Hz, 1H), 5.61 (s, 2H).
Example 86
Preparation of
5-((2-(4-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-oxo-1,2-dihydropy-
ridine-4-carbaldehyde (Compound 194)
##STR00366##
[0625] To
2-methoxy-5-((2-(4-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)i-
sonicotinaldehyde (862 mg, 2.66 mmol, 1 equiv) suspend in water
(5.0 mL) was added HCl (6 N, 4.43 mL, 26.6 mmol, 10 eq.). Once the
mixture turned into a homogeneous solution, it was freeze at
-78.degree. C. to an solid and pump under high vacuum O/N. The
yellow solid was continued to pump at 45.degree. C. for 20 h,
dissolved in water (2.0 mL), and basified to pH 11 with NaOH (2 N).
The aqueous layer was washed with DCM three times and the pH of the
mixture was adjusted to pH 6-7. The solid was collected and dried
to give
5-((2-(4-methyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-2-oxo-1,2-dihydropy-
ridine-4-carbaldehyde (180 mg, 44% based on 50% recovered of SM) as
a white solid. .sup.1H NMR (400 MHz, DMSO at 90.degree. C.) .delta.
10.14 (s, 1H), 8.63 (s, 1H), 8.09-8.03 (br, 1H), 7.56-7.50 (br,
2H), 7.42-7.35 (br, 1H), 6.70 (s, 1H), 5.39 (s, 2H), 2.18 (s, 3H).
LRMS (M+H.sup.+) m/z 311.1.
Example 87
Preparation of
2-(5-(3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)pyridin-2-yl)-1H-pyraz-
ol-1-yl)acetic acid (Compound 199)
Step 1
##STR00367##
[0627] To
(E)-1-(3-((tert-butyldimethylsilyloxy)methyl)pyridin-2-yl)-3-(di-
methylamino)prop-2-en-1-one (crude, 350 mg, 1.09 mmol, 1 eq.) in
EtOH (10 mL) was added ethyl 2-hydrazinylacetate hydrochloride (338
mg, 2.18 mmol, 2.0 eq.). The mixture was heated at 80.degree. C.
for 2 h, cooled to rt, added HCl (6 N, 0.5 mL), and stirred O/N.
The mixture was concentrated, and diluted with a mixture of EtOAc
(50 mL) and NaHCO.sub.3(sat) (10 mL). The layers were separated and
the aqueous layer was extracted with EtOAc three times. The
combined organic layers were dried over Na.sub.2SO.sub.4,
concentrated, and purified on silica gel using EtOAc as eluent to
give ethyl
2-(5-(3-(hydroxymethyl)pyridin-2-yl)-1H-pyrazol-1-yl)acetate (212
mg, 74%) as a colorless oil. .sup.1H NMR (400 MHz, CDCl.sub.3)
.delta. 8.61 (dd, J=4.7, 1.6 Hz, 1H), 7.97 (dd, J=7.8, 1.4 Hz, 1H),
7.64 (d, J=1.9 Hz, 1H), 7.36 (dd, J=7.8, 4.8 Hz, 1H), 6.56 (d,
J=1.9 Hz, 1H), 5.21 (s, 2H), 4.79 (d, J=5.8 Hz, 2H), 4.09 (q, J=7.1
Hz, 2H), 2.54 (t, J=6.0 Hz, 1H), 1.18 (t, J=7.1 Hz, 3H). LRMS
(M+H.sup.+) m/z 262.1
Step 2
##STR00368##
[0629] To ethyl
2-(5-(3-(hydroxymethyl)pyridin-2-yl)-1H-pyrazol-1-yl)acetate (182
mg, 0.70 mmol) in DCM (10 mL) was added SOCl.sub.2 (3.0 mL) at rt.
The reaction mixture was stirred at rt for 4 h and concentrated to
dryness. The crude solid was suspended in toluene and concentrated
to dryness. The process was repeated three times and dried under
vacuum to give ethyl
2-(5-(3-(chloromethyl)pyridin-2-yl)-1H-pyrazol-1-yl)acetate
hydrochloride (220 mg) as an off-white solid, which was used for
next step without further purification.
Step 3
##STR00369##
[0631] A mixture of 5-hydroxy-2-methoxyisonicotinaldehyde (107 mg,
0.70 mmol, 1 eq.), ethyl
2-(5-(3-(chloromethyl)pyridin-2-yl)-1H-pyrazol-1-yl)acetate
hydrochloride (220 mg, 0.70 mmol, 1 eq.), and K.sub.2CO.sub.3 (386
mg, 2.8 mmol, 4 eq.) in DMF (6.0 mL) was heated at 70.degree. C.
for 2 h. The mixture was cooled, filtered, concentrated, and
purified on silica gel using a mixture of EtOAc and hexanes as
eluent to give ethyl
2-(5-(3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)pyridin-2-yl)-1H-pyraz-
ol-1-yl)acetate (261 mg, 94%) as a white solid. .sup.1H NMR (400
MHz, CDCl.sub.3) .delta. 10.45 (s, 1H), 8.69 (d, J=3.8 Hz, 1H),
8.02 (s, 1H), 8.01 (d, J=7.5 Hz, 1H), 7.63 (d, J=1.6 Hz, 1H), 7.40
(dd, J=7.6, 4.0 Hz, 1H), 7.13 (s, 1H), 6.53 (d, J=1.6 Hz, 1H), 5.30
(s, 2H), 5.28 (s, 2H), 4.12 (q, J=7.1 Hz, 2H), 3.93 (s, 3H), 1.18
(t, J=7.1 Hz, 3H). LRMS (M+H.sup.+) m/z 397.1.
Step 4
##STR00370##
[0633] To ethyl
2-(5-(3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)pyridin-2-yl)-1H-pyraz-
ol-1-yl)acetate (182 mg, 0.46 mmol, 1 eq.) in a mixture of MeOH/THF
(1/5, 12.0 mL) was added NaOH (2N, 2.3 mL, 4.6 mmol, 10 eq.). The
mixture was stirred at rt for 2 h, acidified to pH 3, and extracted
with EtOAc (3.times.20 mL). The combined organic layers were dried
over Na.sub.2SO.sub.4 and concentrated to give
2-(5-(3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)pyridin-2-yl)-1H-pyraz-
ol-1-yl)acetic acid (135.1 mg, 80%) as a white solid. .sup.1H NMR
(400 MHz, CDCl.sub.3) .delta. 10.42 (s, 1H), 8.71 (d, J=4.7 Hz,
1H), 8.13 (d, J=7.8 Hz, 1H), 7.97 (s, 1H), 7.66 (d, J=1.6 Hz, 1H),
7.52 (dd, J=7.9, 4.9 Hz, 1H), 7.13 (s, 1H), 6.56 (d, J=1.7 Hz, 1H),
5.31 (s, 2H), 5.14 (s, 2H), 3.91 (s, 3H). LRMS (M+H.sup.+) m/z
369.1.
[0634] Examples 88 and 89 were prepared according to example 87
above.
Example 88
Preparation of methyl
3-(5-(3-(((4-formyl-6-methoxypyridin-3-yl)oxy)methyl)pyridin-2-yl)-1H-pyr-
azol-1-yl)propanoate (Compound 200)
[0635] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.44 (s, 1H), 8.75
(dd, J=4.8, 1.6 Hz, 1H), 8.05 (dd, J=7.9, 1.4 Hz, 1H), 7.99 (s,
1H), 7.58 (d, J=1.9 Hz, 1H), 7.44 (dd, J=7.9, 4.8 Hz, 1H), 7.12 (s,
1H), 6.41 (d, J=1.9 Hz, 1H), 5.21 (s, 2H), 4.55 (t, J=7.1 Hz, 2H),
3.92 (s, 3H), 3.62 (s, 3H), 3.00 (t, J=7.1 Hz, 2H).
Example 89
Preparation of
3-(5-(3-(((4-formyl-6-methoxypyridin-3-yl)oxy)methyl)pyridin-2-yl)-1H-pyr-
azol-1-yl)propanoic acid (Compound 202)
[0636] .sup.1H NMR (400 MHz, CDCl3) .delta. 10.33 (s, 1H), 8.66
(dd, J=4.8, 1.6 Hz, 1H), 7.96 (dd, J=7.9, 1.5 Hz, 1H), 7.83 (s,
1H), 7.53 (d, J=1.9 Hz, 1H), 7.37 (dd, J=7.9, 4.8 Hz, 1H), 7.02 (s,
1H), 6.33 (d, J=1.9 Hz, 1H), 5.13 (s, 2H), 4.49 (t, J=6.5 Hz, 2H),
3.81 (s, 3H), 2.94 (t, J=6.5 Hz, 2H).
Example 90
Preparation of
3-(3-(3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)pyridin-2-yl)-1H-pyraz-
ol-1-yl)propanoic acid (Compound 201)
Step 1
##STR00371##
[0638] To
(E)-1-(3-((tert-butyldimethylsilyloxy)methyl)pyridin-2-yl)-3-(di-
methylamino)prop-2-en-1-one (crude, 350 mg, 1.09 mmol, 1 eq.) in
EtOH (5 mL) was added hydrazine (140 mg, 4.36 mmol, 4 eq.). The
mixture was heated at 80.degree. C. for 2 h, cooled, concentrated,
and purified on silica gel using EtOAc as eluent to give
3-((tert-butyldimethylsilyloxy)methyl)-2-(1H-pyrazol-5-yl)pyridine
(282 mg, 90%) as a white solid. LRMS (M+H.sup.+) m/z 290.1
Step 2
##STR00372##
[0640] To a mixture of
3-((tert-butyldimethylsilyloxy)methyl)-2-(1H-pyrazol-5-yl)pyridine
(140 mg, 0.48 mmol, 1 eq.) and Cs.sub.2CO.sub.3 (312 mg, 0.96 mmol,
2 eq.) in DMF (3 mL) was added methyl 3-bromopropanoate (122 mg,
0.73 mmol, 1.5 eq.). The mixture was stirred at rt for 6 h,
filtered, concentrated, and purified on silica gel using a mixture
of EtOAc and hexanes as eluent to give methyl
3-(3-(3-((tert-butyldimethylsilyloxy)methyl)pyridin-2-yl)-1H-pyrazol-1-yl-
)propanoate (110 mg, 61%). LRMS (M+H.sup.+) m/z 376.1.
Step 3
##STR00373##
[0642] To methyl
3-(3-(3-((tert-butyldimethylsilyloxy)methyl)pyridin-2-yl)-1H-pyrazol-1-yl-
)propanoate in MeOH (10 mL) was added HCl (2 N, 1.2 mL, 10 eq.).
The mixture was stirred at rt for 4 h, concentrated, neutralized to
pH 7-8 with NaHCO.sub.3(sat) solution, and extracted with EtOAc
three times. The combined organic layers were washed with brine,
dried over Na.sub.2SO.sub.4, concentrated, and purified on silica
gel using EtOAc as eluent to give methyl
3-(3-(3-(hydroxymethyl)pyridin-2-yl)-1H-pyrazol-1-yl)propanoate (51
mg, 67%) as an oil. LRMS (M+H.sup.+) m/z 262.1.
Step 4
##STR00374##
[0644] To methyl
3-(3-(3-(hydroxymethyl)pyridin-2-yl)-1H-pyrazol-1-yl)propanoate (51
mg, 0.20 mmol) in DCM (5 mL) was added SOCl.sub.2 (1.0 mL) at rt.
The reaction mixture was stirred at rt for 4 h and concentrated to
dryness. The crude solid was suspended in toluene and concentrated
to dryness. The process was repeated three times and dried under
vacuum to give methyl
3-(3-(3-(chloromethyl)pyridin-2-yl)-1H-pyrazol-1-yl)propanoate
hydrochloride (63 mg) as an off-white solid, which was used for
next step without further purification.
Step 5
##STR00375##
[0646] A mixture of 5-hydroxy-2-methoxyisonicotinaldehyde (30 mg,
0.20 mmol, 1 eq.), methyl
3-(3-(3-(chloromethyl)pyridin-2-yl)-1H-pyrazol-1-yl)propanoate
hydrochloride (63 mg, 0.20 mmol, 1 eq.), and K.sub.2CO.sub.3 (100
mg, 10.32 mmol, 4 eq.) in DMF (5.0 mL) was heated at 70.degree. C.
for 2 h. The mixture was cooled, filtered, concentrated, and
purified on silica gel using a mixture of EtOAc and hexanes as
eluent to give methyl
3-(3-(3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)pyridin-2-yl)-1H-pyraz-
ol-1-yl)propanoate (88 mg, quantitative yield) as a white solid.
.sup.1H NMR (400 MHz, CDCl.sub.3) .delta. 10.50 (s, 1H), 8.65 (dd,
J=4.7, 0.9 Hz, 1H), 8.09 (s, 1H), 8.02 (dd, J=7.8, 0.8 Hz, 1H),
7.53 (d, J=2.3 Hz, 1H), 7.31 (dd, J=7.9, 4.8 Hz, 1H), 7.12 (s, 1H),
6.96 (d, J=2.3 Hz, 1H), 5.71 (s, 2H), 4.46 (t, J=6.6 Hz, 2H), 3.93
(s, 3H), 3.69 (s, 3H), 2.91 (t, J=6.6 Hz, 2H). LRMS (M+H.sup.+) m/z
397.1.
Step 6
##STR00376##
[0648] To methyl
3-(3-(3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)pyridin-2-yl)-1H-pyraz-
ol-1-yl)propanoate (72 mg, 0.18 mmol, 1 eq.) in a mixture of
MeOH/THF (1/6, 6.0 mL) was added NaOH (3 N, 0.6 mL, 1.8 mmol, 10
eq.). The mixture was stirred at rt for 2 h, acidified to pH 3,
extracted with EtOAc (3.times.20 mL). The combined organic layers
were dried over Na.sub.2SO.sub.4 and concentrated to give
3-(3-(3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)pyridin-2-yl)-1H-pyraz-
ol-1-yl)propanoic acid (53.4 mg, 78%) as a white solid. .sup.1H NMR
(400 MHz, CDCl.sub.3) .delta. 10.42 (s, 1H), 8.57 (d, J=4.6 Hz,
1H), 8.08 (s, 1H), 7.95 (d, J=7.8 Hz, 1H), 7.46 (d, J=2.3 Hz, 1H),
7.23 (dd, J=7.9, 4.6 Hz, 1H), 7.03 (s, 1H), 6.85 (d, J=2.3 Hz, 1H),
5.64 (s, 2H), 4.42 (t, J=6.1 Hz, 2H), 3.83 (s, 3H), 2.86 (t, J=6.1
Hz, 2H). LRMS (M+H.sup.+) m/z 383.1.
Example 91
Preparation of 6-(((4-formylpyridin-3-yl)oxy)methyl)nicotinonitrile
2,2,2-trifluoroacetate (Compound 204)
Step 1:
##STR00377##
[0650] Into a 250-mL round-bottom flask, was placed a solution of
6-methylpyridine-3-carbonitrile (8 g, 67.72 mmol, 1.00 equiv) in
CCl4 (125 mL). N-Bromosuccinimide (13.4 g, 75.29 mmol, 1.10 equiv),
and AIBN (480 mg, 2.92 mmol, 0.04 equiv) were added to the reaction
solution. The resulting solution was stirred for 5 h at 85.degree.
C. The resulting mixture was concentrated under vacuum. The residue
was applied onto a silica gel column with ethyl acetate/petroleum
ether (1:5) as eluent to yield 5 g (37%) of
6-(bromomethyl)pyridine-3-carbonitrile as a beige solid.
Step 2:
##STR00378##
[0652] Into a 250-mL round-bottom flask, was placed a solution of
6-(bromomethyl)pyridine-3-carbonitrile (3 g, 15.23 mmol, 1.00
equiv) in CH3CN (100 mL). Potassium carbonate (4.24 g, 30.68 mmol,
2.00 equiv) and 4-(dimethoxymethyl)pyridin-3-ol (2.83 g, 16.73
mmol, 1.10 equiv) were added to the reaction mixture. The resulting
solution was stirred for 2 h at 50.degree. C., and then it was
concentrated under vacuum. The residue was applied onto a silica
gel column with ethyl acetate/petroleum ether (1:3) as eluent to
furnish 1.4 g (32%) of
6-([[4-(dimethoxymethyl)pyridin-3-yl]oxy]methyl)pyridine-3-carbonitrile
as a red solid.
Step 2:
##STR00379##
[0654] Into an 8-mL vial, was placed a solution of
6-([[4-(dimethoxymethyl)pyridin-3-yl]oxy]methyl)pyridine-3-carbonitrile
(100 mg, 0.35 mmol, 1.00 equiv) in a mixture of dichloromethane (2
mL) and trifluoroacetic acid (1 mL). The resulting solution was
stirred for 5 h at 45.degree. C., and then it was concentrated
under vacuum. The crude product (50 mg) was purified by Prep-HPLC
with the following conditions (Prep-HPLC-010): Column, SunFire Prep
C18 OBD Column, 5 um, 19*150 mm, mobile phase, Water and MeCN
(10.0% MeCN up to 40.0% in 3 min, up to 100.0% in 2 min, down to
10.0% in 1 min); Detector, Waters 2545 UvDector 254&220 nm.
This resulted in 8 mg (10%) of
6-[[(4-formylpyridin-3-yl)oxy]methyl]pyridine-3-carbonitrile as a
white solid. LC-MS-PH-GBT-ZL-HS-13-0: (ES, m/z):258 [M+1+18].sup.+.
H-NMR-PH-GBT-ZL-HS-13-0: (300 MHz, DMSO, ppm): 10.48 (s, 1H), 9.06
(s, 1H), 8.80 (s, 1H), 8.47 (m, 2H), 7.94 (d, J=8.1 Hz, 1H), 7.65
(d, J=5.1 Hz, 1H), 5.69 (s, 2H).
Example 92
Preparation of 6-(((4-formylpyridin-3-yl)oxy)methyl)nicotinic acid
hydrochloride (Compound 205)
Step 1:
[0655] Into a 100-mL round-bottom flask, was placed a solution of
6-([[4-(dimethoxymethyl)pyridin-3-yl]oxy]methyl)pyridine-3-carbonitrile
(1 g, 3.51 mmol, 1.00 equiv) in water (30 mL). Sodium hydroxide
(1.4 g, 35.00 mmol, 10.00 equiv) was added to the reaction. The
resulting solution was stirred for 4 h at 90.degree. C. The pH
value of the solution was adjusted to 4-5 with hydrogen chloride
(aq. 3 mol/L). The resulting solution was extracted with
3.times.200 ml of ethyl acetate. The aqueous layer was extracted
again with 3.times.200 ml of tetrahydrofuran. The combined organic
layers were concentrated under vacuum. This resulted in 1 g (94%)
of
6-([[4-(dimethoxymethyl)pyridin-3-yl]oxy]methyl)pyridine-3-carboxylic
acid as a yellow solid.
Step 2:
##STR00380##
[0657] Into an 8-mL vial, was placed a solution of
6-([[4-(dimethoxymethyl)pyridin-3-yl]oxy]methyl)pyridine-3-carboxylic
acid (100 mg, 0.33 mmol, 1.00 equiv) in a solvent mixture of
dichloromethane (2 mL) and trifluoroacetic acid (1 mL). The
resulting solution was stirred for 3 h at 40.degree. C., and then
it was concentrated under vacuum. The crude product (70 mg) was
purified by Prep-HPLC with the following conditions
(Prep-HPLC-010): Column, SunFire Prep C18 OBD Column, 5 um, 19*150
mm; mobile phase, water (0.05% HCl) and MeCN (10.0% MeCN up to
40.0% in 3 min, up to 100.0% in 2 min, down to 10.0% in 1 min);
Detector, Waters 2545 UvDector 254&220 nm. This resulted in 30
mg (31%) of
6-[[(4-formylpyridin-3-yl)oxy]methyl]pyridine-3-carboxylic acid
hydrochloride as a white solid. The compound exhibited a melting
point of 192-194.degree. C. LC-MS-PH-GBT-ZL-HS-14-0: (ES, m/z):259
[M+1]+/277 [M+1+18].sup.+. H-NMR-PH-GBT-ZL-HS-14-0: (300 MHz, DMSO,
ppm): 13.42 (s, 1H), 10.48 (s, 1H), 9.03 (s, 1H), 8.74 (s, 1H),
8.40 (d, J=4.8 Hz, 1H), 8.30 (dd, J=8.1 Hz, 1H), 7.80 (d, J=8.7 Hz,
1H), 7.57 (d, J=4.8 Hz, 1H), 5.55 (s, 2H).
Example 93
Preparation of 2,2,2-trifluoroacetic acid
6-(((4-formylpyridin-3-yl)oxy)methyl)-N-(methylsulfonyl)nicotinamide
(2:1) (Compound 206)
Step 1:
##STR00381##
[0659] Into a 100-mL round-bottom flask, was placed a solution of
6-([[4-(dimethoxymethyl)pyridin-3-yl]oxy]methyl)pyridine-3-carbonitrile
(1 g, 3.51 mmol, 1.00 equiv) and sodium hydroxide (1.4 g, 35.00
mmol, 10.00 equiv) in water (30 mL). The resulting solution was
stirred for 4 h at 90.degree. C. The pH value of the solution was
adjusted to 4-5 with hydrogen chloride (3 mol/L). The resulting
solution was extracted with 3.times.200 mL of ethyl acetate and
3.times.200 ml of tetrahydrofuran. The combined organic layers were
concentrated under vacuum. This resulted in 1 g (94%) of
6-([[4-(dimethoxymethyl)pyridin-3-yl]oxy]methyl)pyridine-3-carboxylic
acid as a yellow solid.
Step 2.
##STR00382##
[0661] Into a 100-mL round-bottom flask, was placed a solution of
6-([[4-(dimethoxymethyl)pyridin-3-yl]oxy]methyl)pyridine-3-carboxylic
acid (200 mg, 0.66 mmol, 1.00 equiv) in dichloromethane (30 mL).
EDCI (190 mg, 0.99 mmol, 1.50 equiv), 4-dimethylaminopyridine (120
mg, 0.98 mmol, 1.50 equiv), and methanesulfonamide (80 mg, 0.84
mmol, 1.20 equiv) were added to the reaction mixture. The resulting
solution was stirred for 3 h at room temperature. The resulting
mixture was concentrated under vacuum. The residue was applied onto
a silica gel column with MeOH:DCM (1:10) as eluent. This resulted
in 200 mg (80%) of
6-([[4-(dimethoxymethyl)pyridin-3-yl]oxy]methyl)-N-methanesulfonylpyridin-
e-3-carboxamide as a yellow solid.
Step 3:
##STR00383##
[0663] Into a 50-mL round-bottom flask, which was purged and
maintained with an inert atmosphere of nitrogen, was placed a
solution of
6-([[4-(dimethoxymethyl)pyridin-3-yl]oxy]methyl)-N-methanesulfonylpyridin-
e-3-carboxamide (80 mg, 0.21 mmol, 1.00 equiv) in dichloromethane
(5 mL), and trifluoroacetic acid (2 mL). The resulting solution was
stirred for 3 h at 40.degree. C. in an oil bath, and then it was
concentrated under vacuum. The crude product (60 mg) was purified
by Flash-Prep-HPLC with the following conditions (CombiFlash-1):
Column, C18 silica gel; mobile phase, CH.sub.3CN/H.sub.2O=1/99
increasing to CH.sub.3CN/H.sub.2O=40/60 within 20 min; Detector, UV
254 nm. This resulted in 20 mg (17%) of
6-[[(4-formylpyridin-3-yl)oxy]methyl]-N-methanesulfonylpyridine-3-carboxa-
mide; bis(trifluoroacetic acid) as a white solid. The compound
exhibited a melting point of 102-104.degree. C. LC-MS: (ES,
m/z):336 [M+1]+/354 [M+1+18].sup.+. H-NMR (300 MHz, DMSO, ppm):
10.53 (s, 1H), 9.07 (s, 1H), 8.78 (s, 1H), 8.43 (d, J=4.5 Hz, 1H),
8.36 (dd, J=8.1 Hz, 1H), 7.84 (d, J=8.4 Hz, 1H), 7.62 (d, J=4.5 Hz,
1H), 5.60 (s, 2H), 3.37 (s, 3H).
Example 94
Preparation of Substituted Isonicotinaldehydes
[0664] Compounds 207-217 were prepared according to the methods
described above.
[0665]
2-(2-methoxyethoxy)-5-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl-
)pyridin-3-yl)methoxy)isonicotinaldehyde (Compound 207). .sup.1H
NMR (400 MHz, CDCl.sub.3) .delta. 10.32 (s, 1H), 8.67 (dd, J=4.8,
1.6 Hz, 1H), 7.97 (dd, J=7.9, 1.5 Hz, 1H), 7.87 (s, 1H), 7.59 (d,
J=1.9 Hz, 1H), 7.38 (dd, J=7.9, 4.8 Hz, 1H), 7.11 (s, 1H), 6.47 (d,
J=1.9 Hz, 1H), 5.17 (q, J=8.6 Hz, 2H), 5.10 (s, 2H), 4.39-4.32 (m,
2H), 3.70-3.63 (m, 2H), 3.37 (s, 3H).
[0666]
2-methoxy-5-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyridin--
3-yl)methoxy)isonicotinaldehyde (Compound 208). .sup.1H NMR (400
MHz, CDCl.sub.3) .delta. 10.41 (s, 1H), 8.77 (dd, J=4.7, 1.6 Hz,
1H), 8.06 (dd, J=7.9, 1.6 Hz, 1H), 7.97 (s, 1H), 7.61 (d, J=1.9 Hz,
1H), 7.46 (dd, J=7.9, 4.8 Hz, 1H), 7.13 (s, 1H), 6.46 (d, J=1.9 Hz,
1H), 5.21 (s, 2H), 4.61-4.49 (m, 2H), 3.93 (s, 3H), 2.95-2.79 (m,
2H).
[0667]
2-(2-methoxyethoxy)-5-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-y-
l)pyridin-3-yl)methoxy)isonicotinaldehyde (Compound 209). .sup.1H
NMR (400 MHz, CDCl.sub.3) .delta. 10.40 (s, 1H), 8.76 (dd, J=4.7,
1.6 Hz, 1H), 8.06 (dd, J=7.9, 1.6 Hz, 1H), 7.93 (s, 1H), 7.61 (d,
J=1.9 Hz, 1H), 7.45 (dd, J=7.9, 4.8 Hz, 1H), 7.19 (s, 1H), 6.45 (d,
J=1.9 Hz, 1H), 5.20 (s, 2H), 4.63-4.48 (m, 2H), 4.48-4.36 (m, 2H),
3.75 (dd, J=5.4, 3.9 Hz, 2H), 3.45 (s, 3H), 3.01-2.69 (m, 2H).
[0668]
2-methyl-5-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl)pyridin-3--
yl)methoxy)isonicotinaldehyde (Compound 210). .sup.1H NMR (400 MHz,
CDCl.sub.3) .delta. 10.23 (s, 1H), 8.64 (dd, J=4.7, 1.6 Hz, 1H),
8.16 (dd, J=7.9, 1.5 Hz, 1H), 7.61 (d, J=1.9 Hz, 1H), 7.38 (dd,
J=7.9, 4.8 Hz, 1H), 7.21 (d, J=8.6 Hz, 1H), 7.10 (d, J=8.6 Hz, 1H),
6.47 (d, J=1.9 Hz, 1H), 5.19 (q, J=8.6 Hz, 2H), 5.12 (d, J=6.1 Hz,
2H), 2.51 (s, 3H).
[0669]
2-methyl-5-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyridin-3-
-yl)methoxy)isonicotinaldehyde (Compound 211). .sup.1H NMR (400
MHz, CDCl.sub.3) .delta. 10.31 (s, 1H), 8.75 (dd, J=4.7, 1.7 Hz,
1H), 8.27 (dd, J=7.9, 1.6 Hz, 1H), 7.62 (d, J=1.9 Hz, 1H), 7.49
(dd, J=7.9, 4.8 Hz, 1H), 7.33 (d, J=8.6 Hz, 1H), 7.24 (d, J=8.6 Hz,
1H), 6.46 (d, J=1.9 Hz, 1H), 5.18 (s, 2H), 4.61-4.44 (m, 2H),
2.96-2.75 (m, 2H), 2.62 (s, 3H).
[0670]
3-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl)pyridin-3-yl)methox-
y)isonicotinaldehyde (Compound 212). .sup.1H NMR (400 MHz,
CDCl.sub.3) .delta. 10.26 (s, 1H), 8.65 (dd, J=4.7, 1.5 Hz, 1H),
8.38 (dd, J=4.4, 1.0 Hz, 1H), 8.19 (dd, J=7.9, 1.0 Hz, 1H), 7.61
(d, J=1.9 Hz, 1H), 7.43-7.33 (m, 2H), 7.21 (d, J=8.6 Hz, 1H), 6.48
(d, J=1.9 Hz, 1H), 5.19 (q, J=8.6 Hz, 2H), 5.15 (s, 2H).
[0671]
3-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyridin-3-yl)metho-
xy)isonicotinaldehyde (Compound 213). .sup.1H NMR (400 MHz,
CDCl.sub.3) .delta. 10.24 (s, 1H), 8.66 (dd, J=4.7, 1.6 Hz, 1H),
8.39 (dd, J=4.5, 1.1 Hz, 1H), 8.21 (dd, J=7.9, 1.6 Hz, 1H), 7.53
(d, J=1.9 Hz, 1H), 7.44-7.37 (m, 2H), 7.26 (d, J=8.5 Hz, 1H), 6.37
(d, J=1.9 Hz, 1H), 5.13 (s, 2H), 4.49-4.40 (m, 2H), 2.87-2.64 (m,
2H).
[0672]
3-chloro-5-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)is-
onicotinaldehyde (Compound 2H). .sup.1H NMR (400 MHz, CDCl.sub.3)
.delta. 10.51 (s, 1H), 8.77 (dd, J=4.7, 1.6 Hz, 1H), 8.41 (s, 1H),
8.28 (s, 1H), 8.13 (dd, J=7.9, 1.5 Hz, 1H), 7.63 (d, J=1.8 Hz, 1H),
7.47 (dd, J=7.9, 4.8 Hz, 1H), 6.37 (d, J=1.8 Hz, 1H), 5.23 (s, 2H),
4.66 (sep, J=6.6 Hz, 1H), 1.49 (d, J=6.6 Hz, 6H).
[0673]
3-((2-(1-isopropyl-1H-pyrazol-5-yl)pyridin-3-yl)methoxy)-5-methylis-
onicotinaldehyde (Compound 215). .sup.1H NMR (400 MHz, CDCl.sub.3)
.delta. 10.58 (s, 1H), 8.69 (dd, J=4.7, 1.5 Hz, 1H), 8.18 (d, J=3.7
Hz, 2H), 7.92 (dd, J=7.9, 1.2 Hz, 1H), 7.53 (d, J=1.8 Hz, 1H), 7.36
(dd, J=7.9, 4.8 Hz, 1H), 7.19 (s, 1H), 6.29 (d, J=1.8 Hz, 1H), 5.14
(s, 2H), 4.59 (sep, J=6.6 Hz, 1H), 1.41 (d, J=6.6 Hz, 6H).
[0674]
3-chloro-5-((2-(1-(3,3,3-trifluoropropyl)-1H-pyrazol-5-yl)pyridin-3-
-yl)methoxy)isonicotinaldehyde (Compound 216). .sup.1H NMR (400
MHz, CDCl.sub.3) .delta. 10.43 (s, 1H), 8.67 (dd, J=4.7, 1.5 Hz,
1H), 8.35 (s, 1H), 8.26 (s, 1H), 8.06 (dd, J=7.9, 1.3 Hz, 1H), 7.61
(d, J=1.9 Hz, 1H), 7.40 (dd, J=7.9, 4.8 Hz, 1H), 6.47 (d, J=1.9 Hz,
1H), 5.21-5.10 (m, 4H).
[0675]
3-methyl-5-((2-(1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl)pyridin-3--
yl)methoxy)isonicotinaldehyde (Compound 217). .sup.1H NMR (400 MHz,
CDCl.sub.3) .delta. 10.68 (s, 1H), 8.77 (dd, J=4.7, 1.3 Hz, 1H),
8.35 (s, 1H), 8.30 (s, 1H), 8.04 (d, J=7.9 Hz, 1H), 7.69 (d, J=1.9
Hz, 1H), 7.47 (dd, J=7.9, 4.8 Hz, 1H), 6.55 (d, J=1.9 Hz, 1H),
5.34-5.22 (m, 4H), 2.57 (s, 3H).
In Vitro Testing
Example 95
Modulation of Hemoglobin Oxygen Affinity by Heteroaryl Aldehydes
Assay Procedure
[0676] Oxygen equilibrium curves (OEC) in purified Hemoglobin S
(HbS) were measured by the change in p50, the partial pressure of
oxygen at which the heme binding sites in the HbS sample are 50%
saturated with oxygen. HbS was purified by a modified procedure
(Antonini and Brunori, 1971; Heomoglobin and Myoglobin in their
Reactions with Ligands; North Holland Publishing Company;
Amsterdam, London) from blood obtained from homozygous sickle cell
patients though the Hemoglobinopathy Center at Children's Hospital
Oakland Research Institute (CHORI) with Institutional Review Board
approval. Oxygen equilibrium curves were carried out with a HEMOX
analyzer, (TCS Scientific, New Hope, Pa.). Five hundred .mu.L of
250 .mu.M purified HbS were diluted into 4.5 mL of HEMOX buffer (30
mM TES, 130 mM NaCl, 5 mM KCl, pH=7.4) resulting in a final
hemoglobin concentration of 25 .mu.M. The compounds were added at
the final desired concentrations. The mixture was incubated for 45
min at 37.degree. C. and then transferred to the Hemox sample
chamber. The samples were saturated with oxygen by flushing with
compressed air for 10 minutes. The samples were then flushed with
pure nitrogen and the absorbance of deoxy-Hb was recorded as a
function of the solution pO.sub.2. The oxygen equilibrium data was
then fit to the Hill Model to obtain values for p50. The
deoxygenation curves for both HbS alone (control) and HbS in the
presence of compound were collected with the TCS software. The p50
for purified Hbs was typically 13.8.+-.1.6. Delta p50 values were
obtained from the p50 value for control minus the p50 value for HbS
treated with compound divided by the p50 value for the control. A
positive delta p50 value corresponds to a left shifted curve and a
lower p50 value relative to control, indicating that the compound
acts to modulate HbS to increase its affinity for oxygen.
Example 96
Modulation of Hemoglobin Oxygen Affinity by Heteroaryl
Aldehydes--Assay Results
[0677] The compounds of Table 1 that were where tested in the assay
above were all found to have positive delta p50 values. Delta p50%
is calculated from [[p50(HbS)-p50(HbS treated with
compound)]/p50(HbS)].times.100. Table 2 below lists the delta p50%
values where + indicates a delta p50% of between 0 and 29, ++
indicates a delta p50% of between 30 and 50, and +++ indicates a
delta p50% of 50 or greater. Unless noted otherwise, the compounds
in Table 2 were tested at 30 .mu.M.
TABLE-US-00002 TABLE 2 delta p50 % Compound delta p50 1 + 2 ++ (100
.mu.M) 3 + 4 + 5 ++ 6 + 7 + 12 + (100 .mu.M) 38 + 39 + 40 + (100
.mu.M) 41 + 42 + 43 ++ 44 +++ 45 +++ 46 ++ 47 + 48 ++ (100 .mu.M)
49 ++ 50 + 51 + 52 + (100 .mu.M) 53 ++ 54 ++ (100 .mu.M) 55 + (100
.mu.M) 56 + (100 .mu.M) 57 ++ (100 .mu.M) 58 ++ 59 + 61 + 62 + 63
+++ 64 + 65 ++ 66 ++ 68 + 69 + 70 + 71 + 72 + 73 + 74 ++ 75 + 76 +
77 + 78 + 79 ++ 80 ++ 81 + 82 + 83 + 84 ++ 85 + 86 ++ 87 + 88 + 89
+ 90 + 91 ++ 92 ++ 93 ++ 94 + 95 + 96 + 97 + 98 + 99 + 100 + 101 +
102 + 103 ++ 104 + 105 + 106 ++ 107 + 108 ++ 109 + 110 + 111 + 112
+ 113 + 114 + 115 + 116 + 117 + 118 + 119 ++ 120 ++ 121 + 122 + 123
+ 124 + 125 + 126 + 127 + 128 + 129 ++ 130 ++ 131 ++ 132 +++ 133 ++
134 ++ 135 + 136 + 137 + 138 + 139 + 140 ++ 141 + 142 + 143 ++ 149
+++ 150 +++ 158 ++ 159 +++ 160 +++ 161 ++ 162 +++ 163 +++ 164 ++
165 ++ 169 ++ 172 ++ 173 +++ 174 +++ 175 +++ 176 +++ 177 +++ 178 ++
179 ++ 180 +++ 181 +++ 183 +++ 184 ++ 186 +++ 187 ++ 188 +++ 189 ++
190 +++ 191 +++ 193 ++ 194 ++ 195 +++ 196 +++ 197 ++ 198 +++ 199
+++ 200 ++ 201 ++ 202 +++ 203 +++
Example 97
Polymerization Assay
[0678] Polymerization assays are carried out in vitro using
purified HBS exchanged into 1.8 M potassium phosphate buffer at pH
7.4. Using a slightly modified protocol (Antonini and Brunori,
1971), HbS is purified by the CRO VIRUSYS, from blood obtained from
homozygous sickle cell patients through the Hemoglobinopathy Center
at Children's Hospital Oakland Research Institute (CHORI) with
Institutional Review Board approval. Compounds are prepared in 100%
DMSO and a desired amount is added to 50 .mu.M of purified HBS at a
final DMSO concentration of 0.3%. Final potassium phosphate
concentration is adjusted to 1.8 M using a combination of 2.5 M
potassium phosphate stock solution and water at pH 7.4. The
reaction mixture is incubated for an hour at 37.degree. C. and then
transferred into a 24-well plate for deoxygenation in a glove box
containing 99.5% nitrogen and 0.5% oxygen. The 24-well plate is not
covered and incubated at 4.degree. C. on a plate cooler inside the
glove box for one and a half hours. Fifty .mu.L of the reaction
mixture is transferred into a 96-well plate and the absorbance at
700 nm is measured every minute for one hour at 37.degree. C. in a
plate reader located inside the glove box. A plot of the absorbance
against time is fitted using a Boltzman sigmoidal fit and the delay
time (from zero to time at half Vmax) is measured. To compare and
rank compounds, delay times are expressed as percent delay (% DT),
which is defined as the difference in delay times for HBS/compound
and HBS alone multiplied by 100 and divided by the delay time for
HBS alone.
[0679] Compounds listed below have been tested in the
polymerization assay. Activity ranges are defined by the number of
dagger (.dagger.) symbols indicated. .dagger. denotes
activity.gtoreq.40% but .ltoreq.80%; .dagger..dagger. denotes
activity>80% but .ltoreq.120%; .dagger..dagger..dagger. denotes
activity>120% but .ltoreq.140%; .dagger..dagger..dagger..dagger.
denotes activity>160%.
TABLE-US-00003 TABLE 3 % delta Delay Compound % delta Delay 5
.dagger. 108 130 .dagger. 132 91 149 .dagger. 150
.dagger..dagger..dagger. 158 .dagger. 179 159 .dagger..dagger. 160
.dagger..dagger. 161 162 .dagger..dagger. 173 .dagger. 174
.dagger..dagger. 195 .dagger..dagger..dagger. 197 .dagger. 198
.dagger. 175 .dagger..dagger. 162 .dagger..dagger. 203
.dagger..dagger. 163 .dagger..dagger. 181 .dagger..dagger..dagger.
206 .dagger..dagger..dagger. 178 .dagger. 180 .dagger. 199
.dagger..dagger..dagger. 176 .dagger. 177 .dagger. 202
.dagger..dagger..dagger. 187 .dagger..dagger. 164
.dagger..dagger..dagger. 165 .dagger..dagger..dagger. 169
.dagger..dagger..dagger. 186 .dagger..dagger..dagger..dagger. 188
.dagger..dagger..dagger. 189 .dagger..dagger..dagger. 190
.dagger..dagger..dagger.
Example 98
R/T Assay
[0680] A relaxed-to-tense transition assay ("R/T assay") was used
to determine the ability of substituted benzaldehyde compounds to
maintain the high-oxygen affinity relaxed (R) state of hemoglobin
under deoxygenated conditions. This ability can be expressed as a
"delta R" value (i.e., the change in the time-period of the R state
after hemoglobin is treated with a compound, as compared to the
period without treatment with the compound). Delta R is the % R to
remaining after the compounds treatment compared with no treatment
(e.g. if R % without treatment is 8% while with treatment with a
target compound is 48% R at 30 .mu.M, then % R is 40% for that
compound.
[0681] A mixture of HbS/A was purified from blood obtained from
homozygous sickle cell patients though the Hemoglobinopathy Center
at Children's Hospital Oakland Research Institute (CHORI) with
Institutional Review Board approval. HbS/A (at a final
concentration of 3 .mu.M) was incubated for 1 hr at 37.degree. C.
in presence or absence of compounds in 50 .mu.M potassium phosphate
buffer, pH=7.4 and 30 .mu.M 2, 3 diphosphoglycerate (DPG) in 96
well plates in a final volume of 160 .mu.l. Compounds were added at
different concentrations (3 .mu.M to 100 .mu.M final
concentrations). Plates were covered with a Mylar film. After
incubation was completed the Mylar cover was removed and the plates
were placed in a Spectrostar Nano plate reader previously heated at
37.degree. C. Five minutes later, N.sub.2 (flow rate=20 L/min) was
flowed through the spectrophotometer. Spectroscopic measurements
(300 nm to 700 nm) were taken every 5 min for 2 hours. Data
analysis was performed by using linear regression from the data
retrieved for all wavelengths.
[0682] Table 4 below lists the delta R values where + indicates a
delta R of between 0 and 30, ++ indicates a delta R of between 30
and 50, and +++ indicates a delta R of 50 or greater. Unless noted
otherwise, the compounds in Table 2 were tested at 30 .mu.M.
TABLE-US-00004 TABLE 4 delta R Compound delta R 5 ++ 43 + (9 .mu.M)
45 ++ (9 .mu.M) 46 + (9 .mu.M) 53 + (9 .mu.M) 58 + (9 .mu.M) 63 ++
(9 .mu.M) 193 + (9 .mu.M) 65 + (9 .mu.M) 66 ++ (9 .mu.M) 79 ++ (9
.mu.M) 80 +++ (9 .mu.M) .sup. 84 ++ (9 .mu.M) 86 + (9 .mu.M) 91 +++
(9 .mu.M) .sup. 92 + (9 .mu.M) 93 + (9 .mu.M) 103 ++ (9 .mu.M) 108
+++ (9 .mu.M) .sup. 119 ++ (9 .mu.M) 120 ++ (9 .mu.M) 129 ++ (9
.mu.M) 130 + (9 .mu.M) 131 + (9 .mu.M) 132 ++ 133 ++ (9 .mu.M) 134
+ (9 .mu.M) 140 + (9 .mu.M) 143 + (9 .mu.M) 149 + (9 .mu.M) 150 +++
194 + (9 .mu.M) 158 + (9 .mu.M) 179 + (9 .mu.M) 159 ++ 160 + 161 +
(9 .mu.M) .sup. 172) + (9 .mu.M) 191 + (9 .mu.M) 173 +++ 195 +++
174 ++ 196 ++ 197 + (9 .mu.M) 198 ++ 175 ++ 162 +++ 203 + (9 .mu.M)
163 ++ 181 + (9 .mu.M) 206 + (9 .mu.M) 178 + (9 .mu.M) 180 ++ 199 +
(9 .mu.M) 176 + (9 .mu.M) 177 + (3 .mu.M) 183 ++ 184 ++ 200 + (9
.mu.M) 201 + (9 .mu.M) 202 + (9 .mu.M) 187 +++ (9 .mu.M) .sup. 164
++ (9 .mu.M) 165 + (9 .mu.M) 169 ++ (9 .mu.M) 186 +++
Example 99
Whole Blood Assay
[0683] Oxygen Equilibrium Curves (OEC) of whole blood before and
after treatment with different concentrations of substituted
benzaldehyde compounds were performed as follows using a HEMOX
analyzer (TCS Scientific, New Hope, Pa.). Blood samples from
homozygous sickle cell patients were obtained though the
Hemoglobinopathy Center at Children's Hospital Oakland Research
Institute (CHORI) with Institutional Review Board approval. The
hematocrit was adjusted to 20% using autologous plasma and the
blood samples were incubated for 1 hour at 37.degree. C. in absence
or presence of compounds. 100 .mu.l of these samples were added to
5 mL of Hemox buffer (30 mM TES, 130 mM NaCl, 5 mM KCl, pH=7.4) at
37.degree. C. and then transferred to the Hemox sample chamber. The
samples were saturated with oxygen by flushing with compressed air
for 10 minutes. The samples were then flushed with pure nitrogen
and the respective absorbances of oxy- and deoxy-Hb are recorded as
a function of the solution pO2. The oxygen equilibrium data were
then fitted to the Hill Model to obtain values for p50. The
deoxygenation curves for both whole blood alone (control) and whole
blood in the presence of the compound were collected with the TCS
software.
[0684] Table 5 below lists the delta p50% values where + indicates
a delta p50% of between 0 and 29, ++ indicates a delta p50% of
between 30 and 50, and +++ indicates a delta p50% of 50 or greater.
Unless noted otherwise, the compounds in Table 2 were tested at
1000 .mu.M. A positive delta p50 value corresponds to a left
shifted curve and a lower p50 value relative to control, indicating
that the compound acts to modulate HbS to increase its affinity for
oxygen.
TABLE-US-00005 TABLE 5 delta p50 % Values for Whole Blood Assay
Compound delta p50 % 5 + 44 + 58 + 65 + 74 ++ 79 + 80 + 92 + 93 +
103 + 106 + 108 + 120 + 129 ++ 130 ++ 131 + 132 ++ 133 + 140 + 143
+ 149 +++ 150 +++ 194 + 158 + 179 ++ 159 +++ 160 +++ 191 +++ 173
+++ 174 +++ 195 +++ 196 ++ 197 +++ 198 +++ 175 +++ 162 +++ 209 +
163 +++ 181 +++ 206 +++ 178 ++ 180 +++ 199 + 176 +++ 177 +++ 183
+++ 184 +++ 200 +++ 201 + 202 + 187 + 164 ++ 165 + 169 ++ 186 +++
188 +++ 189 +++ 190 +++
[0685] All patents, patent applications, publications and
presentations referred to herein are incorporated by reference in
their entirety. Any conflict between any reference cited herein and
the teaching of this specification is to be resolved in favor of
the latter. Similarly, any conflict between an art-recognized
definition of a word or phrase and a definition of the word or
phrase as provided in this specification is to be resolved in favor
of the latter.
* * * * *