U.S. patent application number 15/590846 was filed with the patent office on 2017-11-30 for antiviral compounds.
The applicant listed for this patent is Gilead Phamasset LLC. Invention is credited to Elizabeth M. Bacon, Jeromy J. Cottell, John O. Link, Teresa Alejandra Trejo Martin.
Application Number | 20170342085 15/590846 |
Document ID | / |
Family ID | 49581469 |
Filed Date | 2017-11-30 |
United States Patent
Application |
20170342085 |
Kind Code |
A1 |
Bacon; Elizabeth M. ; et
al. |
November 30, 2017 |
ANTIVIRAL COMPOUNDS
Abstract
The disclosure is related to anti-viral compounds, compositions
containing such compounds, and therapeutic methods that include the
administration of such compounds, as well as to processes and
intermediates useful for preparing such compounds.
Inventors: |
Bacon; Elizabeth M.;
(Burlingame, CA) ; Cottell; Jeromy J.; (Redwood
City, CA) ; Link; John O.; (San Francisco, CA)
; Trejo Martin; Teresa Alejandra; (Belmont, CA) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Gilead Phamasset LLC |
Foster City |
CA |
US |
|
|
Family ID: |
49581469 |
Appl. No.: |
15/590846 |
Filed: |
May 9, 2017 |
Related U.S. Patent Documents
|
|
|
|
|
|
Application
Number |
Filing Date |
Patent Number |
|
|
14925203 |
Oct 28, 2015 |
9682989 |
|
|
15590846 |
|
|
|
|
14316573 |
Jun 26, 2014 |
|
|
|
14925203 |
|
|
|
|
13831116 |
Mar 14, 2013 |
|
|
|
14316573 |
|
|
|
|
61647966 |
May 16, 2012 |
|
|
|
Current U.S.
Class: |
1/1 |
Current CPC
Class: |
A61P 43/00 20180101;
A61K 45/06 20130101; A61K 31/7056 20130101; A61P 1/16 20180101;
C07D 491/04 20130101; A61K 31/7068 20130101; A61K 38/21 20130101;
C07D 491/052 20130101; A61P 31/14 20180101; A61P 31/00 20180101;
A61P 31/12 20180101; A61K 31/7072 20130101; A61K 31/4188 20130101;
A61K 31/7056 20130101; A61K 2300/00 20130101; A61K 38/21 20130101;
A61K 2300/00 20130101; A61K 31/7072 20130101; A61K 2300/00
20130101; A61K 31/7068 20130101; A61K 2300/00 20130101 |
International
Class: |
C07D 491/052 20060101
C07D491/052; A61K 45/06 20060101 A61K045/06; A61K 31/7072 20060101
A61K031/7072; A61K 31/4188 20060101 A61K031/4188; A61K 31/7068
20060101 A61K031/7068; A61K 31/7056 20060101 A61K031/7056; C07D
491/04 20060101 C07D491/04; A61K 38/21 20060101 A61K038/21 |
Claims
1-33. (canceled)
34. A compound selected from: ##STR00331## ##STR00332##
##STR00333## ##STR00334## ##STR00335## ##STR00336## ##STR00337##
##STR00338## ##STR00339## ##STR00340## ##STR00341## ##STR00342##
##STR00343## ##STR00344## ##STR00345## ##STR00346## ##STR00347##
##STR00348## or a pharmaceutically acceptable salt thereof.
35. A pharmaceutical composition comprising the compound of claim
34, or a pharmaceutically acceptable salt thereof, and a
pharmaceutically acceptable diluent or carrier, or combination
thereof.
36. The pharmaceutical composition of claim 35, formulated for oral
administration.
37. The pharmaceutical composition of claim 35, formulated in
tablet form.
38. A compound selected from: ##STR00349## ##STR00350##
##STR00351## ##STR00352## ##STR00353## ##STR00354## ##STR00355##
##STR00356## ##STR00357## ##STR00358## ##STR00359## ##STR00360##
##STR00361## ##STR00362## ##STR00363## ##STR00364## ##STR00365##
##STR00366##
39. A pharmaceutical composition comprising the compound of claim
38 and a pharmaceutically acceptable diluent or carrier, or
combination thereof.
40. The pharmaceutical composition of claim 39, formulated for oral
administration.
41. The pharmaceutical composition of claim 39, formulated in
tablet form.
Description
CROSS REFERENCE TO RELATED APPLICATIONS
[0001] This application is a Continuation of application Ser. No.
14/925,203, filed on Oct. 28, 2015, which is now U.S. Pat. No.
9,682,989, which is a Continuation of application Ser. No.
14/316,573, filed on Jun. 26, 2014, which is a Continuation of
application Ser. No. 13/831,116, filed on Mar. 14, 2013, which
claims priority to U.S. Provisional Application No. 61/647,966,
filed on May 16, 2012, the entirety of these applications are
incorporated herein by reference.
BACKGROUND
[0002] Hepatitis C is recognized as a chronic viral disease of the
liver which is characterized by liver disease. Although drugs
targeting the liver are in wide use and have shown effectiveness,
toxicity and other side effects have limited their usefulness.
Inhibitors of hepatitis C virus (HCV) are useful to limit the
establishment and progression of infection by HCV as well as in
diagnostic assays for HCV.
[0003] There is a need for new HCV therapeutic agents. In
particular, there is a need for HCV therapeutic agents that have
broad activity against HCV genotypes (e.g. genotypes 1a, 1b, 2a,
3a, 4a). There is also a particular need for agents that are less
susceptible to viral resistance. Resistance mutations to inhibitors
have been described for HCV NS5A for genotypes 1a and 1b in
Antimicrobial Agents and Chemotherapy, September 2010, Volume 54,
p. 3641-3650.
SUMMARY
[0004] In one embodiment the disclosure provides a compound of
formula (I):
E.sup.1a-V.sup.1a--C(.dbd.O)--P.sup.1a--W.sup.1a--P.sup.1b--C(.dbd.O)--V-
.sup.1b-E.sup.1b (I)
[0005] wherein: [0006] W.sup.1a is
##STR00001##
[0007] and W.sup.1a is optionally substituted with one or more
groups independently selected from halo, alkyl, haloalkyl,
optionally substituted aryl, optionally substituted heterocycle,
and cyano; [0008] Y.sup.5 is --O--CH.sub.2--, --CH.sub.2--O--,
--O--C(.dbd.O)--, or --C(.dbd.O)--O--; X.sup.5 is
--CH.sub.2--CH.sub.2-- or --CH.dbd.CH--; [0009] E.sup.1a is
--N(H)(alkoxycarbonyl), --N(H)(cycloalkylcarbonyl) or
--N(H)(cycloalkyloxycarbonyl); or E.sup.1a-V.sup.1a taken together
are R.sup.9a; [0010] E.sup.1b is --N(H)(alkoxycarbonyl),
--N(H)(cycloalkylcarbonyl) or --N(H)(cycloalkyloxycarbonyl); or
E.sup.1b-V.sup.b taken together are R.sup.9b; [0011] V.sup.1a and
V.sup.1b are each independently elected from
[0011] ##STR00002## ##STR00003## [0012] P.sup.1a is selected
from:
[0012] ##STR00004## ##STR00005## [0013] P.sup.1b is selected
from:
##STR00006## ##STR00007## ##STR00008##
[0014] and [0015] R.sup.9a and R.sup.9b are each independently
selected from:
[0015] ##STR00009## [0016] or a pharmaceutically acceptable salt or
prodrug thereof; [0017] provided that when Y.sup.5 is
--O--CH.sub.2--, or --CH.sub.2--O--, then at least one of the
following occurs: [0018] (1) at least one of V.sup.1a and V.sup.1b
is selected from (af), (ag), (ah), (ai), (aj), (ak), (al), (am),
(an), (ao), (ap) or (aq); or [0019] (2) P.sup.1a is selected from
(be), (bf), (bg), (bh), (bi), (bj), (bk), (bl), (bm), (bn), (bo),
(bq) or (br); or [0020] (3) P.sup.1b is selected from (be), (bf),
(bg), (bh), (bi), (bj), (bk), (bl), (bm), (bn), (bo), (bp), (bq) or
(br).
[0021] The disclosure also provides isotopically enriched compounds
that are compounds of the disclosure that comprise an enriched
isotope at one or more positions in the compound.
[0022] The present disclosure also provides a pharmaceutical
composition comprising a compound of the disclosure or a
pharmaceutically acceptable salt or prodrug thereof and at least
one pharmaceutically acceptable carrier.
[0023] The present disclosure also provides a pharmaceutical
composition for use in treating hepatitis C (HCV). In one
embodiment the composition comprises at least one additional
therapeutic agent for treating HCV. In one embodiment, the
therapeutic agent is selected from ribavirin, an NS3 protease
inhibitor, a nucleoside or nucleotide inhibitor of HCV NS5B
polymerase, an alpha-glucosidase 1 inhibitor, a hepatoprotectant, a
non-nucleoside inhibitor of HCV polymerase, or combinations
thereof. In one embodiment, the composition further comprises a
nucleoside or nucleotide inhibitor of HCV NS5B polymerase. In one
embodiment, the nucleoside or nucleotide inhibitor of HCV NS5B
polymerase is selected from ribavirin, viramidine, levovirin, a
L-nucleoside, or isatoribine.
[0024] In one embodiment, provided is a pharmaceutical composition
comprising a compound as described herein and at least one
nucleoside or nucleotide inhibitor of HCV NS5B polymerase, and at
least one pharmaceutically acceptable carrier. In one embodiment,
the composition further comprises an interferon, a pegylated
interferon, ribavirin or combinations thereof. In one embodiment,
the nucleoside or nucleotide inhibitor of HCV NS5B polymerase is
sofosbuvir. In one embodiment, provided is a pharmaceutical
composition comprising a compound as described herein and at least
one NS3 protease inhibitor, and at least one pharmaceutically
acceptable carrier. In one embodiment, the composition further
comprises sofosbuvir.
[0025] The present disclosure also provides a pharmaceutical
composition further comprising an interferon or pegylated
interferon.
[0026] The present disclosure also provides a pharmaceutical
composition further comprising a nucleoside analog.
[0027] The present disclosure also provides for a pharmaceutical
composition wherein said nucleoside analogue is selected from
ribavirin, viramidine, levovirin, an L-nucleoside, and isatoribine
and said interferon is .alpha.-interferon or pegylated
.alpha.-interferon.
[0028] The present disclosure also provides for a method of
treating hepatitis C, said method comprising administering to a
human patient a pharmaceutical composition which comprises a
therapeutically effective amount of a compound of the
disclosure.
[0029] The present disclosure also provides a method of inhibiting
HCV, comprising administering to a mammal afflicted with a
condition associated with HCV activity, an amount of a compound of
the disclosure, effective to inhibit HCV.
[0030] The present disclosure also provides a compound of the
disclosure for use in medical therapy (e.g. for use in inhibiting
HCV activity or treating a condition associated with HCV activity),
as well as the use of a compound of the disclosure for the
manufacture of a medicament useful for inhibiting HCV or the
treatment of a condition associated with HCV activity in a
mammal.
[0031] The present disclosure also provides synthetic processes and
novel intermediates disclosed herein which are useful for preparing
compounds of the disclosure. Some of the compounds of the
disclosure are useful to prepare other compounds of the
disclosure.
[0032] In another aspect the disclosure provides a compound of the
disclosure, or a pharmaceutically acceptable salt or prodrug
thereof, for use in the prophylactic or therapeutic treatment of
hepatitis C or a hepatitis C associated disorder.
[0033] In another aspect the disclosure provides a method of
inhibiting HCV activity in a sample comprising treating the sample
with a compound of the disclosure.
[0034] Compounds of formula (I) have been found to possess useful
activity against several HCV genotypes. Additionally certain
compounds of formula (I) exhibit significant potency against
resistant variants in, e.g., GT1.
DETAILED DESCRIPTION
[0035] Reference will now be made in detail to certain embodiments
of the disclosure, examples of which are illustrated in the
accompanying structures and formulas. While the disclosure will be
described in conjunction with the enumerated embodiments, it will
be understood that they are not intended to limit the disclosure to
those embodiments. On the contrary, the disclosure is intended to
cover all alternatives, modifications, and equivalents, which may
be included within the scope of the present disclosure as defined
by the embodiments.
Compounds
[0036] The "P" groups (eg P.sup.1a and P.sup.1b) defined for
formula (I) herein have one bond to a --C(.dbd.O)-- of formula (I)
and one bond to a W.sup.1a group. It is to be understood that a
nitrogen of the P group is connected to the --C(.dbd.O)-- group of
formula (I) and that a carbon of the P group is connected to the
W.sup.1a group.
##STR00010##
[0037] In the W.sup.1a group a Y.sup.5 group is present. When that
Y.sup.5 group is defined as --O--CH.sub.2--, or --CH.sub.2--O--
group, those Y.sup.5 groups have a directionality. The Y.sup.5
group is connected to the W.sup.1a group in the same left to right
directionality that each is drawn. So for example, when Y.sup.5 is
--O--CH.sub.2--, the directly following structure is intended:
##STR00011##
[0038] For example, when Y.sup.5 is --CH.sub.2--O--, the directly
following structure is intended:
##STR00012##
[0039] In the structure I, the W.sup.1a group has a left-to-right
directionality as depicted in I and W.sup.1a as they drawn.
E.sup.1a-V.sup.1a--C(.dbd.O)--P.sup.1a--W.sup.1a--P.sup.1b--C(.dbd.O)--V-
.sup.1b-E.sup.1b (I)
[0040] wherein: [0041] W.sup.1a is
##STR00013##
[0042] For example, the P.sup.1a group is connected to the
imidazole group of W.sup.1a, and the P.sup.1b group is connected to
the pentacyclic ring system of W.sup.1a.
[0043] "Alkyl" is C.sub.1-C.sub.18 hydrocarbon containing normal,
secondary, tertiary or cyclic carbon atoms. Examples are methyl
(Me, --CH.sub.3), ethyl (Et, --CH.sub.2CH.sub.3), 1-propyl (n-Pr,
n-propyl, --CH.sub.2CH.sub.2CH.sub.3), 2-propyl (i-Pr, i-propyl,
--CH(CH.sub.3).sub.2), 1-butyl (n-Bu, n-butyl,
--CH.sub.2CH.sub.2CH.sub.2CH.sub.3), 2-methyl-1-propyl (i-Bu,
i-butyl, --CH.sub.2CH(CH.sub.3).sub.2), 2-butyl (s-Bu, s-butyl,
--CH(CH.sub.3)CH.sub.2CH.sub.3), 2-methyl-2-propyl (t-Bu, t-butyl,
--C(CH.sub.3).sub.3), 1-pentyl (n-pentyl,
--CH.sub.2CH.sub.2CH.sub.2CH.sub.2CH.sub.3), 2-pentyl
(--CH(CH.sub.3)CH.sub.2CH.sub.2CH.sub.3), 3-pentyl
(--CH(CH.sub.2CH.sub.3).sub.2), 2-methyl-2-butyl
(--C(CH.sub.3).sub.2CH.sub.2CH.sub.3), 3-methyl-2-butyl
(--CH(CH.sub.3)CH(CH.sub.3).sub.2), 3-methyl-1-butyl
(--CH.sub.2CH.sub.2CH(CH.sub.3).sub.2), 2-methyl-1-butyl
(--CH.sub.2CH(CH.sub.3)CH.sub.2CH.sub.3), 1-hexyl
(--CH.sub.2CH.sub.2CH.sub.2CH.sub.2CH.sub.2CH.sub.3), 2-hexyl
(--CH(CH.sub.3)CH.sub.2CH.sub.2CH.sub.2CH.sub.3), 3-hexyl
(--CH(CH.sub.2CH.sub.3)(CH.sub.2CH.sub.2CH.sub.3)),
2-methyl-2-pentyl (--C(CH.sub.3).sub.2CH.sub.2CH.sub.2CH.sub.3),
3-methyl-2-pentyl (--CH(CH.sub.3)CH(CH.sub.3)CH.sub.2CH.sub.3),
4-methyl-2-pentyl (--CH(CH.sub.3)CH.sub.2CH(CH.sub.3).sub.2),
3-methyl-3-pentyl (--C(CH.sub.3)(CH.sub.2CH.sub.3).sub.2),
2-methyl-3-pentyl (--CH(CH.sub.2CH.sub.3)CH(CH.sub.3).sub.2),
2,3-dimethyl-2-butyl (--C(CH.sub.3).sub.2CH(CH.sub.3).sub.2),
3,3-dimethyl-2-butyl (--CH(CH.sub.3)C(CH.sub.3).sub.3, and
cyclopropylmethyl
##STR00014##
[0044] "Alkenyl" is C.sub.2-C.sub.18 hydrocarbon containing normal,
secondary, tertiary or cyclic carbon atoms with at least one site
of unsaturation, i.e. a carbon-carbon, sp.sup.2 double bond.
Examples include, but are not limited to, ethylene or vinyl
(--CH.dbd.CH.sub.2), allyl (--CH.sub.2CH.dbd.CH.sub.2),
cyclopentenyl (--C.sub.5H.sub.7), and 5-hexenyl
(--CH.sub.2CH.sub.2CH.sub.2CH.sub.2CH.dbd.CH.sub.2).
[0045] "Alkynyl" is C.sub.2-C.sub.18 hydrocarbon containing normal,
secondary, tertiary or cyclic carbon atoms with at least one site
of unsaturation, i.e. a carbon-carbon, sp triple bond. Examples
include, but are not limited to, acetylenic (--C.ident.CH) and
propargyl (--CH.sub.2C.ident.CH).
[0046] "Alkylene" refers to a saturated, branched or straight chain
or cyclic hydrocarbon radical of 1-18 carbon atoms, and having two
monovalent radical centers derived by the removal of two hydrogen
atoms from the same or two different carbon atoms of a parent
alkane. Typical alkylene radicals include, but are not limited to,
methylene (--CH.sub.2--) 1,2-ethyl (--CH.sub.2CH.sub.2--),
1,3-propyl (--CH.sub.2CH.sub.2CH.sub.2--), 1,4-butyl
(--CH.sub.2CH.sub.2CH.sub.2CH.sub.2--), and the like.
[0047] "Alkenylene" refers to an unsaturated, branched or straight
chain or cyclic hydrocarbon radical of 2-18 carbon atoms, and
having two monovalent radical centers derived by the removal of two
hydrogen atoms from the same or two different carbon atoms of a
parent alkene. Typical alkenylene radicals include, but are not
limited to, 1,2-ethylene (--CH.dbd.CH--).
[0048] "Alkynylene" refers to an unsaturated, branched or straight
chain or cyclic hydrocarbon radical of 2-18 carbon atoms, and
having two monovalent radical centers derived by the removal of two
hydrogen atoms from the same or two different carbon atoms of a
parent alkyne. Typical alkynylene radicals include, but are not
limited to, acetylene (--C.ident.C--), propargyl
(--CH.sub.2C.ident.C--), and 4-pentynyl
(--CH.sub.2CH.sub.2CH.sub.2C.dbd.CH).
[0049] The term "alkoxy" or "alkyloxy," as used herein, refers to
an alkyl group attached to the parent molecular moiety through an
oxygen atom.
[0050] The term "alkoxycarbonyl," as used herein, refers to an
alkoxy group attached to the parent molecular moiety through a
carbonyl group.
[0051] The term "cycloalkyl," as used herein, refers to a saturated
monocyclic, hydrocarbon ring system having three to seven carbon
atoms and zero heteroatoms. Representative examples of cycloalkyl
groups include, but are not limited to, cyclopropyl, cyclopentyl,
and cyclohexyl.
[0052] The cycloalkyl groups of the present disclosure are
optionally substituted with one, two, three, four, or five
substituents independently selected from alkoxy, alkyl, aryl,
cyano, halo, haloalkoxy, haloalkyl, heterocyclyl, hydroxy,
hydroxyalkyl, nitro, and --NR.sup.xR.sup.y wherein the aryl and the
heterocyclyl are further optionally substituted with one, two, or
three substituents independently selected from alkoxy, alkyl,
cyano, halo, haloalkoxy, haloalkyl, hydroxy, and nitro.
[0053] The term "cycloalkylcarbonyl," as used herein, refers to a
cycloalkyl group attached to the parent molecular moiety through a
carbonyl group.
[0054] The term "cycloalkyloxy," as used herein, refers to a
cycloalkyl group attached to the parent molecular moiety through an
oxygen atom.
[0055] The term "cycloalkyloxycarbonyl," as used herein, refers to
a cycloalkyloxy group attached to the parent molecular moiety
through a carbonyl group.
[0056] "Aryl" means a monovalent aromatic hydrocarbon radical of
6-20 carbon atoms derived by the removal of one hydrogen atom from
a single carbon atom of a parent aromatic ring system. Typical aryl
groups include, but are not limited to, radicals derived from
benzene, substituted benzene, naphthalene, anthracene, biphenyl,
and the like.
[0057] "Arylalkyl" refers to an acyclic alkyl radical in which one
of the hydrogen atoms bonded to a carbon atom, typically a terminal
or sp.sup.3 carbon atom, is replaced with an aryl radical. Typical
arylalkyl groups include, but are not limited to, benzyl,
2-phenylethan-1-yl, naphthylmethyl, 2-naphthylethan-1-yl,
naphthobenzyl, 2-naphthophenylethan-1-yl and the like. The
arylalkyl group comprises 6 to 20 carbon atoms, e.g., the alkyl
moiety, including alkanyl, alkenyl or alkynyl groups, of the
arylalkyl group is 1 to 6 carbon atoms and the aryl moiety is 5 to
14 carbon atoms.
[0058] "Substituted alkyl", "substituted aryl", and "substituted
arylalkyl" mean alkyl, aryl, and arylalkyl respectively, in which
one or more hydrogen atoms are each independently replaced with a
non-hydrogen substituent. Typical substituents include, but are not
limited to: halo (e.g. F, Cl, Br, I), --R, --OR, --SR, --NR.sub.2,
--CF.sub.3, --CCl.sub.3, --OCF.sub.3, --CN, --NO.sub.2,
--N(R)C(.dbd.O)R, --C(.dbd.O)R, --OC(.dbd.O)R, --C(O)OR,
--C(.dbd.O)NRR, --S(.dbd.O)R, --S(.dbd.O).sub.2OR,
--S(.dbd.O).sub.2R, --OS(.dbd.O).sub.2OR, --S(.dbd.O).sub.2NRR, and
each R is independently --H, alkyl, aryl, arylalkyl, or
heterocycle. Alkylene, alkenylene, and alkynylene groups may also
be similarly substituted.
[0059] The term "optionally substituted" in reference to a
particular moiety of the compound of formula (I), (e.g., an
optionally substituted aryl group) refers to a moiety having 0, 1,
2, or more substituents.
[0060] The symbol "" in a ring structure means that a bond is a
single or double bond. In a non-limiting example,
##STR00015##
can be
##STR00016##
[0061] "Haloalkyl" as used herein includes an alkyl group
substituted with one or more halogens (e.g. F, Cl, Br, or I).
Representative examples of haloalkyl include trifluoromethyl,
2,2,2-trifluoroethyl, and
2,2,2-trifluoro-1-(trifluoromethyl)ethyl.
[0062] "Heterocycle" or "heterocyclyl" as used herein includes by
way of example and not limitation these heterocycles described in
Paquette, Leo A.; Principles of Modern Heterocyclic Chemistry (W.
A. Benjamin, New York, 1968), particularly Chapters 1, 3, 4, 6, 7,
and 9; The Chemistry of Heterocyclic Compounds, A Series of
Monographs" (John Wiley & Sons, New York, 1950 to present), in
particular Volumes 13, 14, 16, 19, and 28; and J. Am. Chem. Soc.
(1960) 82:5566. In one specific embodiment, "heterocycle" includes
a "carbocycle" as defined herein, wherein one or more (e.g. 1, 2,
3, or 4) carbon atoms have been replaced with a heteroatom (e.g. O,
N, or S). The term heterocycle also includes "heteroaryl" which is
a heterocycle wherein at least one heterocyclic rings is
aromatic.
[0063] Examples of heterocycles include by way of example and not
limitation pyridyl, dihydropyridyl, tetrahydropyridyl (piperidyl),
thiazolyl, tetrahydrothiophenyl, sulfur oxidized
tetrahydrothiophenyl, pyrimidinyl, furanyl, thienyl, pyrrolyl,
pyrazolyl, imidazolyl, tetrazolyl, benzofuranyl, thianaphthalenyl,
indolyl, indolenyl, quinolinyl, isoquinolinyl, benzimidazolyl,
piperidinyl, 4-piperidonyl, pyrrolidinyl, 2-pyrrolidonyl,
pyrrolinyl, tetrahydrofuranyl, tetrahydroquinolinyl,
tetrahydroisoquinolinyl, decahydroquinolinyl,
octahydroisoquinolinyl, azocinyl, triazinyl, 6H-1,2,5-thiadiazinyl,
2H,6H-1,5,2-dithiazinyl, thienyl, thianthrenyl, pyranyl,
isobenzofuranyl, chromenyl, xanthenyl, phenoxathinyl, 2H-pyrrolyl,
isothiazolyl, isoxazolyl, pyrazinyl, pyridazinyl, indolizinyl,
isoindolyl, 3H-indolyl, 1H-indazolyl, purinyl, 4H-quinolizinyl,
phthalazinyl, naphthyridinyl, quinoxalinyl, quinazolinyl,
cinnolinyl, pteridinyl, 4H-carbazolyl, carbazolyl, j-carbolinyl,
phenanthridinyl, acridinyl, pyrimidinyl, phenanthrolinyl,
phenazinyl, phenothiazinyl, furazanyl, phenoxazinyl, isochromanyl,
chromanyl, imidazolidinyl, imidazolinyl, pyrazolidinyl,
pyrazolinyl, piperazinyl, indolinyl, isoindolinyl, quinuclidinyl,
morpholinyl, oxazolidinyl, benzotriazolyl, benzisoxazolyl,
oxindolyl, benzoxazolinyl, isatinoyl, and
bis-tetrahydrofuranyl:
##STR00017##
[0064] By way of example and not limitation, carbon bonded
heterocycles are bonded at position 2, 3, 4, 5, or 6 of a pyridine,
position 3, 4, 5, or 6 of a pyridazine, position 2, 4, 5, or 6 of a
pyrimidine, position 2, 3, 5, or 6 of a pyrazine, position 2, 3, 4,
or 5 of a furan, tetrahydrofuran, thiofuran, thiophene, pyrrole or
tetrahydropyrrole, position 2, 4, or 5 of an oxazole, imidazole or
thiazole, position 3, 4, or 5 of an isoxazole, pyrazole, or
isothiazole, position 2 or 3 of an aziridine, position 2, 3, or 4
of an azetidine, position 2, 3, 4, 5, 6, 7, or 8 of a quinoline or
position 1, 3, 4, 5, 6, 7, or 8 of an isoquinoline. Still more
typically, carbon bonded heterocycles include 2-pyridyl, 3-pyridyl,
4-pyridyl, 5-pyridyl, 6-pyridyl, 3-pyridazinyl, 4-pyridazinyl,
5-pyridazinyl, 6-pyridazinyl, 2-pyrimidinyl, 4-pyrimidinyl,
5-pyrimidinyl, 6-pyrimidinyl, 2-pyrazinyl, 3-pyrazinyl,
5-pyrazinyl, 6-pyrazinyl, 2-thiazolyl, 4-thiazolyl, or
5-thiazolyl.
[0065] By way of example and not limitation, nitrogen bonded
heterocycles are bonded at position 1 of an aziridine, azetidine,
pyrrole, pyrrolidine, 2-pyrroline, 3-pyrroline, imidazole,
imidazolidine, 2-imidazoline, 3-imidazoline, pyrazole, pyrazoline,
2-pyrazoline, 3-pyrazoline, piperidine, piperazine, indole,
indoline, 1H-indazole, position 2 of a isoindole, or isoindoline,
position 4 of a morpholine, and position 9 of a carbazole, or
.beta.-carboline. Still more typically, nitrogen bonded
heterocycles include 1-aziridyl, 1-azetedyl, 1-pyrrolyl,
1-imidazolyl, 1-pyrazolyl, and 1-piperidinyl.
[0066] "Carbocycle" refers to a saturated, unsaturated or aromatic
ring having up to about 25 carbon atoms. Typically, a carbocycle
has about 3 to 7 carbon atoms as a monocycle, about 7 to 12 carbon
atoms as a bicycle, and up to about 25 carbon atoms as a polycycle.
Monocyclic carbocycles typically have 3 to 6 ring atoms, still more
typically 5 or 6 ring atoms. Bicyclic carbocycles typically have 7
to 12 ring atoms, e.g., arranged as a bicyclo [4,5], [5,5], [5,6]
or [6,6] system, or 9 or 10 ring atoms arranged as a bicyclo [5,6]
or [6,6] system. The term carbocycle includes "cycloalkyl" which is
a saturated or unsaturated carbocycle. Examples of monocyclic
carbocycles include cyclopropyl, cyclobutyl, cyclopentyl,
1-cyclopent-1-enyl, 1-cyclopent-2-enyl, 1-cyclopent-3-enyl,
cyclohexyl, 1-cyclohex-1-enyl, 1-cyclohex-2-enyl,
1-cyclohex-3-enyl, phenyl, spiryl and naphthyl.
[0067] The term "amino," as used herein, refers to --NH.sub.2.
[0068] The term "chiral" refers to molecules which have the
property of non-superimposability of the mirror image partner,
while the term "achiral" refers to molecules which are
superimposable on their mirror image partner.
[0069] The term "stereoisomers" refers to compounds which have
identical chemical constitution, but differ with regard to the
arrangement of the atoms or groups in space.
[0070] "Diastereomer" refers to a stereoisomer with two or more
centers of chirality and whose molecules are not mirror images of
one another. Diastereomers have different physical properties,
e.g., melting points, boiling points, spectral properties, and
reactivities. Mixtures of diastereomers may separate under high
resolution analytical procedures such as, for example,
electrophoresis and chromatography.
[0071] "Enantiomers" refer to two stereoisomers of a compound which
are non-superimposable mirror images of one another.
[0072] The term "treatment" or "treating," to the extent it relates
to a disease or condition includes preventing the disease or
condition from occurring, inhibiting the disease or condition,
eliminating the disease or condition, and/or relieving one or more
symptoms of the disease or condition.
[0073] Stereochemical definitions and conventions used herein
generally follow S. P. Parker, Ed., McGraw-Hill Dictionary of
Chemical Terms (1984) McGraw-Hill Book Company, New York; and
Eliel, E. and Wilen, S., Stereochemistry of Organic Compounds
(1994) John Wiley & Sons, Inc., New York. Many organic
compounds exist in optically active forms, i.e., they have the
ability to rotate the plane of plane-polarized light. In describing
an optically active compound, the prefixes (D and L) or (R and S)
are used to denote the absolute configuration of the molecule about
its chiral center(s). The prefixes d and l or (+) and (-) are
employed to designate the sign of rotation of plane-polarized light
by the compound, with (-) or l meaning that the compound is
levorotatory. A compound prefixed with (+) or d is dextrorotatory.
For a given chemical structure, these stereoisomers are identical
except that they are mirror images of one another. A specific
stereoisomer may also be referred to as an enantiomer, and a
mixture of such isomers is often called an enantiomeric mixture. A
50:50 mixture of enantiomers is referred to as a racemic mixture or
a racemate, which may occur where there has been no stereoselection
or stereospecificity in a chemical reaction or process. The terms
"racemic mixture" and "racemate" refer to an equimolar mixture of
two enantiomeric species, devoid of optical activity. The
disclosure includes all stereoisomers of the compounds described
herein.
[0074] Prodrugs
[0075] The term "prodrug" as used herein refers to any compound
that when administered to a biological system generates a compound
of the disclosure that inhibits HCV activity ("the active
inhibitory compound"). The compound may be formed from the prodrug
as a result of: (i) spontaneous chemical reaction(s), (ii) enzyme
catalyzed chemical reaction(s), (iii) photolysis, and/or (iv)
metabolic chemical reaction(s).
[0076] "Prodrug moiety" refers to a labile functional group which
separates from the active inhibitory compound during metabolism,
systemically, inside a cell, by hydrolysis, enzymatic cleavage, or
by some other process (Bundgaard, Hans, "Design and Application of
Prodrugs" in A Textbook of Drug Design and Development (1991), P.
Krogsgaard-Larsen and H. Bundgaard, Eds. Harwood Academic
Publishers, pp. 113-191). Enzymes which are capable of an enzymatic
activation mechanism with the prodrug compounds of the disclosure
include, but are not limited to, amidases, esterases, microbial
enzymes, phospholipases, cholinesterases, and phosphases. Prodrug
moieties can serve to enhance solubility, absorption and
lipophilicity to optimize drug delivery, bioavailability and
efficacy. A prodrug moiety may include an active metabolite or drug
itself.
[0077] Exemplary prodrug moieties include the hydrolytically
sensitive or labile acyloxymethyl esters
--CH.sub.2OC(.dbd.O)R.sup.99 and acyloxymethyl carbonates
--CH.sub.2OC(.dbd.O)OR.sup.99 where R.sup.99 is C.sub.1-C.sub.6
alkyl, C.sub.1-C.sub.6 substituted alkyl, C.sub.6-C.sub.20 aryl or
C.sub.6-C.sub.20 substituted aryl. The acyloxyalkyl ester was first
used as a prodrug strategy for carboxylic acids and then applied to
phosphates and phosphonates by Farquhar et al. (1983) J. Pharm.
Sci. 72: 324; also U.S. Pat. Nos. 4,816,570, 4,968,788, 5,663,159
and 5,792,756. Subsequently, the acyloxyalkyl ester was used to
deliver phosphonic acids across cell membranes and to enhance oral
bioavailability. A close variant of the acyloxyalkyl ester, the
alkoxycarbonyloxyalkyl ester (carbonate), may also enhance oral
bioavailability as a prodrug moiety in the compounds of the
combinations of the disclosure. An exemplary acyloxymethyl ester is
pivaloyloxymethoxy, (POM) --CH.sub.2OC(.dbd.O)C(CH.sub.3).sub.3. An
exemplary acyloxymethyl carbonate prodrug moiety is
pivaloyloxymethylcarbonate (POC)
--CH.sub.2OC(.dbd.O)OC(CH.sub.3).sub.3.
[0078] Protecting Groups
[0079] In the context of the present disclosure, protecting groups
include prodrug moieties and chemical protecting groups.
[0080] "Protecting group" refers to a moiety of a compound that
masks or alters the properties of a functional group or the
properties of the compound as a whole. Chemical protecting groups
and strategies for protection/deprotection are well known in the
art. See e.g., Protective Groups in Organic Chemistry, Theodora W.
Greene, John Wiley & Sons, Inc., New York, 1991. Protecting
groups are often utilized to mask the reactivity of certain
functional groups, to assist in the efficiency of desired chemical
reactions, e.g., making and breaking chemical bonds in an ordered
and planned fashion. Protection of functional groups of a compound
alters other physical properties besides the reactivity of the
protected functional group, such as, for example, the polarity,
lipophilicity (hydrophobicity), and other properties which can be
measured by common analytical tools. Chemically protected
intermediates may themselves be biologically active or
inactive.
[0081] Protected compounds may also exhibit altered, and in some
cases, optimized properties in vitro and in vivo, such as, for
example, passage through cellular membranes and resistance to
enzymatic degradation or sequestration. In this role, protected
compounds with intended therapeutic effects may be referred to as
prodrugs. Another function of a protecting group is to convert the
parental drug into a prodrug, whereby the parental drug is released
upon conversion of the prodrug in vivo. Because active prodrugs may
be absorbed more effectively than the parental drug, prodrugs may
possess greater potency in vivo than the parental drug. Protecting
groups are removed either in vitro, in the instance of chemical
intermediates, or in vivo, in the case of prodrugs. With chemical
intermediates, it is not particularly important that the resulting
products after deprotection, e.g., alcohols, be physiologically
acceptable, although in general it is more desirable if the
products are pharmacologically innocuous.
[0082] Protecting groups are available, commonly known and used,
and are optionally used to prevent side reactions with the
protected group during synthetic procedures, i.e. routes or methods
to prepare the compounds of the disclosure. For the most part the
decision as to which groups to protect, when to do so, and the
nature of the chemical protecting group "PG" will be dependent upon
the chemistry of the reaction to be protected against (e.g.,
acidic, basic, oxidative, reductive or other conditions) and the
intended direction of the synthesis. PGs do not need to be, and
generally are not, the same if the compound is substituted with
multiple PG. In general, PG will be used to protect functional
groups such as, for example, carboxyl, hydroxyl, thio, or amino
groups and to thus prevent side reactions or to otherwise
facilitate the synthetic efficiency. The order of deprotection to
yield free deprotected groups is dependent upon the intended
direction of the synthesis and the reaction conditions to be
encountered, and may occur in any order as determined by the
artisan.
[0083] Various functional groups of the compounds of the disclosure
may be protected. For example, protecting groups for --OH groups
(whether hydroxyl, carboxylic acid, phosphonic acid, or other
functions) include "ether- or ester-forming groups". Ether- or
ester-forming groups are capable of functioning as chemical
protecting groups in the synthetic schemes set forth herein.
However, some hydroxyl and thio protecting groups are neither
ether- nor ester-forming groups, as will be understood by those
skilled in the art, and are included with amides, discussed
below.
[0084] A very large number of hydroxyl protecting groups and
amide-forming groups and corresponding chemical cleavage reactions
are described in Protective Groups in Organic Synthesis, Theodora
W. Greene (John Wiley & Sons, Inc., New York, 1991, ISBN
0-471-62301-6) ("Greene"). See also Kocienski, Philip J.;
Protecting Groups (Georg Thieme Verlag Stuttgart, New York, 1994),
which is incorporated by reference in its entirety herein. In
particular Chapter 1, Protecting Groups: An Overview, pages 1-20,
Chapter 2, Hydroxyl Protecting Groups, pages 21-94, Chapter 3, Diol
Protecting Groups, pages 95-117, Chapter 4, Carboxyl Protecting
Groups, pages 118-154, Chapter 5, Carbonyl Protecting Groups, pages
155-184. For protecting groups for carboxylic acid, phosphonic
acid, phosphonate, sulfonic acid and other protecting groups for
acids see Greene as set forth below.
[0085] Stereoisomers
[0086] The compounds of the disclosure may have chiral centers,
e.g., chiral carbon or phosphorus atoms. The compounds of the
disclosure thus include all stereoisomers, including enantiomers,
diastereomers, and atropisomers. In addition, the compounds of the
disclosure include enriched or resolved optical isomers at any or
all asymmetric, chiral atoms. In other words, the chiral centers
apparent from the depictions are provided as the non-racemic or
racemic mixtures. Both racemic and diastereomeric mixtures, as well
as the individual optical isomers isolated or synthesized,
substantially free of their enantiomeric or diastereomeric
partners, are all within the scope of the disclosure. The racemic
mixtures are separated into their individual, substantially
optically pure isomers through well-known techniques such as, for
example, the separation of diastereomeric salts formed with
optically active adjuncts, e.g., acids or bases followed by
conversion back to the optically active substances. In most
instances, the desired optical isomer is synthesized by means of
stereospecific reactions, beginning with the appropriate
stereoisomer of the desired starting material or through
enantioselective reactions.
[0087] The compounds of the disclosure can also exist as tautomeric
isomers in certain cases. Although only one tautomer may be
depicted, all such forms are contemplated within the scope of the
disclosure. For example, ene-amine tautomers can exist for purine,
pyrimidine, imidazole, guanidine, amidine, and tetrazole systems
and all their possible tautomeric forms are within the scope of the
disclosure.
[0088] Salts and Hydrates
[0089] Examples of physiologically or pharmaceutically acceptable
salts of the compounds of the disclosure include salts derived from
an appropriate base, such as, for example, an alkali metal (for
example, sodium), an alkaline earth metal (for example, magnesium),
ammonium and NX.sub.4.sup.+ (wherein X is C.sub.1-C.sub.4 alkyl).
Physiologically acceptable salts of a hydrogen atom or an amino
group include salts of organic carboxylic acids such as, for
example, acetic, benzoic, lactic, fumaric, tartaric, maleic,
malonic, malic, isethionic, lactobionic and succinic acids; organic
sulfonic acids, such as, for example, methanesulfonic,
ethanesulfonic, benzenesulfonic and p-toluenesulfonic acids; and
inorganic acids, such as, for example, hydrochloric, sulfuric,
phosphoric and sulfamic acids. Physiologically acceptable salts of
a compound of a hydroxy group include the anion of said compound in
combination with a suitable cation such as, for example, Na.sup.+
and NX.sub.4.sup.+ (wherein X is independently selected from H or a
C.sub.1-C.sub.4 alkyl group).
[0090] For therapeutic use, salts of active ingredients of the
compounds of the disclosure will typically be physiologically
acceptable, i.e. they will be salts derived from a physiologically
acceptable acid or base. However, salts of acids or bases which are
not physiologically acceptable may also find use, for example, in
the preparation or purification of a physiologically acceptable
compound. All salts, whether or not derived form a physiologically
acceptable acid or base, are within the scope of the present
disclosure.
[0091] Metal salts typically are prepared by reacting the metal
hydroxide with a compound of this disclosure. Examples of metal
salts which are prepared in this way are salts containing Li.sup.+,
Na.sup.+, and K.sup.+. A less soluble metal salt can be
precipitated from the solution of a more soluble salt by addition
of the suitable metal compound.
[0092] In addition, salts may be formed from acid addition of
certain organic and inorganic acids, e.g., HCl, HBr,
H.sub.2SO.sub.4, H.sub.3PO.sub.4 or organic sulfonic acids, to
basic centers, typically amines, or to acidic groups. Finally, it
is to be understood that the compositions herein comprise compounds
of the disclosure in their un-ionized, as well as zwitterionic
form, and combinations with stoichiometric amounts of water as in
hydrates.
[0093] Also included within the scope of this disclosure are the
salts of the parental compounds with one or more amino acids. Any
of the natural or unnatural amino acids are suitable, especially
the naturally-occurring amino acids found as protein components,
although the amino acid typically is one bearing a side chain with
a basic or acidic group, e.g., lysine, arginine or glutamic acid,
or a neutral group such as, for example, glycine, serine,
threonine, alanine, isoleucine, or leucine.
Methods of Inhibition of HCV
[0094] Another aspect of the disclosure relates to methods of
inhibiting the activity of HCV comprising the step of treating a
sample suspected of containing HCV with a compound or composition
of the disclosure.
[0095] The treating step of the disclosure comprises adding the
compound of the disclosure to the sample or it comprises adding a
precursor of the composition to the sample. The addition step
comprises any method of administration as described above.
[0096] If desired, the activity of HCV after application of the
compound can be observed by any method including direct and
indirect methods of detecting HCV activity. Quantitative,
qualitative, and semiquantitative methods of determining HCV
activity are all contemplated.
[0097] Typically one of the screening methods described above are
applied, however, any other method such as, for example,
observation of the physiological properties of a living organism
are also applicable.
[0098] Many organisms contain HCV. The compounds of this disclosure
are useful in the treatment or prophylaxis of conditions associated
with HCV activation in animals or in man.
[0099] However, in screening compounds capable of inhibiting HCV
activity it should be kept in mind that the results of enzyme
assays may not always correlate with cell culture assays. Thus, a
cell based assay should typically be the primary screening
tool.
Pharmaceutical Formulations
[0100] The compounds of this disclosure are formulated with
conventional carriers and excipients, which will be selected in
accord with ordinary practice. Tablets will contain excipients,
glidants, fillers, binders and the like. Aqueous formulations are
prepared in sterile form, and when intended for delivery by other
than oral administration generally will be isotonic. All
formulations will optionally contain excipients such as, for
example, those set forth in the Handbook of Pharmaceutical
Excipients (1986). Excipients include ascorbic acid and other
antioxidants, chelating agents such as, for example, EDTA,
carbohydrates such as, for example, dextrin, hydroxyalkylcellulose,
hydroxyalkylmethylcellulose, stearic acid and the like. The pH of
the formulations ranges from about 3 to about 11, but is ordinarily
about 7 to 10. Typically, the compound will be administered in a
dose from 0.01 milligrams to 2 grams. In one embodiment, the dose
will be from about 10 milligrams to 450 milligrams. It is
contemplated that the compound may be administered once, twice or
three times a day.
[0101] While it is possible for the active ingredients to be
administered alone it may be preferable to present them as
pharmaceutical formulations. The formulations, both for veterinary
and for human use, of the disclosure comprise at least one active
ingredient, as above defined, together with one or more acceptable
carriers therefore and optionally other therapeutic ingredients.
The carrier(s) must be "acceptable" in the sense of being
compatible with the other ingredients of the formulation and
physiologically innocuous to the recipient thereof.
[0102] The formulations include those suitable for the foregoing
administration routes. The formulations may conveniently be
presented in unit dosage form and may be prepared by any of the
methods well known in the art of pharmacy. Techniques and
formulations generally are found in Remington's Pharmaceutical
Sciences (Mack Publishing Co., Easton, Pa.). Such methods include
the step of bringing into association the active ingredient with
the carrier which constitutes one or more accessory ingredients. In
general the formulations are prepared by uniformly and intimately
bringing into association the active ingredient with liquid
carriers or finely divided solid carriers or both, and then, if
necessary, shaping the product.
[0103] Formulations of the present disclosure suitable for oral
administration may be presented as discrete units such as, for
example, capsules, cachets or tablets each containing a
predetermined amount of the active ingredient; as a powder or
granules; as a solution or a suspension in an aqueous or
non-aqueous liquid; or as an oil-in-water liquid emulsion or a
water-in-oil liquid emulsion. The active ingredient may also be
administered as a bolus, electuary or paste.
[0104] A tablet is made by compression or molding, optionally with
one or more accessory ingredients. Compressed tablets may be
prepared by compressing in a suitable machine the active ingredient
in a free-flowing form such as, for example, a powder or granules,
optionally mixed with a binder, lubricant, inert diluent,
preservative, surface active or dispersing agent. Molded tablets
may be made by molding in a suitable machine a mixture of the
powdered active ingredient moistened with an inert liquid diluent.
The tablets may optionally be coated or scored and optionally are
formulated so as to provide slow or controlled release of the
active ingredient therefrom.
[0105] For administration to the eye or other external tissues
e.g., mouth and skin, the formulations are preferably applied as a
topical ointment or cream containing the active ingredient(s) in an
amount of, for example, 0.075 to 20% w/w (including active
ingredient(s) in a range between 0.1% and 20% in increments of 0.1%
w/w such as, for example, 0.6% w/w, 0.7% w/w, etc.), preferably 0.2
to 15% w/w and most preferably 0.5 to 10% w/w. When formulated in
an ointment, the active ingredients may be employed with either a
paraffinic or a water-miscible ointment base. Alternatively, the
active ingredients may be formulated in a cream with an
oil-in-water cream base.
[0106] If desired, the aqueous phase of the cream base may include,
for example, at least 30% w/w of a polyhydric alcohol, i.e. an
alcohol having two or more hydroxyl groups such as, for example,
propylene glycol, butane 1,3-diol, mannitol, sorbitol, glycerol and
polyethylene glycol (including PEG 400) and mixtures thereof. The
topical formulations may desirably include a compound which
enhances absorption or penetration of the active ingredient through
the skin or other affected areas. Examples of such dermal
penetration enhancers include dimethyl sulphoxide and related
analogs.
[0107] The oily phase of the emulsions of this disclosure may be
constituted from known ingredients in a known manner. While the
phase may comprise merely an emulsifier (otherwise known as an
emulgent), it desirably comprises a mixture of at least one
emulsifier with a fat or an oil or with both a fat and an oil.
Preferably, a hydrophilic emulsifier is included together with a
lipophilic emulsifier which acts as a stabilizer. It is also
preferred to include both an oil and a fat. Together, the
emulsifier(s) with or without stabilizer(s) make up the so-called
emulsifying wax, and the wax together with the oil and fat make up
the so-called emulsifying ointment base which forms the oily
dispersed phase of the cream formulations.
[0108] Emulgents and emulsion stabilizers suitable for use in the
formulation of the disclosure include Tween.RTM. 60, Span.RTM. 80,
cetostearyl alcohol, benzyl alcohol, myristyl alcohol, glyceryl
mono-stearate and sodium lauryl sulfate.
[0109] The choice of suitable oils or fats for the formulation is
based on achieving the desired cosmetic properties. The cream
should preferably be a non-greasy, non-staining and washable
product with suitable consistency to avoid leakage from tubes or
other containers. Straight or branched chain, mono- or dibasic
alkyl esters such as, for example, di-isoadipate, isocetyl
stearate, propylene glycol diester of coconut fatty acids,
isopropyl myristate, decyl oleate, isopropyl palmitate, butyl
stearate, 2-ethylhexyl palmitate or a blend of branched chain
esters known as Crodamol CAP may be used, the last three being
preferred esters. These may be used alone or in combination
depending on the properties required.
[0110] Alternatively, high melting point lipids such as, for
example, white soft paraffin and/or liquid paraffin or other
mineral oils are used.
[0111] Pharmaceutical formulations according to the present
disclosure comprise one or more compounds of the disclosure
together with one or more pharmaceutically acceptable carriers or
excipients and optionally other therapeutic agents. Pharmaceutical
formulations containing the active ingredient may be in any form
suitable for the intended method of administration. When used for
oral use for example, tablets, troches, lozenges, aqueous or oil
suspensions, dispersible powders or granules, emulsions, hard or
soft capsules, syrups or elixirs may be prepared. Compositions
intended for oral use may be prepared according to any method known
to the art for the manufacture of pharmaceutical compositions and
such compositions may contain one or more agents including
sweetening agents, flavoring agents, coloring agents and preserving
agents, in order to provide a palatable preparation. Tablets
containing the active ingredient in admixture with non-toxic
pharmaceutically acceptable excipient which are suitable for
manufacture of tablets are acceptable. These excipients may be, for
example, inert diluents, such as, for example, calcium or sodium
carbonate, lactose, lactose monohydrate, croscarmellose sodium,
povidone, calcium or sodium phosphate; granulating and
disintegrating agents, such as, for example, maize starch, or
alginic acid; binding agents, such as, for example, cellulose,
microcrystalline cellulose, starch, gelatin or acacia; and
lubricating agents, such as, for example, magnesium stearate,
stearic acid or talc. Tablets may be uncoated or may be coated by
known techniques including microencapsulation to delay
disintegration and adsorption in the gastrointestinal tract and
thereby provide a sustained action over a longer period. For
example, a time delay material such as, for example, glyceryl
monostearate or glyceryl distearate alone or with a wax may be
employed.
[0112] Formulations for oral use may be also presented as hard
gelatin capsules where the active ingredient is mixed with an inert
solid diluent, for example calcium phosphate or kaolin, or as soft
gelatin capsules wherein the active ingredient is mixed with water
or an oil medium, such as, for example, peanut oil, liquid paraffin
or olive oil.
[0113] Aqueous suspensions of the disclosure contain the active
materials in admixture with excipients suitable for the manufacture
of aqueous suspensions. Such excipients include a suspending agent,
such as, for example, sodium carboxymethylcellulose,
methylcellulose, hydroxypropyl methylcelluose, sodium alginate,
polyvinylpyrrolidone, gum tragacanth and gum acacia, and dispersing
or wetting agents such as, for example, a naturally occurring
phosphatide (e.g., lecithin), a condensation product of an alkylene
oxide with a fatty acid (e.g., polyoxyethylene stearate), a
condensation product of ethylene oxide with a long chain aliphatic
alcohol (e.g., heptadecaethyleneoxycetanol), a condensation product
of ethylene oxide with a partial ester derived from a fatty acid
and a hexitol anhydride (e.g., polyoxyethylene sorbitan
monooleate). The aqueous suspension may also contain one or more
preservatives such as, for example, ethyl or n-propyl
p-hydroxy-benzoate, one or more coloring agents, one or more
flavoring agents and one or more sweetening agents, such as, for
example, sucrose or saccharin.
[0114] Oil suspensions may be formulated by suspending the active
ingredient in a vegetable oil, such as, for example, arachis oil,
olive oil, sesame oil or coconut oil, or in a mineral oil such as,
for example, liquid paraffin. The oral suspensions may contain a
thickening agent, such as, for example, beeswax, hard paraffin or
cetyl alcohol. Sweetening agents, such as, for example, those set
forth above, and flavoring agents may be added to provide a
palatable oral preparation. These compositions may be preserved by
the addition of an antioxidant such as, for example, ascorbic
acid.
[0115] Dispersible powders and granules of the disclosure suitable
for preparation of an aqueous suspension by the addition of water
provide the active ingredient in admixture with a dispersing or
wetting agent, a suspending agent, and one or more preservatives.
Suitable dispersing or wetting agents and suspending agents are
exemplified by those disclosed above. Additional excipients, for
example sweetening, flavoring and coloring agents, may also be
present.
[0116] The pharmaceutical compositions of the disclosure may also
be in the form of oil-in-water emulsions. The oily phase may be a
vegetable oil, such as, for example, olive oil or arachis oil, a
mineral oil, such as, for example, liquid paraffin, or a mixture of
these. Suitable emulsifying agents include naturally-occurring
gums, such as, for example, gum acacia and gum tragacanth,
naturally occurring phosphatides, such as, for example, soybean
lecithin, esters or partial esters derived from fatty acids and
hexitol anhydrides, such as, for example, sorbitan monooleate, and
condensation products of these partial esters with ethylene oxide,
such as, for example, polyoxyethylene sorbitan monooleate. The
emulsion may also contain sweetening and flavoring agents. Syrups
and elixirs may be formulated with sweetening agents, such as, for
example, glycerol, sorbitol or sucrose. Such formulations may also
contain a demulcent, a preservative, a flavoring or a coloring
agent.
[0117] The pharmaceutical compositions of the disclosure may be in
the form of a sterile injectable preparation, such as, for example,
a sterile injectable aqueous or oleaginous suspension. This
suspension may be formulated according to the known art using those
suitable dispersing or wetting agents and suspending agents which
have been mentioned above. The sterile injectable preparation may
also be a sterile injectable solution or suspension in a non-toxic
parenterally acceptable diluent or solvent, such as, for example, a
solution in 1,3-butane-diol or prepared as a lyophilized powder.
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 may conventionally be employed as a
solvent or suspending medium. For this purpose any bland fixed oil
may be employed including synthetic mono- or diglycerides. In
addition, fatty acids such as, for example, oleic acid may likewise
be used in the preparation of injectables.
[0118] The amount of active ingredient that may be combined with
the carrier material to produce a single dosage form will vary
depending upon the host treated and the particular mode of
administration. For example, a time-release formulation intended
for oral administration to humans may contain approximately 1 to
1000 mg of active material compounded with an appropriate and
convenient amount of carrier material which may vary from about 5
to about 95% of the total compositions (weight:weight). The
pharmaceutical composition can be prepared to provide easily
measurable amounts for administration. For example, an aqueous
solution intended for intravenous infusion may contain from about 3
to 500 .mu.g of the active ingredient per milliliter of solution in
order that infusion of a suitable volume at a rate of about 30
mL/hr can occur.
[0119] Formulations suitable for administration to the eye include
eye drops wherein the active ingredient is dissolved or suspended
in a suitable carrier, especially an aqueous solvent for the active
ingredient. The active ingredient is preferably present in such
formulations in a concentration of 0.5 to 20%, advantageously 0.5
to 10% particularly about 1.5% w/w.
[0120] Formulations suitable for topical administration in the
mouth include lozenges comprising the active ingredient in a
flavored basis, usually sucrose and acacia or tragacanth; pastilles
comprising the active ingredient in an inert basis such as, for
example, gelatin and glycerin, or sucrose and acacia; and
mouthwashes comprising the active ingredient in a suitable liquid
carrier.
[0121] Formulations for rectal administration may be presented as a
suppository with a suitable base comprising for example cocoa
butter or a salicylate.
[0122] Formulations suitable for intrapulmonary or nasal
administration have a particle size for example in the range of 0.1
to 500 microns (including particle sizes in a range between 0.1 and
500 microns in increments microns such as, for example, 0.5, 1, 30
microns, 35 microns, etc.), which is administered by rapid
inhalation through the nasal passage or by inhalation through the
mouth so as to reach the alveolar sacs. Suitable formulations
include aqueous or oily solutions of the active ingredient.
Formulations suitable for aerosol or dry powder administration may
be prepared according to conventional methods and may be delivered
with other therapeutic agents such as, for example, compounds
heretofore used in the treatment or prophylaxis of conditions
associated with HCV activity.
[0123] Formulations suitable for vaginal administration may be
presented as pessaries, tampons, creams, gels, pastes, foams or
spray formulations containing in addition to the active ingredient
such carriers as are known in the art to be appropriate.
[0124] Formulations suitable for parenteral administration include
aqueous and non-aqueous sterile injection solutions which may
contain anti-oxidants, buffers, bacteriostats and solutes which
render the formulation isotonic with the blood of the intended
recipient; and aqueous and non-aqueous sterile suspensions which
may include suspending agents and thickening agents.
[0125] The formulations are presented in unit-dose or multi-dose
containers, for example sealed ampoules and vials, and may be
stored in a freeze-dried (lyophilized) condition requiring only the
addition of the sterile liquid carrier, for example water for
injection, immediately prior to use. Extemporaneous injection
solutions and suspensions are prepared from sterile powders,
granules and tablets of the kind previously described. Preferred
unit dosage formulations are those containing a daily dose or unit
daily sub-dose, as herein above recited, or an appropriate fraction
thereof, of the active ingredient.
[0126] It should be understood that in addition to the ingredients
particularly mentioned above the formulations of this disclosure
may include other agents conventional in the art having regard to
the type of formulation in question, for example those suitable for
oral administration may include flavoring agents.
[0127] The disclosure further provides veterinary compositions
comprising at least one active ingredient as above defined together
with a veterinary carrier therefore.
[0128] Veterinary carriers are materials useful for the purpose of
administering the composition and may be solid, liquid or gaseous
materials which are otherwise inert or acceptable in the veterinary
art and are compatible with the active ingredient. These veterinary
compositions may be administered orally, parenterally or by any
other desired route.
[0129] Compounds of the disclosure can also be formulated to
provide controlled release of the active ingredient to allow less
frequent dosing or to improve the pharmacokinetic or toxicity
profile of the active ingredient. Accordingly, the disclosure also
provides compositions comprising one or more compounds of the
disclosure formulated for sustained or controlled release.
[0130] Effective dose of active ingredient depends at least on the
nature of the condition being treated, toxicity, whether the
compound is being used prophylactically (lower doses), the method
of delivery, and the pharmaceutical formulation, and will be
determined by the clinician using conventional dose escalation
studies.
Routes of Administration
[0131] One or more compounds of the disclosure (herein referred to
as the active ingredients) are administered by any route
appropriate to the condition to be treated. Suitable routes include
oral, rectal, nasal, topical (including buccal and sublingual),
vaginal and parenteral (including subcutaneous, intramuscular,
intravenous, intradermal, intrathecal and epidural), and the like.
It will be appreciated that the preferred route may vary with for
example the condition of the recipient. An advantage of the
compounds of this disclosure is that they are orally bioavailable
and can be dosed orally.
HCV Combination Therapy
[0132] In another embodiment, non-limiting examples of suitable
combinations include combinations of one or more compounds of
formula (I) and (A1-A4) with one or more interferons, ribavirin or
its analogs, HCV NS3 protease inhibitors, alpha-glucosidase 1
inhibitors, hepatoprotectants, nucleoside or nucleotide inhibitors
of HCV NS5B polymerase, non-nucleoside inhibitors of HCV NS5B
polymerase, HCV NS5A inhibitors, TLR-7 agonists, cyclophillin
inhibitors, HCV IRES inhibitors, pharmacokinetic enhancers, and
other drugs or therapeutic agents for treating HCV.
[0133] More specifically, one or more compounds of the present as
described herein may be combined with one or more compounds
selected from the group consisting of [0134] 1) interferons, e.g.,
pegylated rIFN-alpha 2b (PEG-Intron.RTM.), pegylated rIFN-alpha 2a
(Pegasys.RTM.), rIFN-alpha 2b (Intron.RTM. A), rIFN-alpha 2a
(Roferon.RTM.-A), interferon alpha (MOR-22, OPC-18,
Alfaferone.RTM., Alfanative.RTM., Multiferon.RTM., subalin),
interferon alfacon-1 (Infergen.RTM.), interferon alpha-n1
(Wellferon), interferon alpha-n3 (Alferon.RTM.), interferon-beta
(Avonex.RTM., DL-8234), interferon-omega (omega DUROS.RTM.,
Biomed.RTM. 510), albinterferon alpha-2b (Albuferon.RTM.), IFN
alpha-2b XL, BLX-883 (Locteron.RTM.), DA-3021, glycosylated
interferon alpha-2b (AVI-005), PEG-Infergen, PEGylated interferon
lambda-1 (PEGylated IL-29), and Belerofon.RTM.; [0135] 2) ribavirin
and its analogs, e.g., ribavirin (Rebetol.RTM., Copegus.RTM.), and
taribavirin (Viramidine.RTM.); [0136] 3) HCV NS3 protease
inhibitors, e.g., boceprevir (SCH-503034, SCH-7), telaprevir
(VX-950), TMC435350, BI-1335, BI-1230, MK-7009, VBY-376, VX-500,
GS-9256, GS-9451, BMS-605339, PHX-1766, AS-101, YH-5258, YH5530,
YH5531, ABT-450, ACH-1625, ITMN-191, AT26893, MK5172, MK6325, and
MK2748; [0137] 4) alpha-glucosidase 1 inhibitors, e.g., celgosivir
(MX-3253), Miglitol, and UT-231B; [0138] 5) hepatoprotectants,
e.g., emericasan (IDN-6556), ME-3738, GS-9450 (LB-84451),
silibilin, and MitoQ; [0139] 6) nucleoside or nucleotide inhibitors
of HCV NS5B polymerase, e.g., R1626, R7128 (R4048), IDX184,
IDX-102, BCX-4678, valopicitabine (NM-283), MK-0608, sofosbuvir
(GS-7977 (formerly PSI-7977)), VLX-135 (formerly ALS-2200), and
INX-189 (now BMS986094); [0140] 7) non-nucleoside inhibitors of HCV
NS5B polymerase, e.g., PF-868554, VCH-759, VCH-916, JTK-652,
MK-3281, GS-9190, VBY-708, VCH-222, A848837, ANA-598, GL60667,
GL59728, A-63890, A-48773, A-48547, BC-2329, VCH-796 (nesbuvir),
GSK625433, BILN-1941, XTL-2125, ABT-072, ABT-333, GS-9669,
PSI-7792, and GS-9190; [0141] 8) HCV NS5A inhibitors, e.g.,
AZD-2836 (A-831), BMS-790052, ACH-3102, ACH-2928, MK8325, MK4882,
MK8742, PSI-461, IDX719, GS-5885, and A-689; [0142] 9) TLR-7
agonists, e.g., imiquimod, 852A, GS-9524, ANA-773, ANA-975
(isatoribine), AZD-8848 (DSP-3025), and SM-360320; [0143] 10)
cyclophillin inhibitors, e.g., DEBIO-025, SCY-635, and NIM811;
[0144] 11) HCV IRES inhibitors, e.g., MCI-067; [0145] 12)
pharmacokinetic enhancers, e.g., BAS-100, SPI-452, PF-4194477,
TMC-41629, GS-9350 (cobicistat), GS-9585, and roxythromycin; and
[0146] 13) other drugs for treating HCV, e.g., thymosin alpha 1
(Zadaxin), nitazoxanide (Alinea, NTZ), BIVN-401 (virostat), PYN-17
(altirex), KPE02003002, actilon (CPG-10101), GS-9525, KRN-7000,
civacir, GI-5005, XTL-6865, BIT225, PTX-111, ITX2865, TT-033i, ANA
971, NOV-205, tarvacin, EHC-18, VGX-410C, EMZ-702, AVI 4065,
BMS-650032, BMS-791325, Bavituximab, MDX-1106 (ONO-4538),
Oglufanide, and VX-497 (merimepodib).
[0147] In yet another embodiment, the present application discloses
pharmaceutical compositions comprising a compound as described
herein, or a pharmaceutically acceptable salt, prodrug, solvate,
and/or ester thereof, in combination with at least one additional
therapeutic agent, and a pharmaceutically acceptable carrier or
excipient.
[0148] In another embodiment is provided a pharmaceutical
composition comprising a compound of formula (I) as described
herein and sofosbuvir and/or GS-5885 and optionally an interferon
or ribavirin.
[0149] In another embodiment is provided a pharmaceutical
composition comprising a compound of formula (I) as described
herein and a nucleoside or nucleotide inhibitor of HCV NS5B
polymerase and optionally an interferon or ribavirin.
[0150] It is contemplated that additional therapeutic agents will
be administered in a manner that is known in the art and the dosage
may be selected by someone of skill in the art. For example,
additional therapeutic agents may be administered in a dose from
about 0.01 milligrams to about 2 grams per day.
Metabolites of the Compounds
[0151] Also falling within the scope of this disclosure are the in
vivo metabolic products of the compounds described herein. Such
products may result for example from the oxidation, reduction,
hydrolysis, amidation, esterification and the like of the
administered compound, primarily due to enzymatic processes.
Accordingly, the disclosure includes compounds produced by a
process comprising contacting a compound of this disclosure with a
mammal for a period of time sufficient to yield a metabolic product
thereof. Such products typically are identified by preparing a
radiolabelled (e.g., C.sup.14 or H.sup.3) compound of the
disclosure, administering it parenterally in a detectable dose
(e.g., greater than about 0.5 mg/kg) to an animal such as, for
example, rat, mouse, guinea pig, monkey, or to man, allowing
sufficient time for metabolism to occur (typically about 30 seconds
to 30 hours) and isolating its conversion products from the urine,
blood or other biological samples. These products are easily
isolated since they are labeled (others are isolated by the use of
antibodies capable of binding epitopes surviving in the
metabolite). The metabolite structures are determined in
conventional fashion, e.g., by MS or NMR analysis. In general,
analysis of metabolites is done in the same way as conventional
drug metabolism studies well-known to those skilled in the art. The
conversion products, so long as they are not otherwise found in
vivo, are useful in diagnostic assays for therapeutic dosing of the
compounds of the disclosure even if they possess no HCV-inhibitory
activity of their own.
[0152] Methods for determining stability of compounds in surrogate
gastrointestinal secretions are known.
Exemplary Methods of Making the Compounds
[0153] The disclosure also relates to methods of making the
compositions of the disclosure. The compositions are prepared by
any of the applicable techniques of organic synthesis. Many such
techniques are well known in the art. However, many of the known
techniques are elaborated in Compendium of Organic Synthetic
Methods (John Wiley & Sons, New York), Vol. 1, Ian T. Harrison
and Shuyen Harrison, 1971; Vol. 2, Ian T. Harrison and Shuyen
Harrison, 1974; Vol. 3, Louis S. Hegedus and Leroy Wade, 1977; Vol.
4, Leroy G. Wade, Jr., 1980; Vol. 5, Leroy G. Wade, Jr., 1984; and
Vol. 6, Michael B. Smith; as well as March, J., Advanced Organic
Chemistry, Third Edition, (John Wiley & Sons, New York, 1985),
Comprehensive Organic Synthesis. Selectivity, Strategy &
Efficiency in Modern Organic Chemistry. In 9 Volumes, Barry M.
Trost, Editor-in-Chief (Pergamon Press, New York, 1993 printing).
Other methods suitable for preparing compounds of the disclosure
are described in International Patent Application Publication
Number WO 2006/020276.
[0154] A number of exemplary methods for the preparation of the
compositions of the disclosure are provided in the schemes and
examples below. These methods are intended to illustrate the nature
of such preparations and are not intended to limit the scope of
applicable methods.
[0155] Generally, the reaction conditions such as, for example,
temperature, reaction time, solvents, work-up procedures, and the
like, will be those common in the art for the particular reaction
to be performed. The cited reference material, together with
material cited therein, contains detailed descriptions of such
conditions. Typically the temperatures will be -100.degree. C. to
200.degree. C., solvents will be aprotic or protic, and reaction
times will be 10 seconds to 10 days. Work-up typically consists of
quenching any unreacted reagents followed by partition between a
water/organic layer system (extraction) and separating the layer
containing the product.
[0156] Oxidation and reduction reactions are typically carried out
at temperatures near room temperature (about 20.degree. C.),
although for metal hydride reductions frequently the temperature is
reduced to 0.degree. C. to -100.degree. C., solvents are typically
aprotic for reductions and may be either protic or aprotic for
oxidations. Reaction times are adjusted to achieve desired
conversions.
[0157] Condensation reactions are typically carried out at
temperatures near room temperature, although for non-equilibrating,
kinetically controlled condensations reduced temperatures
(0.degree. C. to -100.degree. C.) are also common. Solvents can be
either protic (common in equilibrating reactions) or aprotic
(common in kinetically controlled reactions).
[0158] Standard synthetic techniques such as, for example,
azeotropic removal of reaction by-products and use of anhydrous
reaction conditions (e.g., inert gas environments) are common in
the art and will be applied when applicable.
[0159] The terms "treated", "treating", "treatment", and the like,
when used in connection with a chemical synthetic operation, mean
contacting, mixing, reacting, allowing to react, bringing into
contact, and other terms common in the art for indicating that one
or more chemical entities is treated in such a manner as to convert
it to one or more other chemical entities.
[0160] This means that "treating compound one with compound two" is
synonymous with "allowing compound one to react with compound two",
"contacting compound one with compound two", "reacting compound one
with compound two", and other expressions common in the art of
organic synthesis for reasonably indicating that compound one was
"treated", "reacted", "allowed to react", etc., with compound two.
For example, treating indicates the reasonable and usual manner in
which organic chemicals are allowed to react. Normal concentrations
(0.01M to 10M, typically 0.1M to 1M), temperatures (-100.degree. C.
to 250.degree. C., typically -78.degree. C. to 150.degree. C., more
typically -78.degree. C. to 100.degree. C., still more typically
0.degree. C. to 100.degree. C.), reaction vessels (typically glass,
plastic, metal), solvents, pressures, atmospheres (typically air
for oxygen and water insensitive reactions or nitrogen or argon for
oxygen or water sensitive), etc., are intended unless otherwise
indicated. The knowledge of similar reactions known in the art of
organic synthesis is used in selecting the conditions and apparatus
for "treating" in a given process. In particular, one of ordinary
skill in the art of organic synthesis selects conditions and
apparatus reasonably expected to successfully carry out the
chemical reactions of the described processes based on the
knowledge in the art.
[0161] Modifications of each of the exemplary schemes and in the
Examples (hereafter "exemplary schemes") leads to various analogs
of the specific exemplary materials produce. The above-cited
citations describing suitable methods of organic synthesis are
applicable to such modifications.
[0162] In each of the exemplary schemes it may be advantageous to
separate reaction products from one another and/or from starting
materials. The desired products of each step or series of steps is
separated and/or purified (hereinafter separated) to the desired
degree of homogeneity by the techniques common in the art.
Typically such separations involve multiphase extraction,
crystallization from a solvent or solvent mixture, distillation,
sublimation, or chromatography. Chromatography can involve any
number of methods including, for example: reverse-phase and normal
phase; size exclusion; ion exchange; high, medium, and low pressure
liquid chromatography methods and apparatus; small scale
analytical; simulated moving bed (SMB) and preparative thin or
thick layer chromatography, as well as techniques of small scale
thin layer and flash chromatography.
[0163] Another class of separation methods involves treatment of a
mixture with a reagent selected to bind to or render otherwise
separable a desired product, unreacted starting material, reaction
by product, or the like. Such reagents include adsorbents or
absorbents such as, for example, activated carbon, molecular
sieves, ion exchange media, or the like. Alternatively, the
reagents can be acids in the case of a basic material, bases in the
case of an acidic material, binding reagents such as, for example,
antibodies, binding proteins, selective chelators such as, for
example, crown ethers, liquid/liquid ion extraction reagents (LIX),
or the like.
[0164] Selection of appropriate methods of separation depends on
the nature of the materials involved. For example, boiling point,
and molecular weight in distillation and sublimation, presence or
absence of polar functional groups in chromatography, stability of
materials in acidic and basic media in multiphase extraction, and
the like. One skilled in the art will apply techniques most likely
to achieve the desired separation.
[0165] A single stereoisomer, e.g., an enantiomer, substantially
free of its stereoisomer may be obtained by resolution of the
racemic mixture using a method such as, for example, formation of
diastereomers using optically active resolving agents
(Stereochemistry of Carbon Compounds, (1962) by E. L. Eliel, McGraw
Hill; Lochmuller, C. H., (1975) J. Chromatogr., 113, 3) 283-302).
Racemic mixtures of chiral compounds of the disclosure can be
separated and isolated by any suitable method, including: (1)
formation of ionic, diastereomeric salts with chiral compounds and
separation by fractional crystallization or other methods, (2)
formation of diastereomeric compounds with chiral derivatizing
reagents, separation of the diastereomers, and conversion to the
pure stereoisomers, and (3) separation of the substantially pure or
enriched stereoisomers directly under chiral conditions.
[0166] Under method (1), diastereomeric salts can be formed by
reaction of enantiomerically pure chiral bases such as, for
example, brucine, quinine, ephedrine, strychnine,
.alpha.-methyl-.beta.-phenylethylamine (amphetamine), and the like
with asymmetric compounds bearing acidic functionality, such as,
for example, carboxylic acid and sulfonic acid. The diastereomeric
salts may be induced to separate by fractional crystallization or
ionic chromatography. For separation of the optical isomers of
amino compounds, addition of chiral carboxylic or sulfonic acids,
such as, for example, camphorsulfonic acid, tartaric acid, mandelic
acid, or lactic acid can result in formation of the diastereomeric
salts.
[0167] Alternatively, by method (2), the substrate to be resolved
is reacted with one enantiomer of a chiral compound to form a
diastereomeric pair (Eliel, E. and Wilen, S. (1994) Stereochemistry
of Organic Compounds, John Wiley & Sons, Inc., p. 322).
Diastereomeric compounds can be formed by reacting asymmetric
compounds with enantiomerically pure chiral derivatizing reagents,
such as, for example, menthyl derivatives, followed by separation
of the diastereomers and hydrolysis to yield the free,
enantiomerically enriched substrate. A method of determining
optical purity involves making chiral esters, such as, for example,
a menthyl ester, e.g., (-) menthyl chloroformate in the presence of
base, or Mosher ester,
.alpha.-methoxy-.alpha.-(trifluoromethyl)phenyl acetate (Jacob III.
(1982) J. Org. Chem. 47:4165), of the racemic mixture, and
analyzing the NMR spectrum for the presence of the two
atropisomeric diastereomers. Stable diastereomers of atropisomeric
compounds can be separated and isolated by normal- and
reverse-phase chromatography following methods for separation of
atropisomeric naphthyl-isoquinolines (Hoye, T., WO 96/15111). By
method (3), a racemic mixture of two enantiomers can be separated
by chromatography using a chiral stationary phase (Chiral Liquid
Chromatography (1989) W. J. Lough, Ed. Chapman and Hall, New York;
Okamoto, (1990) J. of Chromatogr. 513:375-378). Enriched or
purified enantiomers can be distinguished by methods used to
distinguish other chiral molecules with asymmetric carbon atoms,
such as, for example, optical rotation and circular dichroism.
SCHEMES AND EXAMPLES
[0168] General aspects of these exemplary methods are described
below and in the Examples. Each of the products of the following
processes is optionally separated, isolated, and/or purified prior
to its use in subsequent processes.
[0169] A number of exemplary methods for the preparation of
compounds of the disclosure are provided herein, for example, in
the Examples below. These methods are intended to illustrate the
nature of such preparations and are not intended to limit the scope
of applicable methods. Certain compounds of the disclosure can be
used as intermediates for the preparation of other compounds of the
disclosure. In the exemplary methods described herein, the fragment
E-V-- can also be written as R9-. PG represents a protecting group
common for the given functional group that it is attached. The
installation and removal of the protecting group can be
accomplished using standard techniques, such as, for example, those
described in Wuts, P. G. M., Greene, T. Protective Groups in
Organic Synthesis, 4th ed.; John Wiley & Sons, Inc.: Hoboken,
N.J., 2007.
##STR00018##
[0170] Scheme 1 shows a general synthesis of an
E-V--C(.dbd.O)--P--W--P--C(.dbd.O)--V-E molecule of the invention
wherein, for illustrative purposes, E is methoxycarbonylamino. The
treatment of either 1a or 1c with one or two equivalents
respectively of methyl chloroformate under basic conditions (e.g.
sodium hydroxide) provides the molecule 1b or 1d.
##STR00019##
[0171] Scheme 2 shows a general synthesis of an
E-V--C(.dbd.O)--P--W--P--C(.dbd.O)--V-E molecule of the invention
wherein, for illustrative purposes, P is pyrrolidine. Coupling of
amine 2a with acid 2b is accomplished using a peptide coupling
reagent (e.g. HATU) to afford 2c. Alternatively, amine 2d is
coupled with two equivalents of 2b under similar conditions to
provide 2e.
##STR00020## ##STR00021##
[0172] Scheme 6 shows a general synthesis of an
R.sup.1--V--C(.dbd.O)--P--R.sup.2 intermediate wherein, for
illustrative purposes, P is pyrrolidine, R.sup.1 is a generic group
that is depicted as either -E or a amino protecting group, and
R.sup.2 is a generic group that is depicted as
--W--P--C(.dbd.O)--V-E, W--P--C(.dbd.O)--V--NH-PG, --W--P--NH-PG,
or --W--NH-PG. Coupling of amine 6a (or 6d, 6h, 6k) with acid 6b or
6e is accomplished using a peptide coupling reagent (e.g. HATU) to
afford 6c (or 6f, 6g, 6i, 6j, 6l, 6m) respectively.
##STR00022##
[0173] Scheme 7 shows a general synthesis of an
E-V--C(.dbd.O)--R.sup.1 intermediate wherein, for illustrative
purposes, E is methoxycarbonylamino and R.sup.1 is a generic group
that is depicted as either --P--W--P--C(.dbd.O)--V--NH-PG,
--P--W--P-PG, --P--W-PG, --P-PG, or --O-PG. Treatment of 7a (or 7c,
7e, 7g, 7i) with methyl chloroformate under basic conditions (e.g.
sodium hydroxide) provides the molecule 7b (or 7d, 7f, 7h, 7j).
##STR00023##
[0174] Scheme 9 shows a general synthesis of an R.sup.1--P--R.sup.2
intermediate wherein, for illustrative purposes, R.sup.1 is
--C(.dbd.O)--V-E or a protecting group and R.sup.2 is a substituted
benzamidazole. The formation of the benzimidazole is accomplished
by coupling the acid 9b or 9e with an arylamine 9a, using a peptide
coupling reagent such as HATU, to afford 9c or 9d. Cyclization of
the amide in the presence an acid (such as acetic acid) affords the
benzimidazole containing molecule 9d or 9g.
[0175] The formation of multiple benzimidazoles is performed in the
same manner, starting with a bis-diamine to provide the
corresponding bis-benzamidazole.
##STR00024## ##STR00025##
[0176] Scheme 20 shows a general synthesis of an
R.sup.1--P--W--P--R.sup.2 intermediate of the invention wherein,
for illustrative purposes, R.sup.1 and R.sup.2 are independent
protecting groups and W is a two aromatic ring unit constructed via
a transition metal mediated cyclization. Alkylation of phenol 20b
with an alkyl bromide, such as 20a, provides the ether 20c.
Cyclization of the aromatic rings in the presence of a palladium
catalyst provides the compound 20d. Treatment of 20d with
CuBr.sub.2 provides the .alpha.-haloketone 20e, which provides 20f
upon addition of an acid under basic conditions (e.g. Et.sub.3N).
Reaction of 20f with an amine or amine salt (e.g. ammonium acetate)
affords the imidazole containing molecule 20g. Oxidation of 20g,
20i, or 20l can be accomplished by heating in the presence of
MnO.sub.2 to provide 20h, 20j, or 20m, respectively. Conversion of
20g or 20h with a palladium catalyst, such as Pd.sub.2dba.sub.3 and
X-Phos, and a boron source such as bis(pinacolato)diboron provides
the boronic ester 20i or 20j. The boronic ester is coupled with an
appropriate coupling partner (e.g. 20k) using a palladium catalyst,
such as Pd(PPh.sub.3).sub.4 or PdCl.sub.2(dppf), to afford 20l or
20m. For each transition metal mediated cross-coupling reaction,
the roles of the nucleophile and electrophile can be reversed to
provide the same coupling product. Other transition metal mediated
cross couplings that enable the construction of W, but employ
alternative coupling partners and reagents, include, but are not
limited to, the Negishi, Kumada, Stille, and Ullman couplings. For
the preparation of alternate two aromatic ring containing W groups,
this general scheme can be applied through the appropriate choice
of the starting reagents.
##STR00026## ##STR00027##
[0177] Scheme 21 shows a general synthesis of an
R.sup.1--P--W--P--R.sup.2 intermediate of the invention wherein,
for illustrative purposes, R.sup.1 and R.sup.2 are independent
protecting groups and W is a two aromatic ring unit constructed via
a transition metal mediated cyclization. Treatment of 20d with an
activated vinyl reagent (e.g. potassium vinyltrifluoroborate) in
the presence of a palladium catalyst (e.g. palladium acetate and
S-Phos) provides the vinyl compound 21a. Conversion to the
corresponding .alpha.-halo ketone can be accomplished by
bromination with N-bromosuccinimide, followed by oxidation with
MnO.sub.2. Displacement of the .alpha.-halo ketone proceeds by the
addition of an acid under basic conditions (e.g. Et.sub.3N).
Bromination of 21d proceeds upon treatment with pyridinium
tribromide, and is followed by the addition of a second acid under
basic conditions to provide the diester 21e. Reaction of 21e with
an amine or amine salt (e.g. ammonium acetate) affords the
imidazole containing molecule 21f. Oxidation of 21f can be
accomplished in the presence of MnO.sub.2 to provide 21g.
##STR00028##
[0178] Scheme 22 shows a general synthesis of an
E-V--C(.dbd.O)--P--W--P--R intermediate of the invention wherein,
for illustrative purposes, R is a protecting group and W is a two
aromatic ring unit. Displacement of the .alpha.-halo ketone 21b
proceeds by the addition of an acid under basic conditions (e.g.
Et.sub.3N). Bromination of 22b proceeds upon treatment with
pyridinium tribromide, and is followed by the addition of a second
acid under basic conditions to provide the diester 22c. Reaction of
22c with an amine or amine salt (e.g. ammonium acetate) affords the
imidazole containing molecule 22d. Oxidation of 22d can be
accomplished in the presence of MnO.sub.2 to provide 22e.
##STR00029##
[0179] Scheme 23 shows a general synthesis of an
E-V--C(.dbd.O)--P--W--P--R intermediate of the invention wherein,
for illustrative purposes, R is a protecting group and W is a two
aromatic ring unit. Displacement of the .alpha.-halo ketone 21d
proceeds by the addition of an acid under basic conditions (e.g.
Et.sub.3N). Reaction of 23a with an amine or amine salt (e.g.
ammonium acetate) affords the imidazole containing molecule 23b.
Oxidation of 23b can be accomplished in the presence of MnO.sub.2
to provide 23c.
##STR00030##
[0180] Scheme 25 shows a general synthesis of an
E-V--C(.dbd.O)--P--W--P--C(.dbd.O)--V-E molecule of the invention
wherein, for illustrative purposes, E is ethylcarbonylamino. The
treatment of either 25a or 25c with one or two equivalents
respectively of propionyl chloride under basic conditions (e.g.
sodium hydroxide) provides the molecule 25b or 25d.
##STR00031##
[0181] Scheme 26 shows a general synthesis of an
E-V--C(.dbd.O)--P--R and an R.sup.1--P--R molecule of the invention
wherein, for illustrative purposes R is a haloimidazole. Treatment
of the aldehyde 26a with glyoxal, in the presence of ammonium
hydroxide provides the imidazole 26b. Treatment with either
N-bromosuccinamide or iodine provides the corresponding
haloimidazole 26c and 26d respectively. Separation from the
corresponding bis-halogenated compound can be accomplished by
preparative HPLC chromatography. The conversion of the
bis-haloimidazole to the mono-haloimidazole can also be
accomplished upon heating in the presence of sodium sulfite.
Further functionalization of the P group can be accomplished upon
removal of the protecting group and coupling with an appropriate
acid (E-V--C(.dbd.O)--OH).
##STR00032##
[0182] Scheme 27 shows an alternate general synthesis of an
R.sup.1--P--W--P--R.sup.2 intermediate of the invention wherein,
for illustrative purposes, R.sup.1 and R.sup.2 are independent
protecting groups and W is a two aromatic ring unit constructed via
a transition metal mediated cyclization. Bromination of 21b with a
brominating agent (i.e. pyridinium tribromide) provides the
dibromide 27a. Displacement of the primary bromide then proceeds by
the addition of an acid under basic conditions (e.g.
K.sub.2CO.sub.3) to provide 21d. Conversion to 21f or 21g can be
accomplished following methods described in Scheme 21.
##STR00033##
[0183] Scheme 28 shows an alternate general synthesis of an
E-V--C(.dbd.O)--P--W--P--R intermediate of the invention wherein,
for illustrative purposes, R is a protecting group and W is a two
aromatic ring unit. Bromination of 21b with a brominating agent
(i.e. pyridinium tribromide) provides the dibromide 27a.
Displacement of the primary bromide then proceeds by the addition
of an acid under basic conditions (e.g. K.sub.2CO.sub.3) to provide
22d. Conversion to 22d or 22e can be accomplished following methods
described in Scheme 22.
Specific Embodiments
[0184] In one embodiment, provided is a compound of formula
(I):
E.sup.1a-V.sup.1a--C(.dbd.O)--P.sup.1a--W.sup.1a--P.sup.1b--C(.dbd.O)--V-
.sup.1b-E.sup.1b (I)
[0185] wherein: [0186] W.sup.1a is
##STR00034##
[0187] and W.sup.1a is optionally substituted with one or more
groups independently selected from halo, alkyl, haloalkyl,
optionally substituted aryl, optionally substituted heterocycle,
and cyano; [0188] Y.sup.5 is --O--CH.sub.2--, --CH.sub.2--O--,
--O--C(.dbd.O)--, or --C(.dbd.O)--O--; X.sup.5 is
--CH.sub.2--CH.sub.2-- or --CH.dbd.CH--; [0189] E.sup.1a is
--N(H)(alkoxycarbonyl), --N(H)(cycloalkylcarbonyl) or
--N(H)(cycloalkyloxycarbonyl); or E.sup.1a-V.sup.1a taken together
are R.sup.9a; [0190] E.sup.1b is --N(H)(alkoxycarbonyl),
--N(H)(cycloalkylcarbonyl) or --N(H)(cycloalkyloxycarbonyl); or
E.sup.1b-V.sup.1b taken together are R.sup.9b; [0191] V.sup.1a and
V.sup.1b are each independently selected from:
[0191] ##STR00035## ##STR00036## [0192] P.sup.1a is selected
from:
[0192] ##STR00037## ##STR00038## ##STR00039## [0193] P.sup.1b is
selected from:
##STR00040## ##STR00041## ##STR00042##
[0194] and [0195] R.sup.9a and R.sup.9b are each independently
selected from:
[0195] ##STR00043## [0196] or a pharmaceutically acceptable salt or
prodrug thereof; [0197] provided that when Y.sup.5 is
--O--CH.sub.2--, or --CH.sub.2--O--, then at least one of the
following occurs: [0198] (1) at least one of V.sup.1a and V.sup.1b
is selected from (af), (ag), (ah), (ai), (aj), (ak), (al), (am),
(an), (ao), (ap) or (aq); or [0199] (2) P.sup.1a is selected from
(be), (bf), (bg), (bh), (bi), (bj), (bk), (bl), (bm), (bn), (bo),
(bq) or (br); or [0200] (3) P.sup.1b is selected from (be), (bf),
(bg), (bh), (bi), (bj), (bk), (bl), (bm), (bn), (bo), (bp), (bq) or
(br).
[0201] In one embodiment, the compound of formula (I) is
represented by formula:
##STR00044## [0202] wherein the imidazole ring shown in formula
(A1), (A2), (A3) and (A4) is optionally substituted with one or
more groups independently selected from halo, haloalkyl, cyano, and
alkyl; [0203] or a pharmaceutically acceptable salt or prodrug
thereof.
[0204] In one embodiment, the compound of formula (I) is
represented by formula:
##STR00045## [0205] wherein the imidazole ring shown in formula
(A2) and (A4) is optionally substituted with one or more groups
independently selected from halo, haloalkyl, cyano, and alkyl;
[0206] or a pharmaceutically acceptable salt or prodrug
thereof.
[0207] In one embodiment, at least one of E.sup.1a and E.sup.1b is
--N(H)(alkoxycarbonyl). In one embodiment, at least one of E.sup.1a
and E.sup.1b is --N(H)C(.dbd.O)OMe. In another embodiment, both of
E.sup.1a and E.sup.1b are --N(H)C(.dbd.O)OMe.
[0208] In one embodiment, at least one of E.sup.1a and E.sup.1b is
--N(H)(cycloalkylcarbonyl) or --N(H)(cycloalkyloxycarbonyl). In one
embodiment, at least one of E.sup.1a and E.sup.1b is
cyclopropylcarbonylamino, cyclobutylcarbonylamino,
cyclopropyloxycarbonylamino or cyclobutyloxycarbonylamino. In
another embodiment, E.sup.1a and E.sup.1b are each independently
selected from cyclopropylcarbonylamino, cyclobutylcarbonylamino,
cyclopropyloxycarbonylamino and methoxycarbonylamino.
[0209] In one embodiment, at least one of V.sup.1a and V.sup.1b
is:
##STR00046##
[0210] In one embodiment, E.sup.1a-V.sup.1a taken together are
R.sup.9a or wherein E.sup.1b-V.sup.1b taken together are
R.sup.9b.
[0211] In one embodiment, at least one of P.sup.1a and P.sup.1b is
selected from:
##STR00047##
[0212] In one embodiment, P.sup.1a and P.sup.1b are each
independently selected from:
##STR00048##
[0213] In one embodiment, at least one of
--V.sup.1a--C(.dbd.O)--P.sup.1a-- and
--P.sup.1b--C(.dbd.O)--V.sup.1b-- is:
##STR00049##
[0214] In another embodiment, at least one of
--V.sup.1a--C(.dbd.O)--P.sup.1a-- and
--P.sup.1b--C(.dbd.O)--V.sup.1b-- is:
##STR00050## ##STR00051##
[0215] In yet another embodiment, --V.sup.1a--C(.dbd.O)--P.sup.1a--
and --P.sup.1b--C(.dbd.O)--V.sup.1b-- are each independently:
##STR00052## ##STR00053##
[0216] In one embodiment, one of --V.sup.1a--C(.dbd.O)--P.sup.1a--
and --P.sup.1b--C(.dbd.O)--V.sup.1b-- is:
##STR00054## ##STR00055##
[0217] and the other of --V.sup.1a--C(.dbd.O)--P.sup.1a-- and
--P.sup.1b--C(.dbd.O)--V.sup.1b-- is:
##STR00056## ##STR00057##
[0218] In one embodiment, the disclosure provides a compound of
formula:
##STR00058## ##STR00059## ##STR00060## ##STR00061## ##STR00062##
##STR00063## ##STR00064## ##STR00065## ##STR00066## ##STR00067##
##STR00068## ##STR00069## ##STR00070## ##STR00071## ##STR00072##
##STR00073## ##STR00074## ##STR00075## ##STR00076## ##STR00077##
##STR00078## ##STR00079## ##STR00080## ##STR00081## ##STR00082##
[0219] or a pharmaceutically acceptable salt or prodrug
thereof.
[0220] The disclosure will now be illustrated by the following
non-limiting Examples. The following abbreviations are used
throughout the specification, including the Examples.
TABLE-US-00001 (aq) Aqueous (g) Gas (s) Solid .degree. C. Degree
Celsius Ac Acetate ACN Acetonitrile apprx Approximate Bis-
Bis(pinacolato)diboron pinB/(Bpin).sub.2/(pinB).sub.2 BOC/Boc
tert-Butoxycarbonyl calc'd Calculated CC.sub.50 50% Cytotoxicity
concentration COMU 1-[(1-(Cyano-2-ethoxy-2-
oxoethylideneaminooxy)dimethyl- aminomorpholino)] uronium
hexafluorophosphate d Doublet dba dibenzalacetone DCM
Dichloromethane dd Doublet of doublets ddd Doublet of doublet of
doublets DIPEA/DIEA N,N-Diisopropylethylamine DMA
N,N-Dimethylacetamide DMAP 4-Dimethylaminopyridine DME Dimethoxy
ethane DMEM Eagle's minimal essential medium DMF Dimethylformamide
DMSO/dmso Dimethylsulfoxide dppf 1,1'-bis(diphenylphosphanyl)
ferrocene dt Doublet of triplets EC.sub.50 Half maximal effective
concentration ESI Electrospray ionization Et Ethyl ext. External
FBS Fetal bovine serum g Gram HATU
2-(1H-7-Azabenzotriazol-1-yl)-1,1,3,3- tetramethyl uronium
hexafluorophosphate Methanaminium HPLC High performance liquid
chromatography hr/h Hour Hz Hertz J Coupling constant LCMS Liquid
chromatography mass spectrometry M Molar m Multiplet m/z Mass to
charge M+ Mass peak Me Methyl mg Milligram MHz Megahertz min Minute
mL Milliliter mmol Millimole Moc Methoxycarbonyl MS Mass
spectrometry MTBE Methyl tert-butyl ether N Normal NADPH
Nicotinamide adenine dinucleotide phosphate NBS N-Bromosuccinimide
NMM N-Methylmorpholine NMR Nuclear magnetic resonance o/n Over
night Papp Apparent permeability PBS Phosphate buffer system Pd/C
Palladium on carbon Ph Phenyl Phg/PhGly Phenyl glycine Piv Pivalate
Pro Proline pyr Pyridine q Quartet qd Quartet of doublets quant
Quantitative quint Quintet rt/RT Room temperature s Singlet SPhos
2-Dicyclohexylphosphino-2',6'- dimethoxybiphenyl t Triplet t-Bu
tert-Butyl TEMPO (2,2,6,6-Tetramethyl-piperidin-1-yl)oxyl Tf
Trifluoromethanesulfonate TFA Trifluoroacetic acid THF
Tetrahydrofuran Thr Threonine TLC Thin layer chromatography tol.
Toluene UV Ultraviolet Val Valine w/v Weight to volume w/w Weight
to weight X-Phos/XPOS/Xphos 2-Dicyclohexylphosphino-2',4',6'-
triisopropylbiphenyl .delta. Chemical shift .mu.g Microgram .mu.L
Microliter
EXAMPLES
Example AA
##STR00083## ##STR00084##
[0221] 3,4-dihydronaphthalen-1(2H)-one
[0222] To a stirred solution of 7-hydroxy-1-tetralone (13.9 g, 85.7
mmol) and 1-bromo-2-(bromomethyl)-4-chlorobenzene (25.6 g, 90.0
mmol) in dimethylformamide (850 mL) was added potassium carbonate
(24 g, 172 mmol). The reaction was stirred under argon for 18 hours
then diluted with ethyl acetate (1 L). The organics were washed
three times with water and once with brine. The organic layer was
then dried with magnesium sulfate, filtered and concentrated. To
the resulting oil was added methanol (500 mL) and the suspension
was agitated for thirty minutes.
7-(2-bromo-5-chlorobenzyloxy)-(27.8 g, 89% yield) was isolated by
filtration.
3-chloro-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one
[0223] To a 1 L flask containing palladium(II) pivalate (1.18 g,
3.8 mmol), tri(4-fluorophenyl)phosphine (1.20 g, 3.8 mmol), pivalic
acid (2.33 g, 22.8 mmol) and potassium carbonate (31.8 g, 228 mmol)
was added a solution of
7-(2-bromo-5-chlorobenzyloxy)-3,4-dihydronaphthalen-1 (2H)-one
(27.8 g, 76.2 mmol) in dimethyacetamide (380 mL). The flask was
evacuated and backfilled with argon 5 times and then stirred under
argon at 60.degree. C. for 24 hours. The reaction was cooled to
room temperature and diluted with MTBE and water. The resulting
biphasic mixture was stirred for 3 hours and filtered through
Celite, rinsing with MTBE. The organic layer of the filtrate was
separated and then washed twice with water and once with brine. The
organics were then dried with magnesium sulfate, filtered,
concentrated and purified by flash column chromatography
(Hexanes/DCM) to yield
3-chloro-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one (14.4 g,
67% yield) as an off-white solid.
9-bromo-3-chloro-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one
[0224] To a mixture of
3-chloro-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one (14.8 g, 52
mmol) in chloroform (50 mL) and ethyl acetate (50 mL) was added
copper(II) bromide (24.3 g, 104 mmol). The reaction was heated to
80.degree. C. for 2 hours and then cooled to room temperature. The
mixture was diluted with dichloromethane and washed twice with a
5:1 solution of saturated aqueous ammonium chloride and aqueous
ammonium hydroxide (.about.38%), and washed once with water. The
organic layer was dried with magnesium sulfate, filtered and
concentrated to yield
9-bromo-3-chloro-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one
(18.5 g, >95% yield) with >95% purity.
[0225] Note: This reaction is not always this clean. Sometimes
there is over-bromination and sometimes there is significant
starting material. These impurities can be removed by flash column
chromatography.
tert-butyl
2-(9-chloro-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,-
2-d]imidazol-2-yl)pyrrolidine-1-carboxylate
[0226] To a solution of
(1R)-2-(tert-butoxycarbonyl)cyclopentanecarboxylic acid (10.17 g,
47.25 mmol) and
9-bromo-3-chloro-10,11-dihydro-6H-naphtho[2,3-c]chromen-8(9H)-one
(5.7 mg, 15.7 mmol) in acetonitrile (50 mL) was added
diisopropylethylamine (11.11 mL, 64 mmol). The reaction was stirred
at 50.degree. C. for 4 hours and was then diluted with ethyl
acetate. The organics were washed with water and brine, dried
(MgSO.sub.4) and concentrated. The resulting crude residue was
purified by flash chromatography to yield (2S)-1-tert-butyl
2-(3-chloro-8-oxo-8,9,10,11-tetrahydro-5H-naphtho[c,g]chromen-9-yl)
pyrrolidine-1,2-dicarboxylate (4.52 g, 58%). To a solution of
(2S)-1-tert-butyl
2-(3-chloro-8-oxo-8,9,10,11-tetrahydro-6H-naphtho[2,3-c]chromen-9-yl)
pyrrolidine-1,2-dicarboxylate (3.27 mg, 6.56 mmol) in a mixture of
toluene (11 mL) and 2-methoxyethanol (0.7 mL) was added ammonium
acetate (5.06 g, 65.6 mmol). The reaction mixture was heated to
110.degree. C. for 3 hours, cooled to room temperature and diluted
with ethyl acetate. The organics were washed with water and brine,
dried (Na.sub.2SO.sub.4), and concentrated. The crude residue was
purified by flash chromatography to yield tert-butyl
2-(9-chloro-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]imidaz-
ol-2-yl)pyrrolidine-1-carboxylate (1.95 g, 61%). LCMS-ESI.sup.+:
calculated for C27H28ClN.sub.3O3.sub.4 2: 477.98; observed
[M+1].sup.+: 478.47
tert-butyl
2-(9-chloro-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imi-
dazol-2-yl)pyrrolidine-1-carboxylate
[0227] To a solution of tert-butyl
2-(9-chloro-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]imidaz-
ol-2-yl)pyrrolidine-1-carboxylate (1.9 g, 3.96 mmol) in
dichloromethane (35 mL) was added manganese(IV) oxide (17 g, 198
mmol). The reaction mixture was stirred at room temperature for 18
hours, diluted with ethyl acetate. The organics were washed with
water and brine, dried (Na.sub.2SO.sub.4), and concentrated. The
crude residue was purified by flash chromatography to yield
tert-butyl
2-(9-chloro-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl-
)pyrrolidine-1-carboxylate (1.52 g, 81%). LCMS-ESI.sup.+:
calculated for C27H26ClN3O3.sub.42: 475.9; observed [M+1].sup.+:
476.45.
tert-butyl
2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,11-dihydro-
isochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]pyrrolidine-1-carboxylat-
e
[0228] A degassed mixture of tert-butyl
2-(9-chloro-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl-
)pyrrolidine-1-carboxylate (1.52 g, 3.17 mmol),
bis(pinacolato)diboron (1.21 g, 4.75 mmol), potassium acetate (934
mg, 9.52 mmol), tris(dibenzylideneacetone)palladium (116 mg, 0.13
mmol) and
2-dicyclohexylphosphino-2',4',6'-tri-i-propyl-1,1'-biphenyl (121
mg, 0.08 mmol) in 1,4-dioxane (16 mL) was heated to 90.degree. C.
for 1.5 hours, cooled to room temperature and diluted with ethyl
acetate. The organics were washed with water and brine, dried
(Na.sub.2SO.sub.4), and concentrated. The crude residue was
purified by flash chromatography to yield tert-butyl
2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,11-dihydroisochromen-
o[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]pyrrolidine-1-carboxylate
(1.7 g, 94%)
tert-butyl
2-[9-(2-{1-[N-(methoxycarbonyl)valyl]pyrrolidin-2-yl}-1H-imidaz-
ol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]pyr-
rolidine-1-carboxylate
[0229] To a solution of methyl
(S)-1-((S)-2-(5-bromo-1H-imidazol-2-yl)pyrrolidin-1-yl)-3-methyl-1-oxobut-
an-2-ylcarbamate (1.48 g, 3.97 mmol), tert-butyl
2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,11-dihydroisochromen-
o[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]pyrrolidine-1-carboxylate
(1.88 g, 1.48 mmol), tetrakis(triphenyl phosphine)palladium(0) (191
mg, 0.16 mmol) and dichloro[1,1'-bis(diphenylphosphino)
ferrocene]palladium(II) (242 mg, 0.33 mmol) in a mixture of
1,2-dimethoxyethane (37.0 mL) and dimethylformamide (6 mL) was
added a solution of potassium carbonate (2M in water, 5 mL, 9.93
mmol). The resulting mixture was degassed and then heated to
85.degree. C. under argon for 18 hours. After cooling to room
temperature, the reaction was diluted with ethyl acetate. The
organics were washed with water and brine, dried
(Na.sub.2SO.sub.4), and concentrated. The crude residue was
purified by flash chromatography to yield tert-butyl
2-[9-(2-{1-[N-(methoxycarbonyl)valyl]pyrrolidin-2-yl}-1H-imidazol-5-yl)-1-
,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]pyrrolidine-1-
-carboxylate (1.45 mg, 59%). LCMS-ESI.sup.+: calculated for
C.sub.41H.sub.47N.sub.7O6.sub.73 733.86; observed [M+1].sup.+:
734.87.
[1-(2-{5-[2-(1-{[(methoxycarbonyl)amino](phenyl)acetyl}pyrrolidin-2-yl)-1,-
11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl]-1H-imidazol-2-
-yl}pyrrolidin-1-yl)-3-methyl-1-oxobutan-2-yl]carbamic acid
[0230] A solution of tert-butyl
2-[9-(2-{1-[N-(methoxycarbonyl)valyl]pyrrolidin-2-yl}-1H-imidazol-5-yl)-1-
,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]pyrrolidine-1-
-carboxylate (462 mg, 0.63 mmol), ethanol (6 mL) and concentrated
HCl (2 mL) was heated to 60.degree. C. for 1 hour. The reaction was
concentrated and the crude material dissolved in DCM (6 mL). This
solution was concentrated and to this material was added a solution
of (R)-2-(methoxycarbonylamino)-2-phenylacetic acid (172 mg, 0.82
mmol) and COMU (311 mg, 073 mmol) in DMF (6 mL). To the resulting
solution was added diisopropylethylamine (330 .mu.L, 1.89 mmol).
After stirring for 18 hours at room temperature, the reaction was
diluted with ethyl acetate, washed with water and brine, dried
(Na.sub.2SO.sub.4), concentrated and purified by preparative
reverse phase HPLC (Gemini, 15 to 45% ACN/H.sub.2O+0.1% TFA). The
product fractions were lyophilized to give
[1-(2-{5-[2-(1-{[(methoxycarbonyl)amino](phenyl)acetyl}pyrrolidin-2-yl)-1-
,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl]-1H-imidazol--
2-yl}pyrrolidin-1-yl)-3-methyl-1-oxobutan-2-yl]carbamic acid (231
mg, 45%). LCMS-ESI.sup.+: calculated for C46H48N8O7.sub.8: 824.92;
observed [M+1].sup.+: 826.00
Example AB
##STR00085##
[0231] (2S,4S)-1-tert-butyl 2,4-dimethyl
pyrrolidine-1,2,4-tricaroxylate
[0232] To a solution of (2S,4S)-1-tert-butyl 2-methyl
4-cyanopyrrolidine-1,2-dicarboxylate (9.0 g, 35.4 mmol) in MeOH
(196 mL) was added HCl (4M in 1,4-dioxane, 100 mL, 403 mmol). The
solution was stirred at room temperature for 16h and concentrated
in vacuo. The crude intermediate was dissolved in EtOAc (180 mL)
and basified with aqueous bicarbonate (sat.). Di-tert-butyl
dicarbonate (8.5 g, 38.9 mmol) was added and the biphasic solution
was stirred at room temperature for 12h. The layers were then
separated and the aqueous layer was back extracted with EtOAc. The
combined organic layers were washed with brine, dried over
Na.sub.2SO.sub.4, and concentrated. The crude oil was purified by
silica gel chromatography (15% to 40% to 100% EtOAc/Hexanes) to
provide (2S,4S)-1-tert-butyl 2,4-dimethyl
pyrrolidine-1,2,4-tricarboxylate (9.56 g, 94%).
(3S,5S)-1-(tert-butoxycarbonyl)-5-(methoxycarbonyl)pyrrolidine-3-carboxyli-
c acid
[0233] To a solution of (2S,4S)-1-tert-butyl 2,4-dimethyl
pyrrolidine-1,2,4-tricarboxylate (9.56 g, 33.3 mmol) in THF (70 mL)
at 0.degree. C. (external temperature, ice bath) was added NaOH (1N
aqueous, 33 mL, 33.3 mmol) dropwise over 15 min. The solution was
stirred at 0.degree. C. for 5h before acidification with HCl (1N).
The solution was extracted with EtOAc (3.times.). The combined
organic layers were dried over Na.sub.2SO.sub.4 and concentrated.
The crude oil was purified by silica gel chromatography (2% to 5%
to 10% MeOH/CH.sub.2Cl.sub.2) to provide
(3S,5S)-1-(tert-butoxycarbonyl)-5-(methoxycarbonyl)pyrrolidine-3--
carboxylic acid (6.38g, 70%).
(2S,4S)-1-tert-butyl 2-methyl
4-(hydroxymethyl)pyrrolidine-1,2-dicarboxylate
[0234] To a solution of
(3S,5S)-1-(tert-butoxycarbonyl)-5-(methoxycarbonyl)pyrrolidine-3-carboxyl-
ic acid (6.38 g, 23.3 mmol) in THF (116 mL) at 0.degree. C.
(external temperature, ice bath) was added Et.sub.3N (4.9 mL, 35.0
mmol) and ethyl chloroformate (2.7 mL, 28.0 mmol). The resulting
solution was stirred at 0.degree. C. for 45 min, during which time
a white precipitate forms. The reaction mixture was filtered
through celite and concentrated.
[0235] The crude intermediate was dissolved in THF (59 mL) and
cooled to 0.degree. C. (external temperature, ice bath). NaBH.sub.4
(4.41 g, 116.7 mmol) in H.sub.2O (59 mL) was slowly added and the
resulting solution was stirred at 0.degree. C. for 2 h. The
reaction mixture was diluted with EtOAc and washed with H.sub.2O.
The aqueous layer was backextracted with EtOAc. The combined
organic layers were dried over Na.sub.2SO.sub.4 and concentrated.
The crude oil was purified by silica gel chromatography (42% to 69%
to 100% EtOAc/Hexanes) to provide (2S,4S)-1-tert-butyl 2-methyl
4-(hydroxymethyl)pyrrolidine-1,2-dicarboxylate (3.63 g, 60%).
(2S,4S)-1-tert-butyl 2-methyl
4-(methoxymethyl)pyrrolidine-1,2-dicarboxylate
[0236] To a solution of (2S,4S)-1-tert-butyl 2-methyl
4-(hydroxymethyl)pyrrolidine-1,2-dicarboxylate (2.57 g, 9.9 mmol)
in CH.sub.2Cl.sub.2 (50 mL) was added AgOTf (4.07 g, 15.8 mmol) and
2,6-di-tert-butylpyridine (4.4 mL, 19.8 mmol). The reaction mixture
was cooled to 0.degree. C. (external temperature, ice bath) and MeI
(0.98 mL, 15.8 mmol) was slowly added. The resulting slurry was
stirred at 0.degree. C. for 1.5 h and at room temperature for 1.5
h. The slurry was diluted with CH.sub.2Cl.sub.2 and filtered
through celite. The filtrate was concentrated to dryness, dissolved
in Et.sub.2O, and washed with HCl (1N) and brine. The aqueous
layers were backextracted with Et.sub.2O and the combined organic
layers were dried over Na.sub.2SO.sub.4 and concentrated. The crude
oil was purified by silica gel chromatography (10% to 75% to 100%
EtOAc/Hexanes) to provide (2S,4S)-1-tert-butyl 2-methyl
4-(methoxymethyl)pyrrolidine-1,2-dicarboxylate (2.11 g, 78%).
.sup.1H-NMR: 400 MHz, (CDCl.sub.3) .delta.: (mixture of rotomers,
major reported) 4.20 (t, 1H), 3.71 (s, 3H), 3.67 (m, 1H), 3.34 (m,
2H), 3.30 (s, 3H), 3.16 (t, 1H), 2.43 (m, 2H), 1.74 (m, 1H), 1.38
(s, 9H).
(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrrolidine-2-carboxylic
acid
[0237] To a solution of (2S,4S)-1-tert-butyl 2-methyl
4-(methoxymethyl)pyrrolidine-1,2-dicarboxylate (2.11 g, 7.7 mmol)
in a mixture of THF (38 mL) and MeOH (15 mL) was added LiOH (2.5 M
aqueous, 15 mL, 38.6 mmol). The resulting solution was stirred at
room temperature for 2h, and acidified with aqueous HCl (1N). The
desired product was extracted with CH.sub.2Cl.sub.2 (4.times.). The
combined organic layers were dried over Na.sub.2SO.sub.4 and
concentrated to provide
(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrrolidine-2-carboxylic
acid (2.0 g, 99%). .sup.1H-NMR: 400 MHz, (CDCl.sub.3) .delta.:
(mixture of rotomers, major reported) 4.33 (t, 1H), 3.65 (m, 1H),
3.35 (m, 2H), 3.32 (s, 3H), 3.16 (t, 1H), 2.45 (m, 2H), 2.12 (m,
1H), 1.46 (s, 9H).
Example AB-1
##STR00086## ##STR00087##
[0238]
(2S,4S)-tert-butyl-2-(9-chloro-4,5-dihydro-5H-naphtho[2,3-c]chromen-
o[8,9-d]imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate
[0239] To a solution of
((S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrrolidine-2-carboxylic
acid (5.9 g, 23.1 mmol) and
9-bromo-3-chloro-10,11-dihydro-5H-naphtho[c,g]chromen-8(9H)-one
(5.6 mg, 15.4 mmol) in acetonitrile (60 mL) was added
diisopropylethylamine (5.35 mL, 30.8 mmol). The reaction was
stirred at 50.degree. C. for 18 hours and was then diluted with
ethyl acetate. The organics were washed with water and brine, dried
(MgSO.sub.4) and concentrated. The resulting crude residue was
purified by flash chromatography to yield
(2S)-1-tert-butyl-2-(3-chloro-8-oxo-8,9,10,11-tetrahydro-6H-naphtho[2,3-c-
]chromen-9-yl)-4(methoxymethyl) pyrrolidine-1,2-dicarboxylate (5.12
g, 61%). To a solution of (2S)-1-tert-butyl-2-(3-chloro-8-oxo-8,9,
10,11-tetrahydro-6H-naphtho[2,3-c]chromen-9-yl)-4(methoxymethyl)pyrrolidi-
ne-1,2-dicarboxylate (5.11 mg, 9.42 mmol) in a mixture of toluene
(94 mL) and 2-methoxyethanol (0.1 mL) was added ammonium acetate
(23.5 g, 304 mmol). The reaction mixture was heated to 110.degree.
C. for 18 hours, cooled to room temperature and diluted with ethyl
acetate. The organics were washed with water and brine, dried
(Na.sub.2SO.sub.4), and concentrated. The crude residue was
purified by flash chromatography to yield (2S,4R)-tert-butyl
2-(9-chloro-4,5-dihydro-5H-naphtho[c,g]chromeno[8,9-d]imidazol-2-yl)-4-(m-
ethoxymethyl)pyrrolidine-1-carboxylate (1.05g, 21%) and
(2S,4S)-tert-butyl-2-(9-chloro-4,5-dihydro-6H-naphtho[2,3-c]chromeno[8,9--
d]imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate (2.0 g,
41%). LCMS-ESI.sup.+: calculated for
C.sub.29H.sub.32ClN.sub.3O.sub.42: 522.0; observed [M+1].sup.+:
522.2.
(2S,4S)-tert-butyl-2-(9-chloro-5H-naphtho[c,g]chromeno[8,9-d]imidazol-2-yl-
)-4-(methoxymethyl)pyrrolidine-1-carboxylate
[0240] To a solution of
(2S,4S)-tert-butyl-2-(9-chloro-4,5-dihydro-5H-naphtho[c,g]chromeno[8,9-d]-
imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate (1.99 g,
3.82 mmol) in dichloromethane (30 mL) was added manganese(IV) oxide
(10 g, 115 mmol). The reaction mixture was stirred at room
temperature for 18 hours, diluted with ethyl acetate. The organics
were washed with water and brine, dried (Na.sub.2SO.sub.4), and
concentrated. The crude residue was purified by flash
chromatography to yield
(2S,4S)-tert-butyl-2-(9-chloro-6H-naphtho[2,3-c]chromeno[8,9-d]imidazol-2-
-yl)-4-methoxymethyl)pyrrolidine-1-carboxylate (1.05g, 21%) and
(2S,4S)-tert-butyl-2-(9-chloro-4,5-dihydro-6H-naphtho[2,3-c]chromeno[8,9--
d]imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate (1.64
g, 82%). LCMS-ESI.sup.+: calculated for
C.sub.29H.sub.30ClN.sub.3O.sub.42: 520.02; observed [M+1].sup.+:
520.97.
(2S,4S)-tert-butyl-4-(methoxymethyl)-2-(9-(4,4,5,5-tetramethyl-1,3,2-dioxa-
borolan-2-yl)-5H-naphtho[c,g]chromeno[8,9-d]imidazol-2-yl)pyrrolidine-1-ca-
rboxylate
[0241] A degassed mixture
of--(2S,4S)-tert-butyl-2-(9-chloro-5H-naphtho[c,g]chromeno[8,9-d]imidazol-
-2-yl)-4-(methoxymethyl) pyrrolidine-1-carboxylate (649 mg 1.25
mmol), bis(pinacolato)diboron (635 mg, 2.5 mmol), potassium acetate
(368 mg, 3.7 mmol), tris(dibenzylideneacetone)palladium (46 mg,
0.05 mmol) and
2-dicyclohexylphosphino-2',4',6'-tri-i-propyl-1,1'-biphenyl (60 mg,
0.12 mmol) in 1,4-dioxane (7 mL) was heated to 90.degree. C. for 3
hours, cooled to room temperature and diluted with ethyl acetate.
The organics were washed with water and brine, dried
(Na.sub.2SO.sub.4), and concentrated. The crude residue was
purified by flash chromatography to yield (2S,4S)-tert-butyl
4-(methoxymethyl)-2-(9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5H-n-
aphtho[c,g]chromeno[8,9-d]imidazol-2-yl)pyrrolidine-1-carboxylate
(467 mg, 61%) LCMS-ESI.sup.+: calculated for
C.sub.35H.sub.42BN.sub.3O.sub.6: 611.54; observed [M+1].sup.+:
612.96.
(2S,4S)-tert-butyl
2-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)pyrrolidin--
2-yl)-1H-imidazol-5-yl)-5H-naphtho[c,g]chromeno[8,9-d]imidazol-2-yl)-4(met-
hoxymethyl)pyrrolidine-1-carboxylate
[0242] To a solution of (2S,4S)-tert-butyl
4-(methoxymethyl)-2-(9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5H-n-
aphtho[c,g]chromeno[8,9-d]imidazol-2-yl)pyrrolidine-1-carboxylate
(467 mg, 0.76 mmol), methyl
(S)-1-((S)-2-(5-bromo-1H-imidazol-2-yl)pyrrolidin-1-yl)-3-methyl-1-oxobut-
an-2-ylcarbamate (342 mg, 0.92 mmol), tetrakis(triphenylphosphine)
palladium(0) (44 mg, 0.04 mmol) and
dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) (56 mg,
0.07 mmol) in a mixture of 1,2-dimethoxyethane (11.0 mL) and
dimethylformamide (1.9 mL) was added a solution of potassium
carbonate (2M in water, 1.15 mL, 2.29 mmol). The resulting mixture
was degassed and then heated to 85.degree. C. under argon for 18
hours. After cooling to room temperature, the reaction was diluted
with ethyl acetate. The organics were washed with water and brine,
dried (Na.sub.2SO.sub.4), and concentrated. The crude residue was
purified by flash chromatography to yield (2S,4S)-tert-butyl
2-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)pyrrolidin--
2-yl)-1H-imidazol-5-yl)-5H-naphtho[c,g]chromeno[8,9-d]imidazol-2-yl)-4-(me-
thoxymethyl)pyrrolidine-1-carboxylate (180 mg, 67%).
LCMS-ESI.sup.+: calculated for C.sub.43H.sub.51N.sub.7O.sub.73
777.91; observed [M+1].sup.+: 778.84.
methyl
{2-[2-{9-[2-(1-{2-[(methoxycarbonyl)amino]-3-methylbutanoyl}pyrroli-
din-2-yl)-1H-imidazol-5-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2--
d]imidazol-2-yl}-4-(methoxymethyl)pyrrolidin-1-yl]-2-oxo-1-phenylethyl}car-
bamate
[0243] A solution of (2S,4S)-tert-butyl
2-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)pyrrolidin--
2-yl)-1H-imidazol-5-yl)-5H-naphtho[c,g]chromeno[8,9-d]imidazol-2-yl)-4-(me-
thoxymethyl)pyrrolidine-1-carboxylate (196 mg, 0.25 mmol), ethanol
(3 mL) and concentrated HCl (1 mL) was heated to 60.degree. C. for
1 hour. The reaction was concentrated and the crude material
dissolved in DCM (6 mL). This solution was concentrated and to this
material was added a solution of
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid (69 mg, 0.33 mmol)
and COMU (124 mg, 029 mmol) in DMF (4 mL). To the resulting
solution was added diisopropylethylamine (130 .mu.L, 0.76 mmol).
After stirring for 2 hours at room temperature, the reaction was
diluted with ethyl acetate, washed with water and brine, dried
(Na.sub.2SO.sub.4), concentrated and purified by preparative
reverse phase HPLC (Gemini, 15 to 45% ACN/H.sub.2O+0.1% TFA). The
product fractions were lyophilized to give methyl
{2-[2-{9-[2-(1-{2-[(methoxycarbonyl)amino]-3-methylbutanoyl}pyrrol-
idin-2-yl)-1H-imidazol-5-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-
-d]imidazol-2-yl}-4-(methoxymethyl)pyrrolidin-1-yl]-2-oxo-1-phenylethyl}ca-
rbamate (84 mg, 39%). LCMS-ESI.sup.+: calculated for
C.sub.48H.sub.52N.sub.8O.sub.8: 868.98; observed [M+1].sup.+:
870.11
Example AC
##STR00088##
[0244] methyl
{1-[2-{9-[2-(1-{2-[(methoxycarbonyl)amino]-3-methylbutanoyl}pyrrolidin-2--
yl)-1H-imidazol-5-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imid-
azol-2-yl}-4-(methoxymethyl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carb-
amate
[0245] A solution of (2S,4S)-tert-butyl
2-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)pyrrolidin--
2-yl)-1H-imidazol-5-yl)-5H-naphtho[c,g]chromeno[8,9-d]imidazol-2-yl)-4-(me-
thoxymethyl)pyrrolidine-1-carboxylate (116 mg, 0.15 mmol), ethanol
(5 mL) and concentrated HCl (1 mL) was heated to 60.degree. C. for
1 hour. The reaction was concentrated and the crude material
dissolved in DCM (10 mL). This solution was concentrated and to
this material was added a solution of
2-methoxycarbonylamino-3-methylbutyric acid (38 mg, 0.22 mmol) and
HATU (79 mg, 0.21 mmol) in DMF (1.4 mL). To the resulting solution
was added diisopropylethylamine (270 .mu.L, 1.5 mmol). After
stirring for 18 hours at room temperature, the reaction was diluted
with ethyl acetate, washed with water and brine, dried
(Na.sub.2SO.sub.4), concentrated and purified by preparative
reverse phase HPLC (Gemini, 15 to 45% ACN/H.sub.2O+0.1% TFA). The
product fractions were lyophilized to give methyl
{1-[2-{9-[2-(1-{2-[(methoxycarbonyl)amino]-3-methylbutanoyl}pyrrolidin-2--
yl)-1H-imidazol-5-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imid-
azol-2-yl}-4-(methoxymethyl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carb-
amate (58 mg, 13%). LCMS-ESI.sup.+: calculated for
C.sub.45H.sub.54N.sub.8O.sub.8: 834.96; observed [M+1].sup.+:
835.70.
Example AD
##STR00089##
[0246]
(2S,4S)-tert-butyl-2-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)
methylbutanoyl)azabicyclo[3.1.0]hexan-3-yl)-1H-imidazol-5-yl)-5H-naphtho[-
c,g]chromeno[8,9-d]i
imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate
[0247] To a solution of (2S,4S)-tert-butyl
4-(methoxymethyl)-2-(9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5H-n-
aphtho[c,g]chromeno[8,9-d]imidazol-2-yl)pyrrolidine-1-carboxylate
(557 mg, 0.91 mmol), methyl
(S)-1-((1S,3S,5S)-3-(5-bromo-1H-imidazol-2-yl)-2-azabicyclo[3.1.0]hexan-2-
-yl)-3-methyl-1-oxobutan-2-ylcarbamate (350 mg, 0.91 mmol)
tetrakis(triphenylphosphine) palladium(0) (53 mg, 0.04 mmol) and
dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) (67 mg,
0.07 mmol) in a mixture of 1,2-dimethoxyethane (11.0 mL) and
dimethylformamide (1.9 mL) was added a solution of potassium
carbonate (2M in water, 1.37 mL, 2.7 mmol). The resulting mixture
was degassed and then heated to 85.degree. C. under argon for 18
hours. After cooling to room temperature, the reaction was diluted
with ethyl acetate. The organics were washed with water and brine,
dried (Na.sub.2SO.sub.4), and concentrated. The crude residue was
purified by flash chromatography to yield (2S,4S)-tert-butyl
2-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)azabicyclo[-
3.1.0]hexan-3-yl)-1H-imidazol-5-yl)-5H-naphtho[c,g]chromeno[8,9-d]imidazol-
-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate (271 mg, 38%).
LCMS-ESI.sup.+: calculated for C.sub.44H.sub.51N.sub.7O.sub.7.
789.92; observed [M+1].sup.+: 790.76.
methyl
{2-[2-{9-[2-(2-{2-[(methoxycarbonyl)amino]-3-methylbutanoyl}-2-azab-
icyclo[3.1.0]hex-3-yl)-1H-imidazol-5-yl]-1,11-dihydroisochromeno[4',3':6,7-
]naphtho[1,2-d]imidazol-2-yl}-4-(methoxymethyl)pyrrolidin-1-yl]-2-oxo-1-ph-
enylethyl}carbamate
[0248] A solution of (2S,4S)-tert-butyl
2-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)azabicyclo[-
3.1.0]hexan-3-yl)-1H-imidazol-5-yl)-5H-naphtho[c,g]chromeno[8,9-d]imidazol-
-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate (196 mg, 0.25
mmol), ethanol (3 mL) and concentrated HCl (1 mL) was heated to
60.degree. C. for 1 hour. The reaction was concentrated and the
crude material dissolved in DCM (6 mL). This solution was
concentrated and to this material was added a solution of
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid (69 mg, 0.33 mmol)
and COMU (124 mg, 029 mmol) in DMF (4 mL). To the resulting
solution was added diisopropylethylamine (130 .mu.L, 0.76 mmol).
After stirring for 2 hours at room temperature, the reaction was
diluted with ethyl acetate, washed with water and brine, dried
(Na.sub.2SO.sub.4), concentrated and purified by preparative
reverse phase HPLC (Gemini, 15 to 45% ACN/H.sub.2O+0.1% TFA). The
product fractions were lyophilized to give methyl
{2-[2-{9-[2-(2-{2-[(methoxycarbonyl)amino]-3-methylbutanoyl}-2-aza-
bicyclo[3.1.0]hex-3-yl)-1H-imidazol-5-yl]-1,11-dihydroisochromeno[4',3':6,-
7]naphtho[1,2-d]imidazol-2-yl}-4-(methoxymethyl)pyrrolidin-1-yl]-2-oxo-1-p-
henylethyl}carbamate (84 mg, 39%). LCMS-ESI.sup.+: calculated for
C.sub.49H.sub.52N.sub.8O.sub.8: 880.99; observed [M+1].sup.+:
882.09
Example AE
##STR00090## ##STR00091##
[0249]
5-(2-bromo-5-chlorobenzyloxy)-3,4-dihydronaphthalen-1(2H)-one
[0250] To a stirred solution of 5-hydroxy-1-tetralone (2.0 g, 12.3
mmol) and 1-bromo-2-(bromomethyl)-4-chlorobenzene (3.6 g, 12.7
mmol) in dimethylformamide (125 mL) was added potassium carbonate
(3.5 g, 25.1 mmol). The reaction was stirred under argon for 1 hour
then diluted with ethyl acetate (1 L). The organics were washed
three times with water and once with brine. The organic layer was
then dried with magnesium sulfate, filtered and concentrated. To
the resulting oil was added methanol (100 mL) and the suspension
was agitated for thirty minutes.
5-(2-bromo-5-chlorobenzyloxy)-3,4-dihydronaphthalen-1(2H)-one (4.25
g, 94% yield) was isolated by filtration.
8-chloro-2,3,4,6-tetrahydro-1H-dibenzo[c,h]chromen-1-one
[0251] To a flask containing palladium(II) pivalate (68 mg, 0.22
mmol), tri(4-fluorophenyl)phosphine (70 mg, 0.22 mmol), pivalic
acid (135 mg, 1.3 mmol) and potassium carbonate (1.83 g, 13.1 mmol)
was added a solution of
5-(2-bromo-5-chlorobenzyloxy)-3,4-dihydronaphthalen-1(2H)-one (1.61
g, 4.4 mmol) in dimethyacetamide (23 mL). The flask was evacuated
and backfilled with argon 5 times and then stirred under argon at
60.degree. C. for 24 hours. The reaction was poured directly onto a
silica gel column and purified by flash column chromatography
(hexanes/DCM) to yield
8-chloro-2,3,4,6-tetrahydro-1H-dibenzo[c,h]chromen-1-one (1.22 g,
97% yield) as an off-white solid.
2-bromo-8-chloro-2,3,4,6-tetrahydro-1H-dibenzo[c,h]chromen-1-one
[0252] To a mixture of
8-chloro-2,3,4,6-tetrahydro-1H-dibenzo[c,h]chromen-1-one (2.58 g,
9.1 mmol) in chloroform (9.1 mL) and ethyl acetate (9.1 mL) was
added copper(II) bromide (4.65 g, 19.9 mmol). The reaction was
heated to 80.degree. C. for 5 hours and then cooled to room
temperature. The mixture was diluted with dichloromethane and
washed twice with a 5:1 solution of saturated aqueous ammonium
chloride and aqueous ammonium hydroxide (.about.28%), and washed
once with water. The organic layer was dried with magnesium
sulfate, filtered and concentrated. The crude material was purified
by flash column chromatography (hexanes/DCM) to yield
2-bromo-8-chloro-2,3,4,6-tetrahydro-1H-dibenzo[c,h]chromen-1-one
(2.45 g, 75% yield).
(2S)-1-tert-butyl
2-(8-chloro-1-oxo-2,3,4,6-tetrahydro-1H-dibenzo[c,h]chromen-2-yl)
pyrrolidine-1,2-dicarboxylate
[0253] To a solution of
2-bromo-8-chloro-2,3,4,6-tetrahydro-1H-dibenzo[c,h]chromen-1-one
(1.05 g, 2.9 mmol) and Boc-Pro-OH (1.75 g, 8.1 mmol) in
acetonitrile (9.0 mL) was added diisopropylethylamine (1.5 mL, 8.7
mmol). The solution was stirred under argon at 50.degree. C. for
two hours. Extra Boc-Pro-OH (620 mg, 2.9 mmol) and
diisopropylethylamine (0.5 mL, 2.9 mmol) were added and the
reaction was stirred at 50.degree. C. for 16 hours. The reaction
was cooled to room temperature and diluted with ethyl acetate. The
organics were washed with water and brine, dried with magnesium
sulfate and concentrated. The crude material was purified by flash
column chromatography and the product (2S)-1-tert-butyl
2-(8-chloro-1-oxo-2,3,4,6-tetrahydro-1H-dibenzo[c,h]chromen-2-yl)
pyrrolidine-1,2-dicarboxylate was isolated as a mixture of
diastereomers (0.99 g, 69% yield).
tert-butyl
(2S)-2-(9-chloro-3,4,5,7-tetrahydroisochromeno[3',4':5,6]naphth-
o[1,2-d]imidazol-2-yl)pyrrolidine-1-carboxylate
[0254] To a solution of (2S)-1-tert-butyl
2-(8-chloro-1-oxo-2,3,4,6-tetrahydro-1H-dibenzo[c,h]chromen-2-yl)
pyrrolidine-1,2-dicarboxylate (2.2 g, 4.4 mmol) in toluene (40 mL)
was added ammonium acetate (7 g, 91 mmol). The reaction mixture was
vigorously refluxed for 3 hours, then cooled to room temperature
and diluted with ethyl acetate. The organics were washed with water
and brine, dried with magnesium sulfate and concentrated. The crude
material was purified by flash column chromatography to yield
tert-butyl
(2S)-2-(9-chloro-3,4,5,7-tetrahydroisochromeno[3,4':5,6]naphtho[1,2-d]imi-
dazol-2-yl)pyrrolidine-1-carboxylate (1.13 g, 54% yield) as well as
recovered (2S)-1-tert-butyl
2-(8-chloro-1-oxo-2,3,4,6-tetrahydro-1H-dibenzo[c,h]chromen-2-yl)
pyrrolidine-1,2-dicarboxylate (0.8 g, 36%).). LCMS-ESI.sup.+:
calculated for C.sub.27H.sub.28N.sub.3O.sub.3: 477.98; observed
[M+1].sup.+: 478.54.
tert-butyl
(2S)-2-(9-chloro-3,7-dihydroisochromeno[3',4':5,6]naphtho[1,2-d-
]imidazol-2-yl)pyrrolidine-1-carboxylate
[0255] To a solution of Intermediate tert-butyl
(2S)-2-(9-chloro-3,4,5,7-tetrahydroisochromeno[3',4':5,6]naphtho[1,2-d]im-
idazol-2-yl)pyrrolidine-1-carboxylate (1.43 g, 3.0 mmol) in
dichloromethane (30 mL) was added manganese(IV) oxide (15 g, 198
mmol). The mixture was stirred for four hours at room temperature
then filtered through Celite. The MnO.sub.2 was thoroughly rinsed
with dichloromethane and the total filtrate was concentrated to
yield tert-butyl
(2S)-2-(9-chloro-3,7-dihydroisochromeno[3',4':5,6]naphtho[1,2-d]imidazol--
2-yl)pyrrolidine-1-carboxylate (1.37 g, 96% yield). This material
was used without further purification.
tert-butyl
(2S)-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,7-dih-
ydroisochromeno[3',4':5,6]naphtho[1,2-d]imidazol-2-yl]pyrrolidine-1-carbox-
ylate
[0256] To a solution of tert-butyl
(2S)-2-(9-chloro-3,7-dihydroisochromeno[3',4':5,6]naphtho[1,2-d]imidazol--
2-yl)pyrrolidine-1-carboxylate (1.4 g, 2.9 mmol) in dioxane (20 mL)
was added bis(pinacolato)diboron (1.5 g, 5.9 mmol),
tris(dibenzylideneacetone)dipalladium(0) (110 mg, 0.12 mmol),
X-Phos (145 mg, 0.30 mmol) and potassium acetate (870 mg, 8.9
mmol). The mixture was degassed with a stream of argon for ten
minutes. The degassed reaction was heated under argon to 90.degree.
C. for 2.5 hours then cooled to room temperature and diluted with
ethyl acetate. The organics were washed with water and brine, dried
with magnesium sulfate and concentrated. The crude material was
purified by flash column chromatography (DCM/EtOAc) to yield
tert-butyl
(2S)-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,7-dihydroisochr-
omeno[3',4':5,6]naphtho[1,2-d]imidazol-2-yl]pyrrolidine-1-carboxylate
(1.5 g, 90% yield).
methyl
[(2S)-3-methyl-1-oxo-1-{(2S)-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxab-
orolan-2-yl)-3,7-dihydroisochromeno[3',4':5,6]naphtho[1,2-d]imidazol-2-yl]-
pyrrolidin-1-yl}butan-2-yl]carbamate
[0257] A solution of tert-butyl
(2S)-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,7-dihydroisochr-
omeno[3',4':
5,6]naphtho[1,2-d]imidazol-2-yl]pyrrolidine-1-carboxylate (0.98 g,
1.7 mmol), concentrated HCl (2 mL) and ethanol (20 mL) was heated
to 60.degree. C. for 2 hours. The reaction was concentrated and
redissolved in a minimal amount of methanol. An equal volume of
dichloromethane was added and the solution was again concentrated.
Dichloromethane was added to the resulting residue and concentrated
off two more times. The resulting crude material was dissolved in
dimethylformamide (17 mL). To this solution was added
(S)-2-(methoxycarbonylamino)-3-methylbutanoic acid (455 mg, 2.6
mmol), HATU (955 mg, 2.5 mmol) and diisopropylethylamine (3 mL, 17
mmol). The reaction was stirred at room temperature for one hour
then diluted with ethyl acetate. The organics were washed with
water (.times.2) and brine, dried with magnesium sulfate and
concentrated. The resulting residue was purified by flash column
chromatography to yield Intermediate methyl
[(2S)-3-methyl-1-oxo-1-{(2S)-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-
-2-yl)-3,7-dihydroisochromeno[3',4':5,6]naphtho[1,2-d]imidazol-2-yl]pyrrol-
idin-1-yl}butan-2-yl]carbamate (780 mg, 72% yield over 2
steps).
tert-butyl
(2R)-2-[5-(2-{(2S)-1-[N-(methoxycarbonyl)-L-valyl]pyrrolidin-2--
yl}-3,7-dihydroisochromeno[3',4':5,6]naphtho[1,2-d]imidazol-9-yl)-1H-imida-
zol-2-yl]pyrrolidine-1-carboxylate
[0258] A mixture of Pentacyclic Intermediate methyl
[(2S)-3-methyl-1-oxo-1-{(2S)-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-
-2-yl)-3,7-dihydroisochromeno[3',4':5,6]naphtho[1,2-d]imidazol-2-yl]pyrrol-
idin-1-yl}butan-2-yl]carbamate (780 mg, 1.3 mmol), (S)-tert-butyl
2-(5-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate (450 mg, 1.4
mmol), tetrakis(triphenylphosphine)palladium(0) (30 mg, 0.03 mmol),
PdCl.sub.2(dppf) (60 mg, 0.08 mmol), 2M aqueous potassium carbonate
(1.9 mL, 3.9 mmol), dimethoxyethane (10 mL) and dimethylformamide
(2 mL) was degassed with argon for 15 minutes. The reaction was
then heated to 85.degree. C. for 3 hours. Upon completion, the
reaction was cooled to room temperature, diluted with ethyl acetate
and filtered through Celite. The filtrate was washed with water and
brine, dried (MgSO.sub.4) and concentrated. The resulting crude
material was purified by flash column chromatography (EtOAc/MeOH)
to yield Intermediate tert-butyl
(2R)-2-[5-(2-{(2S)-1-[N-(methoxycarbonyl)-L-valyl]pyrrolidin-2-yl}-3,7-di-
hydroisochromeno[3',4':5,6]naphtho[1,2-d]imidazol-9-yl)-1H-imidazol-2-yl]p-
yrrolidine-1-carboxylate (390 mg, 43% yield).
methyl
{(2S)-1-[(2R)-2-(5-{2-[(2S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-me-
thylbutanoyl}pyrrolidin-2-yl]-3,7-dihydroisochromeno[3',4':5,6]naphtho[1,2-
-d]imidazol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2--
yl}carbamate
[0259] A mixture of Intermediate tert-butyl
(2R)-2-[5-(2-{(2S)-1-[N-(methoxycarbonyl)-L-valyl]pyrrolidin-2-yl}-3,7-di-
hydroisochromeno[3',4':5,6]naphtho[1,2-d]imidazol-9-yl)-1H-imidazol-2-yl]p-
yrrolidine-1-carboxylate (390 mg, 0.53 mmol), concentrated HCl (2
mL) and ethanol (10 mL) was heated to 60.degree. C. for 2 hours.
The reaction was concentrated and redissolved in a minimal amount
of methanol. An equal volume of dichloromethane was added and the
solution was again concentrated. Dichloromethane was added to the
resulting residue and concentrated off two more times. One half of
the crude material (.about.0.27 mmol) was dissolved in
dimethylformamide (2.5 mL). To this solution was added
(S)-2-(methoxycarbonylamino)-3-methylbutanoic acid (66 mg, 0.38
mmol), HATU (140 mg, 0.37 mmol) and diisopropylethylamine (0.48 mL,
2.7 mmol). The reaction was stirred at room temperature for 2
hours, and then diluted with acetonitrile (2 mL) and methanol (2
mL). To this solution was added ten drops of 5M aqueous NaOH
solution and stirring was continued for 30 minutes. The reaction
was diluted with ethyl acetate and the organic layer was washed
with water and brine. The combined aqueous washings were extracted
three times with ethyl acetate, and the combined organic layers
were dried (MgSO.sub.4) and concentrated. The crude material was
purified by reverse phase HPLC (Gemini, 15 to 45% ACN/H.sub.2O+0.1%
TFA) to yield methyl
{(2S)-1-[(2R)-2-(5-{2-[(2S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-methylbu-
tanoyl}pyrrolidin-2-yl]-3,7-dihydroisochromeno[3',4':
5,6]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]-3-meth-
yl-1-oxobutan-2-yl}carbamate (140 mg, 67% yield over 2 steps).
LCMS-ESI.sup.+: calculated for C.sub.43H.sub.50N.sub.8O.sub.7:
790.91; observed [M+1].sup.+: 791.71.
Example AF
##STR00092##
[0261] This compound was made in an analogous manner to Example
methyl
{(2S)-1-[(2R)-2-(5-{2-[(2S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-methylbu-
tanoyl}pyrrolidin-2-yl]-3,7-dihydroisochromeno[3',4':5,6]naphtho[1,2-d]imi-
dazol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}car-
bamate, substituting (R)-2-(methoxycarbonylamino)-2-phenylacetic
acid for (S)-2-(methoxycarbonylamino)-3-methylbutanoic acid and
substituting COMU for HATU in the final amide coupling step.
LCMS-ESI.sup.+: calculated for C.sub.46H.sub.48N.sub.8O.sub.7:
824.92; observed [M+1].sup.+: 825.72.
Example AG
##STR00093##
[0262] tert-butyl
(2S)-2-[9-(2-{(2R)-1-[N-(methoxycarbonyl)-L-valyl]pyrrolidin-2-yl}-1H-imi-
dazol-5-yl)-3,7-dihydroisochromeno[3',4':5,6]naphtho[1,2-d]imidazol-2-yl]p-
yrrolidine-1-carboxylate
[0263] A mixture of tert-butyl
(2S)-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,7-dihydroisochr-
omeno[3',4':
5,6]naphtho[1,2-d]imidazol-2-yl]pyrrolidine-1-carboxylate (450 mg,
0.79 mmol), methyl
(S)-1-((S)-2-(5-bromo-1H-imidazol-2-yl)pyrrolidin-1-yl)-3-methyl-1-oxobut-
an-2-ylcarbamate (325 mg, 0.87 mmol),
tetrakis(triphenylphosphine)palladium(0) (30 mg, 0.02 mmol),
PdCl.sub.2(dppf) (35 mg, 0.05 mmol), 2M aqueous potassium carbonate
(1.2 mL, 2.4 mmol), dimethoxyethane (6.8 mL) and dimethylformamide
(1.2 mL) was degassed with argon for 15 minutes. The reaction was
then heated to 85.degree. C. for 2.5 hours. Upon completion, the
reaction was cooled to room temperature, diluted with ethyl acetate
and filtered through Celite. The filtrate was washed with water and
brine, dried (MgSO.sub.4) and concentrated. The resulting crude
material was purified by flash column chromatography (EtOAc/MeOH)
to yield tert-butyl
(2S)-2-[9-(2-{(2R)-1-[N-(methoxycarbonyl)-L-valyl]pyrrolidin-2-yl}-1H-imi-
dazol-5-yl)-3,7-dihydroisochromeno[3',4':5,6]naphtho[1,2-d]imidazol-2-yl]p-
yrrolidine-1-carboxylate (270 mg, 46% yield).
methyl
{(2S)-1-[(2R)-2-(5-{2-[(2S)-1-{(2R)-2-[(methoxycarbonyl)amino]-2-ph-
enylacetyl}pyrrolidin-2-yl]-3,7-dihydroisochromeno[3',4':5,6]naphtho[1,2-d-
]imidazol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl-
}carbamate
[0264] A mixture of tert-butyl
(2S)-2-[9-(2-{(2R)-1-[N-(methoxycarbonyl)-L-valyl]pyrrolidin-2-yl}-1H-imi-
dazol-5-yl)-3,7-dihydroisochromeno[3',4':5,6]naphtho[1,2-d]imidazol-2-yl]p-
yrrolidine-1-carboxylate (270 mg, 0.37 mmol), concentrated HCl (1.5
mL) and ethanol (8 mL) was heated to 60.degree. C. for 1 hour. The
reaction was concentrated and redissolved in a minimal amount of
methanol. An equal volume of dichloromethane was added and the
solution was again concentrated. Dichloromethane was added to the
resulting residue and concentrated off two more times. The crude
material was dissolved in 5:1 dichloromethane/dimethylformamide
(3.8 mL). To this solution was added
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid (96 mg, 0.46
mmol), COMU (190 mg, 0.44 mmol) and diisopropylethylamine (0.20 mL,
1.1 mmol). The reaction was stirred at 0.degree. C. for 30 minutes
then warmed to room temperature. Upon completion, the reaction was
diluted with acetonitrile (2 mL) and methanol (2 mL). To this
solution was added ten drops of 5M aqueous NaOH solution and
stirring was continued for 30 minutes. The reaction was diluted
with ethyl acetate and the organic layer was washed with water and
brine. The combined aqueous washings were extracted three times
with ethyl acetate, and the combined organic layers were dried
(MgSO.sub.4) and concentrated. The crude material was purified by
reverse phase HPLC (Gemini, 15 to 45% ACN/H.sub.2O+0.1% TFA) to
yield methyl
{(2S)-1-[(2R)-2-(5-{2-[(2S)-1-{(2R)-2-[(methoxycarbonyl)amino]-2-phenylac-
etyl}pyrrolidin-2-yl]-3,7-dihydroisochromeno[3',4':5,6]naphtho[1,2-d]imida-
zol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carba-
mate (155 mg, 51% yield over 2 steps). LCMS-ESI.sup.+: calculated
for C.sub.46H.sub.48N.sub.8O.sub.7: 824.92; observed [M+1].sup.+:
825.67.
Example AH
##STR00094##
[0265] dimethyl
(2S,2'S)-1,1'-((2S,2'S)-2,2'l-pyrrolidin-2-yl)-5H-naphtho[c,g]chromeno[8,-
9-d]imidazol-9-yl)-1H-imidazol-2-yl)pyrrolidin-1-yl))bis(3-methyl-1-oxobut-
ane-2,1-diyl)dicarbamate
[0266] This compound was made in an analogous manner to methyl
{(2S)-1-[(2R)-2-(5-{2-[(2S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-methylbu-
tanoyl}pyrrolidin-2-yl]-3,7-dihydroisochromeno[3',4':5,6]naphtho[1,2-d]imi-
dazol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}car-
bamate, substituting 7-hydroxy-1-tetralone for
5-hydroxy-1-tetralone in the first step of the sequence. All
reactions in the synthesis of Example AH gave similar product
yields as in the synthesis of methyl
{(2S)-1-[(2R)-2-(5-{2-[(2S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-methylbu-
tanoyl}pyrrolidin-2-yl]-3,7-dihydroisochromeno[3',4':5,6]naphtho[1,2-d]imi-
dazol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}car-
bamate. LCMS-ESI.sup.+: calculated for
C.sub.43H.sub.50N.sub.8O.sub.7: 790.91; observed [M+1].sup.+:
791.6.
Example AI
##STR00095##
[0267] methyl
[1-(2-{5-[2-(1-{[(methoxycarbonyl)amino]-3-methyl-1-oxobutan-2-yl}pyrroli-
din-2-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl]-1-
H-imidazol-2-yl}pyrrolidin-1-yl)-phenyl-1-oxoacet-2-yl]carbamate
[0268] This compound was made in an analogous manner to dimethyl
(2S,2'S)-1,1'-((2S,2'S)-2,2'l-pyrrolidin-2-yl)-5H-naphtho[c,g]chromeno[8,-
9-d]imidazol-9-yl)-1H-imidazol-2-yl)pyrrolidin-1-yl))bis(3-methyl-1-oxobut-
ane-2,1-diyl)dicarbamate, substituting
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid for
(S)-2-(methoxycarbonylamino)-3-methylbutanoic acid and substituting
COMU for HATU in the final amide coupling step. LCMS-ESI.sup.+:
calculated for C.sub.46H.sub.48N.sub.8O.sub.7: 824.92; observed
[M+1].sup.+: 825.67.
Example AJ
##STR00096##
[0269] dimethyl
(2S,2'S)-1,1'-((2S,2'S)-2,2'l-pyrrolidin-2-yl)-7H-dihydro-naphtho[c,g]chr-
omeno[8,9-d]imidazol-9-yl)-1H-imidazol-2-yl)pyrrolidin-1-yl))bis(3-methyl--
1-oxobutane-2,1-diyl)dicarbamate
[0270] This compound was made in an analogous manner to dimethyl
(2S,2'S)-1,1'-((2S,2'S)-2,2'l-pyrrolidin-2-yl)-5H-naphtho[c,g]chromeno[8,-
9-d]imidazol-9-yl)-1H-imidazol-2-yl)pyrrolidin-1-yl))bis(3-methyl-1-oxobut-
ane-2,1-diyl)dicarbamate, omitting the MnO.sub.2 oxidation of
tert-butyl
2-(9-chloro-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]imidaz-
ol-2-yl)pyrrolidine-1-carboxylate. LCMS-ESI.sup.+: calculated for
C.sub.43H.sub.52N.sub.8O.sub.7: 792.40; observed [M+1].sup.+:
793.69.
Example AK
##STR00097##
[0271] methyl
[1-(2-{5-[2-(1-{[(methoxycarbonyl)amino]-3-methyl-1-oxobutan-2-yl}pyrroli-
din-2-yl)-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol--
9-yl]-1H-imidazol-2-yl}pyrrolidin-1-yl)-phenyl-1-oxoacet-2-yl]carbamate
[0272] This compound was made in an analogous manner to dimethyl
(2S,2'S)-1,1'-((2S,2'S)-2,2'l-pyrrolidin-2-yl)-7H-dihydro-naphtho[c,g]chr-
omeno[8,9-d]imidazol-9-yl)-1H-imidazol-2-yl)pyrrolidin-1-yl))bis(3-methyl--
1-oxobutane-2,1-diyl)dicarbamate, substituting
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid for
(S)-2-(methoxycarbonylamino)-3-methylbutanoic acid and substituting
COMU for HATU in the final amide coupling step. LCMS-ESI.sup.+:
calculated for C.sub.46H.sub.50N.sub.8O.sub.7: 826.94; observed
[M+1].sup.+: 827.71.
Example AL
##STR00098##
[0273]
[1-(2-{5-[2-(1-{[(methoxycarbonyl)amino](phenyl)acetyl}pyrrolidin-2-
-yl)-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl]-
-1H-imidazol-2-yl}pyrrolidin-1-yl)-3-methyl-1-oxobutan-2-yl]carbamic
acid
[0274] This compound was made in an analogous manner to methyl
{(2S)-1-[(2R)-2-(5-{2-[(2S)-1-{(2R)-2-[(methoxycarbonyl)amino]-2-phenylac-
etyl}pyrrolidin-2-yl]-3,7-dihydroisochromeno[3',4':5,6]naphtho[1,2-d]imida-
zol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carba-
mate, substituting tert-butyl
(2S)-2-[9-(2-{(2R)-1-[N-(methoxycarbonyl)-L-valyl]pyrrolidin-2-yl}-1H-imi-
dazol-5-yl)-3,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazo-
l-2-yl]pyrrolidine-1-carboxylate for tert-butyl
(2S)-2-[9-(2-{(2R)-1-[N-(methoxycarbonyl)-L-valyl]pyrrolidin-2-yl}-1H-imi-
dazol-5-yl)-3,7-dihydroisochromeno[3',4':
5,6]naphtho[1,2-d]imidazol-2-yl]pyrrolidine-1-carboxylate.
LCMS-ESI.sup.+: calculated for C.sub.46H.sub.50N.sub.8O.sub.7:
826.94; observed [M+1].sup.+: 827.64.
Example AM
##STR00099##
[0275] (2S,4S)-methyll
{4-(methoxymethyl)-2-[(9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,-
11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)
pyrrolidin-1yl]-3-methyl-1-oxobutan-2-yl}carbamate
[0276] A solution of (2S,4S)-tert-butyl
4-(methoxymethyl)-2-(9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,11-
-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)pyrrolidine-1-ca-
rboxylate (424 mg, 0.69 mmol), ethanol (6 mL) and concentrated HCl
(2 mL) was heated to 60.degree. C. for 1 hour. The reaction was
concentrated and the crude material dissolved in DCM (10 mL). This
solution was concentrated and to this material was added a solution
of 2-methoxycarbonylamino-3-methylbutyric acid (152 mg, 0.86 mmol)
and HATU (303 mg, 0.79 mmol) in DMF (6 mL). To the resulting
solution was added diisopropylethylamine (360 .mu.L, 2.08 mmol).
After stirring for 2 hours at room temperature, the reaction was
diluted with ethyl acetate, washed with 5% NaHCO.sub.3 solution,
water and brine, dried (Na.sub.2SO.sub.4), concentrated and dried
under vacuum to give (2S,4S)-methyll
{4-(methoxymethyl)-2-[(9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,-
11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)pyrrolidin-1-y-
l]-3-methyl-1-oxobutan-2-yl}carbamate.
tert-butyl(2S)-2-[5-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-4-methylpy-
rrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9--
yl)-1H-imidazol-2-yl]pyrrolidine-1-carboxylate
[0277] To a solution of (2S,4S)-methyll
{4-(methoxymethyl)-2-[(9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,-
11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)pyrrolidin-1yl-
]-3-methyl-1-oxobutan-2-yl}carbamate (0.69 mmol), (S)-tert-butyl
2-(5-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate (220 mg, 0.69
mmol), tetrakis(triphenylphosphine) palladium(0) (24 mg, 0.02 mmol)
and dichloro[1,1'-bis(diphenylphosphino) ferrocene]palladium(II)
(31 mg, 0.04 mmol) in a mixture of 1,2-dimethoxyethane (6.0 mL) and
dimethylformamide (1.0 mL) was added a solution of potassium
carbonate (2M in water, 1.04 mL, 2.0 mmol). The resulting mixture
was degassed and then heated to 85.degree. C. under argon for 18
hours. After cooling to room temperature, the reaction was diluted
with ethyl acetate. The organics were washed with water and brine,
dried (Na.sub.2SO.sub.4), and concentrated. The crude residue was
purified by flash chromatography to yield (tert-butyl
(2S)-2-[5-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-4-methylpyrrolidin--
2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-im-
idazol-2-yl]pyrrolidine-1-carboxylate (145 mg, 27%).
methyl
{(1R)-2-[(2S)-2-(5-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-
-methylbutanoyl}-4-(methoxymethyl)pyrrolidin-2-yl]-1,11-dihydroisochromeno-
[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]--
2-oxo-1-phenylethyl}carbamate
[0278] A solution of tert-butyl
(2S)-2-[5-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-4-methylpyrrolidin--
2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-im-
idazol-2-yl]pyrrolidine-1-carboxylate (145 mg, 0.18 mmol), ethanol
(3 mL) and concentrated HCl (1 mL) was heated to 60.degree. C. for
1 hour. The reaction was concentrated and the crude material
dissolved in DCM (6 mL). This solution was concentrated and to this
material was added a solution of
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid (51 mg, 0.24 mmol)
and COMU (92 mg, 021 mmol) in DMF (3 mL). To the resulting solution
was added diisopropylethylamine (100 .mu.L, 0.56 mmol). After
stirring for 2 hours at room temperature, the reaction was diluted
with ethyl acetate, washed with water and brine, dried
(Na.sub.2SO.sub.4), concentrated and purified by preparative
reverse phase HPLC (Gemini, 15 to 43% ACN/H.sub.2O+0.1% TFA). The
product fractions were lyophilized to give methyl
{(1R)-2-[(2S)-2-(5-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino]--
3-methylbutanoyl}-4-(methoxymethyl)pyrrolidin-2-yl]-1,11-dihydroisochromen-
o[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]-
-2-oxo-1-phenylethyl}carbamate (68 mg, 39%). MS (ESI) m/z 870
[M+H].sup.+. 1H NMR (400 MHz, dmso) .delta. 8.71 (s, 1H), 8.22 (d,
1H, J=8 Hz), 8.09 (m, 1H), 7.88-7.63 (m, 6H), 7.36-7.29 (m, 6H),
5.41 (d, 1H, J=8.4 Hz), 5.30-5.24 (m, 2H), 5.14-5.10 (m, 1H),
4.13-3.09 (m, 15H), 2.47-1.80 (m, 8H), 0.80 (dd, 6H, J=6.4 Hz, J=23
Hz).
Example AN
##STR00100##
[0279]
tert-butyl(2S,4S)-2-[9-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]--
4-methyl
pyrrolidin-2-yl}-1H-imidazol-5-yl)-3,11-dihydroisochromeno[4',3':-
6,7]naphtho[1,2-d]imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylat-
e
[0280] To a solution of (2S,4S)-tert-butyl
4-(methoxymethyl)-2-(9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,11-
-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)pyrrolidine-1-ca-
rboxylate (438 mg, 0.72 mmol), methyl
(S)-1-((2S,4S)-2-(5-bromo-1H-imidazol-2-yl)-4-methylpyrrolidin-1-yl)-3-me-
thyl-1-oxobutan-2-ylcarbamate (276 mg, 0.72 mmol),
tetrakis(triphenylphosphine) palladium(0) (41 mg, 0.04 mmol) and
dichloro[1,1'-bis(diphenylphosphino) ferrocene]palladium(II) (52
mg, 0.07 mmol) in a mixture of 1,2-dimethoxyethane (8.6 mL) and
dimethylformamide (1.5 mL) was added a solution of potassium
carbonate (2M in water, 1.07 mL, 2.15 mmol). The resulting mixture
was degassed and then heated to 85.degree. C. under argon for 18
hours. After cooling to room temperature, the reaction was diluted
with ethyl acetate. The organics were washed with water and brine,
dried (Na.sub.2SO.sub.4), and concentrated. The crude residue was
purified by flash chromatography to yield tert-butyl
(2S,4S)-2-[9-(2-{(2S4S)-1-[N-(methoxycarbonyl)-L-valyl]-4-methylpyrrolidi-
n-2-yl}-1H-imidazol-5-yl)-3,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]-
imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate (182 mg,
32%).
methyl
{(2S)-1-[(2S,4S)-2-(5-{2-[(2S,4S)-1-{(2R)-2-[(methoxycarbonyl)amino-
]-2-phenylacetyl}-4-(methoxymethyl)pyrrolidin-2-yl]-1,11-dihydroisochromen-
o[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-methylpyrroli-
din-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate
[0281] A solution of tert-butyl
(2S,4S)-2-[9-(2-{(2S4S)-1-[N-(methoxycarbonyl)-L-valyl]-4-methylpyrrolidi-
n-2-yl}-1H-imidazol-5-yl)-3,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]-
imidazol-2-yl]-4-(methoxy methyl)pyrrolidine-1-carboxylate (182 mg,
0.18 mmol), ethanol (3 mL) and concentrated HCl (1 mL) was heated
to 60.degree. C. for 1 hour. The reaction was concentrated and the
crude material dissolved in DCM (6 mL). This solution was
concentrated and to this material was added a solution of
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid (47 mg, 0.23 mmol)
and COMU (85 mg, 0.2 mmol) in DMF (3 mL). To the resulting solution
was added diisopropylethylamine (90 .mu.L, 0.52 mmol). After
stirring for 2 hours at room temperature, the reaction was diluted
with ethyl acetate, washed with water and brine, dried
(Na.sub.2SO.sub.4), concentrated and purified by preparative
reverse phase HPLC (Gemini, 15 to 49% ACN/H.sub.2O+0.1% TFA). The
product fractions were lyophilized to give methyl
{(2S)-1-[(2S,4S)-2-(5-{2-[(2S,4S)-1-{(2R)-2-[(methoxycarbonyl)amino]-2-ph-
enylacetyl}-4-(methoxymethyl)pyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3-
':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-methylpyrrolidin-1-yl-
]-3-methyl-1-oxobutan-2-yl}carbamate (32 mg, 39%). MS (ESI) m/z 884
[M+H].sup.+. .sup.1H NMR (400 MHz, dmso) .delta. 8.70 (s, 1H), 8.21
(d, 1H, J=8 Hz), 8.08 (s, 1H), 7.90-7.64 (m, 6H), 7.34-7.31 (m,
3H), 7.64 (d, 1H, J=8.4 Hz), 5.47 (d, 1H, J=7.6 Hz), 5.28-5.25 (m,
3H), 5.05-5.01 (m, 1H), 4.19-4.04 (m, 3H), 3.67-3.15 (m, 15H),
2.51-2.46 (m, 4H), 1.95-1.92 (m, 2H), 1.82-1.76 (m, 1H), 1.10 (d,
3H, J=6 Hz), 0.75 (dd, 6H, J=6.8 Hz, J=14 Hz).
Example AO
##STR00101##
[0282] methyl
{(2S)-1-[(2S,4S)-2-(5-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-me-
thylbutanoyl}-4-methoxymethylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3-
':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-methylpyrrolidin-1--
yl]-3-methyl-1-oxobutan-2-yl}carbamate
[0283] To a solution of methyl
{(2S)-1-[(2S,4S)-2-(5-{2-[(2S,4S)-4-(methoxymethyl)pyrrolidin-2-yl]-1,11--
dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl-
)-4-(methyl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate (57
mg, 0.08 mmol), 2-methoxycarbonylamino-3-methylbutyric acid (19 mg,
0.1 mmol), HATU (303 mg, 0.79 mmol) in DMF (1 mL) was added
diisopropylethylamine (43 .mu.L, 0.24 mmol). After stirring for 2
hours at room temperature, the reaction was diluted with ethyl
acetate, washed with 5% NaHCO.sub.3 solution, water and brine,
dried (Na.sub.2SO.sub.4), concentrated and purified by preparative
reverse phase HPLC (Gemini, 15 to 43% ACN/H.sub.2O+0.1% TFA). The
product fractions were lyophilized to give methyl
{(2S)-1-[(2S,4S)-2-(5-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-me-
thyl
butanoyl}-4-methoxymethylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',-
3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazo-2-yl)-4-methylpyrrolidin-1--
yl]-3-methyl-1-oxobutan-2-yl}carbamate. (13 mg, 19%). MS (ESI) m/z
850 [M+H].sup.+. 1H NMR (400 MHz, dmso) .delta. 8.66 (s, 1H),
8.28-8.13 (m, 1H), 8.12-7.99 (m, 1H), 7.90-7.75 (m, 3H), 7.73-7.65
(m, 1H), 7.63-7.57 (m, 1H), 7.34-7.19 (m, 2H), 5.30-5.24 (m, 2H),
5.21-4.95 (m, 2H), 4.33-3.93 (m, 6H), 3.23-3.58 (m, 12H), 2.76-2.59
(m, 2H), 2.02-1.73 (m, 6H), 1.12-1.07 (m, 3H), 0.86-0.68 (m,
12H).
Example AP
##STR00102##
[0284]
tert-butyl(2S,4S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]--
5-methyl
pyrrolidin-2-yl}-1H-imidazol-5-yl)-3,11-dihydroisochromeno[4',3':-
6,7]naphtho[1,2-d]imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylat-
e
[0285] To a solution of (2S,4S)-tert-butyl
4-(methoxymethyl)-2-(9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,11-
-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)pyrrolidine-1-ca-
rboxylate (217 mg, 0.35 mmol), methyl
(S)-1-((2S,5S)-2-(5-bromo-1H-imidazol-2-yl)-5-methylpyrrolidin-1-yl)-3-me-
thyl-1-oxobutan-2-ylcarbamate (170 mg, 0.39 mmol),
tetrakis(triphenylphosphine) palladium(0) (21 mg, 0.02 mmol) and
dichloro[1,1'-bis(diphenylphosphino) ferrocene]palladium(II) (26
mg, 0.04 mmol) in a mixture of 1,2-dimethoxyethane (4.3 mL) and
dimethylformamide (0.75 mL) was added a solution of potassium
carbonate (2M in water, 0.53 mL, 1.06 mmol). The resulting mixture
was degassed and then heated to 85.degree. C. under argon for 18
hours. After cooling to room temperature, the reaction was diluted
with ethyl acetate. The organics were washed with water and brine,
dried (Na.sub.2SO.sub.4), and concentrated. The crude residue was
purified by flash chromatography to yield tert-butyl
(2S,4S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1H-imidazol-5-yl)-3,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d-
]imidazol-2-yl]-4-(methoxy methyl)pyrrolidine-1-carboxylate (110
mg, 39%).
methyl{(2S)-1-[(2S,5S)-2-(5-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino]-
-3-methylbutanoyl}-4-methoxymethylpyrrolidin-2-yl]-1,11-dihydroisochromeno-
[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-5-methylpyrrolid-
in-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate
[0286] A solution of tert-butyl
(2S,4S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1H-imidazol-5-yl)-3,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d-
]imidazol-2-yl]-4-(methoxy methyl)pyrrolidine-1-carboxylate (108
mg, 0.14 mmol), ethanol (2 mL) and concentrated HCl (0.7 mL) was
heated to 60.degree. C. for 1 hour. The reaction was concentrated
and the crude material dissolved in DCM (10 mL). This solution was
concentrated and to this material was added a solution of
2-methoxycarbonylamino-3-methylbutyric acid (31 mg, 0.18 mmol) and
HATU (60 mg, 0.16 mmol) in DMF (2 mL). To the resulting solution
was added diisopropylethylamine (70 .mu.L, 0.41 mmol). After
stirring for 2 hours at room temperature, the reaction was diluted
with ethyl acetate, washed with 5% NaHCO.sub.3 solution, water and
brine, dried (Na.sub.2SO.sub.4), After stirring for 2 hours at room
temperature, the reaction was diluted with ethyl acetate, washed
with 5% NaHCO.sub.3 solution, water and brine, dried
(Na.sub.2SO.sub.4), concentrated and purified by preparative
reverse phase HPLC (Gemini, 15 to 43% ACN/H.sub.2O+0.1% TFA). The
product fractions were lyophilized to give methyl
{(2S)-1-[(2S,5S)-2-(5-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-me-
thylbutanoyl}-4-methoxy
methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]im-
idazol-9-yl}-1H-imidazol-2-yl)-5-methylpyrrolidin-1-yl]-3-methyl-1-oxobuta-
n-2-yl}carbamate (52 mg, 45%). MS (ESI) m/z 850 [M+H].sup.+.
.sup.1H NMR (400 MHz, dmso) .delta. 8.69 (s, 1H), 8.18 (d, 1H,
J=7.6 Hz), 7.99-7.86 (m, 4H), 7.72 (s, 1H), 7.64 (d, 1H, J=8.8 Hz),
7.51 (d, 1H, J=8 Hz), 7.23 (d, 1H, J=8.4 Hz), 5.29 (s, 2H),
5.22-5.18 (m, 1H), 5.01-4.70 (m, 1H), 4.64-4.61 (m, 1H), 4.21-4.17
(m, 1H), 4.09-4.05 (m, 1H), 3.92-3.88 (m, 1H), 3.59-3.08 (m, 14H),
2.67-1.83 (m, 7H), 1.43 (d, 3H, J=6.4 Hz), 0.91-0.71 (m, 12H).
Example AQ
##STR00103##
[0287]
(2S,4R)-tert-butyl-4-(methoxymethyl)-2-(9-(4,4,5,5-tetramethyl-1,3,-
2-dioxaborolan-2-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imida-
zol-2-yl) pyrrolidine-1-carboxylate
[0288] A degassed mixture
of--(2S,4R)-tert-butyl-2-(9-chloro-1,11-dihydroisochromeno[4',3':6,7]naph-
tho[1,2-d]imidazol-2-yl)-4-(methoxymethyl)
pyrrolidine-1-carboxylate (335 mg, 0.64 mmol),
bis(pinacolato)diboron (246 mg, 0.96 mmol), potassium acetate (190
mg, 1.9 mmol), tris(dibenzylideneacetone) palladium (24 mg, 0.02
mmol) and
2-dicyclohexylphosphino-2',4',6'-tri-i-propyl-1,1'-biphenyl (31 mg,
0.06 mmol) in 1,4-dioxane (3.3 mL) was heated to 90.degree. C. for
3 hours, cooled to room temperature and diluted with ethyl acetate.
The organics were washed with water and brine, dried
(Na.sub.2SO.sub.4), and concentrated. The crude residue was
purified by flash chromatography to yield (2S,4R)-tert-butyl
4-(methoxymethyl)-2-(9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,11-
-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)pyrrolidine-1-ca-
rboxylate (379 mg, 96%).
(2S,4R)-tert-butyl2-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)-3-methyl
butanoyl)pyrrolidin-2-yl)-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3'-
:6,7]naphtho[1,2-d]imidazol-2-yl)-4(methoxymethyl)
pyrrolidine-1-carboxylate
[0289] To a solution of (2S,4R)-tert-butyl
4-(methoxymethyl)-2-(9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,11-
-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)
pyrrolidine-1-carboxylate (299 mg, 0.49 mmol), methyl
(S)-1-((S)-2-(5-bromo-1H-imidazol-2-yl)pyrrolidin-1-yl)-3-methyl-1-oxobut-
an-2-ylcarbamate (217 mg, 0.58 mmol), tetrakis(triphenylphosphine)
palladium(0) (28 mg, 0.02 mmol) and
dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) (35 mg,
0.04 mmol) in a mixture of 1,2-dimethoxyethane (4.3 mL) and
dimethylformamide (0.75 mL) was added a solution of potassium
carbonate (2M in water, 0.73 mL, 1.46 mmol). The resulting mixture
was degassed and then heated to 85.degree. C. under argon for 18
hours. After cooling to room temperature, the reaction was diluted
with ethyl acetate. The organics were washed with water and brine,
dried (Na.sub.2SO.sub.4), and concentrated. The crude residue was
purified by flash chromatography to yield (2S,4R)-tert-butyl
2-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)pyrrolidin--
2-yl)-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]im-
idazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate (170 mg,
45%).
methyl{(1R)-2-[(2S,4R)-2-(9-{2-[(2S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3--
methylbutanoyl}pyrrolidin-2-yl)-1H-imidazol-5-yl]-1,11-dihydroisochromeno[-
4',3':6,7]naphtho[1,2-d]imidazol-2-yl}-4-(methoxymethyl)pyrrolidin-1-yl]-2-
-oxo-phenylethyl}carbamate
[0290] A solution of (2S,4S)-tert-butyl
2-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)pyrrolidin--
2-yl)-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]im-
idazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxy late (170 mg,
0.22 mmol), ethanol (3 mL) and concentrated HCl (1 mL) was heated
to 60.degree. C. for 1 hour. The reaction was concentrated and the
crude material dissolved in DCM (6 mL). This solution was
concentrated and to this material was added a solution of
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid (59 mg, 0.28 mmol)
and COMU (108 mg, 025 mmol) in DMF (3 mL). To the resulting
solution was added diisopropylethylamine (110 .mu.L, 0.66 mmol).
After stirring for 2 hours at room temperature, the reaction was
diluted with ethyl acetate, washed with water and brine, dried
(Na.sub.2SO.sub.4), concentrated and purified by preparative
reverse phase HPLC (Gemini, 15 to 44% ACN/H.sub.2O+0.1% TFA). The
product fractions were lyophilized to give methyl
{(1R)-2-[(2S,4R)-2-(9-{2-[(2S)-1-{(2S)-2-[(methoxycarbonyl)amino]--
3-methylbutanoyl}pyrrolidin-2-yl)-1H-imidazol-5-yl]-1,11-dihydroisochromen-
o[4',3':6,7]-naphtho[1,2-d]imidazol-2-yl}-(methoxymethyl)
pyrrolidin-1-yl]-2-oxo-phenylethyl}carbamate (67 mg, 35%). MS (ESI)
m/z 870 [M+H].sup.+. 1H NMR (400 MHz, dmso) .delta. 8.71 (s, 1H),
8.20 (d, 1H, J=8.4 Hz), 8.01 (m, 1H), 7.91-7.64 (m, 6H), 7.38-7.28
(m, 6H), 6.85 (s, 1H), 5.51 (d, 1H, J=7.2 Hz), 5.39-5.29 (m, 3H),
5.13-5.09 (m, 1H), 4.11-3.04 (m, 15H), 2.77-1.98 (m, 8H), 0.79 (dd,
6H, J=6.8 Hz, J=12.8 Hz).
Example AR
##STR00104##
[0291]
(2S,4S)-tert-butyl4-(methoxymethyl)-2-(9-(4,4,5,5-tetramethyl-1,3,2-
-dioxaborolan-2-yl)-4,5-dihydro-1,11-dihydroisochromeno[4',3':6,7]naphtho[-
1,2-d]imidazol-2-yl)pyrrolidine-1-carboxylate
[0292] A degassed mixture of (2S,4S)-tert-butyl
2-(9-chloro-4,5-dihydro-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]i-
midazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate (322 mg,
0.61 mmol), bis(pinacolato) diboron (235 mg, 0.92 mmol), potassium
acetate (182 mg, 1.9 mmol), tris(dibenzylideneacetone)palladium (23
mg, 0.02 mmol) and
2-dicyclohexylphosphino-2',4',6'-tri-i-propyl-1,1'-biphenyl (29 mg,
0.06 mmol) in 1,4-dioxane (3.3 mL) was heated to 90.degree. C. for
3 hours, cooled to room temperature and diluted with ethyl acetate.
The organics were washed with water and brine, dried
(Na.sub.2SO.sub.4), and concentrated. The crude residue was
purified by flash chromatography to yield (2S,4S)-tert-butyl
4-(methoxymethyl)-2-(9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4,5--
dihydro-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)pyrr-
olidine-1-carboxylate (267 mg, 70%).
(2S,4S)-tert-butyl2-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)-3-methylbut-
anoyl)pyrrolidin-2-yl)-1H-imidazol-5-yl-4,5-dihydro-1,11-dihydroisochromen-
o[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-ca-
rboxy late
[0293] To a solution of (2S,4S)-tert-butyl
4-(methoxymethyl)-2-(9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4,5--
dihydro-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)pyrr-
olidine-1-carboxylate (267 mg, 0.52 mmol), methyl
(S)-1-((S)-2-(5-bromo-1H-imidazol-2-yl)pyrrolidin-1-yl)-3-methyl-1-oxobut-
an-2-ylcarbamate (195 mg, 0.52 mmol), tetrakis (triphenylphosphine)
palladium(0) (25 mg, 0.02 mmol) and
dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) (32 mg,
0.04 mmol) in a mixture of 1,2-dimethoxyethane (4.3 mL) and
dimethylformamide (0.75 mL) was added a solution of potassium
carbonate (2M in water, 0.65 mL, 1.3 mmol). The resulting mixture
was degassed and then heated to 85.degree. C. under argon for 18
hours. After cooling to room temperature, the reaction was diluted
with ethyl acetate. The organics were washed with water and brine,
dried (Na.sub.2SO.sub.4), and concentrated. The crude residue was
purified by flash chromatography to yield (2S,4S)-tert-butyl
2-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)pyrrolidin--
2-yl)-1H-imidazol-5-yl-4,5-dihydro-1,11-dihydroisochromeno[4',3':6,7]napht-
ho[1,2-d]imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxy late
(75 mg, 22%).
methyl{(1R)-2-[(2S,4S)-2-(9-{2-[(2S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3--
methylbutanoyl}pyrrolidin-2-yl)-1H-imidazol-5-yl]-1,11-dihydroisochromeno[-
4',3':6,7]-4,5-dihydro-naphtho[1,2-d]imidazol-2-yl}-(methoxymethyl)pyrroli-
din-1-yl]-2-oxo-1-phenylethyl}carbamate
[0294] A solution of (2S,4S)-tert-butyl
2-(9-(2-((S)-1-((S)-2-(methoxy
carbonylamino)-3-methylbutanoyl)pyrrolidin-2-yl)-1H-imidazol-5-yl-4,5-dih-
ydro-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-(met-
hoxymethyl) pyrrolidine-1-carboxylate (75 mg, 0.09 mmol), ethanol
(2 mL) and concentrated HCl (0.6 mL) was heated to 60.degree. C.
for 1 hour. The reaction was concentrated and the crude material
dissolved in DCM (6 mL). This solution was concentrated and to this
material was added a solution of
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid (26 mg, 0.13 mmol)
and COMU (47 mg, 0.11 mmol) in DMF (2 mL). To the resulting
solution was added diisopropylethylamine (50 .mu.L, 0.29 mmol).
After stirring for 2 hours at room temperature, the reaction was
diluted with ethyl acetate, washed with water and brine, dried
(Na.sub.2SO.sub.4), concentrated and purified by preparative
reverse phase HPLC (Gemini, 15 to 44% ACN/H.sub.2O+0.1% TFA). The
product fractions were lyophilized to give methyl
{(1R)-2-[(2S,4S)-2-(9-{2-[(2S)-1-{(2S)-2-[(methoxycarbonyl)amino]--
3-methylbutanoyl}pyrrolidin-2-yl)-1H-imidazol-5-yl]-1,11-dihydroisochromen-
o[4',3':6,7]-4,5-dihydro-naphtho[1,2-d]imidazol-2-yl}-4-(methoxymethyl)pyr-
rolidin-1-yl]-2-oxo-1-phenylethyl}carbamate (15 mg, 18%).
[0295] MS (ESI) m/z 872 [M+H].sup.+. .sup.1H NMR (400 MHz, dmso)
.delta. 7.95-7.63 (m, 6H), 7.35-7.25 (m, 7H), 6.97 (s, 1H), 5.42
(d, 1H, J=6.8 Hz), 5.18 (s, 2H), 5.09 (s, 2H), 4.28-2.63 (m, 19H),
2.47-1.80 (m, 8H), 0.77 (dd, 6H, J=4.8 Hz, J=12.4 Hz).
Example AS
##STR00105##
[0296]
(2S,4S)-tert-butyl2-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)-3-me-
thylbutanoyl)pyrrolidin-2-yl)-1H-benzo[d]imidazol-6-yl)-1,11-dihydroisochr-
omeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-(methoxymethyl)
pyrrolidine-1-carboxylate
[0297] To a solution of (2S,4S)-tert-butyl
4-(methoxymethyl)-2-(9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,11-
-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)pyrrolidine-1-ca-
rboxylate (400 mg, 0.85 mmol), methyl
(S)-1-((S)-2-(6-bromo-1H-benzo[d]imidazol-2-yl)pyrrolidin-1-yl)-3-methyl--
1-oxobutan-2-ylcarbamate (360 mg, 0.85 mmol),
tetrakis(triphenylphosphine) palladium(0) (38 mg, 0.03 mmol) and
dichloro[1,1'-bis(diphenylphosphino) ferrocene]palladium(II) (48
mg, 0.07 mmol) in a mixture of 1,2-dimethoxyethane (8.0 mL) and
dimethylformamide (1.4 mL) was added a solution of potassium
carbonate (2M in water, 0.98 mL, 1.96 mmol). The resulting mixture
was degassed and then heated to 85.degree. C. under argon for 18
hours. After cooling to room temperature, the reaction was diluted
with ethyl acetate. The organics were washed with water and brine,
dried (Na.sub.2SO.sub.4), and concentrated. The crude residue was
purified by flash chromatography to (2S,4S)-tert-butyl
2-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)pyrrolidin--
2-yl)-1H-benzo[d]imidazol-6-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[-
1,2-d]imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate
(156 mg, 29%).
methyl{(2S)-2-[[(2S,4S)-2-{9-[2-((2S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-
-methylbutanoyl}pyrrolidin-2-yl)-1H-benzo[d]imidazol-6-y]-1,11-dihydroisoc-
hromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl}-4-(methoxymethyl)pyrrolidin-
-1-yl]-2-oxo-1-phenylethyl}carbamate
[0298] A solution of (2S,4S)-tert-butyl
2-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)pyrrolidin--
2-yl)-1H-benzo[d]imidazol-6-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[-
1,2-d]imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate
(156 mg, 0.18 mmol), ethanol (3 mL) and concentrated HCl (1 mL) was
heated to 60.degree. C. for 1 hour. The reaction was concentrated
and the crude material dissolved in DCM (6 mL). This solution was
concentrated and to (90 mg, 0.12 mmol) of this material was added a
solution of (R)-2-(methoxycarbonylamino)-2-phenylacetic acid (34
mg, 0.16 mmol) and COMU (61 mg, 014 mmol) in DMF (2 mL). To the
resulting solution was added diisopropylethylamine (60 .mu.L, 0.37
mmol). After stirring for 2 hours at room temperature, the reaction
was diluted with ethyl acetate, washed with water and brine, dried
(Na.sub.2SO.sub.4), concentrated and purified by preparative
reverse phase HPLC (Gemini, 15 to 49% ACN/H.sub.2O+0.1% TFA). The
product fractions were lyophilized to give methyl
{(2S)-2-[[(2S,4S)-2-{9-[2-((2S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-meth-
ylbutanoyl}pyrrolidin-2-yl)-1H-benzo[d]imidazol-6-y]-1,11-dihydroisochrome-
no[4',3':6,7]naphtho[1,2-d]imidazol-2-yl}-4-(methoxymethyl)pyrrolidin-1-yl-
]-2-oxo-1-phenylethyl}carbamate (62 mg, 56%). MS (ESI) m/z 920
[M+H].sup.+. .sup.1H NMR (400 MHz, dmso) .delta. 8.73 (s, 1H), 8.17
(d, 2H, J=8.4 Hz), 7.94 (d, 3H, J=8.8 Hz), 7.84-7.67 (m, 6H),
7.37-7.29 (m, 6H), 5.48 (d, 1H, J=7.6 Hz), 5.35-5.20 (m, 5H),
4.14-3.12 (m, 15H), 2.52-1.92 (m, 8H), 0.80 (dd, 6H, J=6.8 Hz,
J=6.4 Hz).
Example AT
##STR00106##
[0299]
methyl{(2S)-2-[(2S,4S)-2-{9-[2-((2S)-1-{(2S)-2-[(methoxycarbonyl)am-
ino]-3-methylbutanoyl}pyrrolidin-2-yl)-1H-benzo[d]imidazol-6-y]-1,11-dihyd-
roisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl}-4-(methoxymethyl)pyrr-
olidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate
[0300] A solution of
(2S,4S)-tert-butyl-2-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)-3-methylb-
utanoyl)pyrrolidin-2-yl)-1H-benzo[d]imidazol-6-yl)-1,11-dihydroisochromeno-
[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-car-
boxylate (156 mg, 0.18 mmol), ethanol (3 mL) and concentrated HCl
(1 mL) was heated to 60.degree. C. for 1 hour. The reaction was
concentrated and the crude material dissolved in DCM (6 mL). This
solution was concentrated and to (68 mg, 0.09 mmol) of this
material was added a solution of
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid (21 mg, 0.12 mmol)
and COMU (41 mg, 01 mmol) in DMF (1 mL). To the resulting solution
was added diisopropylethylamine (50 .mu.L, 0.28 mmol). After
stirring for 2 hours at room temperature, the reaction was diluted
with ethyl acetate, washed with water and brine, dried
(Na.sub.2SO.sub.4), concentrated and purified by preparative
reverse phase HPLC (Gemini, 15 to 44% ACN/H.sub.2O+0.1% TFA). The
product fractions were lyophilized to give methyl
{(2S)-2-[(2S,4S)-2-{9-[2-((2S)-1-{(2S)-2-[(methoxycarbonyl)amino]--
3-methylbutanoyl}pyrrolidin-2-yl)-1H-benzo[d]imidazol-6-y]-1,11-dihydroiso-
chromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl}-4-(methoxymethyl)pyrrolidi-
n-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate (32 mg, 40%). MS (ESI)
m/z 886 [M+H].sup.+. .sup.1H NMR (400 MHz, dmso) .delta. 8.71 (s,
1H), 8.15 (d, 1H, J=8 Hz), 7.95-7.64 (m, 8H), 7.28 (dd, 2H, J=8.8
Hz, J=14.4 Hz), 5.31 (s, 2H), 5.23-5.19 (m, 2H), 4.09-3.85 (m, 5H),
3.58-3.28 (m, 14H), 2.47-1.89 (m, 9H), 0.83-0.72 (m, 12H).
Example AU
##STR00107##
[0301] tert-butyl
(2S,4S)-2-[5-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-pyrrolidin-2-yl}-
-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imidazo-
l-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
[0302] To a solution of (2S)-methyll
{-2-[(9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,11-dihydroisochro-
meno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)pyrrolidin-1yl]-3-methyl-1-oxob-
utan-2-yl}carbamate (460 mg, 0.74 mmol), (2S,4S)-tert-butyl
2-(5-bromo-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate
(250 mg, 0.61 mmol), tetrakis (triphenylphosphine) palladium(0) (35
mg, 0.03 mmol) and dichloro[1,1'-bis (diphenylphosphino)
ferrocene]palladium(II) (45 mg, 0.06 mmol) in a mixture of
1,2-dimethoxyethane (9.0 mL) and dimethylformamide (1.5 mL) was
added a solution of potassium carbonate (2M in water, 0.92 mL, 1.84
mmol). The resulting mixture was degassed and then heated to
85.degree. C. under argon for 18 hours. After cooling to room
temperature, the reaction was diluted with ethyl acetate. The
organics were washed with water and brine, dried
(Na.sub.2SO.sub.4), and concentrated. The crude residue was
purified by flash chromatography to tert-butyl
(2S,4S)-2-[5-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-pyrrolidin-2-yl}-
-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imidazo-
l-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate (123 mg, 26
methyl{(1R)-2-[(2S,4S)-2-(5-{2-[(2S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3--
methylbutanoyl}-pyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho-
[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidin-1-yl]--
2-oxo-1-phenylethyl}carbamate
[0303] A solution tert-butyl (2S,4S)-2-[5-(2-{(2S,4S)-1-[N-(methoxy
carbonyl)-L-valyl]-pyrrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]nap-
htho[1,2-d]imidazol-9-yl)-1H-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-c-
arboxylate (122 mg, 0.16 mmol), ethanol (3 mL) and concentrated HCl
(1 mL) was heated to 60.degree. C. for 1 hour. The reaction was
concentrated and the crude material dissolved in DCM (3 mL). This
solution was concentrated and to this material was added a solution
of (R)-2-(methoxycarbonylamino)-2-phenylacetic acid (43 mg, 0.2
mmol) and COMU (77 mg, 018 mmol) in DMF (3 mL). To the resulting
solution was added diisopropylethylamine (80 .mu.L, 0.37 mmol).
After stirring for 2 hours at room temperature, the reaction was
diluted with ethyl acetate, washed with water and brine, dried
(Na.sub.2SO.sub.4), concentrated and purified by preparative
reverse phase HPLC (Gemini, 15 to 44% ACN/H.sub.2O+0.1% TFA). The
product fractions were lyophilized to give methyl
{(1R)-2-[(2S,4S)-2-(5-{2-[(2S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-methy-
lbutanoyl}-pyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2--
d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidin-1-yl]-2-oxo-
-1-phenylethyl}carbamate (60 mg, 44%). MS (ESI) m/z 870
[M+H].sup.+. .sup.1H NMR (400 MHz, dmso) .delta. 8.71 (s, 1H), 8.22
(d, 1H, J=8 Hz), 8.09 (m, 1H), 7.88-7.63 (m, 6H), 7.36-7.29 (m,
6H), 5.41 (d, 1H, J=8.4 Hz), 5.30-5.24 (m, 2H), 5.14-5.10 (m, 1H),
4.13-3.09 (m, 15H), 2.47-1.80 (m, 8H), 0.80 (dd, 6H, J=6.4 Hz, J=23
Hz).
Example AV
##STR00108##
[0304]
(1R,3S,5R)-tert-butyl3-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)-3-
-methylbutanoyl)-4-methoxymethylpyrrolidin-2-yl)-1H-imidazol-5-yl)-1,11-di-
hydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-2-azabicyclo[3.1.0-
]hexane-2-carboxylate
[0305] To a solution of
(1R,3S,5R)-tert-butyl-3-(9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)--
1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-2-azabicycl-
o[3.1.0]hexane-2-carboxylate (213 mg, 0.37 mmol), methyl
(S)-1-((2S,4S)-2-(5-bromo-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidin-1-
-yl)-3-methyl-1-oxobutan-2-ylcarbamate (142 mg, 0.31 mmol),
tetrakis (triphenylphosphine) palladium(0) (35 mg, 0.03 mmol) and
dichloro[1,1'-bis (diphenylphosphino) ferrocene]palladium(II) (22
mg, 0.03 mmol) in a mixture of 1,4-dioxane (3.0 mL) and
dimethylsulfoxide (3.0 mL) was added a solution of potassium
carbonate (2M in water, 0.46 mL, 0.9 mmol). The resulting mixture
was degassed and then heated to 95.degree. C. under argon for 7
hours. After cooling to room temperature, the reaction was diluted
with ethyl acetate. The organics were washed with water and brine,
dried (Na.sub.2SO.sub.4), and concentrated. The crude residue was
purified by flash chromatography to (1R,3S,5R)-tert-butyl
3-(9-(2-((S)-1-((S)-2-(methoxycarbonyl
amino)-3-methylbutanoyl)-4-methoxymethylpyrrolidin-2-yl)-1H-imidazol-5-yl-
)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-2-azabicy-
clo[3.1.0]hexane-2-carboxylate (101 mg, 42%).
methyl{(1R)-2-[(1R,3S,5R)-2-(9-{2-[(2S,5S)-1-{(2S)-2-[(methoxycarbonyl)ami-
no]-3-methylbutanoyl}-4-methoxymethylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,-
11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-azabicyclo[3.-
1.0]hex-3-yl]-2-oxo-1-phenylethyl}carbamate
[0306] A solution (1R,3S,5R)-tert-butyl
3-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-4-methoxym-
ethylpyrrolidin-2-yl)-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]-
naphtho[1,2-d]imidazol-2-yl)-2-azabicyclo[3.1.0]hexane-2-carboxylate
(101 mg, 0.16 mmol), ethanol (3 mL) and concentrated HCl (1 mL) was
heated to 60.degree. C. for 1 hour. The reaction was concentrated
and the crude material dissolved in DCM (3 mL). This solution was
concentrated and to this material was added a solution of
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid (35 mg, 0.17 mmol)
and COMU (63 mg, 015 mmol) in DMF (3 mL). To the resulting solution
was added diisopropylethylamine (70 .mu.L, 0.38 mmol). After
stirring for 2 hours at room temperature, the reaction was diluted
with ethyl acetate, washed with water and brine, dried
(Na.sub.2SO.sub.4), concentrated and purified by preparative
reverse phase HPLC (Gemini, 15 to 44% ACN/H.sub.2O+0.1% TFA). The
product fractions were lyophilized to give methyl methyl
{(1R)-2-[(1R,3S,5R)-2-(9-{2-[(2S,5S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-
-methylbutanoyl}-4-methoxymethylpyrrolidin-2-yl]-1H-imidazol-5
yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-2-azab-
icyclo[3.1.0]hex-3-yl]-2-oxo-1-phenylethyl}carbamate (71 mg, 63).
MS (ESI) m/z 882 [M+H].sup.+. .sup.1H NMR (400 MHz, dmso) .delta.
8.66 (s, 1H), 8.17 (d, 1H, J=8.8 Hz), 8.04 (s, 1H), 7.87-7.59 (m,
6H), 7.39-7.22 (m, 6H), 5.72 (d, 1H, J=7.6 Hz), 5.68 (s, 1H), 5.25
(s, 1H), 5.13-5.01 (m, 2H), 4.12-4.00 (m, 2H), 3.81-3.00 (m, 13H),
2.60 (m, 1H), 2.43-2.37 (m, 3H), 1.92-1.82 (m, 3H), 0.83-0.58 (m,
7H), 0.59 (s, 1H), 0.00 (s, 1H).
Example AW
##STR00109##
[0308] This compound was synthesized using the same conditions as
Example BX substituting with the respective
(1R,3S,5R)-2-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-2-azabicyclo-
[3.1.0]hexane-3-carboxylic acid and
(2S,4S)-1-(tert-butoxycarbonyl)-4-((difluoromethoxy)methyl)pyrrolidine-2--
carboxylic acid as appropriate. MS (ESI) m/z 918 [M+H].sup.+.
Example AX
##STR00110##
[0310] This compound was synthesized using the same conditions as
Example BX substituting with the respective
(1R,3S,5R)-2-((2S,3S)-3-methoxy-2 (methoxycarbonylamino)
butanoyl)-2-azabicyclo[3.1.0]hexane-3-carboxylic acid and
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid as
appropriate. MS (ESI) m/z 898 [M+H].sup.+.
Example AY
##STR00111##
[0311] (2S,4S)-1-tert-butyl
2-(3-chloro-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-9-yl)
4-methylpyrrolidine-1,2-dicarboxylate
[0312] To a solution of
9-bromo-3-chloro-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one
(1.32 g, 3.63 mmol) in MeCN (40 mL) was added
(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidine-2-carboxylic
acid (1.0 g, 4.36 mmol) and DIPEA (0.7 mL, 3.99 mmol). After
stirring for 18 h, the solution was diluted with EtOAc and washed
successively with saturated aqueous NaHCO.sub.3 and brine. The
organics were dried over MgSO.sub.4, filtered and concentrated
under reduced pressure. The crude residue was purified by silica
column chromatography (10% to 40% EtOAc/hexanes) to afford
(2S,4S)-1-tert-butyl
2-(3-chloro-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-9-yl)
4-methylpyrrolidine-1,2-dicarboxylate (1.31 g, 70%).
(2S,4S)-tert-butyl
2-(9-chloro-4,5-dihydro-5H-naphtho[c,g]chromeno[8,9-d]imidazol-2-yl)-4-me-
thylpyrrolidine-1-carboxylate
[0313] (2S,4S)-1-tert-butyl
2-(3-chloro-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-9-yl)
4-methylpyrrolidine-1,2-dicarboxylate (1.31 g, 2.56 mmol) was added
xylenes (25 mL) and ammonium acetate (3.95 g, 51.2 mmol) and the
solution was heated to 136.degree. C. and stirred overnight. The
following morning, the solution was cooled to rt and was diluted
with EtOAc and washed successively with water, saturated aqueous
NaHCO.sub.3 and brine. The organics were dried over MgSO.sub.4,
filtered and concentrated under reduced pressure. The crude residue
was purified by silica column chromatography (60% to 100%
EtOAc/hexanes) to afford (2S,4S)-tert-butyl
2-(9-chloro-4,5-dihydro-5H-naphtho[c,g]chromeno[8,9-d]imidazol-2-yl)-4-me-
thylpyrrolidine-1-carboxylate (711 mg, 56%).
(2S,4S)-tert-butyl
2-(9-chloro-5H-naphtho[c,g]chromeno[8,9-d]imidazol-2-yl)-4-methylpyrrolid-
ine-1-carboxylate
[0314] To a solution of (2S,4S)-tert-butyl
2-(9-chloro-4,5-dihydro-5H-naphtho[c,g]chromeno[8,9-d]imidazol-2-yl)-4-(m-
ethyl)pyrrolidine-1-carboxylate (935 mg, 1.9 mmol) in
CH.sub.2Cl.sub.2 (20 mL) was added MnO.sub.2 (8.25 g, 95 mmol). The
reaction mixture was stirred for 3 h, and then filtered over
celite. The filter cake was washed with copious CH.sub.2Cl.sub.2
and MeOH, and the filtrate was concentrated under reduced pressure.
The crude residue was purified by silica column chromatography (0%
to 10% MeOH/EtOAc) to afford (2S,4S)-tert-butyl
2-(9-chloro-5H-naphtho[c,g]chromeno[8,9-d]imidazol-2-yl)-4-methylpyrrolid-
ine-1-carboxylate (692 mg, 74%).
(2S,4S)-tert-butyl-2-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)methylbutan-
oyl)azabicyclo[3.1.0]hexan-3-yl)-1H-imidazol-5-yl)-5H-naphtho[c,g]chromeno-
[8,9-d]imidazol-2-yl)-4-methylpyrrolidine-1-carboxylate
[0315] (2S,4S)-tert-butyl
2-(9-chloro-5H-naphtho[c,g]chromeno[8,9-d]imidazol-2-yl)-4-methylpyrrolid-
ine-1-carboxylate (692 mg, 1.41 mmol) in dioxane (15 mL) was added
bis(pinacolato)diboron (1.07 g, 4.23 mmol), KOAc (415 mg, 4.23
mmol), X-Phos (52 mg, 0.11 mmol), and Pd.sub.2dba.sub.3 (26 mg,
0.03 mmol). The solution was degassed with N.sub.2 for 10 min, then
heated to 100.degree. C. for 16 h. The solution was cooled to rt,
diluted with EtOAc, washed with saturated aqueous NaHCO.sub.3,
brine, dried with MgSO.sub.4, and concentrated. Purified by silica
gel chromatography (0% to 30% MeOH/EtOAc) to afford
(2S,4S)-tert-butyl-2-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)methylbuta-
noyl)azabicyclo[3.1.0]hexan-3-yl)-1H-imidazol-5-yl)-5H-naphtho[c,g]chromen-
o[8,9-d]imidazol-2-yl)-4-methylpyrrolidine-1-carboxylate (821 mg,
quant).
(2S,4S)-tert-butyl
2-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)pyrrolidin--
2-yl)-1H-imidazol-5-yl)-5H-naphtho[c,g]chromeno[8,9-d]imidazol-2-yl)-4(met-
hyl)pyrrolidine-1-carboxylate
[0316] To a solution of
(2S,4S)-tert-butyl-2-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)methylbuta-
noyl)azabicyclo[3.1.0]hexan-3-yl)-1H-imidazol-5-yl)-5H-naphtho[c,g]chromen-
o[8,9-d]imidazol-2-yl)-4-methylpyrrolidine-1-carboxylate (821 mg,
1.41 mmol), methyl
(S)-1-((S)-2-(5-bromo-1H-imidazol-2-yl)pyrrolidin-1-yl)-3-methyl-1-oxobut-
an-2-ylcarbamate (1.05 g, 2.82 mmol), tetrakis(triphenylphosphine)
palladium(0) 162 mg, 0.14 mmol) and
dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) (102
mg, 0.14 mmol) in DME (15 mL) was added a solution of potassium
carbonate (2M in water, 2.32 mL, 4.65 mmol). The resulting mixture
was degassed and then heated to 85.degree. C. for 18 hours. After
cooling to room temperature, the reaction was diluted with ethyl
acetate. The organics were washed with saturated sodium bicarbonate
and brine, dried over MgSO.sub.4 and concentrated. The crude
residue was purified by flash chromatography to yield
(2S,4S)-tert-butyl
2-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)pyrrolidin--
2-yl)-1H-imidazol-5-yl)-5H-naphtho[c,g]chromeno[8,9-d]imidazol-2-yl)-4meth-
ylpyrrolidine-1-carboxylate (386 mg, 37%).
Methyl
{2-[2-{9-[2-(1-{2-[(methoxycarbonyl)amino]-3-methylbutanoyl}pyrroli-
din-2-yl)-1H-imidazol-5-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2--
d]imidazol-2-yl}-4-(methyl)pyrrolidin-1-yl]-2-oxo-1-phenylethyl}carbamate
[0317] A solution of (2S,4S)-tert-butyl
2-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)pyrrolidin--
2-yl)-1H-imidazol-5-yl)-5H-naphtho[c,g]chromeno[8,9-d]imidazol-2-yl)-4meth-
ylpyrrolidine-1-carboxylate (386 mg, 0.52 mmol), CH.sub.2Cl.sub.2
(8 mL), MeOH (2 mL) and HCl (4M in Dioxane, 2 mL) and was stirred
overnight. The reaction was concentrated and the crude material
dissolved in DMF (8 mL). This solution was concentrated and to this
material was added a solution of
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid (108 mg, 0.52
mmol) and COMU (248 mg, 0.52 mmol). To the resulting solution was
added diisopropylethylamine (0.45 mL, 2.6 mmol). After stirring for
2 hours at room temperature, the reaction was diluted with 10%
MeOH/EtOAc, washed with saturated NaHCO.sub.3 water and brine,
dried (Na.sub.2SO.sub.4), concentrated and purified by HPLC to give
methyl
{2-[2-{9-[2-(1-{2-[(methoxycarbonyl)amino]-3-methylbutanoyl}pyrrolidin-2--
yl)-1H-imidazol-5-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imid-
azol-2-yl}-4-methylpyrrolidin-1-yl]-2-oxo-1-phenylethyl}carbamate
(27 mg, 6%). LCMS-ESI.sup.+: calculated for
C.sub.47H.sub.50N.sub.8O.sub.7: 838.38; observed [M+1].sup.+:
840.12
Example AZ
##STR00112##
[0318] Methyl
[(2S)-3-methyl-1-{(2S,4S)-4-methyl-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxab-
orolan-2-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl-
]pyrrolidin-1-yl}-1-oxobutan-2-yl]carbamate
[0319]
(2S,4S)-tert-butyl-2-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)meth-
ylbutanoyl)azabicyclo[3.1.0]hexan-3-yl)-1H-imidazol-5-yl)-5H-naphtho[c,g]c-
hromeno[8,9-d]imidazol-2-yl)-4-(methyl)pyrrolidine-1-carboxylate
(950 mg, 1.63 mmol) was dissolved in DCM (12 mL), MeOH (3 mL) and
HCl (4 M in dioxane, 3 mL) was added. The reaction mixture was
stirred for 4 h and then concentrated under reduced pressure. The
crude residue was treated with
(S)-2-(methoxycarbonylamino)-3-methylbutanoic acid (285 mg, 1.63
mmol), HATU (620 mg, 1.63 mmol) and DMF (15 mL), then DIPEA (1.42
mL, 8.15 mmol) was added dropwise. After 1 h, the mixture was
diluted with EtOAc and washed successively with saturated aqueous
NaHCO.sub.3 and brine. The organics were dried over MgSO.sub.4,
filtered and concentrated under reduced pressure. The crude residue
was purified by silica column chromatography (0% to 30% MeOH/EtOAc)
to afford methyl
[(2S)-3-methyl-1-{(2S,4S)-4-methyl-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxab-
orolan-2-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl-
]pyrrolidin-1-yl}-1-oxobutan-2-yl]carbamate (596 mg, 57%).
Tert-butyl
(2S)-2-[5-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-4-methylp-
yrrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-
-yl)-1H-imidazol-2-yl]pyrrolidine-1-carboxylate
[0320] Methyl
[(2S)-3-methyl-1-{(2S,4S)-4-methyl-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxab-
orolan-2-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl-
]pyrrolidin-1-yl}-1-oxobutan-2-yl]carbamate (298 mg, 0.47 mmol),
(S)-tert-butyl
2-(5-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate (443 mg, 1.4
mmol), Pd(PPh.sub.3).sub.4 (54 mg, 0.05 mmol),
PdCl.sub.2(dppf).sub.2 (36 mg, 0.05 mmol), and K.sub.2CO.sub.3 (2M
in H.sub.2O, 0.78 mL, 1.55 mmol) were combined in DME (5 mL). The
mixture was degassed with bubbling N.sub.2 for 10 min the heated to
85.degree. C. for 16 h. After cooling, the reaction mixture was
diluted with EtOAc, and washed successively with saturated aqueous
NaHCO.sub.3 and brine. The organics were dried over MgSO.sub.4,
filtered and concentrated under reduced pressure. The crude residue
was purified by silica column chromatography (0% to 30% MeOH/EtOAc)
to afford tert-butyl
(2S)-2-[5-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-4-methylpyrrolidin--
2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-im-
idazol-2-yl]pyrrolidine-1-carboxylate (84 mg, 24%).
Methyl
{(1R)-2-[(2S)-2-(5-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-
-methylbutanoyl}-4-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6,-
7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]-2-oxo-1-p-
henylethyl}carbamate
[0321] Tert-butyl
(2S)-2-[5-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-4-methylpyrrolidin--
2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-im-
idazol-2-yl]pyrrolidine-1-carboxylate (84 mg, 0.11 mmol) was
dissolved in DCM (2.5 mL), MeOH (0.5 mL) and HCl (4 M in dioxane,
0.5 mL) was added. The reaction mixture was stirred for 18 h and
then concentrated under reduced pressure. The crude residue was
treated with (R)-2-(methoxycarbonylamino)-2-phenylacetic acid (23
mg, 0.11 mmol), COMU (53 mg, 0.11 mmol) and DMF (3 mL), then DIPEA
(0.10 mL, 0.56 mmol) was added dropwise. After 30 min, the mixture
was diluted with 10% MeOH/EtOAc and washed successively with
saturated aqueous NaHCO.sub.3 and brine. The organics were dried
over MgSO.sub.4, filtered and concentrated under reduced pressure.
The crude residue was purified by HPLC to afford methyl
{(1R)-2-[(2S)-2-(5-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-methy-
lbutanoyl}-4-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6,7]naph-
tho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]-2-oxo-1-phenyle-
thyl}carbamate (41 mg, 45%). LCMS-ESI.sup.+: calculated for
C.sub.47H.sub.50N.sub.8O.sub.7: 838.38; observed [M+1].sup.+:
839.39
Example BA
##STR00113##
[0322] Methyl
{(2S)-1-[(2S,5S)-2-(5-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-me-
thylbutanoyl}-4-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6,7]n-
aphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-5-methylpyrrolidin-1-yl]-3-m-
ethyl-1-oxobutan-2-yl}carbamate
[0323] Tert-butyl
(2S,4S)-2-[9-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d-
]imidazol-2-yl]-4-methylpyrrolidine-1-carboxylate (164 mg, 0.23
mmol) was dissolved in DCM (2.57 mL), MeOH (0.7 mL) and HCl (4 M in
dioxane, 0.7 mL) was added. The reaction mixture was stirred for 16
h and then concentrated under reduced pressure. The crude residue
was treated with (S)-2-(methoxycarbonylamino)-3-methylbutanoic acid
(30 mg, 0.17 mmol), HATU (65 mg, 0.17 mmol) and DMF (3 mL), then
DIPEA (0.15 mL, 0.85 mmol) was added dropwise. After 45 min, the
mixture was diluted with 10% MeOH/EtOAc and washed successively
with saturated aqueous NaHCO.sub.3 and brine. The organics were
dried over MgSO.sub.4, filtered and concentrated under reduced
pressure. The crude residue was purified by HPLC to afford methyl
{(2S)-1-[(2S,5S)-2-(5-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amin-
o]-3-methylbutanoyl}-4-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3-
':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-5-methylpyrrolidin-1--
yl]-3-methyl-1-oxobutan-2-yl}carbamate (23 mg, 16%).
LCMS-ESI.sup.+: calculated for C.sub.45H.sub.54N.sub.8O.sub.7:
818.41; observed [M+1].sup.+: 820.70.
Example BB
##STR00114##
[0324] Tert-butyl
(2S,4S)-2-(5-{2-[(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidin-2-yl]-
-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazo-
l-2-yl)-4-methylpyrrolidine-1-carboxylate
[0325]
(2S,4S)-tert-butyl-2-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)meth-
ylbutanoyl)azabicyclo[3.1.0]hexan-3-yl)-1H-imidazol-5-yl)-5H-naphtho[c,g]c-
hromeno[8,9-d]imidazol-2-yl)-4-methylpyrrolidine-1-carboxylate (293
mg, 0.0.78 mmol), (2S,4S)-tert-butyl
2-(5-iodo-1H-imidazol-2-yl)-4-methylpyrrolidine-1-carboxylate (300
mg, 0.52 mmol), Pd(PPh.sub.3).sub.4(60 mg, 0.052 mmol),
PdCl.sub.2(dppf).sub.2 (38 mg, 0.052 mmol), and K.sub.2CO.sub.3 (2M
in H.sub.2O, 0.86 mL, 1.72 mmoL) were combined in DME (6 mL). The
mixture was degassed with bubbling N.sub.2 for 10 min the heated to
85.degree. C. for 16 h. After cooling, the reaction mixture was
diluted with EtOAc, and washed successively with saturated aqueous
NaHCO.sub.3 and brine. The organics were dried over MgSO.sub.4,
filtered and concentrated under reduced pressure. The crude residue
was purified by silica column chromatography (100% EtOAc) to afford
tert-butyl
(2S,4S)-2-(5-{2-[(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidin-2-yl]-
-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazo-
l-2-yl)-4-methylpyrrolidine-1-carboxylate (183 mg, 50%).
Methyl
{(2S)-1-[(2S,5S)-2-(5-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino-
]-3-methylbutanoyl}-4-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3'-
:6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-methylpyrrolidin-1-y-
l]-3-methyl-1-oxobutan-2-yl}carbamate
[0326] Tert-butyl
(2S,4S)-2-(5-{2-[(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidin-2-yl]-
-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazo-
l-2-yl)-4-methylpyrrolidine-1-carboxylate (183 mg, 0.26 mmol) was
dissolved in DCM (4 mL), MeOH (1 mL) and HCl (4 M in dioxane, 1 mL)
was added. The reaction mixture was stirred for 2 h and then
concentrated under reduced pressure. The crude residue was treated
with (S)-2-(methoxycarbonylamino)-3-methylbutanoic acid (91 mg,
0.52 mmol), HATU (198 mg, 0.52 mmol) and DMF (5 mL), then DIPEA
(0.45 mL, 2.6 mmol) was added dropwise. After 1 h, the mixture was
diluted with 10% MeOH/EtOAc and washed successively with saturated
aqueous NaHCO.sub.3 and brine. The organics were dried over
MgSO.sub.4, filtered and concentrated under reduced pressure. The
crude residue was purified by HPLC to afford methyl
{(2S)-1-[(2S,5S)-2-(5-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amin-
o]-3-methylbutanoyl}-4-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3-
':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-methylpyrrolidin-1--
yl]-3-methyl-1-oxobutan-2-yl}carbamate (6 mg, 3%). LCMS-ESI.sup.+:
calculated for C.sub.45H.sub.54N.sub.8O.sub.7: 818.41; observed
[M+1].sup.+: 819.41.
Example BC
##STR00115##
[0327] Tert-butyl
(2S,4S)-2-[9-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-4-methylpyrrolid-
in-2-yl}-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d-
]imidazol-2-yl]-4-methylpyrrolidine-1-carboxylate
[0328]
(2S,4S)-tert-butyl-2-(9-(2-((S)-1-((S)-2-(methoxycarbonylamino)meth-
ylbutanoyl)azabicyclo[3.1.0]hexan-3-yl)-1H-imidazol-5-yl)-5H-naphtho[c,g]c-
hromeno[8,9-d]imidazol-2-yl)-4-methylpyrrolidine-1-carboxylate (558
mg, 0.96 mmol), methyl
(S)-1-((2S,4S)-2-(5-iodo-1H-imidazol-2-yl)-4-methylpyrrolidin-1-yl)-3-met-
hyl-1-oxobutan-2-ylcarbamate (501 mg, 1.15 mmol),
Pd(PPh.sub.3).sub.4(111 mg, 0.096 mmol), PdCl.sub.2(dppf).sub.2 (70
mg, 0.096 mmol), and K.sub.2CO.sub.3 (2M in H.sub.2O, 1.6 mL, 3.17
mmoL) were combined in DMSO (6 mL) and dioxane (6 mL). The mixture
was degassed with bubbling N.sub.2 for 10 min the heated to
95.degree. C. for 14 h. After cooling, the reaction mixture was
diluted with EtOAc, and washed successively with saturated aqueous
NaHCO.sub.3 and brine. The organics were dried over MgSO.sub.4,
filtered and concentrated under reduced pressure. The crude residue
was purified by silica column chromatography (0%-30% MeOH/EtOAc) to
afford tert-butyl
(2S,4S)-2-[9-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-4-methylpyrrolid-
in-2-yl}-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d-
]imidazol-2-yl]-4-methylpyrrolidine-1-carboxylate (257 mg,
35%).
Methyl
{(2S)-1-[(2S,4S)-2-(5-{2-[(2S,4S)-1-{(2R)-2-[(methoxycarbonyl)amino-
]-2-phenylacetyl}-4-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6-
,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-methylpyrrolidin-1-yl]-
-3-methyl-1-oxobutan-2-yl}carbamate
[0329] Tert-butyl
(2S,4S)-2-[9-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-4-methylpyrrolid-
in-2-yl}-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d-
]imidazol-2-yl]-4-methylpyrrolidine-1-carboxylate (257 mg, 0.34
mmol) was dissolved in DCM (4 mL), MeOH (1 mL) and HCl (4 M in
dioxane, 1 mL) was added. The reaction mixture was stirred for 3 h
and then concentrated under reduced pressure. The crude residue was
treated with (R)-2-(methoxycarbonylamino)-2-phenylacetic acid (71
mg, 0.34 mmol), COMU (161 mg, 0.34 mmol) and DMF (6 mL), then DIPEA
(0.3 mL, 1.67 mmol) was added dropwise. After 15 h, the mixture was
diluted with 10% MeOH/EtOAc and washed successively with saturated
aqueous NaHCO.sub.3 and brine. The organics were dried over
MgSO.sub.4, filtered and concentrated under reduced pressure. The
crude residue was purified by HPLC to afford methyl
{(2S)-1-[(2S,4S)-2-(5-{2-[(2S,4S)-1-{(2R)-2-[(methoxycarbonyl)amino]-2-ph-
enylacetyl}-4-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6,7]nap-
htho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-methylpyrrolidin-1-yl]-3-met-
hyl-1-oxobutan-2-yl}carbamate (152 mg, 53%). LCMS-ESI.sup.+:
calculated for C.sub.48H.sub.52N.sub.8O.sub.7: 852.40; observed
[M+1].sup.+: 854.26. .sup.1H NMR (CD.sub.3OD): 8.677 (s, 1H),
8.232-7.837 (m, 5H), 7.695-7.673 (m, 2H), 7.496-7.426 (m, 5H),
5.499 (s, 1H), 5.445-5.401 (m, 1H), 5.337 (s, 1H), 5.253-5.208 (q,
1H, J=7.2 Hz), 4.870 (m, 1H), 4.230 (d, 1H, J=7.2 Hz), 3.781 (m,
1H), 3.671 (s, 3H), 3.607 (s, 3H), 3.425 (m, 3H), 2.750-2.689 (m,
2H), 2.683 (m, 2H), 2.384 (m, 1H), 1.894 (quint, 2H, J=12 Hz),
1.249-1.151 (m, 6H), 0.974-0.890 (m, 6H).
Example BD
##STR00116##
[0330] (2S,5S)-1-tert-butyl
2-(2-oxo-2-(8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-3-yl)ethyl)
5-methylpyrrolidine-1,2-dicarboxylate
[0331] To a solution of
3-(2-bromoacetyl)-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one in
MeCN (30 mL) was added
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid (1.2 g, 3.23 mmol) and triethyl amine (0.48 mL, 3.55 mmol) and
the solution was heated to 50.degree. C. After stirring for 15 h,
the solution was cooled to rt, and diluted with EtOAc and washed
successively with saturated aqueous NaHCO.sub.3 and brine. The
organics were dried over MgSO.sub.4, filtered and concentrated
under reduced pressure. The crude residue was purified by silica
column chromatography (20% to 50% EtOAc/hexanes) to afford
(2S,5S)-1-tert-butyl
2-(2-oxo-2-(8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-3-yl)ethyl)
5-methylpyrrolidine-1,2-dicarboxylate (1.09 g, 65%).
(2S,5S)-2-(2-(9-bromo-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-3--
yl)-2-oxoethyl) 1-tert-butyl
5-methylpyrrolidine-1,2-dicarboxylate
[0332] (2S,5S)-1-tert-butyl
2-(2-oxo-2-(8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-3-yl)ethyl)
5-methylpyrrolidine-1,2-dicarboxylate (1.29 g, 2.48 mmol) was
dissolved in a solution of DCM (17.5 mL) and MeOH (7 mL), then
treated with pyridinium tribromide (873 mg, 2.73 mmol). After
stirring at RT for 1 h, the reaction mixture was diluted with DCM
and 10% HCl, and extracted with DCM. The organic phase was dried
over MgSO.sub.4, filtered and concentrated under reduced pressure
and the crude material was carried on without further
purification.
(2S,5S)-2-(2-(9-((2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-car-
bonyloxy)-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-3-yl)-2-oxoeth-
yl) 1-tert-butyl 5-methylpyrrolidine-1,2-dicarboxylate
[0333]
(2S,5S)-2-(2-(9-bromo-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chr-
omen-3-yl)-2-oxoethyl) 1-tert-butyl
5-methylpyrrolidine-1,2-dicarboxylate (700 mg, 1.17 mmol) was
treated with a solution of
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid (375 mg, 1.64 mmol) in acetone (6 mL) and Cs.sub.2CO.sub.3
(267 mg, 0.82 mmol). The stirred reaction mixture was heated to
40.degree. C. for 16 h, then cooled to RT and diluted with
CH.sub.2Cl.sub.2 and extracted 3.times.. The organic phase was
washed with brine, then dried over MgSO.sub.4, filtered and
concentrated under reduced pressure. The crude residue was purified
by silica column chromatography (40% to 100% EtOAc/hexanes) to
afford
(2S,5S)-2-(2-(9-((2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-ca-
rbonyloxy)-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-3-yl)-2-oxoet-
hyl) 1-tert-butyl 5-methylpyrrolidine-1,2-dicarboxylate (464 mg,
53%).
Tert-butyl
(2S,5S)-2-(9-{2-[(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrol-
idin-2-yl]-1H-imidazol-5-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naph-
tho[1,2-d]imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate
[0334]
(2S,5S)-2-(2-(9-((2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidin-
e-2-carbonyloxy)-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-3-yl)-2-
-oxoethyl) 1-tert-butyl 5-methylpyrrolidine-1,2-dicarboxylate (464
mg, 0.62 mmol) and NH.sub.4OAc (8.48 g, 110.0 mmol) were suspended
in a solution of 10:1 PhMe/2-methoxyethanol (22 mL). The stirred
reaction mixture was heated to 110.degree. C. for 20 h, then cooled
to RT and diluted with EtOAc. The organic phase was washed with
water, saturated aqueous NaHCO.sub.3, and brine, then dried over
MgSO.sub.4, filtered and concentrated under reduced pressure. The
crude residue was purified by silica column chromatography (0% to
30% MeOH/EtOAc) to afford tert-butyl
(2S,5S)-2-(9-{2-[(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidin-2-yl]-
-1H-imidazol-5-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]-
imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate (393 mg, 90%).
Tert-butyl
(2S,4S)-2-(5-{2-[(2S,4S)-1-(tert-butoxycarbonyl)-5-methylpyrrol-
idin-2-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}--
1H-imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate
[0335] Tert-butyl
(2S,5S)-2-(9-{2-[(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidin-2-yl]-
-1H-imidazol-5-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]-
imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate (393 mg, 0.55
mmol) was suspended in DCM (7 mL) and activated MnO.sub.2 (1.45 g,
16.7 mmol) was added in a single portion. The reaction mixture was
heated to 40.degree. C. After stirring for 2.5 h, the mixture was
cooled to rt and the slurry was filtered over celite. The filter
cake was washed with copious CH.sub.2Cl.sub.2 and MeOH and the
filtrate was concentrated under reduced pressure. The crude
material was taken on to the next step without further purification
to afford tert-butyl
(2S,4S)-2-(5-{2-[(2S,4S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidin-2-yl]-
-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazo-
l-2-yl)-5-methylpyrrolidine-1-carboxylate (328 g, 85%).
Methyl
{(2S)-1-[(2S,5S)-2-(5-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino-
]-3-methylbutanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3'-
:6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-5-methylpyrrolidin-1-y-
l]-3-methyl-1-oxobutan-2-yl}carbamate
[0336] Tert-butyl
(2S,4S)-2-(5-{2-[(2S,4S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidin-2-yl]-
-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazo-
l-2-yl)-5-methylpyrrolidine-1-carboxylate (164 mg, 0.23 mmol) was
dissolved in DCM (7 mL), MeOH (1.5 mL) and HCl (4 M in dioxane, 1.5
mL) was added. The reaction mixture was stirred for 16 h and then
concentrated under reduced pressure. The crude residue was treated
with (S)-2-(methoxycarbonylamino)-3-methylbutanoic acid (81 mg,
0.46 mmol), HATU (175 mg, 0.46 mmol) and DMF (5 mL), then DIPEA
(0.4 mL, 2.34 mmol) was added dropwise. After 35 min, the mixture
was diluted with 10% MeOH/EtOAc and washed successively with
saturated aqueous NaHCO.sub.3 and brine. The organics were dried
over MgSO.sub.4, filtered and concentrated under reduced pressure.
The crude residue was purified by HPLC to afford methyl
{(2S)-1-[(2S,5S)-2-(5-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amin-
o]-3-methylbutanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3-
':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-5-methylpyrrolidin-1--
yl]-3-methyl-1-oxobutan-2-yl}carbamate (132 mg, 69%).
LCMS-ESI.sup.+: calculated for C.sub.45H.sub.54N.sub.8O.sub.7:
818.41; observed [M+1].sup.+: 820.19. .sup.1H NMR (CD.sub.3OD):
8.492 (m, 1H), 8.179-7.538 (m, 7H), 5.267-5.201 (m, 3H),
5.125-5.082 (m, 1H), 4.070 (m, 1H), 3.383-3.592 (m, 4H), 3.225 (s,
3H), 2.466-2.249 (m, 5H), 1.992-1.892 (m, 3H), 1.568 (d, 3H, J=6.4
Hz), 1.490 (d, 3H, J=6.8 Hz), 1.266 (m, 2H), 1.020-0.806 (m,
14H).
Example BE
##STR00117##
[0337] Methyl
[(2S,3R)-3-methoxy-1-{(2S,5S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-O-m-
ethyl-L-threonyl]-5-methylpyrrolidin-2-yl}-1H-imidazol-5-yl)-1,11-dihydroi-
sochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]-5-methylpyrrolidin-1-yl}-
-1-oxobutan-2-yl]carbamate
[0338] Tert-butyl
(2S,4S)-2-(5-{2-[(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidin-2-yl]-
-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazo-
l-2-yl)-4-methylpyrrolidine-1-carboxylate (164 mg, 0.23 mmol) was
dissolved in DCM (7 mL), MeOH (1.5 mL) and HCl (4 M in dioxane, 1.5
mL) was added. The reaction mixture was stirred for 16 h and then
concentrated under reduced pressure. The crude residue was treated
with (2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid (90
mg, 0.46 mmol), HATU (175 mg, 0.46 mmol) and DMF (6 mL), then DIPEA
(0.4 mL, 2.34 mmol) was added dropwise. After 30 min, the mixture
was diluted with 10% MeOH/EtOAc and washed successively with
saturated aqueous NaHCO.sub.3 and brine. The organics were dried
over MgSO.sub.4, filtered and concentrated under reduced pressure.
The crude residue was purified by HPLC to afford methyl
[(2S,3R)-3-methoxy-1-{(2S,5S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbon-
yl)-O-methyl-L-threonyl]-5-methylpyrrolidin-2-yl}-1H-imidazol-5-yl)-1,11-d-
ihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]-5-methylpyrrolidi-
n-1-yl}-1-oxobutan-2-yl]carbamate (97 mg, 50%). LCMS-ESI.sup.+:
calculated for C.sub.45H.sub.54N.sub.8O.sub.9: 850.40; observed
[M+1].sup.+: 851.58. .sup.1H NMR (CD.sub.3OD): 8.631 (s, 1H),
8.191-7.938 (m, 7H), 6.100 (m, 1H), 5.925 (m, 1H), 5.303 (m, 3H),
5.179 (t, 1H, J=6.8 Hz), 4.406-4.358 (m, 2H), 3.754-3.598 (m, 8H),
3.376 (s, 3H), 3.263 (s, 3H), 2.625-2.256 (m, 6H), 2.038-1.955 (m,
2H), 1.598 (d, 3H, J=6.4 Hz), 1.530 (d, 3H, J=6.8 Hz), 1.302-1.099
(m, 6H).
Example BF
##STR00118## ##STR00119##
[0339]
(2S,5S)-2-(2-(9-((2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)p-
yrrolidine-2-carbonyloxy)-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chrome-
n-3-yl)-2-oxoethyl) 1-tert-butyl
5-methylpyrrolidine-1,2-dicarboxylate
[0340]
(2S,5S)-2-(2-(9-bromo-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chr-
omen-3-yl)-2-oxoethyl) 1-tert-butyl
5-methylpyrrolidine-1,2-dicarboxylate (800 mg, 1.34 mmol) was
treated with a solution of
(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrrolidine-2-carboxylic
acid (485 mg, 1.87 mmol) in acetone (6 mL) and Cs.sub.2CO.sub.3
(306 mg, 0.94 mmol). The stirred reaction mixture was heated to
40.degree. C. for 16 h, then cooled to RT and diluted with
CH.sub.2Cl.sub.2 and extracted 3.times.. The organic phase was
washed with brine, then dried over MgSO.sub.4, filtered and
concentrated under reduced pressure. The crude residue was purified
by silica column chromatography (40% to 100% EtOAc/hexanes) to
afford
(2S,5S)-2-(2-(9-((2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-ca-
rbonyloxy)-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-3-yl)-2-oxoet-
hyl) 1-tert-butyl 5-methylpyrrolidine-1,2-dicarboxylate (680 mg,
65%).
Tert-butyl
(2S,5S)-2-(9-{2-[(2S,5S)-1-(tert-butoxycarbonyl)-4-(methoxymeth-
yl)pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,4,5,11-tetrahydroisochromeno[4',3'-
:6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate
[0341]
(2S,5S)-2-(2-(9-((2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidin-
e-2-carbonyloxy)-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-3-yl)-2-
-oxoethyl) 1-tert-butyl 5-methylpyrrolidine-1,2-dicarboxylate (680
mg, 0.87 mmol) and NH.sub.4OAc (10.0 g, 130.0 mmol) were suspended
in a solution of 10:1 PhMe/2-methoxyethanol (22 mL). The stirred
reaction mixture was heated to 110.degree. C. for 24 h, then cooled
to RT and diluted with EtOAc. The organic phase was washed with
water, saturated aqueous NaHCO.sub.3, and brine, then dried over
MgSO.sub.4, filtered and concentrated under reduced pressure. The
crude residue was purified by silica column chromatography (0% to
30% MeOH/EtOAc) to afford tert-butyl
(2S,5S)-2-(9-{2-[(2S,5S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrroli-
din-2-yl]-1H-imidazol-5-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]napht-
ho[1,2-d]imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate (461 mg,
72%).
Tert-butyl
(2S,4S)-2-(5-{2-[(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymeth-
yl)pyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidaz-
ol-9-yl}-1H-imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate
[0342] Tert-butyl
(2S,5S)-2-(9-{2-[(2S,5S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrroli-
din-2-yl]-1H-imidazol-5-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]napht-
ho[1,2-d]imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate (461 mg,
0.62 mmol) was suspended in DCM (7 mL) and activated MnO.sub.2 (1.6
g, 18.8 mmol) was added in a single portion. The reaction mixture
was heated to 40.degree. C. After stirring for 5.5 h, the mixture
was cooled to rt and the slurry was filtered over celite. The
filter cake was washed with copious CH.sub.2Cl.sub.2 and MeOH and
the filtrate was concentrated under reduced pressure. The crude
material was taken on to the next step without further purification
to afford tert-butyl
(2S,4S)-2-(5-{2-[(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrroli-
din-2-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1-
H-imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate (414 g,
90%).
Methyl
{(2S,3S)-1-[(2S,5S)-2-(5-{2-[(2S,4S)-1-{(2S,3S)-2-[(methoxycarbonyl-
)amino]-3-methylpentanoyl}-4-(methoxymethyl)pyrrolidin-2-yl]-1,11-dihydroi-
sochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-5-meth-
ylpyrrolidin-1-yl]-3-methyl-1-oxopentan-2-yl}carbamate
[0343] Tert-butyl
(2S,4S)-2-(5-{2-[(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrroli-
din-2-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1-
H-imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate (207 mg, 0.28
mmol) was dissolved in DCM (4 mL), MeOH (1 mL) and HCl (4 M in
dioxane, 1 mL) was added. The reaction mixture was stirred for 1.5
h and then concentrated under reduced pressure. The crude residue
was treated with (2S,3S)-2-(methoxycarbonylamino)-3-methylpentanoic
acid (106 mg, 0.56 mmol), HATU (214 mg, 0.56 mmol) and DMF (5 mL),
then DIPEA (0.49 mL, 2.8 mmol) was added dropwise. After 30 min,
the mixture was diluted with 10% MeOH/EtOAc and washed successively
with saturated aqueous NaHCO.sub.3 and brine. The organics were
dried over MgSO.sub.4, filtered and concentrated under reduced
pressure. The crude residue was purified by HPLC to afford methyl
{(2S,3S)-1-[(2S,5S)-2-(5-{2-[(2S,4S)-1-{(2S,3
S)-2-[(methoxycarbonyl)amino]-3-methylpentanoyl}-4-(methoxymethyl)pyrroli-
din-2-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1-
H-imidazol-2-yl)-5-methylpyrrolidin-1-yl]-3-methyl-1-oxopentan-2-yl}carbam-
ate (132 mg, 69%). LCMS-ESI.sup.+: calculated for
C.sub.45H.sub.54N.sub.8O.sub.7: 876.45; observed [M+1].sup.+:
879.02
Example BG
##STR00120## ##STR00121##
[0344] (2S,4S)-1-tert-butyl
2-(2-oxo-2-(8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-3-yl)ethyl)
4-methylpyrrolidine-1,2-dicarboxylate
[0345] To a solution of
3-(2-bromoacetyl)-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one
(647 mg, 1.74 mmol) in MeCN (20 mL) was added
((2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidine-2-carboxylic
acid (559 mg, 2.44 mmol) and DIPEA (0.36 mL, 2.09 mmol) and the
solution was heated to 60.degree. C. After stirring for 3 h, the
solution was cooled to rt, and diluted with EtOAc and washed
successively with saturated aqueous NaHCO.sub.3 and brine. The
organics were dried over MgSO.sub.4, filtered and concentrated
under reduced pressure. The crude residue was purified by silica
column chromatography (20% to 50% EtOAc/hexanes) to afford
(2S,4S)-1-tert-butyl
2-(2-oxo-2-(8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-3-yl)ethyl)
4-methylpyrrolidine-1,2-dicarboxylate (621 mg, 69%).
(2S,4S)-2-(2-(9-bromo-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-3--
yl)-2-oxoethyl) 1-tert-butyl
4-methylpyrrolidine-1,2-dicarboxylate
[0346] (2S,4S)-1-tert-butyl
2-(2-oxo-2-(8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-3-yl)ethyl)
4-methylpyrrolidine-1,2-dicarboxylate (621 mg, 1.19 mmol) was
dissolved in a solution of DCM (10 mL) and MeOH (4 mL), then
treated with pyridinium tribromide (421 mg, 1.3 mmol). After
stirring at RT for 1.5 h, the reaction mixture was diluted with DCM
and 10% HCl, and extracted with DCM. The organic phase was dried
over MgSO.sub.4, filtered and concentrated under reduced pressure
and the crude material was carried on without further
purification.
(2S,4S)-2-(2-(9-((2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrrolid-
ine-2-carbonyloxy)-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-3-yl)-
-2-oxoethyl) 1-tert-butyl 4-methylpyrrolidine-1,2-dicarboxylate
[0347]
(2S,4S)-2-(2-(9-bromo-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chr-
omen-3-yl)-2-oxoethyl) 1-tert-butyl
4-methylpyrrolidine-1,2-dicarboxylate (709 mg, 1.18 mmol) was
treated with a solution of
(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrrolidine-2-carboxylic
acid (614 mg, 2.36 mmol) in Me-THF (12 mL) and Cs.sub.2CO.sub.3
(384 mg, 1.18 mmol). The stirred reaction mixture was heated to
50.degree. C. for 16 h, then cooled to RT and diluted with
CH.sub.2Cl.sub.2 and extracted 3.times.. The organic phase was
washed with brine, then dried over MgSO.sub.4, filtered and
concentrated under reduced pressure. The crude residue was purified
by silica column chromatography (40% to 100% EtOAc/hexanes) to
afford
(2S,4S)-2-(2-(9-((2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrroli-
dine-2-carbonyloxy)-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-3-yl-
)-2-oxoethyl) 1-tert-butyl 4-methylpyrrolidine-1,2-dicarboxylate
(651 mg, 71%).
Tert-butyl
(2S,5S)-2-(9-{2-[(2S,5S)-1-(tert-butoxycarbonyl)-4-(methoxymeth-
yl)pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,4,5,11-tetrahydroisochromeno[4',3'-
:6,7]naphtho[1,2-d]imidazol-2-yl)-4-methylpyrrolidine-1-carboxylate
[0348]
(2S,4S)-2-(2-(9-((2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)p-
yrrolidine-2-carbonyloxy)-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chrome-
n-3-yl)-2-oxoethyl) 1-tert-butyl
4-methylpyrrolidine-1,2-dicarboxylate (651 mg, 0.84 mmol) and
NH.sub.4OAc (10.0 g, 129.7 mmol) were suspended in a solution of
10:1 PhMe/2-methoxyethanol (22 mL). The stirred reaction mixture
was heated to 110.degree. C. for 20 h, then cooled to RT and
diluted with EtOAc. The organic phase was washed with water,
saturated aqueous NaHCO.sub.3, and brine, then dried over
MgSO.sub.4, filtered and concentrated under reduced pressure. The
crude residue was purified by silica column chromatography (0% to
30% MeOH/EtOAc) to afford tert-butyl
(2S,5S)-2-(9-{2-[(2S,5S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrroli-
din-2-yl]-1H-imidazol-5-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]napht-
ho[1,2-d]imidazol-2-yl)-4-methylpyrrolidine-1-carboxylate (382 mg,
62%).
Tert-butyl
(2S,4S)-2-[5-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-4-(met-
hoxymethyl)pyrrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2--
d]imidazol-9-yl)-1H-imidazol-2-yl]-4-methylpyrrolidine-1-carboxylate
[0349] Tert-butyl
(2S,5S)-2-(9-{2-[(2S,5S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrroli-
din-22-yl]-1H-imidazol-5-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naph-
tho[1,2-d]imidazol-2-yl)-4-methylpyrrolidine-1-carboxylate (382 mg,
0.52 mmol) was suspended in DCM (8 mL) and activated MnO.sub.2
(1.35 g, 15.5 mmol) was added in a single portion. The reaction
mixture was heated to 35.degree. C. After stirring for 15 h, the
mixture was cooled to rt and the slurry was filtered over celite.
The filter cake was washed with copious CH.sub.2Cl.sub.2 and MeOH
and the filtrate was concentrated under reduced pressure. The crude
material was taken on to the next step without further purification
to afford tert-butyl
(2S,4S)-2-[5-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-4-(methoxymethyl-
)pyrrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-
-9-yl)-1H-imidazol-2-yl]-4-methylpyrrolidine-1-carboxylate (347 g,
91%).
Methyl
{(2S,3R)-3-methoxy-1-[(2S,4S)-2-[9-(2-{(2S,4S)-1-[N-(methoxycarbony-
l)-O-methyl-L-threonyl]-4-methylpyrrolidin-2-yl}-1H-imidazol-5-yl)-1,11-di-
hydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]-4-(methoxymethyl)p-
yrrolidin-1-yl]-1-oxobutan-2-yl}carbamate
[0350] Tert-butyl
(2S,4S)-2-[5-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-4-(methoxymethyl-
)pyrrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-
-9-yl)-1H-imidazol-2-yl]-4-methylpyrrolidine-1-carboxylate (174 mg,
0.24 mmol) was dissolved in DCM (4 mL), MeOH (1 mL) and HCl (4 M in
dioxane, 1 mL) was added. The reaction mixture was stirred for 5 h
and then concentrated under reduced pressure. The crude residue was
treated with ((2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic
acid (92 mg, 0.48 mmol), HATU (182 mg, 0.48 mmol) and DMF (5 mL),
then DIPEA (0.31 mL, 2.4 mmol) was added dropwise. After 35 min,
the mixture was diluted with 10% MeOH/EtOAc and washed successively
with saturated aqueous NaHCO.sub.3 and brine. The organics were
dried over MgSO.sub.4, filtered and concentrated under reduced
pressure. The crude residue was purified by HPLC to afford methyl
{(2S,3R)-3-methoxy-1-[(2S,4S)-2-[9-(2-{(2S,4S)-1-[N-(methoxycarbon-
yl)-O-methyl-L-threonyl]-4-methylpyrrolidin-2-yl}-1H-imidazol-5-yl)-1,11-d-
ihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]-4-(methoxymethyl)-
pyrrolidin-1-yl]-1-oxobutan-2-yl}carbamate (72 mg, 34%).
LCMS-ESI.sup.+: calculated for C46H56N8O10: 880.41; observed
[M+1].sup.+: 882.39. .sup.1H NMR (CD.sub.3OD): 8.558 (s, 1H),
8.123-7.572 (m, 7H), 5.436-5.391 (dd, 1H, J=7.2, 3.6 Hz), 5.252 (s,
2H), 5.220 (m, 1H), 4.493-4.444 (m, 2H), 4.287-4.206 (m, 2H),
3.756-3.256 (m, 21H), 2.834 (m, 1H), 2.717-2.621 (m, 2H), 2.500 (m,
1H), 2.150 (m, 1H), 1.882 (m, 1H), 1.208 (d, 3H, J=6.4 Hz),
1.159-1.099 (m, 6H).
Example BH
##STR00122## ##STR00123##
[0351]
(2S,5S)-2-oxo-2-(8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen--
3-yl)ethyl
1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrro-
lidine-2-carboxylate
[0352] To a solution of
3-(2-bromoacetyl)-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one
(750 mg, 2.02 mmol) in MeCN (20 mL) was added
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid (600 mg, 2.09 mmol) and DIPEA (0.35 mL, 2.02
mmol) and the solution was heated to 60.degree. C. After stirring
for 4 h, the solution was cooled to rt, and diluted with EtOAc and
washed successively with saturated aqueous NaHCO.sub.3 and brine.
The organics were dried over MgSO.sub.4, filtered and concentrated
under reduced pressure. The crude residue was purified by silica
column chromatography (40% to 80% EtOAc/hexanes) to afford
(2S,5S)-2-oxo-2-(8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-3-yl)e-
thyl
1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrrolidine-
-2-carboxylate (1.16 g, quant.).
(2S,5S)-2-(9-bromo-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-3-yl)-
-2-oxoethyl
1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrrolidine-2-c-
arboxylate
[0353]
(2S,5S)-2-oxo-2-(8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen--
3-yl)ethyl
1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrro-
lidine-2-carboxylate (400 mg, 0.61 mmol) was dissolved in a
solution of DCM (15 mL) and MeOH (6 mL), then treated with
pyridinium tribromide (409 mg, 1.28 mmol). At 2 h, an additional
portion of pyridinium tribromide (40 mg) was added. After stirring
at RT for another 20 min, the reaction mixture was diluted with DCM
and 10% HCl, and extracted with DCM. The organic phase was dried
over MgSO.sub.4, filtered and concentrated under reduced pressure
and the crude material was carried on without further
purification.
(2S,4S)-1-tert-butyl
2-(3-(2-((2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-meth-
ylpyrrolidine-2-carbonyloxy)acetyl)-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[-
c,g]chromen-9-yl) 4-methylpyrrolidine-1,2-dicarboxylate
[0354]
(2S,5S)-2-(9-bromo-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chrome-
n-3-yl)-2-oxoethyl
1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrrolidine-2-c-
arboxylate) was treated with a solution of
(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidine-2-carboxylic
acid (280 mg, 1.22 mmol) in Me-THF (6 mL) and Cs.sub.2CO.sub.3 (199
mg, 0.61 mmol). The stirred reaction mixture was heated to
50.degree. C. for 2.5 h, then cooled to RT and diluted with
CH.sub.2Cl.sub.2 and extracted 3.times.. The organic phase was
washed with brine, then dried over MgSO.sub.4, filtered and
concentrated under reduced pressure. The crude residue was purified
by silica column chromatography (50% to 100% EtOAc/hexanes) to
afford (2S,4S)-1-tert-butyl
2-(3-(2-((2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-meth-
ylpyrrolidine-2-carbonyloxy)acetyl)-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[-
c,g]chromen-9-yl) 4-methylpyrrolidine-1,2-dicarboxylate (441 mg,
90%).
Tert-butyl
(2S,4S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-meth-
ylpyrrolidin-2-yl}-1H-imidazol-5-yl)-1,4,5,11-tetrahydroisochromeno[4',3':-
6,7]naphtho[1,2-d]imidazol-2-yl]-4-methylpyrrolidine-1-carboxylate
[0355] (2S,4S)-1-tert-butyl
2-(3-(2-((2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-meth-
ylpyrrolidine-2-carbonyloxy)acetyl)-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[-
c,g]chromen-9-yl) 4-methylpyrrolidine-1,2-dicarboxylate (441 mg,
0.55 mmol) and NH.sub.4OAc (5 g, 65.0 mmol) were suspended in a
solution of 10:1 PhMe/2-methoxyethanol (11 mL). The stirred
reaction mixture was heated to 110.degree. C. for 7 h, then cooled
to RT and diluted with EtOAc. The organic phase was washed with
water, saturated aqueous NaHCO.sub.3, and brine, then dried over
MgSO.sub.4, filtered and concentrated under reduced pressure. The
crude residue was purified by silica column chromatography (0% to
30% MeOH/EtOAc) to afford tert-butyl
(2S,4S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1H-imidazol-5-yl)-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphth-
o[1,2-d]imidazol-2-yl]-4-methylpyrrolidine-1-carboxylate (266 mg,
63%).
Tert-butyl
(2S,4S)-2-[9-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-4-meth-
ylpyrrolidin-2-yl}-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]nap-
htho[1,2-d]imidazol-2-yl]-4-methylpyrrolidine-1-carboxylate
[0356] Tert-butyl
(2S,4S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1H-imidazol-5-yl)-1,4,5,11
tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]-4-methylpyrr-
olidine-1-carboxylate (266 mg, 0.35 mmol) was suspended in DCM (7
mL) and activated MnO.sub.2 (908 mg, 10.45 mmol) was added in a
single portion. The reaction mixture was stirred overnight. After
stirring for 15 h, additional activated MnO.sub.2 (500 mg, 5.75
mmol) was added in a single portion.
[0357] After stirring 2 h at 35.degree. C., the mixture was cooled
to rt and the slurry was filtered over celite. The filter cake was
washed with copious CH.sub.2Cl.sub.2 and MeOH and the filtrate was
concentrated under reduced pressure. The crude material was taken
on to the next step without further purification to afford
tert-butyl
(2S,4S)-2-[9-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-4-methylpyrrolid-
in-2-yl}-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d-
]imidazol-2-yl]-4-methylpyrrolidine-1-carboxylate (266 mg,
quant).
Methyl
{(2S)-1-[(2S,5S)-2-(5-{2-[(2S,4S)-1-{(2S,3R)-3-methoxy-2-[(methoxyc-
arbonyl)amino]butanoyl}-4-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4-
',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-5-methylpyrrolidin-
-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate
[0358] Tert-butyl
(2S,4S)-2-[9-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-4-methylpyrrolid-
in-2-yl}-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d-
]imidazol-2-yl]-4-methylpyrrolidine-1-carboxylate (266 mg, 0.23
mmol) was dissolved in DCM (4 mL), MeOH (1 mL) and HCl (4 M in
dioxane, 1 mL) was added. The reaction mixture was stirred for 1.5
h and then concentrated under reduced pressure. The crude residue
was treated with (2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic
acid (44 mg, 0.23 mmol), HATU (87 mg, 0.23 mmol) and DMF (5 mL),
then DIPEA (0.3 mL, 1.75 mmol) was added dropwise. After 30 min,
the mixture was diluted with 10% MeOH/EtOAc and washed successively
with saturated aqueous NaHCO.sub.3 and brine. The organics were
dried over MgSO.sub.4, filtered and concentrated under reduced
pressure. The crude residue was purified by HPLC to afford methyl
{(2S)-1-[(2S,5S)-2-(5-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amin-
o]-3-methylbutanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3-
':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-5-methylpyrrolidin-1--
yl]-3-methyl-1-oxobutan-2-yl}carbamate (59 mg, 31%).
LCMS-ESI.sup.+: calculated for C.sub.45H.sub.54N.sub.8O.sub.8:
834.41; observed [M+1].sup.+: 836.89. .sup.1H NMR (CD.sub.3OD):
8.186 (s, 1H), 7.800-7.291 (m, 7H), 5.258-5.213 (dd, 1H, J=7.2, 3.6
Hz), 5.027-4.918 (m, 4H), 4.620 (t, 1H, J=6.8 Hz), 4.246 (m, 1H),
4.116 (m, 1H), 3.972 (d, 1H, J=8.8 Hz), 3.701-3.675 (m, 1H), 3.503
(s, 3H), 3.479 (s, 3H), 3.177 (s, 3H), 2.554-2.191 (m, 3H),
1.906-1.821 (m, 6H), 1.392 (d, 2H, J=6.4 Hz), 1.113-0.728 (m,
12H).
Example BI
##STR00124##
[0359] Tert-butyl
(2S,4S)-2-[5-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-4-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
[0360] Methyl
[(2S)-3-methyl-1-{(2S,4S)-4-methyl-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxab-
orolan-2-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl-
]pyrrolidin-1-yl}-1-oxobutan-2-yl]carbamate (312 mg, 0.49 mmol),
methyl
(S)-1-((2S,4S)-2-(5-iodo-1H-imidazol-2-yl)-4-methylpyrrolidin-1-yl)-3-met-
hyl-1-oxobutan-2-ylcarbamate (219 mg, 0.54 mmol),
Pd(PPh.sub.3).sub.4(58 mg, 0.05 mmol), PdCl.sub.2(dppf).sub.2 (36
mg, 0.05 mmol), and K.sub.2CO.sub.3 (2M in H.sub.2O, 0.8 mL, 1.6
mmoL) were combined in DMSO (5 mL) and dioxane (5 mL). The mixture
was degassed with bubbling N.sub.2 for 10 min the heated to
95.degree. C. for 5 h. After cooling, the reaction mixture was
diluted with EtOAc, and washed successively with saturated aqueous
NaHCO.sub.3 and brine. The organics were dried over MgSO.sub.4,
filtered and concentrated under reduced pressure. The crude residue
was purified by silica column chromatography (0%-30% MeOH/EtOAc) to
afford tert-butyl
(2S,4S)-2-[5-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-4-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate (166 mg,
43%).
Methyl
{(1R)-2-[(2S,4S)-2-(5-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino-
]-3-methylbutanoyl}-4-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3'-
:6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)pyrro-
lidin-1-yl]-2-oxo-1-phenylethyl}carbamate
[0361] Tert-butyl
(2S,4S)-2-[5-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-4-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate (166 mg,
0.21 mmol) was dissolved in DCM (4 mL), MeOH (1 mL) and HCl (4 M in
dioxane, 1 mL) was added. The reaction mixture was stirred for 2 h
and then concentrated under reduced pressure. The crude residue was
treated with (R)-2-(methoxycarbonylamino)-2-phenylacetic acid (44
mg, 0.21 mmol), COMU (100 mg, 0.21 mmol) and DMF (5 mL), then DIPEA
(0.18 mL, 1.05 mmol) was added dropwise. After 1 h, the mixture was
diluted with 10% MeOH/EtOAc and washed successively with saturated
aqueous NaHCO.sub.3 and brine. The organics were dried over
MgSO.sub.4, filtered and concentrated under reduced pressure. The
crude residue was purified by HPLC to afford methyl
{(1R)-2-[(2S,4S)-2-(5-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-me-
thylbutanoyl}-4-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6,7]n-
aphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidin--
1-yl]-2-oxo-1-phenylethyl}carbamate (71 mg, 38%). LCMS-ESI.sup.+:
calculated for C.sub.49H.sub.54N.sub.8O.sub.8: 882.41; observed
[M+1].sup.+: 884.34. .sup.1H NMR (CD.sub.3OD): 8.462 (s, 1H),
8.029-7.471 (m, 7H), 7.394-7.343 (m, 5H), 5.410 (d, 2H, J=6.8 Hz),
5.300 (m, 1H), 5.233 (m, 2H), 4.341 (m, 1H), 4.236 (d, 1H, J=7.2
Hz), 3.603 (s, 3H), 3.551 (s, 3H), 3.522-3.241 (m, 8H), 2.650 (m,
1H), 2.550 (m, 2H), 1.977-1.926 (m, 4H), 1.221 (d, 3H, J=3.2 Hz),
0.897-0.779 (dd, 6H, J=19.2, 6.8 Hz).
Example BJ
##STR00125## ##STR00126##
[0362] (S)-ethyl 2-(tert-butoxycarbonylamino)-5-oxohexanoate
[0363] A solution of ethyl N-Boc (S)-pyroglutamate (20.0 g, 77.7
mmol) was in anhydrous THF (150 mL) in a two neck round bottom
under argon was cooled to -40.degree. C. Methyl-magnesium bromide
solution (3.0 M in Ether, 28.5 mL, 85.5 mmol) was added to the
reaction mixture dropwise over 30 minutes. The reaction was stirred
for 4 hrs at -40 OC then for 1 hr at 0.degree. C. The reaction was
partitioned between ethyl acetate and saturated ammonium chloride
solution and acidified with 1 N HCl. The aqueous layer was
extracted two more times with ethylacetate. The organic layers were
combined and dried with sodium sulfate. The crude material was
purified by column chromatography (20%-40% EtOAc/hexanes) to yield
(S)-ethyl 2-(tert-butoxycarbonylamino)-5-oxohexanoate as a viscous
oil and was used directly in the following step.
(S)-ethyl 5-methyl-3,4-dihydro-2H-pyrrole-2-carboxylate
[0364] (S)-ethyl 2-(tert-butoxycarbonylamino)-5-oxohexanoate in a 1
L flask was treated with a trifluoro acetic acid/dichloromethane
solution (1:1 mixture, 100 mL). Effervescence was observed and the
mixture was allowed to stir for 4 hours at room temperature. After
which time the volatiles were removed in vacuo to yield (S)-ethyl
5-methyl-3,4-dihydro-2H-pyrrole-2-carboxylate as an oil, and used
directly in the following step.
(2S,5S)-ethyl 5-methylpyrrolidine-2-carboxylate
[0365] The crude imine 3 in a 1 L flask was dissolved with ethanol
(400 mL) was evacuated and charged with argon three times
(3.times.). Palladium on carbon (apprx. 750 mg, 10% w/w, dry) was
added and the reaction was evacuated of gas and charged with
hydrogen gas (3.times.). The reaction was allowed to stir under
atmospheric hydrogen for 16 hours. The mixture was filtered through
a plug of celite and the filtrate was concentrated in vacuo.
Diethyl ether was added to the oil and a precipitate formed. The
mixture was filtered to yield (2S,5S)-ethyl
5-methylpyrrolidine-2-carboxylate, as a white solid (10.6 g, 67.4
mmol, 86.7% over three steps). .sup.1H NMR (400 MHz, cdcl.sub.3)
.delta. 4.48 (dd, 1H), 4.27 (q, 2H), 3.92-3.80 (m, 1H), 2.52-2.36
(m, 1H), 2.32-2.13 (m, 2H), 1.75-1.60 (m, 1H), 1.51 (d, 3H), 1.30
(t, 3H).
(2S,5S)-1-tert-butyl 2-ethyl
5-methylpyrrolidine-1,2-dicarboxylate
[0366] To a solution of (2S,5S)-ethyl
5-methylpyrrolidine-2-carboxylate (7.0 g, 44.5 mmol) in
dichloromethane (250 mL), ditertbutylanhydride (10.7 g, 49.0 mmol),
diisopropylethylamine (17.1 mL, 98.0 mmol) dropwise over 10
minutes, and dimethyl amino pyridine (0.27 g, 2.23 mmol) were added
successively. Effervescence was observed and the mixture was
allowed to stir for 16 hours at room temperature. The reaction was
washed with HCl (250 mL, of 1N). The organic layer was then dried
with sodium sulfate. The crude material was purified by column
chromatography (5%-25% EtOAc/hexanes) to yield (2S,5S)-1-tert-butyl
2-ethyl 5-methylpyrrolidine-1,2-dicarboxylate as an oil (6.46 g,
25.1 mmol, 56%). LCMS-ESI.sup.+: calc'd for
C.sub.13H.sub.23NO.sub.4: 257.16 (M.sup.+); Found: 258.70
(M+H.sup.+).
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid
[0367] To a solution of (2S,5S)-1-tert-butyl 2-ethyl
5-methylpyrrolidine-1,2-dicarboxylate (6.46 g, 25.1 mmol) in
ethanol (20 mL) was added lithium hydroxide mono hydrate (2.11 g,
50.2 mmol) and deionized water (12 mL). The mixture was allowed to
stir for 16 hours then partitioned between ethylacetate and a 1:1
mixture of saturated brine and 1N HCl. The aqueous layer was
extracted an additional time with ethyl acetate. The organic layers
were combined, dried with sodium sulfate and the solvent was
removed in vacuo to yield
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid as a white solid (quant.) and was used directly in the
following step.
(2S,5S)-tert-butyl
2-(hydroxymethyl)-5-methylpyrrolidine-1-carboxylate
[0368] To a solution of
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid (5.91 g, 25.8 mmol) in tetrahydrofuran at 0.degree. C., was
added borane in dimethylsulfide (1.0 M, 3.4 mL, 34 mmol) dropwise.
The reaction was stirred for 4 hours at 0.degree. C. then 18 hours
at room temperature. The mixture was then cooled to 0.degree. C.
and methanol (70 mL) was added dropwise. The reaction was warmed to
room temperature and the solvents were removed in vacuo. The
residue was taken up in dichloromethane (200 mL) and extracted with
saturated sodium bicarbonate. The organic layer was dried with
sodium sulfate and the solvent was removed in vacuo to yield
(2S,5S)-tert-butyl
2-(hydroxymethyl)-5-methylpyrrolidine-1-carboxylate as a clear oil
(5.15 g, 23.9 mmol, 93%) and was used directly in the following
step.
(2S,5S)-tert-butyl 2-formyl-5-methylpyrrolidine-1-carboxylate
[0369] To a solution of (2S,5S)-tert-butyl
2-(hydroxymethyl)-5-methylpyrrolidine-1-carboxylate (5.15 g, 23.9
mmol) in dichloromethane, was added TEMPO (0.075 g, 0.48 mmol),
sodium bromide (0.246 g, 2.39 mmol) and sodium bicarbonate (0.442
g, 5.26 mmol). Sodium hypochlorite (2.67 g, 35.9 mmol) of a 6%
solution was added and the biphasic mixture was vigorously stirred
for 2 hours at room temperature. The reaction mixture was extracted
two times with dichloromethane (2.times.100 mL). The organic layers
were combined and washed with saturated sodium thiosulfate
solution, dried with sodium sulfate and the solvent was removed in
vacuo to yield (2S,5S)-tert-butyl
2-formyl-5-methylpyrrolidine-1-carboxylate (3.9 g, 18.29 mmol, 77%)
as a slight colored oil and was used directly in the following
step.
(2S,5S)-tert-butyl
2-(1H-imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate
[0370] To a solution of (2S,5S)-tert-butyl
2-formyl-5-methylpyrrolidine-1-carboxylate (3.9g, 18.30 mmol) in
MeOH (15 mL) and ammonium hydroxide (15 mL, 99.9%), glyoxal (11.7
mL, 40% w/v in water, 102.40 mmol) was added dropwise. The biphasic
mixture turned orange and turbid. The reaction was stirred
vigorously overnight at room temperature. The solvent was removed
in vacuo. The crude mixture was redissolved in ethyl acetate and
washed with water. The aqueous layer was washed an additional time
with ethyl acetate. The organic layers were combined and washed
with brine, dried with sodium sulfate and the solvent was removed
in vacuo. The crude material was purified by column chromatography
85% to 100% ethyl acetate in hexanes to yield (2S,5S)-tert-butyl
2-(1H-imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate as an off
white solid (3.47 g, 13.8 mmol, 75%). LCMS-ESI.sup.+: calc'd for
C.sub.13H.sub.21N.sub.3O.sub.2: 251.16 (M.sup.+); Found: 252.20
(M+H.sup.+).
(2S,5S)-tert-butyl
2-(4,5-diiodo-1H-imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate
[0371] A 500 ml round bottom flask was charged with
(2S,5S)-tert-butyl
2-(1H-imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate (3.47 g,
13.8 mmol), iodine (7.7 g, 30.4 mmol) and sodium carbonate (4.54 g,
42.8 mmol). Dioxane (70 mL) and water (45 mL) was added to mixture
and the reaction was stirred vigorously overnight in the dark. The
reaction was then partitioned between ethyl acetate and a 10%
aqueous solution of sodium thiosulfate and extracted. The aqueous
layer was extracted an additional time with ethyl acetate. The
organic layers were combined, dried with sodium sulfate and the
solvent was removed in vacuo. The crude material was filtered
through a plug of silica with 25% ethyl acetate in hexanes to yield
(2S,5S)-tert-butyl
2-(4,5-diiodo-1H-imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate
as a white solid (4.28 g, 8.50 mmol, 62%). LCMS-ESI.sup.+: calc'd
for C.sub.13H.sub.19I.sub.2N.sub.3O.sub.2: 502.96 (M.sup.+); Found:
503.94 (M+H.sup.+).
(2S,5S)-tert-butyl
2-(5-iodo-1H-imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate
[0372] To a solution of (2S,5S)-tert-butyl
2-(4,5-diiodo-1H-imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate
(4.28 g, 8.50 mmol) in ethanol (75 mL) and water (75 mL), sodium
thiosulfate (10.72 g, 85.1 mmol) was added and the reaction mixture
was stirred vigorously for 1 hour at 100.degree. C., 16 hours at
90.degree. C., and 5 hours at 100.degree. C. The reaction mixture
was partitioned between ethyl acetate and water. The aqueous layer
was washed additionally with ethyl acetate and the organic layers
were combined. The organic layer was dried with sodium sulfate,
concentrated and the crude material was purified by column
chromatography to yield (2S,5S)-tert-butyl
2-(5-iodo-1H-imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate as a
white solid (2.34 g, 6.20 mmol, 73%). .sup.1H NMR (400 MHz,
cdcl.sub.3) .delta. 7.04 (s, 1H), 4.89 (dd, 1H), 3.92 (m, 1H), 2.91
(s, 1H), 2.18-2.06 (m, 2H), 1.78 (m, 1H), 1.52 (m, 1H), 1.48 (s,
9H), 1.13 (d, 3H).
(2S)-1-[(2S,5S)-2-(5-iodo-1H-imidazol-2-yl)-5-methylpyrrolidin-1-yl]-2-[(1-
-methoxyethenyl)amino]-3-methylbutan-1-one
[0373] A round bottom flask was charged with (2S,5S)-tert-butyl
2-(5-iodo-1H-imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate (1.5
g, 3.98 mmol) and treated with an excess of hydrochloric acid (100
mL of 4.0M in dioxane). The mixture was stirred vigorously for 3
hours in which time a precipitate formed and the solvent was
removed in vacuo. To a mixture of the crude intermediate,
(S)-2-(methoxycarbonylamino)-3-methylbutanoic acid (0.836 g, 4.77
mmol), HATU (1.81 g, 4.77 mmol) in dichloromethane (25 mL),
diisopropylethylamine (3.46 mL, 19.9 mmol) was then added dropwise
and was stirred over night under nitrogen. The reaction mixture was
partitioned ethyl acetate and saturated sodium bicarbonate. The
organic layer was dried with sodium sulfate, the solvent removed in
vacuo. The crude product was purified by column chromatography to
yield
(2S)-1-[(2S,5S)-2-(5-iodo-1H-imidazol-2-yl)-5-methylpyrrolidin-1-yl]-2-[(-
1-methoxyethenyl)amino]-3-methylbutan-1-one as a white solid (1.63
g, 3.75 mmol, 94%). LCMS-ESI.sup.+: calc'd for
C.sub.15H.sub.23IN.sub.4O.sub.3: 434.08 (M.sup.+); Found: 435.51
(M+H.sup.+).
Example BK
##STR00127##
[0374] Methyl
{(2S)-1-[(2S,5S)-2-(5-{2-[(2S,4S)-1-{(2R)-2-[(methoxycarbonyl)amino]-2-ph-
enylacetyl}-4-(methoxymethyl)pyrrolidin-2-yl]-1,11
dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-y-
l)-5-methylpyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate
[0375] The synthesis of this compound was prepared according to the
procedure of Example AB-1 with the following modification. During
the suzuki coupling,
(2S)-1-[(2S,5S)-2-(5-iodo-1H-imidazol-2-yl)-5-methylpyrrolidin-1-yl]-2-[(-
1-methoxyethenyl)amino]-3-methylbutan-1-one was used in lieu of
(2S)-1-[(2S)-2-(5-bromo-1H-imidazol-2-yl)pyrrolidin-1-yl]-2-[(1-methoxyet-
henyl)amino]-3-methylbutan-1-one. The crude material was purified
by preparative HPLC to provide methyl
{(2S)-1-[(2S,5S)-2-(5-{2-[(2S,4S)-1-{(2R)-2-[(methoxycarbonyl)amino]-2-ph-
enylacetyl}-4-(methoxymethyl) pyrrolidin-2-yl]-1,11
dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-y-
l)-5-methylpyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate as a
white solid (17 mg, 0.019 mmol, 17%). .sup.1H NMR (400 MHz,
cd.sub.3od) .delta. 8.63 (s, 1H), 8.19 (d, 1H), 8.04 (m, 1H), 7.87
(m, 2H), 7.66 (m, 2H), 7.52-7.39 (m, 6H), 5.50 (m, 2H), 5.32 (s,
2H), 5.16 (m, 1H), 4.12 (m, 1H), 3.80 (m, 4H), 3.66 (s, 6H), 3.43
(m, 4H), 3.23 (s, 3H), 2.72-1.99 (m, 9H), 1.56 (d, 3H), 1.29 (m,
1H), 0.99 (d, 3H), 0.88 (d, 3H).
Example BL
##STR00128##
[0376] Methyl
{(2S)-1-[(2S,5S)-2-(5-{2-[(2S)-1-{(2R)-2-[(methoxycarbonyl)amino]-2-pheny-
lacetyl}pyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]i-
midazol-9-yl}-1H-imidazol-2-yl)-5-methylpyrrolidin-1-yl]-3-methyl-1-oxobut-
an-2-yl}carbamate
[0377] The synthesis of this compound was prepared according to the
procedure of Example AA with the following modification. During the
Suzuki coupling,
(2S)-1-[(2S,5S)-2-(5-iodo-1H-imidazol-2-yl)-5-methylpyrrolidin-1-yl]-2-[(-
1-methoxyethenyl)amino]-3-methylbutan-1-one was used in lieu of
(2S)-1-[(2S)-2-(5-bromo-1H-imidazol-2-yl)pyrrolidin-1-yl]-2-[(1-methoxyet-
henyl)amino]-3-methylbutan-1-one. The crude material was purified
by preparative HPLC to provide methyl
{(2S)-1-[(2S,5S)-2-(5-{2-[(2S)-1-{(2R)-2-[(methoxycarbonyl)amino]-2-pheny-
lacetyl}pyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]i-
midazol-9-yl}-1H-imidazol-2-yl)-5-methylpyrrolidin-1-yl]-3-methyl-1-oxobut-
an-2-yl}carbamate as a white solid (110 mg, 0.131 mmol, 57%).
.sup.1H NMR (400 MHz, cd.sub.3od) .delta. 8.65 (s, 1H), 8.21 (d,
1H), 8.04 (m, 2H), 7.91 (s, 1H), 7.81 (m, 1H), 7.67 (m, 2H), 7.46
(m, 6H), 5.59 (s, 1H), 5.50 (dd, 1H), 5.33 (s, 2H), 5.22-5.09 (m,
1H), 4.14 (m, 2H), 3.74 (s, 1H), 3.65 (m, 6H), 3.52-3.37 (m, 2H),
2.60-1.89 (m, 11H), 1.56 (d, 3H), 1.29 (d, 1H), 0.99 (d, 3H), 0.88
(d, 3H).
Example BM
##STR00129##
[0378] Methyl
[(2S)-1-{(2S,5S)-2-[5-(2-{(2S)-1-[(2R)-2-amino-2-phenylacetyl]pyrrolidin--
2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-im-
idazol-2-yl]-5-methylpyrrolidin-1-yl}-3-methyl-1-oxobutan-2-yl]carbamate
[0379] The synthesis of this compound was prepared according to
Example BL with the following modifications. During the amide
coupling, (R)-2-(tert-butoxycarbonylamino)-2-phenylacetic acid was
used in lieu of (R)-2-(methoxycarbonylamino)-2-phenylacetic acid.
This was then treated with an excess of hydrochloric acid (15 ml,
4.0 M in Dioxane) for 2 hours. The crude product was purified by
HPLC to provide methyl
[(2S)-1-{(2S,5S)-2-[5-(2-{(2S)-1-[(2R)-2-amino-2-phenylacetyl]pyrrolidin--
2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-im-
idazol-2-yl]-5-methylpyrrolidin-1-yl}-3-methyl-1-oxobutan-2-yl]carbamate
as a white solid (153 mg, 0.196 mmol, 74%). .sup.1H NMR (400 MHz,
cd.sub.3od) .delta. 8.63 (s, 1H), 8.20 (d, 1H), 7.99 (m, 1H), 7.93
(m, 2H), 7.80 (m, 2H), 7.72-7.64 (m, 2H), 7.63-7.52 (m, 5H), 5.52
(dd, 1H), 5.44 (m, 1H), 5.33 (s, 2H), 5.21-5.10 (m, 1H), 4.80 (m,
2H), 4.14 (m, 1H), 4.02 (m, 1H), 3.75 (s, 1H), 3.67 (s, 3H), 3.12
(dd, 1H), 2.72-2.13 (m, 7H), 2.00 (m, 3H), 1.56 (d, 3H), 1.30 (d,
1H), 0.98 (d, 3H), 0.88 (d, 3H).
Example BN
##STR00130##
[0380] (2S,5S)-Ethyl
1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrrolidine-2-c-
arboxylate
[0381] (2S,5S)-Ethyl 5-methylpyrrolidine-2-carboxylate-TFA (10.0 g,
39.3 mmol), (S)-2-(methoxycarbonylamino)-3-methylbutanoic acid
(6.88 g, 39.3 mmol) and HATU (14.9 g, 39.3 mmol) were combined in
DMF (100 mL) and DIPEA (15.0 mL, 86.5 mmol) was added. After
stirring for 1 h at RT, the reaction mixture was diluted with
EtOAc. The organic phase was washed successively with 10% HCl,
saturated aqueous NaHCO.sub.3 and brine, then dried over
MgSO.sub.4, filtered and concentrated under reduced pressure to
afford (2S,5S)-ethyl
1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrrolidine-2-c-
arboxylate. The crude material was carried on without further
purification.
(2S,5S)-1-((S)-2-(Methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrrolid-
ine-2-carboxylic acid
[0382] (2S,5S)-Ethyl
1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrrolidine-2-c-
arboxylate (39.3 mmol, assuming complete conversion from the
previous transformation) was suspended in MeOH (200 mL) and aqueous
LiOH (1.0 M, 100 mL, 100 mmol) was added. The reaction mixture was
stirred o/n, then concentrated under reduced pressure to remove
most of the MeOH. The aqueous solution was washed 2.times. with DCM
before being acidified to pH-1-2 with 10% HCl. The acidic aqueous
phase was then extracted 5.times. with EtOAc. The combined EtOAc
extracts were dried over MgSO.sub.4 filtered and concentrated under
reduced pressure to afford
(2S,5S)-1-((S)-2-(Methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid (6.89 g, 56% over 2 steps).
Example BO
##STR00131## ##STR00132##
[0383] 3-Vinyl-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one
[0384] A 3-neck oven-dried 500 mL round-bottom flask was cooled
under Ar, then charged with
3-Chloro-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one (12.0 g,
42.1 mmol), potassium vinyltrifluoroborate (8.47 g, 6.32 mmol),
Pd(OAc).sub.2 (473 mg, 2.11 mmol), SPhos (1.74 g, 4.25 mmol),
K.sub.2CO.sub.3 (17.5 g, 126 mmol) and anhydrous propanol (120 mL).
The reaction mixture was sparged with Ar for 16 min, then heated to
reflux for 5.5 h. Upon completion, the reaction mixture was cooled
to RT and concentrated under reduced pressure. The crude residue
was suspended in DCM, then washed with H.sub.2O and brine. The
organic solution was dried over MgSO.sub.4, filtered and
concentrated under reduced pressure. The resulting residue was
further purified via silica plug, eluting with DCM to afford
3-vinyl-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one (10.2 g,
87%).
3-(2-Bromoacetyl)-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one
[0385] 3-Vinyl-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one (9.98
g, 36.1 mmol) was dissolved in a stirred solution of THF (70 mL),
DMSO (70 mL) and H.sub.2O (35 mL). NBS (6.75 g, 37.9 mmol) was
added in a single portion and the reaction mixture was stirred at
RT for 33 min. Upon completion, the reaction medium was diluted
with EtOAc and washed twice with H.sub.2O and once with brine. The
organic phase was dried over MgSO.sub.4, filtered and concentrated
under reduced pressure. The resulting crude bromohydrin was
suspended in DCM (200 mL) and treated with activated MnO.sub.2
(62.7 g, 722 mmol). After stirring for 15 h at RT, the reaction
mixture was filtered over celite and the filter cake was rinsed
several times with DCM. The combined filtrate (.about.400 mL) was
treated with MeOH (.about.100 mL) and the mixture was gradually
concentrated under reduced pressure, causing solid material to
precipitate from solution. When the liquid volume reached -200 mL,
the solid was filtered off and rinsed with MeOH. The
concentration/precipitation/filtration/rinsing sequence was
performed 2.times. more, resulting in the collection of 3 crops of
powdered
3-(2-bromoacetyl)-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one
(7.49 g, 56% over 2 steps).
(4S)-1-tert-Butyl
2-(2-oxo-2-(8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-3-yl)ethyl)
4-(methoxymethyl)pyrrolidine-1,2-dicarboxylate
[0386]
3-(2-Bromoacetyl)-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one
(7.47 g, 20.1 mmol) and
(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrrolidine-2-carboxylic
acid (5.22 g, 20.1 mmol) were suspended in 2-Me-THF (75 mL) and
treated with Cs.sub.2CO.sub.3 (3.27 g, 10.1 mmol). After stirring 4
h at RT, the reaction mixture was diluted with diluted with DCM.
The organic layer was washed with H.sub.2O. The aqueous layer was
then back extracted 2.times. with DCM. The combined organics were
dried over MgSO.sub.4, filtered and concentrated under reduced
pressure. The crude residue was purified by silica column
chromatography (10% to 50% EtOAc/DCM) to afford (4S)-1-tert-butyl
2-(2-oxo-2-(8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-3-yl)ethyl)
4-(methoxymethyl)pyrrolidine-1,2-dicarboxylate (7.73 g, 70%).
(2S,4S)-2-(2-(9-Bromo-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-3--
yl)-2-oxoethyl) 1-tert-butyl
4-(methoxymethyl)pyrrolidine-1,2-dicarboxylate
[0387] (4S)-1-tert-Butyl
2-(2-oxo-2-(8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-3-yl)ethyl)
4-(methoxymethyl)pyrrolidine-1,2-dicarboxylate (7.66 g, 13.9 mmol)
was dissolved in a solution of DCM (100 mL) and MeOH (40 mL), then
treated with pyridinium tribromide (4.90 g, 15.3 mmol). After
stirring at RT for 1.75 h, the reaction mixture was diluted with
DCM and washed successively with 10% HCl, saturated aqueous
NaHCO.sub.3 and brine. The organic phase was dried over MgSO.sub.4,
filtered and concentrated under reduced pressure and the crude
material was carried on without further purification.
(2R,4R)-1-tert-Butyl
2-(2-(9-((2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-meth-
ylpyrrolidine-2-carbonyloxy)-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chr-
omen-3-yl)-2-oxoethyl)
4-(methoxymethyl)pyrrolidine-1,2-dicarboxylate
[0388]
(2S,4S)-2-(2-(9-Bromo-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chr-
omen-3-yl)-2-oxoethyl) 1-tert-butyl
4-(methoxymethyl)pyrrolidine-1,2-dicarboxylate (8.76 g, 13.94 mmol)
was treated with a solution of
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid (6.85 g, 23.92 mmol) in 2-Me-THF (70 mL) and
Cs.sub.2CO.sub.3 (3.63 g, 11.15 mmol). The stirred reaction mixture
was heated to 50.degree. C. for 20 h, then cooled to RT and diluted
with EtOAc. The organic phase was washed with H.sub.2O and brine,
then dried over MgSO.sub.4, filtered and concentrated under reduced
pressure. The crude residue was purified by silica column
chromatography (0% to 30% MeOH/EtOAc) to afford
(2R,4R)-1-tert-butyl
2-(2-(9-((2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-meth-
ylpyrrolidine-2-carbonyloxy)-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chr-
omen-3-yl)-2-oxoethyl)
4-(methoxymethyl)pyrrolidine-1,2-dicarboxylate (10.47 g, 90%).
tert-Butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-meth-
ylpyrrolidin-2-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]-
imidazol-9-yl)-1H-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylat-
e
[0389] (2R,4R)-1-tert-Butyl
2-(2-(9-((2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-meth-
ylpyrrolidine-2-carbonyloxy)-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chr-
omen-3-yl)-2-oxoethyl)
4-(methoxymethyl)pyrrolidine-1,2-dicarboxylate (10.47 g, 12.56
mmol) and NH.sub.4OAc (50.9 g, 660 mmol) were suspended in a
solution of 10:1 PhMe/2-methoxyethanol (132 mL). The stirred
reaction mixture was heated to 110.degree. C. for 4.5 h, then
cooled to RT and diluted with EtOAc. The organic phase was washed
3.times. with saturated aqueous NaHCO.sub.3, then dried over
MgSO.sub.4, filtered and concentrated under reduced pressure. The
crude residue was purified by silica column chromatography (0% to
30% MeOH/EtOAc) to afford tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-
-yl)-1H-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
(8.33 g, 84%).
tert-Butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-meth-
ylpyrrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazo-
l-9-yl)-1H-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
[0390] tert-Butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-
-yl)-1H-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
(8.33 g, 1.049 mmol) was suspended in DCM and activated MnO.sub.2
(55.0 g, 630 mmol) was added in a single portion. After 13 h, MeOH
(200 mL) was added and the slurry was filtered over celite. The
filter cake was washed with MeOH (600 mL) and the filtrate was
concentrated under reduced pressure. The crude material was
purified by silica column chromatography (0% to 45% MeOH/EtOAc) to
afford tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate (4.85 g,
58%).
Methyl
{(2S,3S)-1-[(2S,4S)-2-(5-{2-[(2S,5S)-1-{(2S)-2-[(methoxycarbonyl)am-
ino]-3-methylbutanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4'-
,3':6,7]naphtho[1,2-d]imidazol-9-yl}-H-imidazol-2-yl)-4-(methoxymethyl)pyr-
rolidin-1-yl]-3-methyl-1-oxopentan-2-yl}carbamate
[0391] tert-Butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate (179 mg,
0.226 mmol) was dissolved in DCM (4 mL) and HCl (4.0 M in dioxane,
1 mL) was added. The reaction mixture was stirred for 1 h at RT
then concentrated under reduced pressure. The resulting residue was
treated with (2S,3S)-2-(methoxycarbonylamino)-3-methylpentanoic
acid (51 mg, 0.27 mmol), HATU (95 mg, 0.25 mmol), DMF (2 mL) and
DIPEA (0.39 mL, 2.3 mmol). After stirring for 6 min, the reaction
was quenched with H.sub.2O, filtered and purified by reverse phase
HPLC to afford methyl
{(2S,3S)-1-[(2S,4S)-2-(5-{2-[(2S,5S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-
-methylbutanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6,-
7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolid-
in-1-yl]-3-methyl-1-oxopentan-2-yl}carbamate (116 mg, 59%). MS
(ESI) m/z 864 [M+H].sup.+. .sup.1H NMR (400 MHz, cd.sub.3od)
.delta. 8.57 (d, J=14.7 Hz, 1H), 8.45 (s, 1H), 8.20 (d, J=14.4 Hz,
1H), 8.15-7.98 (m, 2H), 7.91 (dd, J=21.8, 14.1 Hz, 2H), 7.85-7.69
(m, 2H), 7.69-7.48 (m, 2H), 5.42-5.12 (m, 5H), 4.34 (dd, J=22.3,
13.7 Hz, 1H), 4.30-4.10 (m, 2H), 3.87-3.73 (m, 1H), 3.73-3.63 (m,
7H), 3.62-3.48 (m, 2H), 3.48-3.38 (m, 4H), 3.35 (s, 3H), 2.95-2.70
(m, 1H), 2.70-2.55 (m, 2H), 2.55-2.20 (m, 2H), 2.20-1.91 (m, 3H),
1.77 (d, J=42.0 Hz, 1H), 1.65 (d, J=6.6 Hz, 3H), 1.43 (t, J=24.6
Hz, 1H), 1.28 (d, J=6.2 Hz, 1H), 1.23-1.01 (m, 3H), 0.98 (d, J=6.6
Hz, 3H), 0.90 (dd, J=13.1, 5.9 Hz, 10H).
Example BP
##STR00133##
[0392] Methyl
{(2S)-1-[(2S,5S)-2-(9-{2-[(2S,4S)-1-[N-(methoxycarbonyl)-L-alloisoleucyl]-
-4-(methoxymethyl)pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydroisochrome-
no[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidin-1-yl]-3-methy-
l-1-oxobutan-2-yl}carbamate
[0393] was prepared from tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate by the
same method employed in the synthesis of {(2S,3
S)-1-[(2S,4S)-2-(5-{2-[(2S,5S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-methy-
lbutanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6,7]naph-
tho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidin-1-y-
l]-3-methyl-1-oxopentan-2-yl}carbamate, replacing
(2S,3S)-2-(methoxycarbonylamino)-3-methylpentanoic acid with
(2S,3R)-2-(methoxycarbonylamino)-3-methylpentanoic acid. MS (ESI)
m/z 864 [M+H].sup.+. .sup.1H NMR (400 MHz, cd.sub.3od) .delta.
8.62-8.41 (m, 1H), 8.22 (s, 1H), 8.07 (dt, J=20.1, 10.0 Hz, 1H),
7.89 (dt, J=35.6, 15.6 Hz, 2H), 7.77 (dd, J=20.3, 7.0 Hz, 2H),
7.68-7.48 (m, 2H), 5.95 (d, J=5.0 Hz, 1H), 5.42-5.13 (m, 4H), 4.47
(t, J=5.5 Hz, 1H), 4.40-4.09 (m, 2H), 3.80-3.73 (m, 1H), 3.73-3.62
(m, 6H), 3.57 (dt, J=16.1, 9.7 Hz, 2H), 3.40 (s, 3H), 3.34 (d,
J=7.5 Hz, 1H), 2.81 (dd, J=18.4, 12.5 Hz, 1H), 2.63 (td, J=13.3,
6.8 Hz, 2H), 2.55-2.18 (m, 2H), 2.16-1.77 (m, 4H), 1.65 (d, J=6.6
Hz, 3H), 1.50-1.31 (m, 1H), 1.26 (dd, J=15.6, 6.7 Hz, 2H),
1.17-1.03 (m, 2H), 0.98 (dd, J=6.7, 4.5 Hz, 5H), 0.89 (dd, J=15.5,
7.8 Hz, 3H), 0.86-0.74 (m, 3H).
Example BQ
##STR00134##
[0394] Methyl
{(1R)-2-[(2S,4S)-2-(5-{2-[(2S,5S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-me-
thylbutanoyl}-5-methylpyrrolidin-2-yl]-1,4,5,11-tetrahydroisochromeno[4',3-
':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)pyrr-
olidin-1-yl]-2-oxo-1-phenylethyl}carbamate
[0395] tert-Butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-
-yl)-1H-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
(102 mg, 0.128 mmol) was dissolved in DCM (4 mL) and HCl (4.0 M in
dioxane, 2.0 mL, 8.0 mmol) was added. After stirring at RT for 30
min, the solution was concentrated under reduced pressure. The
residue was treated with
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid (29 mg, 0.141
mmol), COMU (60 mg, 0.141 mmol), DMF (3.0 mL) and DIPEA (0.223 mL,
1.28 mmol). After stirring at RT for 20 min, the reaction mixture
was diluted with EtOAc. The organic solution was washed with
saturated aqueous NaHCO.sub.3 and brine, then dried over
MgSO.sub.4, filtered and concentrated under reduced pressure. The
crude material was purified by reverse-phase HPLC to afford methyl
{(1R)-2-[(2S,4S)-2-(5-{2-[(2S,5S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-me-
thylbutanoyl}-5-methylpyrrolidin-2-yl]-1,4,5,11-tetrahydroisochromeno[4',3-
':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)pyrr-
olidin-1-yl]-2-oxo-1-phenylethyl}carbamate as the bis-TFA salt
(82.4 mg, 60%). MS (ESI) m/z 866 [M+H].sup.+. .sup.1H NMR (400 MHz,
cd.sub.3od) .delta. 7.94-7.67 (m, 4H), 7.59 (d, J=9.1 Hz, 1H), 7.52
(s, 1H), 7.48-7.33 (m, 4H), 7.11 (d, J=18.7 Hz, 1H), 5.68 (d, J=6.3
Hz, 1H), 5.48-5.33 (m, 1H), 5.23 (dd, J=24.1, 15.7 Hz, 1H),
5.17-5.03 (m, 3H), 4.22 (dd, J=17.0, 9.6 Hz, 1H), 4.16-4.01 (m,
1H), 3.91 (d, J=24.1 Hz, 1H), 3.83-3.68 (m, 1H), 3.68-3.59 (m, 3H),
3.59-3.49 (m, 3H), 3.38 (ddd, J=15.9, 9.6, 5.7 Hz, 2H), 3.28-3.14
(m, 5H), 3.10 (dd, J=14.0, 8.2 Hz, 1H), 3.00 (dd, J=17.8, 9.6 Hz,
1H), 2.92 (dd, J=14.5, 6.7 Hz, 1H), 2.73-2.41 (m, 2H), 2.40-2.11
(m, 2H), 2.11-1.83 (m, 2H), 1.54 (t, J=9.7 Hz, 2H), 1.24 (d, J=6.2
Hz, 1H), 1.06 (t, J=8.0 Hz, 1H), 0.99 (d, J=6.8 Hz, 1H), 0.94 (d,
J=6.6 Hz, 2H), 0.85 (d, J=6.7 Hz, 2H).
Example BR
##STR00135##
[0396] tert-Butyl
(2S,4S)-2-(5-{2-[(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrroli-
din-2-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1-
H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate
[0397] was prepared from
(2S,4S)-2-(2-(9-bromo-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-3-
-yl)-2-oxoethyl) 1-tert-butyl
4-(methoxymethyl)pyrrolidine-1,2-dicarboxylate by the same method
employed in the synthesis of tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate,
replacing
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid with
(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrrolidine-2-carboxylic
acid.
Methyl
{(2S)-1-[(2S,4S)-2-(5-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino-
]-3-methylbutanoyl}-4-(methoxymethyl)pyrrolidin-2-yl]-1,11-dihydroisochrom-
eno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymet-
hyl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate
[0398] tert-Butyl
(2S,4S)-2-(5-{2-[(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrroli-
din-2-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1-
H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate (137
mg, 0.179 mmol) was dissolved in DCM (5 mL) and HCl (4.0 M in
dioxane, 1 mL) was added. After stirring at RT for 1.5 h, the
reaction mixture was concentrated under reduced pressure. The crude
residue was treated with
(S)-2-(methoxycarbonylamino)-3-methylbutanoic acid (69 mg, 0.39
mmol), HATU (149 mg, 0.393 mmol), DMF (2.0 mL) and DIPEA (0.31 mL,
1.8 mmol). After stirring for 15 min at RT, the reaction mixture
was quenched with water and purified by HPLC to provide methyl
{(2S)-1-[(2S,4S)-2-(5-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-me-
thylbutanoyl}-4-(methoxymethyl)pyrrolidin-2-yl]-1,11-dihydroisochromeno[4'-
,3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)py-
rrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate (123 mg). MS
(ESI) m/z 880 [M+H].sup.+. .sup.1H NMR (400 MHz, cd.sub.3od)
.delta. 8.48 (s, 1H), 8.05 (t, J=11.2 Hz, 1H), 7.92 (dd, J=19.7,
10.1 Hz, 2H), 7.74 (s, 2H), 7.59-7.44 (m, 2H), 5.49 (s, 1H), 5.40
(dt, J=16.3, 8.1 Hz, 1H), 5.31-5.15 (m, 3H), 4.47-4.10 (m, 4H),
3.86-3.44 (m, 12H), 3.39 (dd, J=13.2, 7.1 Hz, 6H), 2.94-2.57 (m,
4H), 2.25-1.94 (m, 4H), 1.02-0.82 (m, 12H).
Example BS
##STR00136##
[0399] Methyl
{(2S,3S)-1-[(2S,4S)-2-(5-{2-[(2S,4S)-1-{(2S,3S)-2-[(methoxycarbonyl)amino-
]-3-methylpentanoyl}-4-(methoxymethyl)pyrrolidin-2-yl]-1,11-dihydroisochro-
meno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxyme-
thyl)pyrrolidin-1-yl]-3-methyl-1-oxopentan-2-yl}carbamate
[0400] was prepared from tert-Butyl
(2S,4S)-2-(5-{2-[(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrroli-
din-2-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1-
H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate using
the same method employed in the synthesis of methyl
{(2S)-1-[(2S,4S)-2-(5-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-me-
thylbutanoyl)}-4-(methoxymethyl)pyrrolidin-2-yl]-1,11-dihydroisochromeno[4-
',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)p-
yrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate, replacing with
(S)-2-(methoxycarbonylamino)-3-methylbutanoic acid with
(2S,3S)-2-(methoxycarbonylamino)-3-methylpentanoic acid. MS (ESI)
m/z 908 [M+H].sup.+.
Example BT
##STR00137##
[0401] tert-Butyl
(2S,4S)-2-[5-(2-{(2S)-1-[N-(methoxycarbonyl)-L-valyl]pyrrolidin-2-yl}-1,4-
,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imid-
azol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
[0402] was synthesized from
(2S,4S)-2-(2-(9-bromo-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-3-
-yl)-2-oxoethyl) 1-tert-butyl
4-(methoxymethyl)pyrrolidine-1,2-dicarboxylate using the same
methods described for the synthesis of tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-
-yl)-1H-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate,
substituting
(S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)pyrrolidine-2-carbox-
ylic acid for
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid.
Methyl
{(1R)-2-[(2S,4S)-2-(5-{2-[(2S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-
-methylbutanoyl}pyrrolidin-2-yl]-1,4,5,11-tetrahydroisochromeno[4',3':6,7]-
naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidin-
-1-yl]-2-oxo-1-phenylethyl}carbamate
[0403] was synthesized from tert-butyl
(2S,4S)-2-[5-(2-{(2S)-1-[N-(methoxycarbonyl)-L-valyl]pyrrolidin-2-yl}-1,4-
,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imid-
azol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate using the
same method employed for the synthesis of methyl
{(1R)-2-[(2S,4S)-2-(5-{2-[(2S,5S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-me-
thylbutanoyl}-5-methylpyrrolidin-2-yl]-1,4,5,11-tetrahydroisochromeno[4',3-
':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)pyrr-
olidin-1-yl]-2-oxo-1-phenylethyl}carbamate substituting tert-butyl
(2S,4S)-2-[5-(2-{(2S)-1-[N-(methoxycarbonyl)-L-valyl]pyrrolidin-2-yl}-1,4-
,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imid-
azol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate for
tert-Butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-
-yl)-1H-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate.
MS (ESI) m/z 871 [M+H].sup.+. .sup.1H NMR (400 MHz, cd.sub.3od)
.delta. 7.87 (ddd, J=20.5, 15.3, 6.8 Hz, 4H), 7.65 (s, 1H),
7.50-7.38 (m, 5H), 7.17 (s, 1H), 5.41 (d, J=24.5 Hz, 1H), 5.28 (t,
J=8.3 Hz, 1H), 5.20 (d, J=7.3 Hz, 3H), 4.24 (d, J=7.2 Hz, 1H), 4.12
(d, J=10.3 Hz, 1H), 4.03-3.94 (m, 1H), 3.89 (dd, J=15.4, 8.6 Hz,
1H), 3.77 (t, J=9.6 Hz, 1H), 3.72-3.64 (m, 4H), 3.63-3.52 (m, 4H),
3.43 (qd, J=9.5, 5.6 Hz, 3H), 3.30 (s, 3H), 3.24-3.08 (m, 2H), 2.97
(dd, J=11.6, 5.4 Hz, 2H), 2.59 (dt, J=21.1, 7.8 Hz, 3H), 2.29 (s,
1H), 2.24-2.14 (m, 2H), 2.11-1.85 (m, 2H), 0.92 (dd, J=15.8, 6.7
Hz, 6H).
Example BU
##STR00138##
[0404] tert-Butyl
(2S,4S)-2-[5-(2-{(2S)-1-[N-(methoxycarbonyl)-L-valyl]pyrrolidin-2-yl}-1,1-
1-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imidazol-2--
yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
[0405] was prepared according to the method described for the
synthesis of tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate,
substituting tert-butyl
(2S,4S)-2-[5-(2-{(2S)-1-[N-(methoxycarbonyl)-L-valyl]pyrrolidin-2-yl}-1,1-
1-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imidazol-2--
yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate for tert-Butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-
-yl)-1H-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate.
Methyl
{(2S)-1-[(2S)-2-(9-{2-[(2S,4S)-1-[(2R)-2-amino-2-phenylacetyl]-4-(m-
ethoxymethyl)pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydroisochromeno[4'-
,3':6,7]naphtho[1,2-d]imidazol-2-yl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-
-yl}carbamate
[0406] was prepared according to the method described for the
synthesis of methyl
(S)-1-((2S,4S)-2-(2'-((2S,4S)-1-((R)-2-amino-2-phenylacetyl)-4-(me-
thoxymethyl)pyrrolidin-2-yl)-1H,
1'H-7,7'-binaphtho[1,2-d]imidazol-2-yl)-4-methylpyrrolidin-1-yl)-3-methyl-
-1-oxobutan-2-ylcarbamate, substituting methyl
(S)-1-((2S,4S)-2-(2'-((2S,4S)-1-((R)-2-tert-butoxycarbonylamino-2-phenyla-
cetyl)-4-(methoxymethyl)pyrrolidin-2-yl)-1H,
1'H-7,7'-binaphtho[1,2-d]imidazol-2-yl)-4-methylpyrrolidin-1-yl)-3-methyl-
-1-oxobutan-2-ylcarbamate with tert-butyl
(2S,4S)-2-[5-(2-{(2S)-1-[N-(methoxycarbonyl)-L-valyl]pyrrolidin-2-yl}-1,1-
1-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imidazol-2--
yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate. MS (ESI) m/z 811
[M+H].sup.+.
Example BV
##STR00139##
[0407] tert-Butyl
(2S,4S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1H-imidazol-5-yl)-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphth-
o[1,2-d]imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
[0408] was synthesized from
3-(2-bromoacetyl)-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one,
by the same methods employed in the synthesis of tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-
-yl)-1H-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate,
substituting
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid for
(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrrolidine-2-carboxylic
acid and
(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrrolidine-2-c-
arboxylic acid for
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid.
tert-Butyl
(2S,4S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-meth-
ylpyrrolidin-2-yl}-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]nap-
htho[1,2-d]imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
[0409] was prepared according to the method described for the
synthesis of tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate,
substituting tert-butyl
(2S,4S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1H-imidazol-5-yl)-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphth-
o[1,2-d]imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
for tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-
-yl)-1H-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate.
Methyl
{(2S)-1-[(2S,4S)-2-(5-{2-[(2S,5S)-1-{(2S,3R)-3-methoxy-2-[(methoxyc-
arbonyl)amino]butanoyl}-4-(methoxymethyl)pyrrolidin-2-yl]-1,11-dihydroisoc-
hromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-5-methylp-
yrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate
[0410] was prepared from tert-butyl
(2S,4S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d-
]imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
according to the same method described for the synthesis of methyl
(S)-1-((2S,4S)-2-(2'-((2S,4S)-1-((2S,3R)-2-methoxycarbonylamino-3-methoxy-
butanoyl)-4-(methoxymethyl)pyrrolidin-2-yl)-1H,
1'H-7,7'-binaphtho[1,2-d]imidazol-2-yl)-4-methylpyrrolidin-1-yl)-3-methyl-
-1-oxobutan-2-ylcarbamate, substituting (2S,4S)-tert-Butyl
2-(2'-((2S,4S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-4-methyl-
pyrrolidin-2-yl)-1H,
1'H-7,7'-binaphtho[1,2-d]imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-ca-
rboxylate with tert-butyl
(2S,4S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d-
]imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate. MS
(ESI) m/z 866 [M+H].sup.+. .sup.1H NMR (400 MHz, cd.sub.3od)
.delta. 8.44 (d, J=19.8 Hz, 1H), 8.02 (t, J=8.6 Hz, 2H), 7.98-7.81
(m, 3H), 7.74 (dd, J=22.2, 13.6 Hz, 2H), 7.63-7.41 (m, 2H), 5.79
(d, J=6.0 Hz, 1H), 5.42 (dt, J=43.3, 21.5 Hz, 2H), 5.31-5.10 (m,
5H), 4.85-4.70 (m, 1H), 4.52 (d, J=3.8 Hz, 1H), 4.31 (t, J=8.2 Hz,
1H), 4.17 (dd, J=20.8, 8.8 Hz, 1H), 3.80 (dt, J=19.0, 7.3 Hz, 2H),
3.73-3.63 (m, 7H), 3.63-3.49 (m, 3H), 3.39 (d, J=9.7 Hz, 4H), 3.35
(s, 5H), 3.28 (d, J=4.4 Hz, 3H), 2.84 (d, J=8.8 Hz, 1H), 2.72 (dd,
J=12.5, 6.6 Hz, 1H), 2.59-2.45 (m, 1H), 2.45-2.11 (m, 4H),
2.11-1.82 (m, 2H), 1.56 (d, J=6.6 Hz, 3H), 1.35-1.21 (m, 1H),
1.22-1.12 (m, 4H), 1.10-1.01 (m, 2H), 0.99 (d, J=6.6 Hz, 3H), 0.91
(d, J=6.7 Hz, 3H).
Example BW
##STR00140##
[0411] Methyl
{(2S)-1-[(2S,4S)-2-(5-{2-[(2S,5S)-1-{(2S,3S)-2-[(methoxycarbonyl)amino]-3-
-methylpentanoyl}-4-(methoxymethyl)-2-yl]-1,11-dihydroisochromeno[4',3':6,-
7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-5-methylpyrrolidin-1-yl]--
3-methyl-1-oxobutan-2-yl}carbamate
[0412] was prepared according to the method described for the
synthesis of methyl {(2S,3 S)-1-[(2S,4S)-2-(5-{2-[(2S,4S)-1-{(2S,3
S)-2-[(methoxycarbonyl)amino]-3-methylpentanoyl}-4-(methoxymethyl)pyrroli-
din-2-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1-
H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidin-1-yl]-3-methyl-1-oxopentan-2--
yl}carbamate substituting tert-butyl
(2S,4S)-2-[9-(2-{(2S)-1-[N-(methoxycarbonyl)-L-valyl]pyrrolidin-2-yl}-1H--
imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2--
yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate for tert-Butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate. MS
(ESI) m/z 863 [M+H].sup.+. .sup.1H NMR (400 MHz, cd.sub.3od)
.delta. 8.43 (d, J=24.6 Hz, 1H), 8.01 (dt, J=16.1, 8.0 Hz, 1H),
7.95-7.78 (m, 2H), 7.77-7.64 (m, 2H), 7.59-7.41 (m, 2H), 5.79 (d,
J=5.8 Hz, 1H), 5.39 (dt, J=46.2, 23.1 Hz, 1H), 5.27-5.07 (m, 3H),
4.85-4.72 (m, 1H), 4.42 (t, J=8.6 Hz, 1H), 4.31 (d, J=7.9 Hz, 1H),
4.17 (dd, J=19.7, 8.7 Hz, 1H), 3.81 (dd, J=23.6, 13.3 Hz, 1H), 3.69
(d, J=10.0 Hz, 5H), 3.60 (dd, J=14.7, 7.8 Hz, 2H), 3.42 (s, 3H),
3.17 (d, J=6.1 Hz, 1H), 3.07 (s, 1H), 2.99-2.91 (m, 1H), 2.85 (s,
1H), 2.73 (dd, J=12.5, 6.4 Hz, 1H), 2.62-2.48 (m, 1H), 2.45-2.14
(m, 3H), 2.10-1.91 (m, 2H), 1.83 (s, 1H), 1.57 (d, J=6.6 Hz, 3H),
1.44 (d, J=7.4 Hz, 1H), 1.34-1.23 (m, 1H), 1.20-0.96 (m, 5H), 0.90
(dt, J=14.8, 6.7 Hz, 9H).
Example BX
##STR00141##
[0413] Methyl
{(2S)-1-[(2S)-2-(5-{2-[(2S,4S)-1-[(2R)-2-amino-2-phenylacetyl]-4-(methoxy-
methyl)pyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]im-
idazol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}ca-
rbamate
[0414] was prepared according to the method described for the
synthesis of methyl
(S)-1-((2S,4S)-2-(2'-((2S,4S)-1-((R)-2-amino-2-phenylacetyl)-4-(me-
thoxymethyl)pyrrolidin-2-yl)-1H,1'H-7,7'-binaphtho[1,2-d]imidazol-2-yl)-4--
methylpyrrolidin-1-yl)-3-methyl-1-oxobutan-2-ylcarbamate,
substituting tert-butyl
(2S,4S)-2-[9-(2-{(2S)-1-[N-(methoxycarbonyl)-L-valyl]pyrrolidin-2-yl}-1H--
imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2--
yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate for
(2S,4S)-tert-butyl
2-(2'-((2S,4S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-4-methyl-
pyrrolidin-2-yl)-1H,
1'H-7,7'-binaphtho[1,2-d]imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-ca-
rboxylate. MS (ESI) m/z 811 [M+H].sup.+.
Example BY
##STR00142##
[0415] Methyl
{(1R)-2-[(2S,4S)-2-(9-{2-[(2S,5S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-me-
thylbutanoyl}-5-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,4,5,11-tetrahyd-
roisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-(methoxymethyl)pyrr-
olidin-1-yl]-2-oxo-1-phenylethyl}carbamate
[0416] was synthesized according to the protocol described for the
preparation of methyl
{(1R)-2-[(2S,4S)-2-(5-{2-[(2S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-methy-
lbutanoyl}pyrrolidin-2-yl]-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphth-
o[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidin-1-yl]-
-2-oxo-1-phenylethyl}carbamate, substituting tert-butyl
(2S,4S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1H-imidazol-5-yl)-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphth-
o[1,2-d]imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
for tert-butyl
(2S,4S)-2-[5-(2-{(2S)-1-[N-(methoxycarbonyl)-L-valyl]pyrrolidin-2-yl}-1,4-
,5,11
tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imid-
azol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate. MS (ESI) m/z
886 [M+H].sup.+. .sup.1H NMR (400 MHz, cd.sub.3od) .delta.
8.02-7.85 (m, 2H), 7.85-7.68 (m, 2H), 7.58 (d, J=21.5 Hz, 1H),
7.55-7.35 (m, 4H), 7.31 (d, J=13.6 Hz, 1H), 5.43 (d, J=19.1 Hz,
1H), 5.28 (t, J=8.3 Hz, 1H), 5.25-5.10 (m, 3H), 4.13 (t, J=9.5 Hz,
1H), 3.93-3.54 (m, 7H), 3.42 (qd, J=9.5, 5.5 Hz, 2H), 3.34 (d,
J=7.9 Hz, 1H), 3.28 (s, 3H), 3.19 (t, J=7.8 Hz, 2H), 3.00 (t, J=7.8
Hz, 2H), 2.74-2.46 (m, 3H), 2.44-2.15 (m, 2H), 2.12-1.86 (m, 2H),
1.56 (d, J=6.7 Hz, 2H), 1.29 (d, J=6.3 Hz, 1H), 1.15-1.01 (m, 1H),
0.98 (d, J=6.7 Hz, 2H), 0.88 (d, J=6.8 Hz, 2H).
Example BZ
##STR00143## ##STR00144##
[0417] (2S,4S)-1-Tert-butyl
2-(3-chloro-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-9-yl)
4-ethoxypyrrolidine-1,2-dicarboxylate
[0418] To a slurry of
9-bromo-3-chloro-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one
(2.50 g, 6.8 mmol) in MeCN (20 mL) was added
(2S,4S)-1-(tert-butoxycarbonyl)-4-ethoxypyrrolidine-2-carboxylic
acid (2.68 g, 10.3 mmol) and DIPEA (1.3 mL, 7.5 mmol). The reaction
was heated with stirring to 50.degree. C. for 18 h. The reaction
was then cooled to room temperature and diluted with EtOAc. The
solution was washed with HCl (1N) and brine. The aqueous layers
were backextracted with EtOAc and the resulting organic layers were
combined, dried (Na.sub.2SO.sub.4) and concentrated under reduced
pressure. The crude residue was purified by silica column
chromatography (15% to 50% EtOAc/Hexanes) to afford
(2S,4S)-1-tert-butyl
2-(3-chloro-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-9-yl)
4-ethoxypyrrolidine-1,2-dicarboxylate (2.08 g, 56%).
Tert-butyl
(2S,4S)-2-(9-chloro-1,4,5,11-tetrahydroisochromeno[4',3':6,7]na-
phtho[1,2-d]imidazol-2-yl)-4-ethoxypyrrolidine-1-carboxylate
[0419] To a solution of (2S,4S)-1-tert-butyl
2-(3-chloro-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-9-yl)
4-ethoxypyrrolidine-1,2-dicarboxylate (2.08 g, 3.8 mmol) in a
mixture of toluene (30 mL) and methoxyethanol (4 mL) was added
ammonium acetate (2.90 g, 37.7 mmol). The solution was heated with
stirring to 80.degree. C. for 18 h. The reaction was then cooled to
room temperature and diluted with EtOAc. The solution was washed
with brine, and the resulting aqueous layer was backextracted with
EtOAc. The resulting organic layers were combined, dried
(Na.sub.2SO.sub.4), and concentrated under reduced pressure. The
crude residue was purified by silica column chromatography (10% to
75% EtOAc (w/5% MeOH)/Hexanes) to afford tert-butyl
(2S,4S)-2-(9-chloro-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2--
d]imidazol-2-yl)-4-ethoxypyrrolidine-1-carboxylate (0.99 g,
50%).
Tert-butyl
(2S,4S)-2-(9-chloro-1,11-dihydroisochromeno[4',3':6,7]naphtho[1-
,2-d]imidazol-2-yl)-4-ethoxypyrrolidine-1-carboxylate
[0420] To a solution of
(2S,4S)-2-(9-chloro-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2--
d]imidazol-2-yl)-4-ethoxypyrrolidine-1-carboxylate (0.99 g, 1.9
mmol) in CH.sub.2Cl.sub.2 (18 mL) was added MnO.sub.2 (4.52 g, 52.0
mmol). The resulting slurry was stirred at room temperature for 18
h. The reaction was filtered through celite, washed with
CH.sub.2Cl.sub.2, and concentrated under reduced pressure. The
crude residue was purified by silica column chromatography (10% to
75% EtOAc (w/5% MeOH)/Hexanes) to afford tert-butyl
(2S,4S)-2-(9-chloro-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imida-
zol-2-yl)-4-ethoxypyrrolidine-1-carboxylate (0.71 g, 72%)
Methyl
{(2S)-1-[(2S,4S)-2-(9-chloro-1,11-dihydroisochromeno[4',3':6,7]naph-
tho[1,2-d]imidazol-2-yl)-4-ethoxypyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl-
}carbamate
[0421] To a solution of
(2S,4S)-2-(9-chloro-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imida-
zol-2-yl)-4-ethoxypyrrolidine-1-carboxylate (0.46 g, 0.9 mmol) in a
mixture of CH.sub.2Cl.sub.2 (9.0 mL) and MeOH (1.5 mL) was added
HCl (in dioxanes, 4M, 6.5 mL, 26.0 mmol). The resulting solution
was stirred at room temperature for 2 h. The solution was
concentrated to dryness under reduced pressure. To the crude
intermediate in CH.sub.2Cl.sub.2 (10.0 mL) was added
(S)-2-(methoxycarbonylamino)-3-methylbutanoic acid (0.17 g, 0.9
mmol), HATU (0.41 g, 1.1 mmol), and DIPEA (0.5 mL, 2.9 mmol). The
resulting solution was stirred at room temperature for 48 h and
diluted with CH.sub.2Cl.sub.2. The solution was washed with aqueous
HCl (1N) and brine. The aqueous layers were backextracted with
CH.sub.2Cl.sub.2 (2.times.). The resulting organic layers were
combined, dried (Na.sub.2SO.sub.4), and concentrated under reduced
pressure. The crude residue was purified by silica column
chromatography (20% to 100% EtOAc (w/5% MeOH)/Hexanes to 80%
MeOH/EtOAc) to afford methyl
{(2S)-1-[(2S,4S)-2-(9-chloro-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,-
2-d]imidazol-2-yl)-4-ethoxypyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carba-
mate (0.46 g, 90%).
Methyl
[(2S)-1-{(2S,4S)-4-ethoxy-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaboro-
lan-2-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]py-
rrolidin-1-yl}-3-methyl-1-oxobutan-2-yl]carbamate
[0422] To a solution of methyl
{(2S)-1-[(2S,4S)-2-(9-chloro-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,-
2-d]imidazol-2-yl)-4-ethoxypyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carba-
mate (0.46 g, 0.84 mmol) in dioxane (8.5 mL) was added
4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(1,3,2-dioxaborolane) (0.32
g, 1.3 mmol), potassium acetate (0.25 g, 2.5 mmol),
bis(dibenzylideneacetone)palladium (0.032 g, 0.035 mmol), and
2-dicyclohexylphosphino-2',4',6'-triisopropylbiphenyl (Xphos, 0.032
g, 0.067 mmol). The resulting solution was degassed with argon for
5 min and heated, with stirring, to 90.degree. C. for 6 h. The
reaction was cooled to room temperature, diluted with EtOAc, and
filtered through celite. The crude residue was purified by silica
column chromatography (20% to 100% EtOAc (w/5% MeOH)/Hexanes to 90%
MeOH/EtOAc) to afford methyl
[(2S)-1-{(2S,4S)-4-ethoxy-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2--
yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]pyrrolid-
in-1-yl}-3-methyl-1-oxobutan-2-yl]carbamate (0.41 g, 73%).
Tert-butyl
(2S)-2-[5-(2-{(2S,4S)-4-ethoxy-1-[N-(methoxycarbonyl)-L-valyl]p-
yrrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-
-yl)-1H-imidazol-2-yl]pyrrolidine-1-carboxylate
[0423] To a solution of methyl
[(2S)-1-{(2S,4S)-4-ethoxy-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2--
yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]pyrrolid-
in-1-yl}-3-methyl-1-oxobutan-2-yl]carbamate (0.41 g, 0.61 mmol) in
a mixture of DME (6.1 mL) and DMF (1.0 mL) was added (S)-tert-butyl
2-(5-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate (0.39 g, 1.2
mmol), tetrakis(triphenylphosphine)palladium (0.021 g, 0.018 mmol),
[1,1'-bis(diphenylphosphino)ferrocene]dichloropalladium (0.030 g,
0.041 mmol), and aqueous potassium carbonate (2M, 1.0 mL, 2.0
mmol). The solution was degasses with argon for 5 min and heated,
with stirring, to 85.degree. C. for 6 h. The solution was cooled to
room temperature and diluted with EtOAc. The organic layer was
washed with water and brine. The aqueous layers were backextracted
with EtOAc (3.times.). The combined organic layers were dried over
Na.sub.2SO.sub.4 and concentrated under reduced pressure. The crude
residue was purified by silica column chromatography (20% to 100%
EtOAc (w/5% MeOH)/Hexanes to 80% MeOH/EtOAc) to afford tert-butyl
(2S)-2-[5-(2-{(2S,4S)-4-ethoxy-1-[N-(methoxycarbonyl)-L-valyl]pyrrolidin--
2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-im-
idazol-2-yl]pyrrolidine-1-carboxylate (0.16 g, 33%).
Methyl
{(2S)-1-[(2S)-2-(5-{2-[(2S,4S)-4-ethoxy-1-{(2S)-2-[(methoxycarbonyl-
)amino]-3-methylbutanoyl}pyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6,-
7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]-3-methyl--
1-oxobutan-2-yl}carbamate
[0424] To a solution of tert-butyl
(2S)-2-[5-(2-{(2S,4S)-4-ethoxy-1-[N-(methoxycarbonyl)-L-valyl]pyrrolidin--
2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-im-
idazol-2-yl]pyrrolidine-1-carboxylate (0.048 g, 0.062 mmol) in a
mixture of CH.sub.2Cl.sub.2 (1.0 mL) and MeOH (0.25 mL) was added
HCl (in dioxanes, 4M, 0.47 mL, 1.9 mmol). The solution was stirred
at room temperature for 3 h, and then concentrated to dryness under
reduced pressure. To the crude intermediate suspended in
CH.sub.2Cl.sub.2 (1.5 mL) was added
(S)-2-(methoxycarbonylamino)-3-methylbutanoic acid (0.012 g, 0.069
mmol), HATU (0.029 g, 0.076 mmol), and DIPEA (0.050 mL, 0.28 mmol).
The resulting solution was stirred at room temperature for 1.5 h.
The reaction was diluted with DMF and aqueous LiOH (2.5 M, 4 drops)
was added. The solution was concentrated to remove the
CH.sub.2Cl.sub.2 and the crude residue was purified by preparative
reverse phase HPLC (10% to 52% MeCN/water with 0.1% TFA). The
desired fractions were combined and concentrated under reduced
pressure to remove volatile organics. The addition of aqueous
sodium bicarbonate with stirring resulted in precipitation of a
white solid. The precipitate was filtered through a membrane filter
and washed with water. Drying under reduced pressure afforded
methyl
{(2S)-1-[(2S)-2-(5-{2-[(2S,4S)-4-ethoxy-1-{(2S)-2-[(methoxycarbonyl)amino-
]-3-methylbutanoyl}pyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6,7]naph-
tho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]-3-methyl-1-oxob-
utan-2-yl}carbamate (0.008 g, 17%). 1H-NMR: 400 MHz, (MeOD)
.delta.: (Mixture of rotomers) 8.37 (s, 1H), 7.97 (s, 2H),
7.37-7.76 (m, 5H), 5.38-5.54 (m, 1H), 5.18 (s, 2H), 5.14-5.16 (m,
1H), 4.21-4.31 (m, 4H), 3.87-4.09 (m, 1H), 3.79-3.85 (m, 2H), 3.66
(s, 3H), 3.64 (s, 3H), 3.46-3.55 (m, 2H), 2.30-2.35 (m, 3H),
2.04-2.06 (m, 3H), 1.11 (m, 2H), 0.95 (d, 3H), 0.88 (d, 3H). MS
(ESI) m/z 836.02 [M+H].sup.+.
Example CA
##STR00145##
[0425] Methyl
{(1R)-2-[(2S)-2-(5-{2-[(2S,4S)-4-ethoxy-1-{(2S)-2-[(methoxycarbonyl)amino-
]-3-methylbutanoyl}pyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6,7]naph-
tho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]-2-oxo-1-phenyle-
thyl}carbamate
[0426] To a solution of tert-butyl
(2S)-2-[5-(2-{(2S,4S)-4-ethoxy-1-[N-(methoxycarbonyl)-L-valyl]pyrrolidin--
2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-im-
idazol-2-yl]pyrrolidine-1-carboxylate (0.11 g, 0.14 mmol) in a
mixture of CH.sub.2Cl.sub.2 (2.0 mL) and MeOH (0.5 mL) was added
HCl (in dioxanes, 4M, 1.0 mL, 4.0 mmol). The solution was stirred
at room temperature for 3 h, and then concentrated to dryness under
reduced pressure. To the crude intermediate suspended in
CH.sub.2Cl.sub.2 (1.5 mL) was added
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid (0.044 g, 0.21
mmol) and DIPEA (0.075 mL, 0.43 mmol). The resulting solution was
cooled to -40.degree. C. and COMU (0.096 g, 0.22 mmol) was added.
The reaction was allowed to slowly warm to 0.degree. C. over 1 h.
The reaction was diluted with DMF. The solution was concentrated to
remove the CH.sub.2Cl.sub.2 and the crude residue was purified by
preparative reverse phase HPLC (10% to 55% MeCN/water with 0.1%
TFA). The desired fractions were combined and concentrated under
reduced pressure to remove volatile organics. The addition of
aqueous sodium bicarbonate with stirring resulted in precipitation
of a white solid. The precipitate was filtered through a membrane
filter and washed with water.
[0427] Drying under reduced pressure afforded methyl
{(1R)-2-[(2S)-2-(5-{2-[(2S,4S)-4-ethoxy-1-{(2S)-2-[(methoxycarbonyl)amino-
]-3-methylbutanoyl}pyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6,7]naph-
tho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]-2-oxo-1-phenyle-
thyl}carbamate (0.022 g, 18%). 1H-NMR: 400 MHz, (MeOD) .delta.:
(Mixture of rotomers) 8.28 (d, 1H), 7.88 (d, 1H), 7.52-7.70 (m,
3H), 7.28-7.38 (m, 5H), 6.90-6.96 (m, 2H), 5.44-5.47 (m, 1H), 5.31
(s, 1H), 5.12 (s, 2H), 4.16-4.48 (m, 3H), 3.81-3.19 (m, 1H),
3.62-3.76 (m, 2H), 3.58 (s, 3H), 2.56 (s, 3H), 2.42-2.57 (m, 1H),
2.31 (m, 1H), 1.81-2.41 (m, 5H), 1.04 (t, 3H), 0.87 (d, 3H), 0.81
(d, 3H). MS (ESI) m/z 869.55 [M+H].sup.+.
Example CB
##STR00146##
[0428] Methyl
(2S,3R)-1-((S)-2-(5-bromo-1H-imidazol-2-yl)pyrrolidin-1-yl)-3-methoxy-1-o-
xobutan-2-ylcarbamate
[0429] To a solution of (S)-tert-butyl
2-(5-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate (1.00 g, 3.2
mmol) in a mixture of CH.sub.2Cl.sub.2 (30 mL) and MeOH (5 mL) was
added HCl (in dioxane, 4 M, 11.5 mL, 46.0 mmol). The solution was
stirred at 40.degree. C. for 1 h, cooled to room temperature, and
concentrated to dryness under reduced pressure. To the crude
intermediate suspended in CH.sub.2Cl.sub.2 (30 mL) was added
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid (0.67 g,
3.5 mmol), HATU (1.47 g, 3.8 mmol), and DIPEA (1.00 mL, 6.0 mmol),
The resulting solution was stirred at room temperature for 24 h.
DMF (2 mL) and aqueous LiOH (2.5 M, 1 mL) were added and the
reaction was concentrated to dryness under reduced pressure. The
crude material was diluted with EtOAc and washed with H.sub.2O and
brine. The aqueous layers were backextracted with EtOAc. The
combined organic layers were dried over Na.sub.2SO.sub.4 and
concentrated under reduced pressure. The crude residue was purified
by silica column chromatography (20% to 100% EtOAc (w/5%
MeOH)/CH.sub.2Cl.sub.2) to afford methyl
(2S,3R)-1-((S)-2-(5-bromo-1H-imidazol-2-yl)pyrrolidin-1-yl)-3-methoxy-1-o-
xobutan-2-ylcarbamate (1.2g, 100%).
Example CC
##STR00147##
[0430] Tert-butyl
(2S,4S)-2-[9-(2-{(2S)-1-[N-(methoxycarbonyl)-O-methyl-L-threonyl]pyrrolid-
in-2-yl}-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d-
]imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
[0431] To a solution of tert-butyl
4-(methoxymethyl)-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,11-
-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]pyrrolidine-1-ca-
rboxylate (1.0 g, 3.2 mmol) in a mixture of DMSO (2.0 mL) and
dioxanes (2.0 mL) was added methyl
(2S,3R)-1-((S)-2-(5-bromo-1H-imidazol-2-yl)pyrrolidin-1-yl)-3-methoxy-1-o-
xobutan-2-ylcarbamate (0.24 g, 0.62 mmol),
tetrakis(triphenylphosphine)palladium (0.050 g, 0.043 mmol),
[1,1'-bis(diphenylphosphino)ferrocene]dichloropalladium (0.030 g,
0.041 mmol), and aqueous potassium carbonate (2M, 0.65 mL, 1.3
mmol). The solution was degasses with argon for 5 min and heated,
with stirring, to 85.degree. C. for 6 h. The solution was cooled to
room temperature and diluted with EtOAc. The organic layer was
washed with water and brine. The aqueous layers were backextracted
with EtOAc (3.times.). The combined organic layers were dried over
Na.sub.2SO.sub.4 and concentrated under reduced pressure. The crude
residue was purified by silica column chromatography (20% to 100%
EtOAc (w/5% MeOH)/Hexanes to 60% MeOH/EtOAc) to afford tert-butyl
(2S,4S)-2-[9-(2-{(2S)-1-[N-(methoxycarbonyl)-O-methyl-L-threonyl]pyrrolid-
in-2-yl}-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d-
]imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate (0.20 g,
63%).
Methyl
{(1R)-2-[(2S,4S)-2-(9-{2-[(2S)-1-{(2S,3R)-3-methoxy-2-[(methoxycarb-
onyl)amino]butanoyl}pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydroisochro-
meno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-(methoxymethyl)pyrrolidin-1--
yl]-2-oxo-1-phenylethyl}carbamate
[0432] To a solution of tert-butyl
(2S,4S)-2-[9-(2-{(2S)-1-[N-(methoxycarbonyl)-O-methyl-L-threonyl]pyrrolid-
in-2-yl}-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d-
]imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate (0.20 g,
0.26 mmol) in a mixture of CH.sub.2Cl.sub.2 (3.0 mL) and MeOH (0.5
mL) was added HCl (in dioxanes, 4M, 2.0 mL, 8.0 mmol). The solution
was stirred at 40.degree. C. for 1 h, and then cooled to room
temperature and concentrated to dryness under reduced pressure. To
the crude intermediate suspended in CH.sub.2Cl.sub.2 (3.0 mL) was
added (R)-2-(methoxycarbonylamino)-2-phenylacetic acid (0.081 g,
0.39 mmol) and DIPEA (0.150 mL, 0.86 mmol). The resulting solution
was cooled to -40.degree. C. and COMU (0.180 g, 0.42 mmol) was
added. The reaction was allowed to slowly warm to room temperature
over 30 min and maintained for 1.5 h. The solution was diluted with
CH.sub.2Cl.sub.2 and washed with aqueous bicarb. The aqueous layer
was backextracted with CH.sub.2Cl.sub.2. The combined organic
layers were dried over Na.sub.2SO.sub.4 and concentrated under
reduced pressure. The crude residue was purified by preparative
reverse phase HPLC (10% to 50% MeCN/water with 0.1% TFA). The
desired fractions were combined and concentrated under reduced
pressure to remove volatile organics. The addition of aqueous
sodium bicarbonate with stirring resulted in precipitation of a
white solid. The precipitate was filtered through a membrane filter
and washed with water. Drying under reduced pressure afforded
methyl
{(1R)-2-[(2S,4S)-2-(9-{2-[(2S)-1-{(2S,3R)-3-methoxy-2-[(methoxycarbonyl)a-
mino]butanoyl}pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydroisochromeno[4-
',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-(methoxymethyl)pyrrolidin-1-yl]-2--
oxo-1-phenylethyl}carbamate (0.10 g, 46%). 1H-NMR: 400 MHz, (MeOD)
.delta.: (Mixture of rotomers) 8.34 (s, 1H), 7.92-7.97 (m, 2H),
7.33-7.69 (m, 10H), 5.53 (s, 1H), 5.36-5.39 (m, 1H), 5.15-5.21 (m,
3H), 4.44 (d, 1H), 3.86-3.93 (m, 2H), 3.68-3.75 (m, 2H), 3.66 (s,
3H), 3.65 (s, 3H), 3.46-3.57 (m, 2H), 3.28 (s, 3H), 3.19 (s, 3H),
2.47-2.60 (m, 3H), 2.22-2.36 (m, 4H), 1.99-2.08 (m, 3H), 1.15 (d,
3H). MS (ESI) m/z 886.19 [M+H].sup.+.
Example CD
##STR00148##
[0433] Methyl
(1-{4-(methoxymethyl)-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)--
1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]pyrrolidin-1-
-yl}-3-methoxy-1-oxobutan-2-yl)carbamate
[0434] To a solution of tert-butyl
4-(methoxymethyl)-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,11-
-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]pyrrolidine-1-ca-
rboxylate (0.25 g, 0.41 mmol) in a mixture of CH.sub.2Cl.sub.2 (4.0
mL) and MeOH (1.0 mL) was added HCl (in dioxanes, 4M, 3.0 mL, 12.0
mmol). The resulting solution was stirred at 40.degree. C. for 45
min. The solution was cooled to room temperature and concentrated
to dryness under reduced pressure. To the crude intermediate in
CH.sub.2Cl.sub.2 (4.0 mL) was added
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid (0.08 g,
0.42 mmol), HATU (0.17 g, 0.45 mmol), and DIPEA (0.4 mL, 2.3 mmol).
The resulting solution was stirred at room temperature for 48 h and
diluted with CH.sub.2Cl.sub.2. The solution was washed with brine.
The aqueous layer was backextracted with CH.sub.2Cl.sub.2
(2.times.). The resulting organic layers were combined, dried
(Na.sub.2SO.sub.4), and concentrated under reduced pressure. The
crude residue was purified by silica column chromatography (30% to
100% EtOAc (w/5% MeOH)/Hexanes to 80% MeOH/EtOAc) to afford methyl
(1-{4-(methoxymethyl)-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)--
1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]pyrrolidin-1-
-yl}-3-methoxy-1-oxobutan-2-yl)carbamate (0.24 g, 92%).
Tert-butyl
(2S)-2-(5-{2-[(2S,4S)-1-[N-(methoxycarbonyl)-O-methyl-L-threony-
l]-4-(methoxymethyl)pyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6,7]nap-
htho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)pyrrolidine-1-carboxylate
[0435] To a solution of methyl
(1-{4-(methoxymethyl)-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)--
1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]pyrrolidin-1-
-yl}-3-methoxy-1-oxobutan-2-yl)carbamate (0.15 g, 0.22 mmol) in a
mixture of DMSO (2.0 mL) and dioxane (2.0 mL) was added
(S)-tert-butyl 2-(5-iodo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate
(0.15 g, 0.40 mmol), tetrakis(triphenylphosphine)palladium (0.028
g, 0.024 mmol),
[1,1'-bis(diphenylphosphino)ferrocene]dichloropalladium (0.018 g,
0.025 mmol), and aqueous potassium carbonate (2M, 0.35 mL, 0.70
mmol). The solution was degasses with argon for 5 min and heated,
with stirring, to 90.degree. C. for 6 h. The solution was cooled to
room temperature and diluted with EtOAc. The organic layer was
washed with water and brine. The aqueous layers were backextracted
with EtOAc (3.times.). The combined organic layers were dried over
Na.sub.2SO.sub.4 and concentrated under reduced pressure. The crude
residue was purified by preparative reverse phase HPLC (10% to 55%
MeCN/water with 0.1% TFA). The desired fractions were combined and
concentrated under reduced pressure to remove volatile organics.
The remaining solution was basified with aqueous bicarbonate and
extracted with CH.sub.2Cl.sub.2 (3.times.). The combined organic
layers were dried over Na.sub.2SO.sub.4 and concentrated under
reduced pressure to provide tert-butyl
(2S)-2-(5-{2-[(2S,4S)-1-[N-(methoxycarbonyl)-O-methyl-L-threonyl]-4-(meth-
oxymethyl)pyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d-
]imidazol-9-yl}-1H-imidazol-2-yl)pyrrolidine-1-carboxylate (0.013
g, 7%).
Methyl
{(1R)-2-[(2S)-2-(5-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-
-methoxybutanoyl}-4-(methoxymethyl)pyrrolidin-2-yl]-1,11-dihydroisochromen-
o[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]-
-2-oxo-1-phenylethyl}carbamate
[0436] To a solution of tert-butyl
(2S)-2-(5-{2-[(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-4-(methoxymethyl)py-
rrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9--
yl}-1H-imidazol-2-yl)pyrrolidine-1-carboxylate (0.013 g, 0.016
mmol) in a mixture of CH.sub.2Cl.sub.2 (0.5 mL) and MeOH (0.02 mL)
was added HCl (in dioxanes, 4M, 0.20 mL, 0.80 mmol). The solution
was stirred at room temperature for 1 h, and then concentrated to
dryness under reduced pressure. To the crude intermediate suspended
in CH.sub.2Cl.sub.2 (0.5 mL) was added
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid (0.006 g, 0.029
mmol) and DIPEA (0.05 mL, 0.28 mmol). The resulting solution was
cooled to 0.degree. C. and COMU (0.012 g, 0.028 mmol) was added.
The reaction was stirred at 0.degree. C. for 30 min. The solution
was diluted with DMF and aqueous LiOH (2.5 M, 2 drops) and
concentrated under reduced pressure to remove the CH.sub.2Cl.sub.2.
The crude residue was purified by preparative reverse phase HPLC
(10% to 55% MeCN/water with 0.1% TFA). The desired fractions were
combined and concentrated under reduced pressure to remove volatile
organics. The addition of aqueous sodium bicarbonate with stirring
resulted in precipitation of a white solid. The precipitate was
filtered through a membrane filter and washed with water. Drying
under reduced pressure afforded methyl
{(1R)-2-[(2S)-2-(5-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-metho-
xybutanoyl}-4-(methoxymethyl)pyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3-
':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]-2-oxo-
-1-phenylethyl}carbamate (0.008 g, 61%). .sup.1H-NMR: 400 MHz,
(MeOD) .delta.: (Mixture of rotomers) 8.37 (m, 1H), 7.96-7.98 (m,
2H), 7.60-7.79 (m, 3H), 7.35-7.52 (m, 6H), 6.98-7.03 (m, 1H), 5.52
(s, 1H), 5.26-5.39 (m, 2H), 5.20 (s, 2H), 4.44 (m, 1H), 4.27 (m,
1H), 3.64 (s, 6H), 3.50-3.57 (m, 3H), 3.37 (s, 3H), 3.29-3.44 (m,
3H), 3.20 (s, 3H), 2.68-2.72 (m, 2H), 2.57-2.62 (m, 2H), 1.89-2.15
(m, 6H), 1.18 (d, 3H). MS (ESI) m/z 885.73 [M+H].sup.+.
Example CE
##STR00149##
[0437] Methyl
[(2S)-1-{(2S,4S)-3-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,11--
dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]-2-azabicyclo[3.1-
.0]hex-2-yl}-3-methyl-1-oxobutan-2-yl]carbamate
[0438] Methyl
[(2S)-1-{(2S,4S)-3-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,11--
dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]-2-azabicyclo[3.1-
.0]hex-2-yl}-3-methyl-1-oxobutan-2-yl]carbamate was prepared
following the procedure for methyl
[(2S)-1-{(2S,4S)-4-ethoxy-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2--
yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]pyrrolid-
in-1-yl}-3-methyl-1-oxobutan-2-yl]carbamate by substitution of
(1S,3S,5S)-2-(tert-butoxycarbonyl)-2-azabicyclo[3.1.0]hexane-3-carboxylic
acid for
(2S,4S)-1-(tert-butoxycarbonyl)-4-ethoxypyrrolidine-2-carboxylic
acid.
Tert-butyl
(2S,4S)-2-[5-(2-{(1S,3S,5S)-2-[N-(methoxycarbonyl)-L-valyl]-2-a-
zabicyclo[3.1.0]hex-3-yl-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidaz-
ol-9-yl)-1H-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
[0439] To a solution of methyl
[(2S)-1-{(2S,4S)-3-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,11--
dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]-2-azabicyclo[3.1-
.0]hex-2-yl}-3-methyl-1-oxobutan-2-yl]carbamate (0.19 g, 0.30 mmol)
in a mixture of DMSO (2.0 mL) and dioxane (2.0 mL) was added
(2S,4S)-tert-butyl
2-(5-iodo-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate
(0.20 g, 0.55 mmol), tetrakis(triphenylphosphine)palladium (0.035
g, 0.030 mmol),
[1,1'-bis(diphenylphosphino)ferrocene]dichloropalladium (0.025 g,
0.034 mmol), and aqueous potassium carbonate (2M, 0.5 mL, 1.0
mmol). The solution was degasses with argon for 5 min and heated,
with stirring, to 90.degree. C. for 6 h. The solution was cooled to
room temperature, diluted with EtOAc, and filtered through celite.
The filtrate was concentrated under reduced pressure and purified
by silica column chromatography (2% to 25% CH.sub.2Cl.sub.2/MeOH)
and preparative reverse phase HPLC (10% to 55% MeCN/water with 0.1%
TFA). The desired fractions were combined and concentrated under
reduced pressure to remove volatile organics. The aqueous layer was
basified with aqueous sodium bicarbonate and extracted with
CH.sub.2Cl.sub.2 (3.times.). The organic layers were combine, dried
over Na.sub.2SO.sub.4, and concentrated under reduced pressure to
afford tert-butyl (2S,4S)-2-[5-(2-{(1
S,3S,5S)-2-[N-(methoxycarbonyl)-L-valyl]-2-azabicyclo[3.1.0]hex-3-yl}-1,1-
1-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imidazol-2--
yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate (0.025 g, 11%).
Methyl
{(1R)-2-[(2S,4S)-2-(5-{2-[(1S,3S,5S)-2-{(2S)-2-[(methoxycarbonyl)am-
ino]-3-methylbutanoyl}-2-azabicyclo[3.1.0]hex-3-yl]-1,11-dihydroisochromen-
o[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethy-
l)pyrrolidin-1-yl]-2-oxo-1-phenylethyl}carbamate
[0440] To a solution of tert-butyl (2S,4S)-2-[5-(2-{(1
S,3S,5S)-2-[N-(methoxycarbonyl)-L-valyl]-2-azabicyclo[3.1.0]hex-3-yl}-1,1-
1-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imidazol-2--
yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate (0.025 g, 0.032
mmol) in a mixture of CH.sub.2Cl.sub.2 (1.0 mL) and MeOH (0.25 mL)
was added HCl (in dioxanes, 4M, 0.50 mL, 2.0 mmol). The solution
was stirred at room temperature for 12 h, and then concentrated to
dryness under reduced pressure. To the crude intermediate suspended
in CH.sub.2Cl.sub.2 (0.5 mL) was added
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid (0.012 g, 0.057
mmol) and DIPEA (0.05 mL, 0.28 mmol). The resulting solution was
cooled to 0.degree. C. and COMU (0.023 g, 0.054 mmol) was added.
The reaction was stirred at 0.degree. C. for 30 min. The solution
was diluted with DMF and aqueous LiOH (2.5 M, 2 drops) and
concentrated under reduced pressure to remove the CH.sub.2Cl.sub.2.
The crude residue was purified by preparative reverse phase HPLC
(10% to 55% MeCN/water with 0.1% TFA). The desired fractions were
combined and concentrated under reduced pressure to remove volatile
organics. The addition of aqueous sodium bicarbonate with stirring
resulted in precipitation of a white solid. The precipitate was
filtered through a membrane filter and washed with water. Drying
under reduced pressure afforded methyl {(1R)-2-[(2S,4S)-2-(5-{2-[(1
S,3S,5S)-2-{(2S)-2-[(methoxycarbonyl)amino]-3-methylbutanoyl}-2-azabicycl-
o[3.1.0]hex-3-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-
-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidin-1-yl]-2-oxo-1-phenyle-
thyl}carbamate (0.015 g, 55%). .sup.1H-NMR: 400 MHz, (MeOD)
.delta.: (Mixture of rotomers) 8.35 (m, 1H), 7.94-7.96 (m, 2H),
7.54-7.78 (m, 6H), 6.93-7.00 (m, 1H), 5.72 (m, 1H), 5.46 (s, 1H),
5.19 (s, 2H), 5.14-5.16 (m, 1H), 3.95 (m, 1H), 3.67 (s, 3H), 3.63
(s, 3H), 3.42-3.49 (m, 2H), 3.24 (s, 3H), 2.67-2.78 (m, 2H),
2.41-2.62 (m, 3H), 2.01-2.13 (m, 2H), 1.86-1.99 (m, 3H), 0.99-1.03
(m, 2H), 0.90 (d, 3H). MS (ESI) m/z 882.23 [M+H].sup.+.
Example CF
##STR00150##
[0441] Tert-butyl
(2S,4S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-isoleucyl]-5-methylpyrr-
olidin-2-yl}-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1-
,2-d]imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
[0442] To a solution of methyl
(1-{4-(methoxymethyl)-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)--
1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]pyrrolidin-1-
-yl}-3-methyl-1-oxobutan-2-yl)carbamate (0.47 g, 0.78 mmol) in a
mixture of DMSO (4.0 mL) and dioxane (4.0 mL) was added methyl
(2S,3S)-1-((2S,5S)-2-(5-iodo-1H-imidazol-2-yl)-5-methylpyrrolidin-1-yl)-3-
-methyl-1-oxopentan-2-ylcarbamate (0.26 g, 0.72 mmol),
tetrakis(triphenylphosphine)palladium (0.090 g, 0.078 mmol),
[1,1'-bis(diphenylphosphino)ferrocene]dichloropalladium (0.061g,
0.083 mmol), and aqueous potassium carbonate (2M, 1.2 mL, 2.4
mmol). The solution was degasses with argon for 5 min and heated,
with stirring, to 90.degree. C. for 6 h. The solution was cooled to
room temperature, diluted with EtOAc, and filtered through celite.
The filtrate was concentrated under reduced pressure and diluted
with EtOAc. The organic solution was washed water and brine and the
aqueous layers were backextracted with EtOAc. The combined organic
layers were dried over Na.sub.2SO.sub.4 and concentrated under
reduced pressure. The crude residue was purified by silica column
chromatography (10% to 100% EtOAc (5% MeOH)/CH.sub.2Cl.sub.2) to
afford tert-butyl
(2S,4S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-isoleucyl]-5-methylpyrr-
olidin-2-yl}-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1-
,2-d]imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
(0.25 g, 40%).
Methyl
{(1R)-2-[(2S,4S)-2-(9-{2-[(2S,5S)-1-{(2S,3S)-2-[(methoxycarbonyl)am-
ino]-3-methylpentanoyl}-5-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-di-
hydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-(methoxymethyl)p-
yrrolidin-1-yl]-2-oxo-1-phenylethyl}carbamate
[0443] To a solution of tert-butyl
(2S,4S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-isoleucyl]-5-methylpyrr-
olidin-2-yl}-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1-
,2-d]imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
(0.175 g, 0.21 mmol) in a mixture of CH.sub.2Cl.sub.2 (2.0 mL) and
MeOH (0.5 mL) was added HCl (in dioxanes, 4M, 1.6 mL, 6.4 mmol).
The solution was stirred at 40.degree. C. for 1 h, cooled to room
temperature, and then concentrated to dryness under reduced
pressure. To the crude intermediate suspended in CH.sub.2Cl.sub.2
(3.0 mL) was added (R)-2-(methoxycarbonylamino)-2-phenylacetic acid
(0.070 g, 0.34 mmol) and DIPEA (0.15 mL, 0.86 mmol). The resulting
solution was cooled to -40.degree. C. and COMU (0.15 g, 0.35 mmol)
was added. The reaction was warmed to room temperature over 30 min
and diluted with CH.sub.2Cl.sub.2. The solution was washed with
saturated aqueous sodium bicarbonate. The aqueous layer was
backextracted with CH.sub.2Cl.sub.2, and the combined organic
layers were dried over Na.sub.2SO.sub.4 and concentrated under
reduced pressure. The crude residue was purified by preparative
reverse phase HPLC (10% to 58% MeCN/water with 0.1% TFA). The
desired fractions were combined and concentrated under reduced
pressure to remove volatile organics. The addition of aqueous
sodium bicarbonate with stirring resulted in precipitation of a
white solid. The precipitate was filtered through a membrane filter
and washed with water. Drying under reduced pressure afforded
methyl {(1R)-2-[(2S,4S)-2-(9-{2-[(2S,5S)-1-{(2S,3
S)-2-[(methoxycarbonyl)amino]-3-methylpentanoyl}-5-methylpyrrolidin-2-yl]-
-1H-imidazol-5-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazo-
l-2-yl)-4-(methoxymethyl)pyrrolidin-1-yl]-2-oxo-1-phenylethyl}carbamate
(0.079 g, 41%). .sup.1H-NMR: 400 MHz, (MeOD) .delta.: (Mixture of
rotomers) 8.36 (m, 1H), 7.93-7.98 (m, 2H), 7.66-7.84 (m, 3H),
7.35-7.48 (m, 7H), 5.53 (s, 1H), 5.36-5.39 (m, 1H), 5.17 (d, 2H),
5.08 (m, 1H), 4.14-4.35 (m, 1H), 3.74 (m, 4H), 3.64 (s, 3H), 3.62
(s, 3H), 3.46 (m, 1H), 3.19 (s, 3H), 2.76 (m, 1H), 2.46-2.60 (m,
3H), 2.24-2.35 (m, 1H), 2.08-2.18 (m, 2H), 1.91 (m, 1H), 1.61-1.87
(m, 2H), 1.48 (d, 3H), 1.13-1.21 (m, 3H), 0.80-0.97 (m, 3H). MS
(ESI) m/z 898.24 [M+H].sup.+.
Example CG
##STR00151##
[0444] Methyl
{(2S)-1-[(2S,4S)-2-(9-{2-[(2S,5S)-1-{(2S,3S)-2-[(methoxycarbonyl)amino]-3-
-methylpentanoyl}-5-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydroi-
sochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-(methoxymethyl)pyrroli-
din-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate
[0445] To a solution of tert-butyl
(2S,4S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-isoleucyl]-5-methylpyrr-
olidin-2-yl}-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1-
,2-d]imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
(0.075 g, 0.09 mmol) in a mixture of CH.sub.2Cl.sub.2 (1.0 mL) and
MeOH (0.25 mL) was added HCl (in dioxanes, 4M, 0.7 mL, 2.8 mmol).
The solution was stirred at 40.degree. C. for 1 h, cooled to room
temperature, and then concentrated to dryness under reduced
pressure. To the crude intermediate suspended in CH.sub.2Cl.sub.2
(3.0 mL) was added (S)-2-(methoxycarbonylamino)-3-methylbutanoic
acid (0.020 g, 0.14 mmol), HATU (0.043 g, 0.11 mmol) and DIPEA
(0.10 mL, 0.57 mmol). The reaction was stirred at room temperature
for 2 h. The reaction was diluted with DMF and aqueous LiOH (2.5 M,
3 drops) and the CH.sub.2Cl.sub.2 was removed under reduced
pressure. The crude residue was purified by preparative reverse
phase HPLC (10% to 58% MeCN/water with 0.1% TFA). The desired
fractions were combined and concentrated under reduced pressure to
remove volatile organics. The addition of aqueous sodium
bicarbonate with stirring resulted in precipitation of a white
solid. The precipitate was filtered through a membrane filter and
washed with water. Drying under reduced pressure afforded methyl
{(2S)-1-[(2S,4S)-2-(9-{2-[(2S,5S)-1-{(2S,3S)-2-[(methoxycarbonyl)amino]-3-
-methylpentanoyl}-5-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydroi-
sochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-(methoxymethyl)pyrroli-
din-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate (0.031 g, 38%).
.sup.1H-NMR: 400 MHz, (MeOD) .delta.: (Mixture of rotomers) 8.34
(m, 1H), 7.91-9.97 (m, 2H), 7.50-7.81 (m, 3H), 7.35-7.38 (m, 2H),
5.17-5.26 (m, 3H), 5.08 (m, 1H), 4.14-4.33 (m, 4H), 3.64 (s, 3H),
3.63 (s, 3H), 3.51-3.59 (m, 3H), 3.37 (s, 3H), 2.71 (m, 1H),
2.55-2.59 (m, 1H), 2.23-2.33 (m, 1H), 1.92-2.10 (m, 2H), 1.77-1.89
(m, 1H), 1.60 (m, 1H), 1.48 (d, 1H), 1.11-1.22 (m, 2H), 0.81-0.98
(m, 12H). MS (ESI) m/z 864.27 [M+H].sup.+.
Example CH
##STR00152## ##STR00153##
[0446] tert-butyl
(2S,4S)-4-(methoxymethyl)-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2--
yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]pyrrolid-
ine-1-carboxylate
[0447] The title compound was obtained as in Example AA but using
(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrrolidine-2-carboxylic
acid in place of
(S)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid.
2-[4-(methoxymethyl)pyrrolidin-2-yl]-9-(4,4,5,5-tetramethyl-1,3,2-dioxabor-
olan-2-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazole
[0448] Tert-butyl
(2S,4S)-4-(methoxymethyl)-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2--
yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]pyrrolid-
ine-1-carboxylate (310 mg, 0.507 mmol) was treated with 2 mL 1.25N
HCl in ethanol and stirred at room temperature for 2h then at
50.degree. C. for 2h. The reaction mixture was concentrated under
reduced pressure to give a dark yellow solid that was directly in
the next step.
methyl
[(2S)-1-{(2S,4S)-4-ethoxy-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaboro-
lan-2-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]py-
rrolidin-1-yl}-3-methyl-1-oxobutan-2-yl]carbamate
[0449] A mixture of (S)-2-(methoxycarbonylamino)-3-methylbutanoic
acid (107 mg, 0.608 mmol), HATU (231 mg, 0.608 mmol) and 6 mL 10%
DIPEA in DMF was pre-activated for 5 minutes, then it was added to
the amine salt from the step above and allowed to stir overnight.
The reaction mixture was partitioned between ethyl acetate and
saturated sodium bicarbonate. The organic phase was concentrated
and purified by silica gel chromatography. (103 mg)
tert-butyl
2-[5-(2-{1-[N-(methoxycarbonyl)valyl]-4-(methoxymethyl)pyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-methylpyrrolidine-1-carboxylate
[0450] the title compound was obtained as in Example AA but using
methyl
[(2S)-1-{(2S,4S)-4-ethoxy-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2--
yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]pyrrolid-
in-1-yl}-3-methyl-1-oxobutan-2-yl]carbamate (103 mg, 0.154 mmol) in
place of tert-butyl
2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,11-dihydroisochromen-
o[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]pyrrolidine-1-carboxylate
and methyl
(S)-1-((S)-2-(5-iodo-1H-imidazol-2-yl)pyrrolidin-1-yl)-3-methyl-1--
oxobutan-2-ylcarbamate (58 mg, 0.154 mmol) in place of methyl
(S)-1-((S)-2-(5-bromo-1H-imidazol-2-yl)pyrrolidin-1-yl)-3-methyl-1-oxobut-
an-2-ylcarbamate. (50.0 mg)
methyl
{1-[4-(methoxymethyl)-2-{9-[2-(4-methylpyrrolidin-2-yl)-1H-imidazol-
-5-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl}pyrro-
lidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate
[0451] tert-butyl
2-[5-(2-{1-[N-(methoxycarbonyl)valyl]-4-(methoxymethyl)pyrrolidin-2-yl}-1-
,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imidazol--
2-yl]-4-methylpyrrolidine-1-carboxylate (50 mg, 0.063 mmol) was
treated with 2 mL 1.25N HCl in ethanol and heated at 60.degree. C.
for 2h, then it was concentrated under reduced pressure and pumped
dry under high vacuum and used directly in the next step.
methyl
{1-[2-{9-[2-(1-{[(methoxycarbonyl)amino](phenyl)acetyl}-4-methylpyr-
rolidin-2-yl)-1H-imidazol-5-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[-
1,2-d]imidazol-2-yl}-4-(methoxymethyl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-
-2-yl}carbamate
[0452] A mixture of (R)-2-(methoxycarbonylamino)-2-phenylacetic
acid (13 mg, 0.063 mmol), COMU (30 mg, 0.069 mmol) in 0.500 mL DMF
and DIPEA (0.033 mL, 0.189 mmol) was allowed to preactivate for 15
minutes before it was added to the solid crude amine salt from the
previous step and stirred overnight. The product was purified by
reverse phase HPLC. The product was converted to the free base by
dissolution in 2 mL 1:1 acetonitrile:methanol and passage through a
prepacked cartridge of polymer supported carbonate. Concentration
and drying gave an off white powder. (23.3 mg). MS (ESI) m/z 883.8
[M+H].sup.+. .sup.1H NMR (CD.sub.3CN) 8.176 (s, 1H), 7.778 (m, 1H),
7.596-7.521 (m, 4H), 7.455-7.347 (m, 6H), 7.218 (s, 1H), 5.482 (s,
1H), 5.310 (m, 1H), 5.192 (m, 1H), 4.999 (q, 2H, J=14 Hz), 4.372
(d, 1H, J=6.4 Hz), 4.279 (m, 1H), 3.800-3.697 (m, 2H), 3.632 (s,
3H) 3.597-3.445 (m, 7H), 3.355 (s, 3H), 2.876 (m, 2H), 2.761 (m,
1H), 2.583 (m, 2H), 2.220 (m, 2H), 1.764 (m, 1H), 1.070 (d, 3H,
J=6.4 Hz), 1.020 (d, 3H, J 6.4 Hz), 0.898 (d, 3H, J=6.4 Hz).
Example CI
##STR00154##
[0453] tert-butyl
(2S,4S)-2-[5-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-4-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-methylpyrrolidine-1-carboxylate
[0454] The title compound was obtained as in Example AA but using
methyl
[(2S)-3-methyl-1-{(2S,4S)-4-methyl-2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxab-
orolan-2-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl-
]pyrrolidin-1-yl}-1-oxobutan-2-yl]carbamate (307 mg, 0.481 mmol) in
place of tert-butyl
2-[9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,11-dihydroisochromen-
o[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]pyrrolidine-1-carboxylate
and methyl
(S)-1-((S)-2-(5-iodo-1H-imidazol-2-yl)pyrrolidin-1-yl)-3-methyl-1--
oxobutan-2-ylcarbamate (181 mg, 0.481 mmol) in place of methyl
(S)-1-((S)-2-(5-bromo-1H-imidazol-2-yl)pyrrolidin-1-yl)-3-methyl-1-oxobut-
an-2-ylcarbamate. (200.8 mg)
methyl
{(2S)-3-methyl-1-[(2S,4S)-4-methyl-2-(9-{2-[(2S,4S)-4-methylpyrroli-
din-2-yl]-1H-imidazol-5-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2--
d]imidazol-2-yl)pyrrolidin-1-yl]-1-oxobutan-2-yl}carbamate
[0455] Tert-butyl
(2S,4S)-2-[5-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-4-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-methylpyrrolidine-1-carboxylate (200 mg, 0.262
mmol) was treated with 2 mL 1.25N HCl in ethanol and heated at
60.degree. C. for 2h, then it was concentrated under reduced
pressure and pumped dry under high vacuum and used directly in the
next step.
methyl
{(1R)-2-[(2S,4S)-2-(5-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino-
]-3-methylbutanoyl}-4-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3'-
:6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-methylpyrrolidin-1-y-
l]-2-oxo-1-phenylethyl}carbamate
[0456] A mixture of (R)-2-(methoxycarbonylamino)-2-phenylacetic
acid (13 mg, 0.063 mmol), COMU (30 mg, 0.069 mmol) in 1.5 mL DMF
was allowed to preactivate for 5 minutes before it was added to a
solution of the amine from the previous salt in 1.5 mL DMF and
DIPEA (0.137 mL, 0.786 mmol) and stirred overnight. The product was
purified by reverse phase HPLC. The product was converted to the
free base by dissolution in 2 mL 1:1 acetonitrile:methanol and
passage through a prepacked cartridge of polymer supported
carbonate. Concentration and drying gave an off white powder. (25.8
mg). MS (ESI) m/z 853.8 [M+H].sup.+. .sup.1H NMR (CD.sub.3CN) 8.164
(s, 1H), 7.781 (m, 1H), 7.609 (m, 2H), 7.535 (m, 2H), 7.433-7.305
(m, 6H), 7.229 (s, 1H), 5.482 (s, 1H), 5.290 (m, 1H), 5.191 (m,
1H), 4.997 (m, 2H), 4.372 (d, 1H, J=6.4 Hz), 4.267 (m, 1H),
3.735-3.445 (m, 10H), 2.573 (m, 4H), 2.197 (m, 2H), 2.017 (m, 1H),
1.760 (m, 1H), 1.204 (d, 3H, J=6.4 Hz), 1.068 (d, 3H, J=6.4 Hz),
1.010 (d, 3H, J=6.8 Hz), 0.887 (d, 3H, J=6.8 Hz).
Example CJ
##STR00155##
[0457] tert-butyl
(2S,4S)-2-[5-(2-{(2S)-1-[(benzyloxy)carbonyl]pyrrolidin-2-yl}-1,11-dihydr-
oisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imidazol-2-yl]-4-(m-
ethoxymethyl)pyrrolidine-1-carboxylate
[0458] The title compound was obtained as in Example BO (compound
tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-
-yl)-1H-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate)
but using (S)-1-(benzyloxycarbonyl)pyrrolidine-2-carboxylic acid in
place of
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid in step 6
tert-butyl
(2S,4S)-4-(methoxymethyl)-2-(5-{2-[(2S)-pyrrolidin-2-yl]-1,11-d-
ihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-
pyrrolidine-1-carboxylate
[0459] A mixture of tert-butyl
(2S,4S)-2-[5-(2-{(25)-1-[(benzyloxy)carbonyl]pyrrolidin-2-yl}-1,11-dihydr-
oisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imidazol-2-yl]-4-(m-
ethoxymethyl)pyrrolidine-1-carboxylate (724 mg, 0.96 mmol) and 70
mg 10% Pd/C in 20 mL ethanol was hydrogenated at 1 atm overnight.
Additional 10% Pd/C (300 mg) and a portion of solid NaHCO3 was
added and hydrogenation continued for 4 hours. Filtration through
celite and concentration of the filtrate under reduced pressure
gave the product as a dark brown solid, 454 mg. Purification by
reverse phase HPLC gave 65 mg purified product.
methyl
{(1R)-2-[(2S)-2-(9-{2-[(2S,4S)-4-(methoxymethyl)pyrrolidin-2-yl]-1H-
-imidazol-5-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-
-yl)pyrrolidin-1-yl]-2-oxo-1-phenylethyl}carbamate
[0460] A mixture of (R)-2-(methoxycarbonylamino)-2-phenylacetic
acid (22 mg, 0.105 mmol), COMU (45 mg, 0.069 mmol), and tert-butyl
(2S,4S)-4-(methoxymethyl)-2-(5-{2-[(2S)-pyrrolidin-2-yl]-1,11-dihydroisoc-
hromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)pyrrolidin-
e-1-carboxylate (65 mg, 0.105 mmol) in 1.5 mL 10% DIPEA in DMF was
stirred for 1.5h. The reaction mixture was partitioned between
ethyl acetate and saturated sodium bicarbonate. The organic phase
was dried over sodium sulphate, filtered and concentrated under
reduced pressure. The crude intermediate was treated with 8 mL
1.25N HCl in ethanol at 50.degree. C. for 4h. Added saturated
sodium bicarbonate and extracted the free base into
dichloromethane. (106 mg)
methyl
{(2S)-1-[(2S,4S)-2-(5-{2-[(2S)-1-{(2R)-2-[(methoxycarbonyl)amino]-2-
-phenylacetyl}pyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1-
,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidin-1-yl]-3--
methyl-1-oxobutan-2-yl}carbamate
[0461] A mixture of methyl
{(1R)-2-[(2S)-2-(9-{2-[(2S,4S)-4-(methoxymethyl)pyrrolidin-2-yl]-1H-imida-
zol-5-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)py-
rrolidin-1-yl]-2-oxo-1-phenylethyl}carbamate (55 mg, 0.077 mmol),
(S)-2-(methoxycarbonylamino)-3-methylbutanoic acid (14 mg, 0.077
mmol), HATU (32 mg, 0.085 mmol) and 0.4 mL 10% DIPEA in DMF was
stirred at room temperature for 1 hour. The product was purified by
reverse phase HPLC. The product was converted to the free base by
dissolution in 2 mL 1:1 acetonitrile:methanol and passage through a
prepacked cartridge of polymer supported carbonate. The eluent was
concentrated, the taken up in 1% TFA in 1:1 acetonitrile:water,
frozen, and lyophilized to give the product as a trifluoroacetate
salt. (30.7 mg) MS (ESI) m/z 869.9 [M+H].sup.+.
methyl
{(1R)-2-[(2S)-2-(9-{2-[(2S,4S)-1-[N-(methoxycarbonyl)-O-methyl-L-th-
reonyl]-4-(methoxymethyl)pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydrois-
ochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)pyrrolidin-1-yl]-2-oxo-1-p-
henylethyl}carbamate
[0462] A mixture of methyl
{(1R)-2-[(2S)-2-(9-{2-[(2S,4S)-4-(methoxymethyl)pyrrolidin-2-yl]-1H-imida-
zol-5-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)py-
rrolidin-1-yl]-2-oxo-1-phenylethyl}carbamate (51 mg, 0.072 mmol),
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid (14 mg,
0.072 mmol), HATU (30 mg, 0.079 mmol) and 0.4 mL 10% DIPEA in DMF
was stirred at room temperature for 1 hour. The product was
purified by reverse phase HPLC. The product was converted to the
free base by dissolution in 2 mL 1:1 acetonitrile:methanol and
passage through a prepacked cartridge of polymer supported
carbonate. The eluent was concentrated, the taken up in 1% TFA in
1:1 acetonitrile:water, frozen, and lyophilized to give the product
as a trifluoroacetate salt. (24 mg). MS (ESI) m/z 885.8
[M+H].sup.+; .sup.1H NMR (CD.sub.3CN) 7.635 (s, 1H), 7.434 (m, 3H),
7.330 (m, 4H), 7.233 (m, 1H), 7.164 (m, 1H), 6.983 (m, 1H), 6.747
(m, 2H), 6.127 (m, 1H), 5.584 (d, 1H, J=6.4 Hz), 5.431 (m, 1H),
5.145 (m, 1H), 4.729 (s, 2H), 4.442 (m, 1H), 4.029 (m, 2H), 3.838
(m, 1H), 3.662-3.534 (m, 2H), 3.572 (s, 3H) 3.552 (s, 3H),
3.444-3.310 (m, 3H), 3.240 (s, 3H), 3.225 (s, 3H), 2.618 (m, 1H),
2.464 (m, 1H), 2.304 (m, 1H), 2.129 (m, 1H), 2.041 (m, 1H), 1.899
(m, 2H), 1.107 (d, 3H, J 6.4 Hz).
Example CK
##STR00156##
[0463] tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[(benzyloxy)carbonyl]-5-methylpyrrolidin-2-yl}-
-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imidazo-
l-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
[0464] The title compound was obtained as in Example BO (compound
tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,4,5,11-tetrahydroisochromeno[4',3'
6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imidazol-2-yl]-4-(methoxymethyl)pyrro-
lidine-1-carboxylate) but using
(2S,5S)-1-(benzyloxycarbonyl)-5-methylpyrrolidine-2-carboxylic acid
in place of
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-meth-
ylpyrrolidine-2-carboxylic acid.
tert-butyl
(2S,4S)-4-(methoxymethyl)-2-(5-{2-[(2S,5S)-5-methylpyrrolidin-2-
-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imi-
dazol-2-yl)pyrrolidine-1-carboxylate
[0465] A mixture of 683A (830 mg, 1.08 mmol) and 100 mg 10% Pd/C in
20 mL ethanol was hydrogenated at 1 atm overnight. Additional 10%
Pd/C (300 mg) and a portion of solid NaHCO3 was added and
hydrogenation continued for 4 hours. Filtration through celite and
concentration of the filtrate under reduced pressure gave the
product as a dark brown solid, 722 mg. Purification by reverse
phase HPLC gave 100 mg purified product.
tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-O-methyl-L-thre-
onyl]-5-methylpyrrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1-
,2-d]imidazol-9-yl)-1H-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carbo-
xylate
[0466] A mixture of tert-butyl
(2S,4S)-4-(methoxymethyl)-2-(5-{2-[(2S,5S)-5-methylpyrrolidin-2-yl]-1,11--
dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl-
)pyrrolidine-1-carboxylate (101 mg, 0.159 mmol),
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid (30 mg,
0.159 mmol), HATU (61 mg, 0.159 mmol) and 2 mL 10% DIPEA in DMF was
stirred at room temperature for 1.5 hours. Saturated sodium
bicarbonate was added and the product was extracted into
dichloromethane, dried over sodium sulphate, filtered and
concentrated under reduced pressure. This crude product was treated
with 5 mL 1.25N HCl in ethanol at 50.degree. C. for 4h and then it
was concentrated under reduced pressure. Saturated sodium
bicarbonate was added and the product was extracted into
dichloromethane, dried over sodium sulphate, filtered and
concentrated under reduced pressure. (74.6 mg)
methyl
{(2S)-1-[(2S,4S)-2-(5-{2-[(2S,5S)-1-{(2S,3R)-3-methoxy-2-[(methoxyc-
arbonyl)amino]butanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4-
',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)p-
yrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate
[0467] A mixture of methyl
{(2S,3R)-3-methoxy-1-[(2S,5S)-2-(9-{2-[(2S,4S)-4-(methoxymethyl)pyrrolidi-
n-2-yl]-1H-imidazol-5-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]-
imidazol-2-yl)-5-methylpyrrolidin-1-yl]-1-oxobutan-2-yl}carbamate
(74.6 mg, 0.105 mmol),
(S)-2-(methoxycarbonylamino)-3-methylbutanoic acid (18.5 mg, 0.105
mmol), HATU (44 mg, 0.116 mmol) and 0.6 mL 10% DIPEA in DMF was
stirred at room temperature for 1 hour. The product was purified by
reverse phase HPLC. (48.1 mg) MS (ESI) m/z 866.1 [M+H].sup.+.
Example CL
##STR00157##
[0468] tert-butyl
(2S,4S)-2-(9-{2-[(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-4-(trifluorometh-
yl)pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydroisochromeno[4',3':6,7]na-
phtho[1,2-d]imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate
[0469] the title compound was prepared as in Example BO for
compound tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate, by
using
(2S,4S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-4-(trifluoromet-
hyl)pyrrolidine-2-carboxylic acid in place of
(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrrolidine-2-carboxylic
acid and
(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrrolidine-2-c-
arboxylic acid in place of
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid.
methyl
{(1R)-2-[(2S,4S)-2-(9-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino-
]-3-methylbutanoyl}-4-(trifluoromethyl)pyrrolidin-2-yl]-1H-imidazol-5-yl}--
1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-(methoxym-
ethyl)pyrrolidin-1-yl]-2-oxo-1-phenylethyl}carbamate
[0470] tert-butyl
(2S,4S)-2-(9-{2-[(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-4-(trifluorometh-
yl)pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydroisochromeno[4',3':6,7]na-
phtho[1,2-d]imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate
(<0.412 mmol, crude from previous step) was treated with 6 mL 4N
HCl in dioxane at room temperature overnight and then at 50.degree.
C. for 1 hour. Diethyl ether (20 mL) was added and the precipitate
of hydrochloride salt was collected by vacuum filtration. (126 mg,
0.16 mmol). This material was combined with
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid (34 mg, 0.16
mmol), COMU (70 mg, 0.16 mmol), and 1.6 mL of 10% DIPEA in DMF.
After 1 hour at room temperature, the mixture was added dropwise
into 25 mL saturated sodium bicarbonate, with stirring and the
resulting precipitate was collected by vacuum filtration and washed
with 2 mL water. The product was purified, then re-purified by
reverse phase HPLC. (3.5 mg). MS (ESI) m/z 938.1 [M+H].sup.+.
Example CM
##STR00158##
[0471] (2S,4S)-tert-butyl
2-formyl-4-methylpyrrolidine-1-carboxylate
[0472] A mixture of
(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidine-2-carboxylic
acid (5.2g, 22.7 mmol), O,N-dimethylhydroxylamine hydrochloride
(2.4g, 24.9 mmol), HATU (10.4g, 27.2 mmol) and DIPEA (9.5 mL, 54.5
mmol) in 114 mL DMF was stirred at room temperature overnight. The
mixture was extracted into ethyl acetate and washed with saturated
bicarbonate and water, dried over sodium sulphate, filtered, and
concentrated. It was then dissolved in diethyl ether (100 mL) and
washed with water to remove residual DMF, dried, filtered, and
concentrated to a pale yellow oil (5.30g, 19.5 mmol) of
(2S,4S)-tert-butyl
2-(methoxy(methyl)carbamoyl)-4-methylpyrrolidine-1-carboxylate.
[0473] (2S,4S)-tert-butyl
2-(methoxy(methyl)carbamoyl)-4-methylpyrrolidine-1-carboxylate
(5.30g, 19.5 mmol) was dissolved in 120 mL THF, cooled to
-78.degree. C. and treated with lithium aluminium hydride (1M in
THF, 19.5 mL, 19.5 mmol) dropwise via addition funnel. After 1
hour, the mixture was brought to 0.degree. C. and kept at that
temperature for 2 hours. It was quenched by dropwise addition of a
50 mL solution of 3.0g KHSO4 in water, removed from the ice bath,
and stirred 15 minutes at room temperature. The product was
extracted with three 75 mL portions of ethyl acetate and washed
with brine. The organic phase was dried over sodium sulphate,
filtered, and concentrated to give crude (2S,4S)-tert-butyl
2-formyl-4-methylpyrrolidine-1-carboxylate. (4.89g)
(2S,4S)-tert-butyl
2-(1H-imidazol-2-yl)-4-methylpyrrolidine-1-carboxylate
[0474] To a solution of (2S,4S)-tert-butyl
2-formyl-4-methylpyrrolidine-1-carboxylate (4.89g, 22.9 mmol),
ammonium hydroxide (17 mL) and water (17 mL) was added, dropwise,
glyoxal (40% in water, 14.6 mL, 128 mmol) and the resulting mixture
was stirred at room temperature overnight.
[0475] Saturated sodium bicarbonate (100 mL) was added and the
mixture was extracted with four 75 mL portions of dichloromethane.
The organic phase was washed with water, dried over sodium
sulphate, filtered and concentrated, and then purified by silica
gel chromatography to give a total of 3.76g product.
(2S,4S)-tert-butyl
2-(5-iodo-1H-imidazol-2-yl)-4-methylpyrrolidine-1-carboxylate
[0476] A mixture of (2S,4S)-tert-butyl
2-(1H-imidazol-2-yl)-4-methylpyrrolidine-1-carboxylate (1.0g, 3.97
mmol), iodine (2.22g, 8.75 mmol) and sodium carbonate (1.3g, 12.31
mmol) in 20 mL dioxane and 13.25 mL water was covered in foil and
stirred at room temperature overnight. The mixture was diluted with
ethyl acetate and treated with 10% sodium thiosulfate (5 mL) and
stirred for 10 minutes. The organic phase was washed with brine,
and then the aqueous phase was back extracted with ethyl acetate.
The combined organic phases were dried over sodium sulphate,
filtered and concentrated to provide crude (2S,4S)-tert-butyl
2-(4,5-diiodo-1H-imidazol-2-yl)-4-methylpyrrolidine-1-carboxylate
(2.25g) as a pale yellow solid.
[0477] A solution of (2S,4S)-tert-butyl
2-(4,5-diiodo-1H-imidazol-2-yl)-4-methylpyrrolidine-1-carboxylate
(2.25g, 4.4 mmol) in 18 mL ethanol and 18 mL water was treated with
sodium sulfite (5.59g, 44.4 mmol) and heated at 90.degree. C.
overnight. The mixture was partitioned between ethyl acetate and
water. The aqueous phase was extracted with more ethyl acetate and
the combined organic phase was washed with brine, dried over sodium
sulphate, filtered, concentrated, and purified by silica gel
chromatography to give 766 mg (2S,4S)-tert-butyl
2-(5-iodo-1H-imidazol-2-yl)-4-methylpyrrolidine-1-carboxylate.
Example CN
##STR00159##
[0478] (2S,3aS,6aS)-2-benzyl 1-tert-butyl
hexahydrocyclopenta[b]pyrrole-1,2(2H)-dicarboxylate
[0479] To a solution of commercially available
(2S,3aS,6aS)-2-benzyl 1-tert-butyl
hexahydrocyclopenta[b]pyrrole-1,2(2H)-dicarboxylate (4.70 g, 16.68
mmol) in methylene chloride (42 mL) was added Di-tert-butyl
dicarbonate (7.28 g, 33.36 mmol) N,N-diisopropylethylamine (5.82
mL, 33.36 mmol) and 4-(Dimethylamino)pyridine (0.20 g, 1.67 mmol).
The solution was stirred under air for 16 hours. Upon completion,
the reaction was concentrated in vacuo, diluted in ethyl acetate,
and washed with 1N HCl. The aqueous layers were backextracted twice
with ethyl acetate and the combined organic layers were dried over
sodium sulfate, filtered and concentrated. The resulting residue
was purified by silica gel chromatography (5-40% ethyl acetate in
hexanes) to afford (2S,3aS,6aS)-2-benzyl 1-tert-butyl
hexahydrocyclopenta[b]pyrrole-1,2(2H)-dicarboxylate which was used
without further purification. MS (ESI) m/z 368.47 [M+Na].sup.+.
(2S,3aS,6aS)-1-(tert-butoxycarbonyl)octahydrocyclopenta[b]pyrrole-2-carbox-
ylic acid
[0480] To a 250 mL round bottom flask charged with a stirbar and
(2S,3aS,6aS)-2-benzyl 1-tert-butyl
hexahydrocyclopenta[b]pyrrole-1,2(2H)-dicarboxylate (5.76 g, 16.68
mmol) was added 10% Palladium on carbon (1.77g). Ethanol was poured
over the mixture and the reaction mixture was evacuated and flushed
with hydrogen gas three times. The suspension was stirred at room
temperature under and atmosphere of hydrogen for 24 hours. Upon
completion, the reaction mixture was filtered through celite and
concentrated to give
(2S,3aS,6aS)-1-(tert-butoxycarbonyl)octahydrocyclopenta[b]pyrrole-2-carbo-
xylic acid (4.45g, >99%). MS (ESI) m/z 256.21 [M+H].sup.+.
Example CO
##STR00160## ##STR00161##
[0481] tert-butyl
2-[5-(2-{(2S,3aS,6aS)-1-[N-(methoxycarbonyl)-L-valyl]octahydrocyclopenta[-
b]pyrrol-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9--
yl)-1H-imidazol-2-yl]pyrrolidine-1-carboxylate
[0482] This compound was made in an analogous manner to tert-butyl
(2R)-2-[5-(2-{(2S)-1-[N-(methoxycarbonyl)-L-valyl]pyrrolidin-2-yl}-3,11-d-
ihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imidazol-2-yl]-
pyrrolidine-1-carboxylate substituting
(2S,3aS,6aS)-1-(tert-butoxycarbonyl)octahydrocyclopenta[b]pyrrole-2-carbo-
xylic acid for the initial alkylation of
9-bromo-3-chloro-10,11-dihydro-6H-naphtho[2,3-c]chromen-8(9H)-one.
Reactions in the synthesis of tert-butyl
2-[5-(2-{(2S,3aS,6aS)-1-[N-(methoxycarbonyl)-L-valyl]octahydrocyclopenta[-
b]pyrrol-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9--
yl)-1H-imidazol-2-yl]pyrrolidine-1-carboxylate gave similar product
yields as in the synthesis of tert-butyl
(2R)-2-[5-(2-{(2S)-1-[N-(methoxycarbonyl)-L-valyl]pyrrolidin-2-yl}-3,11-d-
ihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imidazol-2-yl]-
pyrrolidine-1-carboxylate. MS (ESI) m/z 774.1 [M+H].sup.+.
Example CP
##STR00162##
[0483] methyl
{(1R)-2-[2-(5-{2-[(2S,3aS,6aS)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-methy-
lbutanoyl}octahydrocyclopenta[b]pyrrol-2-yl]-1,11-dihydroisochromeno[4',3'-
:6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]-2-oxo--
1-phenylethyl}carbamate
[0484] To a solution of tert-butyl
2-[5-(2-{(2S,3aS,6aS)-1-[N-(methoxycarbonyl)-L-valyl]octahydrocyclopenta[-
b]pyrrol-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9--
yl)-1H-imidazol-2-yl]pyrrolidine-1-carboxylate (0.128 g, 0.165
mmol) in a mixture of CH.sub.2Cl.sub.2(1.6 mL) and MeOH (0.33 mL)
was added HCl (4M in 1,4-dioxane, 1.24 mL, 4.9 mmol). The solution
was stirred at room temperature for 1.5 h and concentrated to
dryness. The intermediate was dissolved in CH.sub.2C12 (1.6 mL).
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid (0.052 g, 0.25
mmol) and DIPEA (0.087 mL, 0.496 mmol) were then added to the
solution. The reaction mixture was cooled to -40.degree. C.
(external temperature, MeCN/CO.sub.2(s) bath). COMU (0.113 g, 0.265
mmol) was then added and solution was allowed to warm to 0.degree.
C. over 1.5 h. Upon completion by LCMS, the solution was diluted
with DMF and concentrated. The crude product was purified by
preparative HPLC (Gemini column, 10-47% MeCN/H.sub.2O with 0.1%
TFA) and the desired fractions were combined. The solution was
concentrated until the aqueous layer remained and aqueous
bicarbonate (sat.) was slowly added until the solution was basic.
The resulting slurry was stirred at room temperature for 2h and
filtered. The resulting solid was dried in vacuo to provide methyl
{(1R)-2-[2-(5-{2-[(2S,3aS,6aS)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-methy-
lbutanoyl}octahydrocyclopenta[b]pyrrol-2-yl]-1,11-dihydroisochromeno[4',3'-
:6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]-2-oxo--
1-phenylethyl}carbamate (0.068 g, 48%). MS (ESI) m/z 865.7
[M+H].sup.+. .sup.1H NMR (400 MHz, cd.sub.3od) .delta. 8.44-8.30
(m, 1H), 8.02-7.82 (m, 2H), 7.81-7.58 (m, 4H), 7.50-7.11 (m, 6H),
7.09-6.83 (m, 2H), 5.72-5.45 (m, 2H), 5.41 (s, 1H), 5.34-5.28 (m,
1H), 5.22 (s, 3H), 4.69-4.64 (m, 1H), 4.26-4.19 (m, 1H), 4.03-3.98
(m, 1H), 3.96-3.91 (m, 1H), 3.66 (d, 4H), 2.98-2.91 (m, 1H),
2.88-2.83 (m, 1H), 2.58-2.48 (m, 1H), 2.27-2.12 (m, 4H), 2.11-2.00
(m, 3H), 2.00-1.89 (m, 2H), 1.77-1.72 (m, 1H), 1.31-1.04 (m, 3H),
0.93 (d, 6H).
Example CQ
##STR00163##
[0485] methyl
{(2S)-1-[2-(5-{2-[(2S,3aS,6aS)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-methy-
lbutanoyl}octahydrocyclopenta[b]pyrrol-2-yl]-1,11-dihydroisochromeno[4',3'-
:6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]-3-meth-
yl-1-oxobutan-2-yl}carbamate
[0486] To a solution of tert-butyl
2-[5-(2-{(2S,3aS,6aS)-1-[N-(methoxycarbonyl)-L-valyl]octahydrocyclopenta[-
b]pyrrol-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9--
yl)-1H-imidazol-2-yl]pyrrolidine-1-carboxylate (0.030 g, 0.039
mmol) in a mixture of CH.sub.2Cl.sub.2 (0.39 mL) and MeOH (0.078
mL) was added HCl (4M in 1,4-dioxane, 0.29 mL, 1.16 mmol). The
solution was stirred at room temperature for 1.5 h and concentrated
to dryness.
[0487] The intermediate was dissolved in CH.sub.2Cl.sub.2 (0.39
mL). (S)-2-(methoxycarbonylamino)-3-methylbutanoic acid (0.007 g,
0.043 mmol) and DIPEA (0.020 mL, 0.116 mmol) were then added to the
solution. HATU (0.018 g, 0.047 mmol) was added and solution was
allowed to stir at room temp. Upon completion, the solution was
diluted with DMF and concentrated. The crude product was purified
by preparative HPLC (Gemini column, 10-47% MeCN/H.sub.2O with 0.1%
TFA) and the desired fractions were combined and lyophilized to
provide methyl
{(2S)-1-[2-(5-{2-[(2S,3aS,6aS)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-methy-
lbutanoyl}octahydrocyclopenta[b]pyrrol-2-yl]-1,11-dihydroisochromeno[4',3'-
:6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]-3-meth-
yl-1-oxobutan-2-yl}carbamate (0.010g, 31%). MS (ESI) m/z 832.2
[M+H].sup.+.
Example CR
##STR00164##
[0488] methyl
[(1S)-2-[2-(5-{2-[(2S,3aS,6aS)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-methy-
lbutanoyl}octahydrocyclopenta[b]pyrrol-2-yl]-1,11-dihydroisochromeno[4',3'-
:6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]-2-oxo--
1-(tetrahydro-2H-pyran-4-yl)ethyl]carbamate
[0489] This compound was made in an analogous manner to methyl
{(2S)-1-[2-(5-{2-[(2S,3aS,6aS)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-methy-
lbutanoyl}octahydrocyclopenta[b]pyrrol-2-yl]-1,11-dihydroisochromeno[4',3'-
:6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]-3-meth-
yl-1-oxobutan-2-yl}carbamate, substituting
(S)-2-(methoxycarbonylamino)-2-(tetrahydro-2H-pyran-4-yl)acetic
acid for (S)-2-(methoxycarbonylamino)-3-methylbutanoic acid to give
methyl
[(1S)-2-[2-(5-{2-[(2S,3aS,6aS)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-methy-
lbutanoyl}octahydrocyclopenta[b]pyrrol-2-yl]-1,11-dihydroisochromeno[4',3'-
:6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)pyrrolidin-1-yl]-2-oxo--
1-(tetrahydro-2H-pyran-4-yl)ethyl]carbamate (0.039, 56%). MS (ESI)
m/z 874.34 [M+H].sup.+. .sup.1H NMR (400 MHz, cd.sub.3od) .delta.
8.58 (s, 2H), 8.26-8.08 (m, 2H), 7.96-7.75 (m, 4H), 7.65-7.54 (m,
5H), 5.36-5.11 (m, 4H), 4.34-4.04 (m, 4H), 3.97-3.79 (m, 4H), 3.65
(s, 4H), 3.53-3.44 (m, 2H), 2.68-2.47 (m, 4H), 2.32-2.02 (m, 7H),
1.95-1.82 (m, 3H), 1.77-1.54 (m, 4H), 1.49-1.24 (m, 5H), 1.10-0.99
(m, 3H), 0.92-0.85 (m, 4H).
Example CS
##STR00165##
[0490] tert-butyl
2-[5-(2-{(2S,4S)-4-[(difluoromethoxy)methyl]-1-[N-(methoxycarbonyl)-L-val-
yl]pyrrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidaz-
ol-9-yl)-1H-imidazol-2-yl]pyrrolidine-1-carboxylate
[0491] This compound was made in an analogous manner to tert-butyl
2-[5-(2-{(2S,3aS,6aS)-1-[N-(methoxycarbonyl)-L-valyl]octahydrocyclopenta[-
b]pyrrol-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9--
yl)-1H-imidazol-2-yl]pyrrolidine-1-carboxylate substituting
(2S,4S)-1-(tert-butoxycarbonyl)-4-((difluoromethoxy)methyl)pyrrolidine-2--
carboxylic acid for the initial alkylation of
9-bromo-3-chloro-10,11-dihydro-6H-naphtho[2,3-c]chromen-8(9H)-one.
Reactions in the synthesis of tert-butyl
2-[5-(2-{(2S,4S)-4-[(difluoromethoxy)methyl]-1-[N-(methoxycarbonyl)-L-val-
yl]pyrrolidin-2-yl})-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imida-
zol-9-yl)-1H-imidazol-2-yl]pyrrolidine-1-carboxylate gave similar
product yields as in the synthesis of tert-butyl
2-[5-(2-{(2S,3aS,6aS)-1-[N-(methoxycarbonyl)-L-valyl]octahydrocyclopenta[-
b]pyrrol-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9--
yl)-1H-imidazol-2-yl]pyrrolidine-1-carboxylate. MS (ESI) m/z 815.04
[M+H].sup.+. .sup.1H NMR (400 MHz, cd.sub.3od) .delta. 8.58 (s,
1H), 8.18 (d, 1H), 7.96-7.85 (m, 3H), 7.70 (s, 1H), 7.60 (d, 1H),
7.50-7.38 (m, 4H), 7.10 (s, 1H), 6.46 (t, 1H), 5.51 (s, 1H),
5.39-5.36 (m, 1H), 5.31-5.28 (m, 2H), 4.43-4.36 (m, 1H), 4.24 (d,
1H), 4.13-4.02 (m, 3H), 3.75-3.62 (m, 7H), 3.51-3.47 (m, 1H),
3.18-3.11 (m, 2H), 2.93-2.83 (m, 2H), 2.75-2.69 (m, 1H), 2.47-2.36
(m, 2H), 2.23-2.09 (m, 3H), 2.01-1.94 (m, 2H), 0.87 (dd, 6H).
Example CT
##STR00166## ##STR00167##
[0492] tert-butyl
(2S,4S)-2-[5-(2-{(1R,3S,5R)-2-[N-(methoxycarbonyl)-L-valyl]-2-azabicyclo[-
3.1.0]hex-3-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-
-yl)-1H-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
[0493] This compound was made in an analogous manner to tert-butyl
(2R)-2-[5-(2-{(2S)-1-[N-(methoxycarbonyl)-L-valyl]pyrrolidin-2-yl}-3,11-d-
ihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imidazol-2-yl]-
pyrrolidine-1-carboxylate substituting
(1R,5R)-2-(tert-butoxycarbonyl)-2-azabicyclo[3.1.0]hexane-3-carboxylic
acid for the initial alkylation of
9-bromo-3-chloro-10,11-dihydro-6H-naphtho[2,3-c]chromen-8(9H)-one,
and substituting (2S,4S)-tert-butyl
2-(5-iodo-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidine-1-carboxylate
for the Suzuki-Miyara coupling. Reactions in the synthesis of
tert-butyl
(2S,4S)-2-[5-(2-{(1R,3S,5R)-2-[N-(methoxycarbonyl)-L-valyl]-2-azabicyclo[-
3.1.0]hex-3-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-
-yl)-1H-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
gave similar product yields as in the synthesis of tert-butyl
(2R)-2-[5-(2-{(2S)-1-[N-(methoxycarbonyl)-L-valyl]pyrrolidin-2-yl}-3,11-d-
ihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imidazol-2-yl]-
pyrrolidine-1-carboxylate. MS (ESI) m/z 791.0 [M+H].sup.+.
methyl
{(1R)-2-[(2S,4S)-2-(5-{2-[(1R,3S,5R)-2-{(2S)-2-[(methoxycarbonyl)am-
ino]-3-methylbutanoyl}-2-azabicyclo[3.1.0]hex-3-yl]-1,11-dihydroisochromen-
o[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethy-
l)pyrrolidin-1-yl]-2-oxo-1-phenylethyl}carbamate
[0494] To a solution of tert-butyl
(2S,4S)-2-[5-(2-{(1R,3S,5R)-2-[N-(methoxycarbonyl)-L-valyl]-2-azabicyclo[-
3.1.0]hex-3-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-
-yl)-1H-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
(0.060 g, 0.076 mmol) in a mixture of CH.sub.2Cl.sub.2 (0.76 mL)
and MeOH (0.15 mL) was added HCl (4M in 1,4-dioxane, 0.570 mL, 2.28
mmol). The solution was stirred at room temperature for 2 h and
concentrated to dryness.
[0495] The intermediate was dissolved in CH.sub.2Cl.sub.2 (0.76
mL). (R)-2-(methoxycarbonylamino)-2-phenylacetic acid (0.024 g,
0.114 mmol) and DIPEA (0.040 mL, 0.228 mmol) were then added to the
solution. The reaction mixture was cooled to -40.degree. C.
(external temperature, MeCN/CO.sub.2(s) bath). COMU (0.052 g, 0.122
mmol) was then added and solution was allowed to warm to 0.degree.
C. over 1.5 h. Upon completion by LCMS, the solution was diluted
with DMF and concentrated. The crude product was purified by
preparative HPLC (Gemini column, 10-45% MeCN/H.sub.2O with 0.1%
TFA) and lyophilized to provide methyl
{(1R)-2-[(2S,4S)-2-(5-{2-[(1R,3S,5R)-2-{(2S)-2-[(methoxycarbonyl)amino]-3-
-methylbutanoyl}-2-azabicyclo[3.1.0]hex-3-yl]-1,11-dihydroisochromeno[4',3-
':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)pyrr-
olidin-1-yl]-2-oxo-1-phenylethyl}carbamate (0.028 g, 42%). MS (ESI)
m/z 881.8 [M+H].sup.+. .sup.1H NMR (400 MHz, cd.sub.3od) .delta.
8.45-8.33 (m, 1H), 8.02-7.94 (m, 1H), 7.91-7.75 (m, 2H), 7.72-7.67
(m, 1H), 7.61 (s, 1H), 7.59-7.34 (m, 6H), 7.09-6.91 (m, 2H),
5.62-5.38 (m, 2H), 5.29 (t, 1H), 5.24-5.09 (m, 3H), 4.61 (d, 1H),
4.37-4.26 (m, 1H), 3.83-3.73 (m, 1H), 3.69-3.56 (m, 6H), 3.50-3.40
(m, 1H), 3.20-3.11 (m, 1H), 2.99 (s, 1H), 2.83 (d, 1H), 2.63-2.50
(m, 2H), 2.47-2.34 (m, 2H), 2.29-2.13 (m, 2H), 2.10-1.95 (m, 2H),
1.37-1.23 (m, 3H), 1.19-1.10 (m, 1H), 1.03-0.78 (m, 7H).
Example CU
##STR00168##
[0496] tert-butyl
(2S,4S)-2-(9-{2-[(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidin-2-yl]-
-1H-imidazol-5-yl}-1,1,1-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidaz-
ol-2-yl)-4-[(difluoromethoxy)methyl]pyrrolidine-1-carboxylate
[0497] This compound was made in an analogous manner to tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid for the initial alkylation of
3-(2-bromoacetyl)-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one,
and substituting
(2S,4S)-1-(tert-butoxycarbonyl)-4-((difluoromethoxy)methyl)pyrrolidine-2--
carboxylic acid for the other alkylation in the sequence. Reactions
in the synthesis of tert-butyl
(2S,4S)-2-(9-{2-[(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidin-2-yl]-
-1H-imidazol-5-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazo-
l-2-yl)-4-[(difluoromethoxy)methyl]pyrrolidine-1-carboxylate gave
similar product yields as in the synthesis of tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate. MS
(ESI) m/z 772.03 [M+H].sup.+.
methyl
{(2S)-1-[(2S,5S)-2-(5-{2-[(2S,4S)-4-[(difluoromethoxy)methyl]-1-{(2-
S)-2-[(methoxycarbonyl)amino]-3-methylbutanoyl}pyrrolidin-2-yl]-1,11-dihyd-
roisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-5-m-
ethylpyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate
[0498] To a solution of tert-butyl
(2S,4S)-2-(9-{2-[(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidin-2-yl]-
-1H-imidazol-5-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazo-
l-2-yl)-4-[(difluoromethoxy)methyl]pyrrolidine-1-carboxylate (0.081
g, 0.105 mmol) in a mixture of CH.sub.2Cl.sub.2 (1.05 mL) and MeOH
(0.210 mL) was added HCl (4M in 1,4-dioxane, 0.788 mL, 3.15 mmol).
The solution was stirred at room temperature for 2 h and
concentrated to dryness.
[0499] The intermediate was dissolved in CH.sub.2Cl.sub.2 (1.05
mL). (S)-2-(methoxycarbonylamino)-3-methylbutanoic acid (0.040 g,
0.231 mmol) and DIPEA (0.055 mL, 0.315 mmol) were then added to the
solution. HATU (0.176 g, 0.462 mmol) was added and solution was
allowed to stir at room temp. Upon completion, the solution was
diluted with DMF and concentrated. The crude product was purified
by preparative HPLC (Gemini column, 10-45% MeCN/H.sub.2O with 0.1%
TFA) and the desired fractions were combined. The solution was
concentrated until the aqueous layer remained and aqueous
bicarbonate (sat.) was slowly added until the solution was basic.
The resulting slurry was stirred at room temperature for 2h and
filtered. The resulting solid was dried in vacuo to provide methyl
{(2S)-1-[(2S,5S)-2-(5-{2-[(2S,4S)-4-[(difluoromethoxy)methyl]-1-{(-
2S)-2-[(methoxycarbonyl)amino]-3-methylbutanoyl}pyrrolidin-2-yl]-1,11-dihy-
droisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-5--
methylpyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate (0.025 g,
27%). MS (ESI) m/z 886.1 [M+H].sup.+. .sup.1H NMR (400 MHz,
cd.sub.3od) .delta. 8.49-8.25 (m, 2H), 8.08-7.82 (m, 2H), 7.79-7.27
(m, 5H), 6.45 (t, 1H), 5.36-5.26 (m, 1H), 5.22-5.07 (m, 3H),
4.78-4.49 (m, 2H), 4.45-4.19 (m, 3H), 4.16-4.05 (m, 2H), 3.99-3.92
(m, 1H), 3.85-3.71 (m, 2H), 3.66 (s, 3H), 2.88-2.70 (m, 2H),
2.69-2.49 (m, 2H), 2.42-2.26 (m, 2H), 2.23-2.10 (m, 2H), 2.07-1.87
(m, 3H), 1.51 (d, 2H), 1.34-1.20 (m, 2H), 1.17-0.76 (m, 12H).
Example CV
##STR00169##
[0500] methyl
{(2S)-1-[(2S,4S)-4-[(difluoromethoxy)methyl]-2-(5-{2-[(2S,5S)-1-{(2S)-2-[-
(methoxycarbonyl)amino]-3-methylbutanoyl}-5-methylpyrrolidin-2-yl]-1,11-di-
hydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)p-
yrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate
[0501] This compound was made in an analogous manner to tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-H--
imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
substituting
(2S,4S)-1-(tert-butoxycarbonyl)-4-((difluoromethoxy)methyl)pyrrolidine-2--
carboxylic acid for the initial alkylation of
3-(2-bromoacetyl)-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one,
and substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid for the other alkylation in the sequence. Reactions in the
synthesis of tert-butyl
(2S,4S)-2-(5-{2-[(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidin-2-yl]-
-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazo-
l-2-yl)-4-[(difluoromethoxy)methyl]pyrrolidine-1-carboxylate gave
similar product yields as in the synthesis of tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate. MS
(ESI) m/z 772.31 [M+H].sup.+.
methyl
{(2S)-1-[(2S,4S)-4-[(difluoromethoxy)methyl]-2-(5-{2-[(2S,5S)-1-{(2-
S)-2-[(methoxycarbonyl)amino]-3-methylbutanoyl}-5-methylpyrrolidin-2-yl]-1-
,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol--
2-yl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate
[0502] To tert-butyl
(2S,4S)-2-(5-{2-[(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidin-2-yl]-
-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazo-
l-2-yl)-4-[(difluoromethoxy)methyl]pyrrolidine-1-carboxylate (0.057
g, 0.074 mmol) in a mixture of CH.sub.2Cl.sub.2 (0.739 mL) and MeOH
(0.148 mL) was added HCl (4M in 1,4-dioxane, 0.555 mL, 2.218 mmol).
The solution was stirred at room temperature for 2 h and
concentrated to dryness.
[0503] The intermediate was dissolved in CH.sub.2Cl.sub.2 (0.739
mL). (S)-2-(methoxycarbonylamino)-3-methylbutanoic acid (0.028 g,
0.163 mmol) and DIPEA (0.039 mL, 0.222 mmol) were then added to the
solution. HATU (0.124 g, 0.325 mmol) was added and solution was
allowed to stir at room temp. Upon completion, the solution was
diluted with DMF and concentrated. The crude product was purified
by preparative HPLC (Gemini column, 10-46% MeCN/H.sub.2O with 0.1%
TFA) and the desired fractions were combined and lyophilized to
provide methyl
{(2S)-1-[(2S,4S)-4-[(difluoromethoxy)methyl]-2-(5-{2-[(2S,5S)-1-{(2S)-2-[-
(methoxycarbonyl)amino]-3-methylbutanoyl}-5-methylpyrrolidin-2-yl]-1,11-di-
hydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)p-
yrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate (0.011 g, 17%).
MS (ESI) m/z 886.1 [M+H].sup.+. .sup.1H NMR (400 MHz, cd.sub.3od)
.delta. 8.67-8.51 (m, 1H), 8.26-8.11 (m, 1H), 8.04-7.75 (m, 3H),
7.69-7.58 (m, 2H), 6.43 (t, 1H), 5.41-5.15 (m, 4H), 4.48-3.90 (m,
6H), 3.82 (s, 1H), 3.71-3.57 (m, 5H), 3.53-3.43 (m, 1H), 3.20-3.01
(m, 2H), 2.92-2.63 (m, 3H), 2.60-2.25 (m, 4H), 2.15-1.86 (m, 4H),
1.57 (d, 3H), 1.24 (d, 2H), 1.07 (dd, 2H), 0.98-0.77 (m, 9H).
Example CW
##STR00170##
[0504] tert-butyl
(2S,4S)-2-[5-(2-{(2S,4S)-1-(tert-butoxycarbonyl)-4-[(difluoromethoxy)meth-
yl]pyrrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidaz-
ol-9-yl)-1H-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
[0505] This compound was made in an analogous manner to tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
substituting
(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrrolidine-2-carboxylic
acid for the initial alkylation of
3-(2-bromoacetyl)-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one,
and substituting
(2S,4S)-1-(tert-butoxycarbonyl)-4-((difluoromethoxy)methyl)pyrrolidine-2--
carboxylic acid for the other alkylation in the sequence. Reactions
in the synthesis of tert-butyl
(2S,4S)-2-[5-(2-{(2S,4S)-1-(tert-butoxycarbonyl)-4-[(difluoromethoxy)meth-
yl]pyrrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidaz-
ol-9-yl)-1H-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
gave similar product yields as in the synthesis of tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate. MS
(ESI) m/z 801.1 [M+H].sup.+.
methyl
{(2S)-1-[(2S,4S)-2-(5-{2-[(2S,4S)-4-[(difluoromethoxy)methyl]-1-{(2-
S)-2-[(methoxycarbonyl)amino]-3-methylbutanoyl}pyrrolidin-2-yl]-1,11-dihyd-
roisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(-
methoxymethyl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate
[0506] To tert-butyl
(2S,4S)-2-[5-(2-{(2S,4S)-1-(tert-butoxycarbonyl)-4-[(difluoromethoxy)meth-
yl]pyrrolidin-2-yl}-1,11
dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imidazol-2-y-
l]-4-(methoxymethyl)pyrrolidine-1-carboxylate (0.092 g, 0.115 mmol)
in a mixture of CH.sub.2Cl.sub.2 (1.15 mL) and MeOH (0.230 mL) was
added HCl (4M in 1,4-dioxane, 0.862 mL, 3.446 mmol). The solution
was stirred at room temperature for 2 h and concentrated to
dryness.
[0507] The intermediate was dissolved in CH.sub.2Cl.sub.2 (1.149
mL). (S)-2-(methoxycarbonylamino)-3-methylbutanoic acid (0.044 g,
0.253 mmol) and DIPEA (0.060 mL, 0.345 mmol) were then added to the
solution. HATU (0.192 g, 0.505 mmol) was added and solution was
allowed to stir at room temp. Upon completion, the solution was
diluted with DMF and concentrated. The crude product was purified
by preparative HPLC (Gemini column, 10-45% MeCN/H.sub.2O with 0.1%
TFA) and the desired fractions were combined. The solution was
concentrated until the aqueous layer remained and aqueous
bicarbonate (sat.) was slowly added until the solution was basic.
The resulting slurry was stirred at room temperature for 2h and
filtered. The resulting solid was dried in vacuo to provide methyl
{(2S)-1-[(2S,4S)-2-(5-{2-[(2S,4S)-4-[(difluoromethoxy)methyl]-1-{(-
2S)-2-[(methoxycarbonyl)amino]-3-methylbutanoyl}pyrrolidin-2-yl]-1,11-dihy-
droisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4--
(methoxymethyl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate
(0.042 g, 40%). MS (ESI) m/z 916.30 [M+H].sup.+. .sup.1H NMR (400
MHz, cd.sub.3od) .delta. 8.55-8.25 (m, 1H), 8.15-7.85 (m, 2H),
7.83-7.26 (m, 5H), 6.44 (t, 1H), 5.37-5.02 (m, 4H), 4.47-4.35 (m,
1H), 4.33-4.18 (m, 3H), 4.15-3.90 (m, 3H), 3.81-3.45 (m, 11H), 3.39
(s, 3H), 2.90-2.27 (m, 5H), 2.22-1.92 (m, 4H), 1.12-0.73 (m,
13H).
Example CX
##STR00171##
[0508] (2S,4S)-1-tert-butyl 2-methyl
4-((difluoromethoxy)methyl)pyrrolidine-1,2-dicarboxylate
[0509] A 100 mL round-bottom flask was charged with
(2S,4S)-1-tert-butyl 2-methyl
4-(hydroxymethyl)pyrrolidine-1,2-dicarboxylate (3.33 g, 12.84
mmol), CuI (0.489 g, 2.56 mmol), and anhydrous acetonitrile (57.1
mL). The reaction was heated to 45.degree. C. (ext. oil bath).
2,2-difluoro-2-(fluorosulfonyl)acetic acid (2.655 mL, 25.68 mmol)
was added at 45.degree. C. over 30 minutes via syringe pump. The
reaction was heated for 30 minutes. Upon completion as monitored by
TLC, the reaction mixture was cooled to room temperature and
concentrated in vacuo. The crude residue was diluted in EtOAc and
washed with sodium bicarbonate (aq). The bicarbonate layer was back
extracted with ethyl acetate twice. Combined organic layers were
washed with brine, dried over sodium sulphate, filtered and
concentrated. The resulting residue was further purified via silica
gel chromatography (10 to 40% EtOAc/Hexanes) to afford
(2S,4S)-1-tert-butyl 2-methyl
4-((difluoromethoxy)methyl)pyrrolidine-1,2-dicarboxylate (2.41 g,
61%). MS (ESI) m/z 210.21 [M+H-Boc].sup.+.
(2S,4S)-1-(tert-butoxycarbonyl)-4-((difluoromethoxy)methyl)pyrrolidine-2-c-
arboxylic acid
[0510] To a solution of (2S,4S)-1-tert-butyl 2-methyl
4-((difluoromethoxy)methyl)pyrrolidine-1,2-dicarboxylate (2.41 g,
7.79 mmol) in a mixture of THF (39 mL) and MeOH (15.6 mL) was added
LiOH (2.5 M aqueous, 15.6 mL, 38.9 mmol). The resulting solution
was stirred at room temperature for 1 h. Upon completion by TLC the
reaction mixture was and acidified with aqueous HCl (1N). The
desired product was extracted with CH.sub.2Cl.sub.2 (3.times.). The
combined organic layers were dried over Na.sub.2SO.sub.4 and
concentrated to provide
(2S,4S)-1-(tert-butoxycarbonyl)-4-((difluoromethoxy)methyl)pyrrolidine-2--
carboxylic acid (2.4 g, 99%). MS (ESI) m/z 294.96 [M-H].sup.-.
.sup.1H-NMR: 400 MHz, (acetone-d.sub.6) .delta. (mixture of
rotomers): 6.50 (t, 1H), 4.36-4.17 (m, 1H), 3.93 (d, 2H), 3.77-3.67
(m, 1H), 3.63-3.59 (m, 1H), 3.26-3.12 (m, 1H), 2.72-2.41 (m, 2H),
1.89-1.73 (m, 2H), 1.41 (s, 9H).
Example CY
##STR00172##
[0511] Methyl
{(2S)-1-[(2S,5S)-2-(9-{2-[(2S,4S)-1-{(2R)-2-[(methoxycarbonyl)amino]-2-ph-
enylacetyl}-4-(methoxymethyl)pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihyd-
roisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidin-1--
yl]-3-methyl-1-oxobutan-2-yl}carbamate
[0512] A solution of tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate (150 mg,
0.19 mmol) in 1.25 N HCl in EtOH (3 mL) was stirred overnight then
heated to 50.degree. C. for 3h. The reaction was concentrated and
the crude material dissolved in DMF (2 mL). To this solution was
added a solution of (R)-2-(methoxycarbonylamino)-2-phenylacetic
acid (52 mg, 0.25 mmol) and COMU (90 mg, 0.21 mmol). To the
resulting solution was added diisopropylethylamine (0.099 mL, 0.57
mmol).
[0513] After stirring for 2h at room temperature, the reaction was
quenched with 1N HCl (0.200 mL) and purified purified by HPLC.
After lyophilization, the TFA salt was dissolved in EtOAc and
washed with saturated NaHCO.sub.3. The organic phase was dried over
Na.sub.2SO.sub.4 and concentrated. The free base was then dissolved
in MeCN/H.sub.2O and lyophilized to afford methyl
{(2S)-1-[(2S,5S)-2-(9-{2-[(2S,4S)-1-{(2R)-2-[(methoxycarbonyl)amino]-2-ph-
enylacetyl}-4-(methoxymethyl)pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihyd-
roisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidin-1l-
-yl]-3-methyl-1-oxobutan-2-yl}carbamate (65 mg, 39%).
LCMS-ESI.sup.+: calculated for C.sub.49H.sub.54N.sub.8O.sub.8:
882.4; observed [M+1].sup.+: 884.1. Diagnostic peaks in NMR .sup.1H
NMR (CD.sub.3OD): 8.28 (s, 1H), 8.21 (s, 1H), 8.04 (s, 1H),
7.91-7.01 (m, 10H), 3.62 (s, 3H), 3.34 (s, 3H), 3.23 (s, 3H), 1.56
(d, 3H), 1.03 (d, 3H), 0.94 (d, 3H).
Example CZ
##STR00173##
[0514] Methyl
{(2S)-1-[(2S,5S)-2-(9-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-me-
thylbutanoyl}-4-(methoxymethyl)pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dih-
ydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidin--
1-yl]-3-methyl-1-oxobutan-2-yl}carbamate
[0515] Tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate (100 mg,
0.13 mmol) in 1.25 N HCl in EtOH (3 mL) was heated to 50.degree. C.
for 3h and then concentrated under reduced pressure. The crude
residue was treated with
(S)-2-(methoxycarbonylamino)-3-methylbutanoic acid (34 mg, 0.20
mmol), HATU (54 mg, 0.14 mmol) and DMF (1.3 mL), then
N-methylmorpholine (0.043 mL, 0.39 mmol) was added dropwise. After
3h, the mixture was quenched with 1N HCl (0.100 mL) and then
purified by HPLC to afford methyl
{(2S)-1-[(2S,5S)-2-(9-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amin-
o]-3-methylbutanoyl}-4-(methoxymethyl)pyrrolidin-2-yl]-1H-imidazol-5-yl}-1-
,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrr-
olidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate (91 mg, 82%).
LCMS-ESI.sup.+: calculated for C.sub.46H.sub.56N.sub.8O.sub.8:
848.4; observed [M+1].sup.+: 850.2.
Example DA
##STR00174##
[0516] Methyl
{(2S)-1-[(2S,5S)-2-(9-{2-[(2S,4S)-1-{(2S,3S)-3-methoxy-2-[(methoxycarbony-
l)amino]butanoyl}-4-(methoxymethyl)pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-
-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrroli-
din-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate
[0517] Tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate (119 mg,
0.15 mmol) in 1.25 N HCl in EtOH (3 mL) was heated to 50.degree. C.
for 3h and then concentrated under reduced pressure. The crude
residue was treated with
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid (43 mg,
0.23 mmol), HATU (63 mg, 0.17 mmol) and DMF (2 mL), then
N-methylmorpholine (0.050 mL, 0.45 mmol) was added dropwise. After
3 hr, the mixture was quenched with 1N HCl (0.100 mL) and then
purified by HPLC to afford methyl
{(2S)-1-[(2S,5S)-2-(9-{2-[(2S,4S)-1-{(2S,3S)-3-methoxy-2-[(methoxy-
carbonyl)amino]butanoyl}-4-(methoxymethyl)pyrrolidin-2-yl]-1H-imidazol-5-y-
l}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methyl-
pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate (76 mg, 59%).
LCMS-ESI.sup.+: calculated for C.sub.46H.sub.56N.sub.8O.sub.9:
864.4; observed [M+1].sup.+: 866.1.
Example DB
##STR00175##
[0518] Methyl
(2S,3S)-1-((2S,4S)-2-(5-bromo-1H-imidazol-2-yl)-4-methylpyrrolidin-1-yl)--
3-methyl-1-oxopentan-2-ylcarbamate
[0519] (2S,4S)-tert-butyl
2-(5-bromo-1H-imidazol-2-yl)-4-methylpyrrolidine-1-carboxylate (100
mg, 0.13 mmol) in 1.25 N HCl in EtOH (15 mL) was heated to
50.degree. C. for 3h and then concentrated under reduced pressure.
The crude residue was treated with
(2S,3S)-2-(methoxycarbonylamino)-3-methylpentanoic acid (625 mg,
3.30 mmol), HATU (1.05 g, 2.77 mmol) and DMF (10 mL), then DIPEA
(1.33 mL, 7.62 mmol) was added dropwise. After 2h, the mixture was
poured into saturated aqueous NaHCO.sub.3 and then extracted with
EtOAc. The organic phase was washed with successively with 5%
aqueous LiCl and Brine. The organics were dried over
Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure.
The crude residue was purified by silica column chromatography (30
to 90% of 10% MeOH/EtoAc to Hexanes) afforded methyl
(2S,3S)-1-((2S,4S)-2-(5-bromo-1H-imidazol-2-yl)-4-methylpyrrolidin-1-yl)--
3-methyl-1-oxopentan-2-ylcarbamate (932 mg, 81%).
Tert-butyl
(2S,4S)-2-[9-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-alloisoleucyl-
]-4-methylpyrrolidin-2-yl}-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3'-
:6,7]naphtho[1,2-d]imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxyla-
te
[0520] (2S,4S)-Tert-butyl
4-(methoxymethyl)-2-(9-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,11-
-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)pyrrolidine-1-ca-
rboxylate (856 mg, 1.4 mmol), methyl
(2S,3S)-1-((2S,4S)-2-(5-bromo-1H-imidazol-2-yl)-4-methylpyrrolidin-1-yl)--
3-methyl-1-oxopentan-2-ylcarbamate (932 mg, 2.1 mmol),
Pd(PPh.sub.3).sub.4(162 mg, 0.14 mmol), PdCl.sub.2(dppf).sub.2 (102
mg, 0.14 mmol), and K.sub.2CO.sub.3 (2M in H.sub.2O, 2.31 mL, 4.62
mmol) were combined in DMSO (8 mL) and dioxanes (8 mL). The mixture
was degassed with bubbling Argon for 10 min the heated to
95.degree. C. for 1 h. After cooling, the reaction mixture was
diluted with EtOAc, and washed successively with saturated aqueous
NaHCO.sub.3 and brine. The organics were dried over
Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure.
The crude residue was purified by silica column chromatography (1%
to 20% MeOH/EtOAc) to afford tert-butyl
(2S,4S)-2-[9-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-alloisoleucyl]-4-methyl-
pyrrolidin-2-yl}-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]napht-
ho[1,2-d]imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
(701 mg, 62%).
Methyl
{(1R)-2-[(2S,4S)-2-(9-{2-[(2S,4S)-1-{(2S,3R)-2-[(methoxycarbonyl)am-
ino]-3-methylpentanoyl}-4-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-di-
hydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-(methoxymethyl)p-
yrrolidin-1-yl]-2-oxo-1-phenylethyl}carbamate
[0521] A solution of tert-butyl
(2S,4S)-2-[9-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-alloisoleucyl]-4-methyl-
pyrrolidin-2-yl}-H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphth-
o[1,2-d]imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
(218 mg, 0.27 mmol) in 1.25 N HCl in EtOH (3 mL) was heated to
50.degree. C. for 3h. The reaction was concentrated and the crude
material dissolved in DMF (3 mL). To this solution was added a
solution of (R)-2-(methoxycarbonylamino)-2-phenylacetic acid (73
mg, 0.35 mmol) and COMU (127 mg, 0.30 mmol). To the resulting
solution was added diisopropylethylamine (0.141 mL, 0.81 mmol).
After stirring for 2h at room temperature, the reaction was
quenched with 1N HCl (0.200 mL) and purified purified by HPLC.
After lyophilization, the TFA salt was dissolved in EtOAc and
washed with saturated NaHCO.sub.3. The organic phase was dried over
Na.sub.2SO.sub.4 and concentrated. The free base was then dissolved
in MeCN/H.sub.2O and lyophilized to afford methyl
{(1R)-2-[(2S,4S)-2-(9-{2-[(2S,4S)-1-{(2S,3R)-2-[(methoxycarbonyl)amino]-3-
-methylpentanoyl}-4-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydroi-
sochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-(methoxymethyl)pyrroli-
din-1-yl]-2-oxo-1-phenylethyl}carbamate: (121 mg, 50%).
LCMS-ESI.sup.+: calculated for C.sub.50H.sub.56N.sub.8O.sub.8:
896.4; observed [M+1].sup.+: 897.5.
Example DC
##STR00176##
[0522] Methyl
{(2S)-1-[(2S,4S)-2-(9-{2-[(2S,4S)-1-{(2S,3R)-2-[(methoxycarbonyl)amino]-3-
-methylpentanoyl}-4-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydroi-
sochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-(methoxymethyl)pyrroli-
din-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate
[0523] tert-butyl
(2S,4S)-2-[9-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-alloisoleucyl]-4-methyl-
pyrrolidin-2-yl}-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]napht-
ho[1,2-d]imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
(105 mg, 0.13 mmol) in 1.25 N HCl in EtOH (3 mL) was heated to
50.degree. C. for 3h and then concentrated under reduced pressure.
The crude residue was treated with
(S)-2-(methoxycarbonylamino)-3-methylbutanoic acid (32 mg, 0.18
mmol), HATU (59 mg, 0.16 mmol) and DMF (1.3 mL), then
N-methylmorpholine (0.043 mL, 0.39 mmol) was added dropwise. After
3h, the mixture was quenched with 1N HCl (0.100 mL) and then
purified by HPLC to afford methyl
{(2S)-1-[(2S,4S)-2-(9-{2-[(2S,4S)-1-{(2S,3R)-2-[(methoxycarbonyl)amino]-3-
-methylpentanoyl}-4-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydroi-
sochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-(methoxymethyl)pyrroli-
din-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate (80 mg, 71%).
LCMS-ESI.sup.+: calculated for C.sub.47H.sub.58N.sub.8O.sub.8:
862.4; observed [M+1].sup.+: 864.2.
Example DD
##STR00177##
[0524] Methyl
{(2S,3R)-1-[(2S,4S)-2-(5-{2-[(2S,4S)-1-[N-(methoxycarbonyl)-O-methyl-L-al-
lothreonyl]-4-(methoxymethyl)pyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3-
':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-methylpyrrolidin-1--
yl]-3-methyl-1-oxopentan-2-yl}carbamate
[0525] tert-butyl
(2S,4S)-2-[9-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-alloisoleucyl]-4-methyl-
pyrrolidin-2-yl}-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]napht-
ho[1,2-d]imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
(105 mg, 0.13 mmol) in 1.25 N HCl in EtOH (3 mL) was heated to
50.degree. C. for 3h and then concentrated under reduced pressure.
The crude residue was treated with
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid (35 mg,
0.18 mmol), HATU (59 mg, 0.16 mmol) and DMF (1.3 mL), then
N-methylmorpholine (0.043 mL, 0.39 mmol) was added dropwise. After
3 hr, the mixture was quenched with 1N HCl (0.100 mL) and then
purified by HPLC to afford methyl
{(2S,3R)-1-[(2S,4S)-2-(5-{2-[(2S,4S)-1-[N-(methoxycarbonyl)-O-methyl-L-al-
lothreonyl]-4-(methoxymethyl)pyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3-
':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-methylpyrrolidin-1--
yl]-3-methyl-1-oxopentan-2-yl}carbamate (92 mg, 81%).
LCMS-ESI.sup.+: calculated for C.sub.47H.sub.58N.sub.8O.sub.9:
878.4; observed [M+1].sup.+: 879.3.
Example DE
##STR00178##
[0526] Methyl
{(3R)-1-[(2S,4S)-2-(9-{2-[(2S,4S)-1-{(2S,3R)-2-[(methoxycarbonyl)amino]-3-
-methylpentanoyl}-4-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydroi-
sochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-(methoxymethyl)pyrroli-
din-1-yl]-3-methyl-1-oxopentan-2-yl}carbamate
[0527] tert-butyl
(2S,4S)-2-[9-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-alloisoleucyl]-4-methyl-
pyrrolidin-2-yl}-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]napht-
ho[1,2-d]imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
(105 mg, 0.13 mmol) in 1.25 N HCl in EtOH (3 mL) was heated to
50.degree. C. for 3h and then concentrated under reduced pressure.
The crude residue was treated with
(2S,3S)-2-(methoxycarbonylamino)-3-methylpentanoic acid (34 mg,
0.18 mmol), HATU (59 mg, 0.16 mmol) and DMF (1.3 mL), then
N-methylmorpholine (0.043 mL, 0.39 mmol) was added dropwise. After
3h, the mixture was quenched with 1N HCl (0.100 mL) and then
purified by HPLC to afford methyl
{(3R)-1-[(2S,4S)-2-(9-{2-[(2S,4S)-1-{(2S,3R)-2-[(methoxycarbonyl)amino]-3-
-methylpentanoyl}-4-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydroi-
sochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-(methoxymethyl)pyrroli-
din-1-yl]-3-methyl-1-oxopentan-2-yl}carbamate (98 mg, 86%).
LCMS-ESI.sup.+: calculated for C.sub.48H.sub.60N.sub.8O.sub.8:
876.5; observed [M+1].sup.+: 878.2.
Example DF
##STR00179## ##STR00180## ##STR00181##
[0528] (2S,5S)-1-tert-butyl
2-(3-chloro-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-9-yl)
5-methylpyrrolidine-1,2-dicarboxylate
[0529] To a solution of
9-bromo-3-chloro-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one
(1.41 g, 3.88 mmol) in MeCN (17 mL) was added
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid (980 mg, 4.27 mmol) and DIPEA (1.49 mL, 8.54 mmol). After
stirring for 18 h at 50.degree. C., the solution was diluted with
EtOAc and washed successively with 1N HCl, saturated aqueous
NaHCO.sub.3 and brine. The organics were dried over
Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure.
The crude residue was purified by silica column chromatography (10%
to 30% EtOAc/hexanes) to afford (2S,5S)-1-tert-butyl
2-(3-chloro-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-9-yl)
5-methylpyrrolidine-1,2-dicarboxylate (1.63 g, 81%).
(2S,5S)-tert-butyl
2-(9-chloro-4,5-dihydro-5H-naphtho[c,g]chromeno[8,9-d]imidazol-2-yl)-5-(m-
ethyl)pyrrolidine-1-carboxylate
[0530] (2S,5S)-1-tert-butyl
2-(3-chloro-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-9-yl)
5-methylpyrrolidine-1,2-dicarboxylate (1.63 g, 3.18 mmol) was added
toluene (30 mL), 2-methoxyethanol (3 mL), and ammonium acetate
(3.68 g, 77.1 mmol) and the solution was heated to reflux
overnight. The following morning, the solution was cooled to rt and
was diluted with EtOAc and washed successively with water,
saturated aqueous NaHCO.sub.3 and brine. The organics were dried
over Na.sub.2SO.sub.4, filtered and concentrated under reduced
pressure. The crude residue was purified by silica column
chromatography (40% to 80% EtOAc/hexanes) to afford
(2S,5S)-tert-butyl
2-(9-chloro-4,5-dihydro-5H-naphtho[c,g]chromeno[8,9-d]imidazol-2-yl)-5-me-
thylpyrrolidine-1-carboxylate (1.13 g, 72%).
((2S,5S)-tert-butyl
2-(9-chloro-5H-naphtho[c,g]chromeno[8,9-d]imidazol-2-yl)-5-methylpyrrolid-
ine-1-carboxylate
[0531] To a solution of (2S,5S)-tert-butyl
2-(9-chloro-4,5-dihydro-5H-naphtho[c,g]chromeno[8,9-d]imidazol-2-yl)-5-(m-
ethyl)pyrrolidine-1-carboxylate (1.13 g, 2.3 mmol) in
CH.sub.2Cl.sub.2 (25 mL) was added MnO.sub.2 (9.98 g, 115 mmol).
The reaction mixture was stirred overnight then filtered over
celite. The filter cake was washed with copious CH.sub.2Cl.sub.2
and MeOH, and the filtrate was concentrated under reduced pressure
to afford the crude product (2S,5S)-tert-butyl
2-(9-chloro-5H-naphtho[c,g]chromeno[8,9-d]imidazol-2-yl)-5-methylpyrrolid-
ine-1-carboxylate (931 mg, 83%).
Methyl
{(2S)-1-[(2S,5S)-2-(9-chloro-1,11-dihydroisochromeno[4',3':6,7]naph-
tho[1,2-d]imidazol-2-yl)-5-methylpyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl-
}carbamate
[0532] (2S,5S)-tert-butyl
2-(9-chloro-5H-naphtho[c,g]chromeno[8,9-d]imidazol-2-yl)-5-methylpyrrolid-
ine-1-carboxylate (931 mg, 1.9 mmol) in 1.25 N HCl in EtOH (8 mL)
was heated to 50.degree. C. for 3h and then concentrated under
reduced pressure. The crude residue was treated with
(S)-2-(methoxycarbonylamino)-3-methylbutanoic acid (499 mg, 2.9
mmol), HATU (795 mg, 2.1 mmol) and DMF (10 mL), then
N-methylmorpholine (0.627 mL, 5.7 mmol) was added dropwise. After
stirring for 1 h, the reaction was diluted with EtOAc and washed
successively with saturated aqueous NaHCO.sub.3, 5% LiCl, and
brine. The organics were dried over Na.sub.2SO.sub.4, filtered and
concentrated under reduced pressure. The crude residue was purified
by silica column chromatography (50% to 100% EtOAc/hexanes) to
afford methyl
{(2S)-1-[(2S,5S)-2-(9-chloro-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,-
2-d]imidazol-2-yl)-5-methylpyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carba-
mate (950 mg, 91%).
Methyl
[(2S)-3-methyl-1-{(2S,5S)-2-methyl-5-[9-(4,4,5,5-tetramethyl-1,3,2--
dioxaborolan-2-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazo-
l-2-yl]pyrrolidin-1-yl}-1-oxobutan-2-yl]carbamate
[0533] To methyl
{(2S)-1-[(2S,5S)-2-(9-chloro-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,-
2-d]imidazol-2-yl)-5-methylpyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carba-
mate (950 mg, 1.74 mmol) in dioxane (17 mL) was added
bis(pinacolato)diboron (662 mg, 2.61 mmol), KOAc (512 mg, 5.22
mmol), X-Phos (25 mg, 0.05 mmol), and Pd.sub.2dba.sub.3 (80 mg,
0.08 mmol). The solution was degassed with N.sub.2 for 10 min, then
heated to 90.degree. C. for 16 h. The solution was cooled to rt,
diluted with EtOAc, washed with saturated aqueous NaHCO.sub.3,
brine, dried with Na.sub.2SO.sub.4, and concentrated. Purification
by silica gel chromatography (30% to 75% gradient using 5%
MeOH/EtOAc to Hexanes) to afford methyl
[(2S)-3-methyl-1-{(2S,5S)-2-methyl-5-[9-(4,4,5,5-tetramethyl-1,3,2-dioxab-
orolan-2-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl-
]pyrrolidin-1-yl}-1-oxobutan-2-yl]carbamate (800 mg, 72%).
tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-meth-
ylpyrrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazo-
l-9-yl)-1H-imidazol-2-yl]-4-methylpyrrolidine-1-carboxylate
[0534] To a solution of
[(2S)-3-methyl-1-{(2S,5S)-2-methyl-5-[9-(4,4,5,5-tetramethyl-1,3,2-dioxab-
orolan-2-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl-
]pyrrolidin-1-yl}-1-oxobutan-2-yl]carbamate (269 mg, 0.42 mmol),
methyl
(S)-1-((2S,4S)-2-(5-bromo-1H-imidazol-2-yl)-4-methylpyrrolidin-1-yl)-3-me-
thyl-1-oxobutan-2-ylcarbamate (206 mg, 0.54 mmol),
tetrakis(triphenylphosphine) palladium(0) (49 mg, 0.042 mmol) and
dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) (31 mg,
0.042 mmol) in DMSO (3 mL) and dioxanes (3 mL) was added a solution
of potassium carbonate (2M in water, 0.69 mL, 1.39 mmol). The
resulting mixture was degassed and then heated to 95.degree. C. for
2h. After cooling to room temperature, the reaction was diluted
with ethyl acetate. The organics were washed with saturated sodium
bicarbonate and brine, dried over Na.sub.2SO.sub.4 and
concentrated. The crude residue was purified by flash
chromatography (1 to 20% MeOH/EtOAc) to yield tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-methylpyrrolidine-1-carboxylate (202 mg,
63%).
Methyl
{(2S)-1-[(2S,5S)-2-(9-{2-[(2S,4S)-1-{(2R)-2-[(methoxycarbonyl)amino-
]-2-phenylacetyl}-4-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydroi-
sochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidin-1-yl]-
-3-methyl-1-oxobutan-2-yl}carbamate
[0535] A solution of tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-methylpyrrolidine-1-carboxylate (80 mg, 0.11
mmol) in 1.25 N HCl in EtOH (2 mL) was heated to 50.degree. C. for
3h. The reaction was concentrated and the crude material dissolved
in DMF (1.5 mL). To this solution was added a solution of
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid (29 mg, 0.14 mmol)
and COMU (52 mg, 0.12 mmol). To the resulting solution was added
diisopropylethylamine (0.057 mL, 0.33 mmol). After stirring for 2h
at room temperature, the reaction was quenched with 1N HCl (0.200
mL) and purified purified by HPLC. After lyophilization, the TFA
salt was dissolved in EtOAc and washed with saturated NaHCO.sub.3.
The organic phase was dried over Na.sub.2SO.sub.4 and concentrated.
The free base was then dissolved in MeCN/H.sub.2O and lyophilized
to afford methyl
{(2S)-1-[(2S,5S)-2-(9-{2-[(2S,4S)-1-{(2R)-2-[(methoxycarbonyl)amino]-2-ph-
enylacetyl}-4-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydroisochro-
meno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidin-1-yl]-3-met-
hyl-1-oxobutan-2-yl}carbamate: (42 mg, 45%). LCMS-ESI.sup.+:
calculated for C.sub.48H.sub.52N.sub.8O.sub.7: 852.4; observed
[M+1].sup.+: 854.2.
Example DG
##STR00182##
[0536] Methyl
{(2S)-1-[(2S,5S)-2-(9-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-me-
thylbutanoyl}-4-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydroisoch-
romeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidin-1-yl]-3-m-
ethyl-1-oxobutan-2-yl}carbamate
[0537] tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-methylpyrrolidine-1-carboxylate (60 mg, 0.079
mmol) in 1.25 N HCl in EtOH (2 mL) was heated to 50.degree. C. for
3h and then concentrated under reduced pressure. The crude residue
was treated with (S)-2-(methoxycarbonylamino)-3-methylbutanoic acid
(21 mg, 0.12 mmol), HATU (36 mg, 0.095 mmol) and DMF (1.5 mL), then
N-methylmorpholine (0.027 mL, 0.24 mmol) was added dropwise. After
3h, the mixture was quenched with 1N HCl (0.100 mL) and then
purified by HPLC to afford methyl
{(2S)-1-[(2S,5S)-2-(9-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-me-
thylbutanoyl}-4-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydroisoch-
romeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidin-1-yl]-3-m-
ethyl-1-oxobutan-2-yl}carbamate (33 mg, 51%). LCMS-ESI.sup.+:
calculated for C.sub.45H.sub.54N.sub.8O.sub.7: 818.4; observed
[M+1].sup.+: 820.2.
Example DH
##STR00183##
[0538] Methyl
{(2S)-1-[(2S,5S)-2-(9-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-me-
thylbutanoyl}-4-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydroisoch-
romeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidin-1-yl]-3-m-
ethyl-1-oxobutan-2-yl}carbamate
[0539] tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-methylpyrrolidine-1-carboxylate (20 mg, 0.079
mmol) in 1.25 N HCl in EtOH (2 mL) was heated to 50.degree. C. for
3h and then concentrated under reduced pressure. The crude residue
was treated with (2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic
acid (8 mg, 0.04 mmol), HATU (12 mg, 0.03 mmol) and DMF (0.5 mL),
then N-methylmorpholine (0.009 mL, 0.078 mmol) was added dropwise.
After 3h, the mixture was quenched with 1N HCl (0.100 mL) and then
purified by HPLC to afford methyl
{(2S)-1-[(2S,5S)-2-(9-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amin-
o]-3-methylbutanoyl}-4-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihyd-
roisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidin-1--
yl]-3-methyl-1-oxobutan-2-yl}carbamate (7.5 mg, 35%).
LCMS-ESI.sup.+: calculated for C.sub.45H.sub.54N.sub.8O.sub.8:
834.4; observed [M+1].sup.+: 835.7.
Examples DI-DT
[0540] Using procedures similar to those described herein, the
following compounds of the invention were prepared.
TABLE-US-00002 LCMS (observed # Compound (M + H).sup.+) DI
##STR00184## 879.4 DJ ##STR00185## 838.2 DK ##STR00186## 837.3 DL
##STR00187## 835.34 DM ##STR00188## 823.35 DN ##STR00189## 837.35
DO ##STR00190## 865.32 DP ##STR00191## 880.0 DQ ##STR00192## 836.04
DR ##STR00193## 803.2 DS ##STR00194## 806.11 DT ##STR00195##
838.29
Example DU
##STR00196##
[0541]
9-bromo-3-(2-bromoacetyl)-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H-
)-one
[0542] To
3-(2-bromo-1-hydroxyethyl)-10,11-dihydro-5H-dibenzo[c,g]chromen--
8(9H)-one (20.3g, 54.4 mmol) in DCM (365 mL) was added MeOH (22 mL)
and pyridinium tribromide (18.24 g, 57.0 mmol). After 2h, water was
added (100 mL) and after briefly agitating the layers split and the
bottom organic layer was collected. The organic layer was then
washed with 1M HCl (100 mL) and the bottom organic layer containing
9-bromo-3-(2-bromo-1-hydroxyethyl)-10,11-dihydro-5H-dibenzo[c,g]chromen-8-
(9H)-one was collected. 400 MHz .sup.1H NMR (CDCl.sub.3) 7.75 (d,
J=8.1 Hz, 1H), 7.68 (s, 1H), 7.61 (s, 1H), 7.42 (d, J=7.5 Hz, 1H),
7.24 (s, 1H), 5.13 (s, 2H), 4.99-4.96 (m, 1H), 4.73 (dd, J=4.1, 4.1
Hz, 1H), 3.69-3.66 (m, 1H), 3.58-3.53 (m, 1H), 3.35-3.27 (m, 1H),
2.96-2.90 (m, 1H), 2.58-2.44 (m, 2H), C--OH not observed.
[0543] To
9-bromo-3-(2-bromo-1-hydroxyethyl)-10,11-dihydro-5H-dibenzo[c,g]-
chromen-8(9H)-one (approx. 54.4 mmol) in DCM (365 mL) was added
sodium bicarbonate (5.45 g), sodium bromide (6.14 g), TEMPO (16.55
mg) and water (60 mL). The solution was cooled between 0-5.degree.
C. and 6% bleach (91.5 mL) was added. After 1h isopropyl alcohol
(20 mL) was added and the reaction mixture was warmed to room
temperature. Agitation was stopped, the layers separated and the
lower organic layer was collected and concentrated removing
approximately 345 g of solvent.
[0544] The slurry was filtered and the cake washed with 50 mL water
and then 50 mL DCM (pre-cooled to 5.degree. C.). The solids were
collected and dried under vacuum to obtain
9-bromo-3-(2-bromoacetyl)-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one
(18.6 g, 76% yield). 400 MHz .sup.1H NMR (CDCl.sub.3) .delta.
8.03-8.01 (m, 1H), 7.85 (d, J=8.2 Hz, 1H), 7.82 (s, 1H), 7.71 (s,
1H), 7.67 (s, 1H), 5.19 (s, 2H), 4.74 (dd, J=4.1, 4.1 Hz, 1H), 4.45
(s, 2H), 3.37-3.29 (m, 1H), 2.99-2.92 (m, 1H), 2.59-2.46 (m, 2H);
100 MHz .sup.13C NMR (CDCl.sub.3) .delta. 190.4, 189.6, 154.2,
136.6, 134.1, 133.9, 132.9, 131.8, 129.3, 127.2, 125.6, 124.2,
123.3, 117.0, 68.1, 49.9, 31.8, 30.4, 25.5.
Example DV
##STR00197##
[0545]
9-bromo-3-(2-bromoacetyl)-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H-
)-one
[0546] A mixture of
3-(2-bromoacetyl)-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one
(2.58 g, 6.95 mmol), pyridinium tribromide (2.56 g, 8.0 mmol),
dichloromethane (22 mL) and methanol (2.5 mL) was stirred at about
20.degree. C. for 3 hours to obtain a slurry. The precipitated
product was filtered, washed with dichloromethane (10 mL) and dried
in a vacuum oven at 40.degree. C. to give
9-bromo-3-(2-bromoacetyl)-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-
-one (2.62 g, 84% yield). 400 MHz H NMR (CDCl.sub.3) .delta.
8.03-8.01 (m, 1H), 7.85 (d, J=8.2 Hz, 1H), 7.82 (s, 1H), 7.71 (s,
1H), 7.67 (s, 1H), 5.19 (s, 2H), 4.74 (dd, J=4.1, 4.1 Hz, 1H), 4.45
(s, 2H), 3.37-3.29 (m, 1H), 2.99-2.92 (m, 1H), 2.59-2.46 (m,
2H).
Example DW
##STR00198##
[0547]
3-((trimethylsilyl)ethynyl)-10,11-dihydro-5H-dibenzo[c,g]chromen-8(-
9H)-one
[0548] A 300 mL flask equipped with an overhead stirrer and a
reflux condenser under an atmosphere of nitrogen was charged with
3-chloro-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one (10.0g,
35.12 mmol), powdered anhydrous tripotassium phosphate (22.4 g,
105.4 mmol), XPhos (1.34 g, 2.81 mmol), and PdCl.sub.2(MeCN).sub.2
(364 mg, 1.40 mmol). Acetonitrile (140 mL) was added followed by
TMSacetylene (18 mL, 141 mmol). The mixture was heated to
65.degree. C. After 6h, the reaction was judged complete, and the
mixture was cooled to 20.degree. C. The mixture was filtered
through a fritted funnel, and the filtercake was washed with
acetonitrile. The filtrate was concentrated to about 150 mL under
reduced pressure and extracted with heptane (50 mL, 3.times.100
mL). N-Acetyl cysteine (15 g) was added to the acetonitrile phase,
and the mixture was agitated for 5 h at 45.degree. C. The mixture
was cooled to ambient temperature, filtered through a fritted
funnel, and the filtercake was washed with acetonitrile. The
filtrate was concentrated to about 120 mL under reduced pressure.
Water (120 mL) was added and the mixture was agitated for 40
minutes at 45.degree. C. and then cooled to ambient temperature.
After 30 minutes the mixture was filtered through a fritted funnel
to provide
3-((trimethylsilyl)ethynyl)-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-on-
e (4.07 g, 33.4% yield) as a yellow solid: 400 MHz .sup.1H NMR
(CDCl.sub.3) .delta. 7.65 (d, J=8.1 Hz, 1H), 7.60 (s, 1H), 7.55 (s,
1H), 7.47 (dd, J=8.1, 1.4 Hz, 1H), 7.27 (s, 1H), 5.06 (s, 2H), 2.95
(t, J=6.1 Hz, 2H), 2.67-2.59 (m, 2H), 2.18-2.08 (m, 2H), 0.26 (s,
9H).
3-acetyl-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one
[0549] A 20 mL vial with stirbar was charged with
3-((trimethylsilyl)ethynyl)-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-on-
e (850 mg, 2.44 mmol) and formic acid (9.8 mL). The solution was
heated to 65.degree. C. After 3 h, the reaction was judged
complete. The mixture was concentrated under reduced pressure; the
resulting residue was taken up in CH.sub.2Cl.sub.2 and loaded onto
a prepacked 25g silica gel cartridge. The product was purified by
chromatography on a prepacked 80g silica gel column eluting with a
solvent gradient from 5% to 85% EtOAc/hexanes. The product
containing fractions were combined and concentrated to provide
3-acetyl-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one (616 mg,
86%): 400 MHz .sup.1H NMR (CDCl.sub.3) .delta. 8.00-7.94 (m, 1H),
7.81 (d, J=8.2 Hz, 1H), 7.77 (s, 1H), 7.64 (s, 2H), 5.16 (s, 2H),
2.98 (t, J=6.1 Hz, 2H), 2.69-2.64 (m, 2H), 2.63 (s, 3H), 2.21-2.09
(m, 2H).
9-bromo-3-(2-bromoacetyl)-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one
[0550] A 20 mL vial with a stirbar was charged with
3-acetyl-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one (100 mg,
0.366 mmol), 9:1 CH.sub.2Cl.sub.2/MeOH (3.4 mL) and pyridinium
tribromide (246 mg, 0.769 mmol). The solution was heated to
35.degree. C. After 30 minutes, the reaction was judged complete.
The mixture was cooled to ambient temperature, diluted with EtOAc
(50 mL) and sequentially washed with saturated aqueous
Na.sub.2S.sub.2O.sub.3 (20 mL), 2% aqueous NaHCO.sub.3 (20 mL),
water (20 mL), and brine (10 mL). The organic phase was dried over
MgSO.sub.4, filtered and concentrated under reduced pressure
resulting in
9-bromo-3-(2-bromoacetyl)-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one
(68 mg, 41%): 400 MHz .sup.1H NMR (CDCl.sub.3) .delta. 8.03-8.01
(m, 1H), 7.85 (d, J=8.2 Hz, 1H), 7.82 (s, 1H), 7.71 (s, 1H), 7.67
(s, 1H), 5.19 (s, 2H), 4.74 (dd, J=4.1, 4.1 Hz, 1H), 4.45 (s, 2H),
3.37-3.29 (m, 1H), 2.99-2.92 (m, 1H), 2.59-2.46 (m, 2H).
Example DX
##STR00199##
[0551]
(2S,5S)-2-(2-(9-bromo-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chr-
omen-3-yl)-2-oxoethyl) 1-tert-butyl
5-methylpyrrolidine-1,2-dicarboxylate
[0552]
9-bromo-3-(2-bromoacetyl)-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H-
)-one (1.43 g, 3.17 mmol) was treated with a solution of
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid (800 mg, 3.49 mmol) in dichloromethane (14 mL) and
K.sub.2CO.sub.3 (658 mg, 1.18 mmol). The stirred reaction mixture
was stirred at RT and diluted with CH.sub.2Cl.sub.2 and extracted
3.times.. The organic phase was washed with brine, then dried over
MgSO.sub.4, filtered and concentrated under reduced pressure to
afford
((2S,5S)-2-(2-(9-bromo-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen--
3-yl)-2-oxoethyl) 1-tert-butyl
5-methylpyrrolidine-1,2-dicarboxylate (1.61 g, 84%).
(2S,5S)-1-tert-butyl
2-(2-(9-((2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-meth-
ylpyrrolidine-2-carbonyloxy)-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chr-
omen-3-yl)-2-oxoethyl) 5-methylpyrrolidine-1,2-dicarboxylate
[0553]
((2S,5S)-2-(2-(9-bromo-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]ch-
romen-3-yl)-2-oxoethyl) 1-tert-butyl
5-methylpyrrolidine-1,2-dicarboxylate (1.59 g, 2.66 mmol) was
treated with a solution of
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid (1.14 g, 3.99 mmol) in THF (16 mL) and
Cs.sub.2CO.sub.3 (692 mg, 2.12 mmol). The stirred reaction mixture
was heated to 50.degree. C. for 16 h, then cooled to RT and diluted
with CH.sub.2Cl.sub.2 and extracted 3.times.. The organic phase was
washed with brine, then dried over MgSO.sub.4, filtered and
concentrated under reduced pressure. The crude residue was purified
by silica column chromatography (20% EtOAc/hexanes) to afford
(2S,5S)-1-tert-butyl
2-(2-(9-((2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-meth-
ylpyrrolidine-2-carbonyloxy)-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chr-
omen-3-yl)-2-oxoethyl) 5-methylpyrrolidine-1,2-dicarboxylate (1.26
g, 59%).
Tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-meth-
ylpyrrolidin-2-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]-
imidazol-9-yl)-1H-imidazol-2-yl]-5-methylpyrrolidine-1-carboxylate
[0554] (2S,5S)-1-tert-butyl
2-(2-(9-((2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-meth-
ylpyrrolidine-2-carbonyloxy)-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chr-
omen-3-yl)-2-oxoethyl) 5-methylpyrrolidine-1,2-dicarboxylate (1.2
g, 1.49 mmol), hexamethyldisilazane (2.5 mL, 11.9 mmol) and
propionic acid (3.3 mL, 44.8 mmol) were suspended in PhMe (12 mL).
The stirred reaction mixture was heated to 90.degree. C. for 20 h,
then cooled to RT and diluted with EtOAc. The organic phase was
washed with 98:2 water/NH.sub.4OH then dried over MgSO.sub.4,
filtered and concentrated under reduced pressure. The crude residue
was purified by silica column chromatography (0% to 30% MeOH/EtOAc)
to afford tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-
-yl)-1H-imidazol-2-yl]-5-methylpyrrolidine-1-carboxylate (474 mg,
41%).
Tert-butyl
(2S,4S)-2-[5-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-5-meth-
ylpyrrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazo-
l-9-yl)-1H-imidazol-2-yl]-5-methylpyrrolidine-1-carboxylate
[0555]
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpy-
rrolidin-2-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]imid-
azol-9-yl)-1H-imidazol-2-yl]-5-methylpyrrolidine-1-carboxylate (474
mg, 0.70 mmol) was suspended in DCM (5 mL) and activated MnO.sub.2
(2.1 g, 21.7 mmol) was added in a single portion. After stirring
for 15 h, the mixture was was filtered over celite. The filter cake
was washed with copious CH2Cl2 and EtOAc and the filtrate was
concentrated under reduced pressure to afford tert-butyl
(2S,4S)-2-[5-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-5-methylpyrrolidine-1-carboxylate (432 mg, 81%)
which was taken on to the next step without further
purification.
methyl
{(2S)-1-[(2S,4S)-2-(5-{2-[(2S,5S)-1-{(2S,3R)-3-methoxy-2-[(methoxyc-
arbonyl)
amino]butanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[-
4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-5-methylpyrrolidi-
n-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate
[0556] Tert-butyl (2S,4S)-2-[5-(2-{(2S,4S)-1-[N-(methoxy
carbonyl)-L-valyl]-5-methylpyrrolidin-2-yl}-1,11-dihydroisochromeno[4',3'-
:6,7]naphtha[1,2-d]imidazol-9-yl)-1H-imidazol-2-yl]-5-methylpyrrolidine-1--
carboxylate (216 mg, 0.28 mmol) was dissolved in EtOH (3 mL) and
HCl (1 mL) was added. The reaction mixture was stirred for 1 h at
60.degree. C. and then concentrated under reduced pressure. The
crude residue was treated with
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid (71 mg,
0.38 mmol), HATU (126 mg, 0.33 mmol) and DMF (3 mL), then DIPEA
(0.15 mL, 0.86 mmol) was added dropwise. After 2 h, the mixture was
diluted with 10% MeOH/EtOAc and washed successively with saturated
aqueous NaHCO.sub.3 and brine. The organics were dried over
MgSO.sub.4, filtered and concentrated under reduced pressure. The
crude residue was purified by reverse phase HPLC (Gemini, 15 to 43%
ACN/H.sub.2O+0.1% TFA). to afford methyl
{(2S)-1-[(2S,4S)-2-(5-{2-[(2S,5S)-1-{(2S,3R)-3-methoxy-2-[(methoxycarbony-
l)amino]butanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6-
,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-5-methylpyrrolidin-1-yl]-
-3-methyl-1-oxobutan-2-yl}carbamate (96.7 mg, 41%). .sup.1H NMR
(400 MHz, dmso) .delta. 8.64 (s, 1H), 7.74 (m, Hz, 8H), 5.27 (s,
2H), 5.15 (s, 1H), 4.98 (s, 1H), 4.70 (s, 2H), 4.20-3.22 (m, 10H),
3.17 (s, 3H), 2.22 (m, 5H), 1.84 (m, 2H), 1.47 (m, 6H), 1.31-0.97
(m, 3H), 0.92 (d, 3H), 0.83 (d, 3H), 0.72 (d, 3H). MS (ESI) m/z
835.76 [M+H].sup.+.
Example DY
##STR00200##
[0557] methyl
[(2S,3R)-3-methoxy-1-{(2S,5S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-O-m-
ethyl-L-threonyl]-5-methylpyrrolidin-2-yl}-1H-imidazol-5-yl)-1,11-dihydroi-
sochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]-4-methylpyrrolidin-1-yl}-
-1-oxobutan-2-yl]carbamate
[0558] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid with
(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidine-2-carboxylic
acid. .sup.1H NMR (400 MHz, dmso) .delta. 8.70 (s, 1H), 8.31-7.45
(m, 8H), 7.05 (s, 1H), 5.29 (s, 2H), 5.22-5.14 (m, 1H), 5.03-4.92
(m, 1H), 4.68-4.60 (m, 1H), 4.21 (d, 4H), 3.75-3.06 (m, 14H),
2.36-2.02 (m, 2H), 1.94-1.75 (m, 2H), 1.45 (s, 3H), 1.26-1.18 (m,
2H), 1.14 (s, 3H), 1.05 (s, 2H), 0.95 (d, 6H). MS (ESI) m/z 851.79
[M+H].sup.+.
Example DZ
##STR00201##
[0559] methyl
[(2S,3R)-3-methoxy-1-{(2S,5S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-O-m-
ethyl-L-threonyl]-4-methylpyrrolidin-2-yl}-1H-imidazol-5-yl)-1,11-dihydroi-
sochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]-5-methylpyrrolidin-1-yl}-
-1-oxobutan-2-yl]carbamate
[0560] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with
(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidine-2-carboxylic
acid and
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-meth-
ylpyrrolidine-2-carboxylic acid with
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid. .sup.1H NMR (400 MHz, dmso) .delta. 8.62 (s, 1H), 8.34-7.47
(m, 8H), 7.10 (s, 1H), 5.26 (s, 2H), 5.18-5.00 (m, 2H), 4.79-4.66
(m, 2H), 4.54-4.40 (m, 1H), 4.31-4.01 (m, 2H), 3.43 (m, 10H), 3.15
(s, 3H), 2.43-2.23 (m, 4H), 2.18-2.01 (m, 2H), 1.82 (s, 2H), 1.50
(s, 3H), 1.28-1.17 (m, 1H), 1.02 (d, 4H), 0.95 (d, 6H). MS (ESI)
m/z 851.82 [M+H].sup.+.
Example EA
##STR00202##
[0561]
methyl(1-{(2S,5S)-2-[9-(2-{(2S,5S)-1-[(2S)-2-[(methoxycarbonyl)amin-
o]-2-(tetra
hydro-2H-pyran-4-yl)acetyl]-5-methylpyrrolidin-2-yl}-1H-imidazol-5-yl)-1,-
11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]-5-methylpyrro-
lidin-1-yl}-3-methyl-1-oxobutan-2-yl)carbamate
[0562] was synthesized in a similar manner as Example DX
substituting (2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic
acid with
(S)-2-(methoxycarbonylamino)-2-(tetrahydro-2H-pyran-4-yl)acetic
acid. .sup.1H NMR (400 MHz, dmso) .delta. 8.66 (s, 1H), 8.18 (s,
1H), 8.04-7.50 (m, 8H), 5.27 (s, 2H), 5.15 (s, 1H), 4.99 (s, 1H),
4.66 (m, 2H), 4.24-3.43 (m, 9H), 3.15 (s, 2H), 2.35 (s, 3H), 2.15
(s, 3H), 1.98-1.97 (m, 1H), 1.83 (s, 3H), 1.57 (s, 1H), 1.47 (m,
6H), 1.20 (s, 4H), 0.90 (s, 2H), 0.83 (d, 3H), 0.72 (d, 3H). MS
(ESI) m/z 861.82 [M+H].sup.+.
Example EB
##STR00203##
[0563] methyl
[(1S)-2-[(2S,5S)-2-(5-{2-[(2S,5S)-1-{[(methoxycarbonyl)amino](tetrahydro--
2H-pyran-4-yl)acetyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',-
3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-5-methylpyrrolidin-1-
-yl]-2-oxo-1-(tetrahydro-2H-pyran-4-yl)ethyl]carbamate
[0564] Was synthesized in a similar manner as Example DX
substituting (2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methyl
butanoyl)-5-methylpyrrolidine-2-carboxylic acid with
(2S,4S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid and substituting (2S,3R)-3-methoxy-2-(methoxy
carbonylamino)butanoic acid with
(S)-2-(methoxycarbonylamino)-2-(tetrahydro-2H-pyran-4-yl)acetic
acid. .sup.1H NMR (400 MHz, dmso) .delta. 8.67 (s, 1H), 8.19 (d,
J=8.1 Hz, 1H), 8.07-7.50 (m, 8H), 5.27 (s, 2H), 5.19-5.08 (m, 1H),
4.98 (m, 1H), 4.66 (m, 2H), 4.03 (m, 2H), 3.75 (m, 4H), 3.56-3.39
(m, 6H), 3.26-2.95 (m, 4H), 2.22 (m, 6H), 1.83 (s, 3H), 1.58 (d,
2H), 1.47 (m, 6H), 1.21 (m, 8H). MS (ESI) m/z 903.60
[M+H].sup.+.
Example EC
##STR00204##
[0565] methyl
{(2S,3S)-1-[(2S,5S)-2-(9-{2-[(2S,5S)-1-{(2S,3S)-2-[(methoxycarbonyl)amino-
]-3-methylpentanoyl}-5-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihyd-
roisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidin-1--
yl]-3-methyl-1-oxopentan-2-yl}carbamate
[0566] was synthesized in a similar manner as Example DX
substituting
((2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methyl
pyrrolidine-2-carboxylic acid with
(2S,4S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid and substituting (2S,3R)-3-methoxy-2-(methoxycarbonylamino)
butanoic acid with (2S,3S)-2-(methoxy
carbonylamino)-3-methylpentanoic acid. .sup.1H NMR (400 MHz, dmso)
.delta. 8.68 (s, 1H), 8.18 (d, J=8.3 Hz, 1H), 8.02 (m, 1H),
7.94-7.80 (m, 3H), 7.73 (s, 1H), 7.63 (m, 1H), 7.51 (m, 2H), 5.67
(d, J=10.9 Hz, 1H), 5.25 (d, J=6.5 Hz, 2H), 5.18-5.09 (m, 1H),
5.03-4.91 (m, 1H), 4.72-4.56 (m, 2H), 4.23-4.03 (m, 1H), 3.97 (m,
2H), 3.48 (t, 5H), 3.38 (s, 1H), 2.33 (s, 2H), 2.26-2.02 (m, 3H),
2.08 (m, 2H), 1.81 (m, 1H), 1.64 (s, 2H), 1.45 (m, 7H), 1.17 (d,
1H), 1.04 (m, 2H), 0.75 (m, 7H), 0.63 (d, 5H). MS (ESI) m/z 847.78
[M+H].sup.+.
Example ED
##STR00205##
[0567]
methyl{(2S,3S)-1-[(2S,4S)-2-(9-{2-[(2S,5S)-1-{(2S,3R)-3-methoxy-2-[-
(methoxy
carbonyl)amino]butanoyl}-5-methylpyrrolidin-2-yl]-1H-imidazol-5-y-
l}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-(metho-
xymethyl)pyrrolidin-1-yl]-3-methyl-1-oxopentan-2-yl}carbamate
[0568] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with (2S,5S)-1-((2S,3R)-3-methoxy-2-(methoxycarbonylamino)
butanoyl)-5-methylpyrrolidine-2-carboxylic acid;
(2S,5S)-1-((S)-2-(methoxycarbonyl
amino)-3-methylbutanoyl)-5-methylpyrrolidine-2-carboxylic acid with
(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrrolidine-2-carboxylic
acid and (2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid
with (2S,3S)-2-(methoxycarbonyl amino)-3-methylpentanoic acid.
.sup.1H NMR (400 MHz, dmso) .delta. 8.70 (s, 1H), 8.16 (s, 1H),
7.87 (s, 4H), 7.74 (d, 1H), 7.65 (d, 1H), 7.57 (d, 1H), 7.28 (d,
1H), 5.29 (s, 2H), 5.24-5.16 (m, 1H), 4.97 (d, 1H), 4.63 (s, 1H),
4.27-4.02 (m, 2H), 3.60-3.37 (m, 14H), 2.68 (m, 1H), 2.51 (m, 1H),
2.32 (m, 3H), 2.18-1.91 (m, 3H), 1.82 (s, 1H), 1.63 (s, 1H), 1.45
(d, 3H), 1.24 (m, 2H), 0.99 (d, 5H), 0.79-0.64 (m, 7H). MS (ESI)
m/z 879.85 [M+H].sup.+.
Example EE
##STR00206##
[0569]
methyl{(3S)-1-[(2S,5S)-2-(5-{2-[(2S,4S)-1-[N-(methoxycarbonyl)-O-me-
thyl-D-allothreonyl]-4-(methoxymethyl)pyrrolidin-2-yl]-1,11-dihydroisochro-
meno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-5-methylpyrr-
olidin-1-yl]-3-methyl-1-oxopentan-2-yl}carbamate
[0570] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with (2S,5S)-1-((2S,3
S)-2-(methoxycarbonylamino)-3-methylpentanoyl)-5-methylpyrrolidine-2-carb-
oxylic acid and
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid with
(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxy
methyl)pyrrolidine-2-carboxylic acid. .sup.1H NMR (400 MHz, dmso)
.delta. 8.73 (s, 1H), 8.20 (d, 1H), 8.04 (s, 1H), 7.90 (m, 3H),
7.77 (s, 1H), 7.68 (d, 1H), 7.55 (d, 1H), 7.07 (d, 1H), 5.35-5.15
(m, 3H), 5.06-4.94 (m, 1H), 4.64 (s, 1H), 4.33-4.25 (m, 1H), 4.19
(s, 1H), 4.08 (s, 1H), 3.98 (t, 1H), 3.62 (t, 1H), 3.54-3.41 (m,
8H), 3.27 (s, 3H), 3.11 (s, 3H), 2.69 (s, 1H), 2.59-2.49 (m, 1H),
2.48-2.41 (m, 2H), 2.28 (m, 2H), 2.18-1.94 (m, 2H), 1.82 (m, 1H),
1.67 (m, 1H), 1.44 (d, 3H), 1.15-1.01 (m, 1H), 0.98 (d, 3H), 0.79
(m, 4H), 0.65 (d, 3H). MS (ESI) m/z 879.90 [M+H].sup.+.
Example EF
##STR00207##
[0571]
methyl[(1S)-2-[(2S,4S)-2-(9-{2-[(2S,5S)-1-{(2S)-2-[(methoxycarbonyl-
)amino]-3-methylbutanoyl}-5-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11
dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-(methoxymethy-
l)pyrrolidin-1-yl]-2-oxo-1-(tetra
hydro-2H-pyran-4-yl)ethyl]carbamate
[0572] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpy-
rrolidine-2-carboxylic acid;
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methyl-butanoyl)-5-methylpyrrol-
idine-2-carboxylic acid with
(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrrolidine-2-carboxylic
acid and (2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid
with
(S)-2-(methoxycarbonylamino)-2-(tetra-hydro-2H-pyran-4-yl)acetic
acid. .sup.1H NMR (400 MHz, dmso) .delta. 8.66 (s, 1H), 8.15 (m,
1H), 7.97 (s, 1H), 7.78 (m, 4H), 7.59 (d, 1H), 7.49 (d, 2H), 7.27
(d, 1H), 5.30-5.10 (m, 3H), 5.01-4.89 (m, 1H), 4.59 (s, 1H), 4.13
(m, 3H), 3.92-2.95 (m, 9H), 2.65 (s, 2H), 2.52-2.37 (m, 2H), 2.18
(m, 4H), 1.98-1.69 (m, 4H), 1.40 (d, 5H), 1.22 (m, 5H), 0.84 (m,
5H), 0.68 (d, 3H). MS (ESI) m/z 891.65 [M+H].sup.+.
Example EG
##STR00208##
[0573]
methyl{2-[(2S,5S)-2-(9-{2-[(2S,5S)-1-{(2S,3R)-3-methoxy-2-[(methoxy-
carbonyl)
amino]butanoyl}-5-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11--
dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolid-
in-1-yl]-2-oxo-1-(tetrahydro-2H-pyran-4-yl)ethyl}carbamate
[0574] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with (2S,5S)-1-((2S,3R)-3-methoxy-2-(methoxycarbonylamino)
butanoyl)-5-methylpyrrolidine-2-carboxylic acid;
(2S,5S)-1-((S)-2-(methoxycarbonyl
amino)-3-methylbutanoyl)-5-methylpyrrolidine-2-carboxylic acid with
(2S,5S)-1-(tert-butoxy carbonyl)-5-methylpyrrolidine-2-carboxylic
acid and (2S,3R)-3-methoxy-2-(methoxy-carbonylamino)butanoic acid
with
(S)-2-(methoxycarbonylamino)-2-(tetrahydro-2H-pyran-4-yl)acetic
acid. .sup.1H NMR (400 MHz, dmso) .delta. 8.60 (s, 1H), 8.13 (s,
1H), 7.94 (s, 1H), 7.76 (m, 4H), 7.54 (m, 3H), 5.23 (s, 2H), 5.11
(t, 1H), 4.95 (s, 1H), 4.63 (m, 2H), 4.42-4.16-3.95 (m, 2H),
3.86-3.30 (m, 8H), 3.26-2.89 (m, 5H), 2.21 (m, 5H), 1.80 (s, 3H),
1.54 (m, 2H), 1.44 (m, 6H), 1.16 (m, 5H), 1.02 (d, 1H), 0.88 (d,
3H). MS (ESI) m/z 877.77 [M+H].sup.+.
Example EH
##STR00209##
[0575]
methyl{(3S)-1-[(2S,5S)-2-(9-{2-[(2S,5S)-1-{(2S,3R)-3-methoxy-2-[(me-
thoxycarbonyl)
amino]butanoyl}-5-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydrois-
ochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidin-1-yl]--
3-methyl-1-oxopentan-2-yl}carbamate
[0576] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with
(2S,5S)-1-((2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoyl)-5-met-
hylpyrrolidine-2-carboxylic acid;
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid with
(2S,5S)-1-(tert-butoxycarbonyl)-5-methyl pyrrolidine-2-carboxylic
acid and (2S,3R)-3-methoxy-2-(methoxycarbonylamino) butanoic acid
with (2S,3S)-2-(methoxy carbonylamino)-3-methylpentanoic acid.
.sup.1H NMR (400 MHz, dmso) .delta. 8.63 (s, 1H), 8.21-7.49 (m,
8H), 5.26 (s, 2H), 5.13 (m, 1H), 4.98 (s, 1H), 4.68 (m, 2H), 4.14
(s, 1H), 4.02 (m, 1H), 3.34 (m, 9H), 2.36 (m, 2H), 2.11 (m, 4H),
1.84 (m, 2H), 1.70-1.60 (m, 1H), 1.47 (m, 6H), 1.13 (m, 4H), 0.92
(d, 3H), 0.84 (m, 2H), 0.74 (m, 3H), 0.66 (d, 3H). MS (ESI) m/z
849.74 [M+H].sup.+.
Example EI
##STR00210##
[0577]
methyl[(1S)-2-[(2S,4S)-2-(9-{2-[(2S,5S)-1-{(2S)-2-[(methoxycarbonyl-
)amino]-3-methylbutanoyl}-5-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11
dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-methylpyrroli-
din-1-yl]-2-oxo-1-(tetra hydro-2H-pyran-4-yl)ethyl]carbamate
[0578] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with
(2S,5S)-1-((2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoyl)-5-met-
hyl pyrrolidine-2 carboxylic acid;
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methyl
butanoyl)-5-methylpyrrolidine-2-carboxylic acid with
(2S,4S)-1-(tert-butoxy carbonyl)-4-methyl pyrrolidine-2-carboxylic
acid and (2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid
with (S)-2-(methoxycarbonylamino)-2-(tetra
hydro-2H-pyran-4-yl)acetic acid. .sup.1H NMR (400 MHz, dmso)
.delta. 8.73 (s, 1H), 8.21 (m, 1H), 8.06 (s, 1H), 7.98-7.84 (m,
3H), 7.73 (m, 2H), 7.52 (d, 1H), 7.27 (d, 1H), 5.31 (s, 2H),
5.24-5.14 (m, 1H), 5.05-4.96 (m, 1H), 4.62 (s, 1H), 4.29-3.48 (m,
10H), 3.26-3.03 (m, 4H), 2.65-2.52 (m, 2H), 2.41-2.03 (m, 4H),
1.97-1.75 (m, 4H), 1.44 (d, 3H), 1.32 (s, 2H), 1.20 (m, 2H), 1.09
(d, 3H), 0.87 (m, 4H), 0.72 (d, 3H). MS (ESI) m/z 861.75
[M+H].sup.+.
Example EJ
##STR00211##
[0579]
methyl[(2S)-1-{(2S,5S)-2-[9-(2-{(2S,4S)-1-[(2S)-2-[(methoxycarbonyl-
)amino]-2-(tetrahydro-2H-pyran-4-yl)acetyl]-4-methylpyrrolidin-2-yl}-1H-im-
idazol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl-
]-5-methylpyrrolidin-1-yl}-3-methyl-1-oxobutan-2-yl]carbamate
[0580] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with
(2S,5S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidine-2-carboxylic
acid and (2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid
with (S)-2-(methoxycarbonylamino)-2-(tetra
hydro-2H-pyran-4-yl)acetic acid. .sup.1H NMR (400 MHz, dmso)
.delta. 8.68 (s, 1H), 8.18 (d, 1H), 8.09-7.96 (m, 1H), 7.83 (m,
2H), 7.73-7.43 (m, 2H), 7.27 (d, 1H), 5.24 (d, 2H), 5.13 (m, 1H),
5.01 (m, 1H), 4.72-4.59 (m, 1H), 4.21-4.03 (m, 4H), 3.91 (m, 1H),
3.74 (s, 2H), 3.55-3.31 (m, 8H), 3.25-3.03 (m, 3H), 2.51-2.25 (m,
4H), 2.12 (m, 1H), 1.79 (m, 3H), 1.47 (d, 3H), 1.34-1.12 (m, 3H),
1.12-0.93 (m, 4H), 0.86 (s, 1H), 0.79 (d, 3H), 0.69 (d, 3H). MS
(ESI) m/z 861.79 [M+H].sup.+.
Example EK
##STR00212##
[0581] methyl
[(2S,3R)-1-{(2S,5S)-2-[5-(2-{(2S,5S)-5-ethyl-1-[N-(methoxycarbonyl)-O-met-
hyl-L-threonyl]pyrrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[-
1,2-d]imidazol-9-yl)-1H-imidazol-2-yl]-5-methylpyrrolidin-1-yl}-3-methoxy--
1-oxobutan-2-yl]carbamate
[0582] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid with
(2S,5S)-1-(tert-butoxycarbonyl)-5-ethylpyrrolidine-2-carboxylic
acid. .sup.1H NMR (400 MHz, dmso) .delta. 8.66 (s, 1H), 8.19 (d,
1H), 8.00 (d, 1H), 7.81 (m, 3H), 7.59 (m, 2H), 5.27 (s, 2H),
5.20-5.08 (m, 1H), 5.05-4.94 (m, 1H), 4.63 (s, 1H), 4.53 (s, 1H),
4.42 (s, 1H), 4.24-3.98 (m, 4H), 3.61-3.36 (m, 5H), 3.28-3.12 (m,
6H), 2.43-2.08 (m, 6H), 1.92 (m, 4H), 1.45 (d, 3H), 1.05 (m, 12H),
0.71 (s, 1H). MS (ESI) m/z 865.74 [M+H].sup.+.
Example EL
##STR00213##
[0583] methyl
[(2S,3R)-3-methoxy-1-{(2S,5S)-2-[5-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-O-m-
ethyl-L-threonyl]-4-methylpyrrolidin-2-yl}-1,11dihydroisochromeno[4',3':6,-
7]naphtho[1,2-d]imidazol-9-yl)-1H-imidazol-2-yl]-5-methylpyrrolidin-1-yl}--
1-oxo butan-2-yl]carbamate
[0584] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with
(2S,5S)-1-(tert-butoxycarbonyl)-5-ethylpyrrolidine-2-carboxylic
acid and
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyr-
rolidine-2-carboxylic acid with
(2S,5S)-1-(tert-butoxycarbonyl)-5-ethylpyrrolidine-2-carboxylic
acid. .sup.1H NMR (400 MHz, dmso) .delta. 8.66 (s, 1H), 8.19 (d,
1H), 7.99 (d, 1H), 7.93-7.57 (m, 6H), 5.27 (s, 2H), 5.14 (m, 1H),
5.02-4.93 (m, 1H), 4.56-4.26 (m, 2H), 4.22-4.08 (m, 2H), 3.77-3.08
(m, 16H), 2.39-2.08 (m, 4H), 1.91 (m, 6H), 1.16-1.03 (m, 2H),
1.01-0.83 (m, 10H), 0.79-0.64 (m, 3H). MS (ESI) m/z 879.87
[M+H].sup.+.
Example EM
##STR00214##
[0585]
methyl[(2S,3R)-1-{(2S,5S)-2-ethyl-5-[5-(2-{(2S,5S)-1-[N-(methoxycar-
bonyl)-O-methyl-L-threonyl]-5-methylpyrrolidin-2-yl}-1,11dihydroisochromen-
o[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imidazol-2-yl]pyrrolidin-1-yl}-
-3-methoxy-1-oxobutan-2-yl]carbamate
[0586] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid
(2S,5S)-1-(tert-butoxycarbonyl)-5-ethylpyrrolidine-2-carboxylic
acid, and (2S,5S)-1-((S)-2-(methoxy carbonylamino)-3-methyl
butanoyl)-5-methylpyrrolidine-2-carboxylic acid with
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid. .sup.1H NMR (400 MHz, dmso) .delta. 8.66 (s, 1H), 8.19 (d,
1H), 8.06-7.68 (m, 5H), 7.59 (m, 2H), 5.27 (s, 2H), 5.19-5.08 (m,
1H), 5.03-4.94 (m, 1H), 4.71 (s, 1H), 4.47 (s, 1H), 4.31 (s, 1H),
4.23-4.05 (m, 3H), 3.87-3.09 (m, 16H), 2.34 (s, 3H), 2.15 (s, 3H),
1.98 (s, 2H), 1.85 (s, 3H), 1.50 (d, 2H), 1.25 (s, 1H), 1.08 (d,
2H), 0.94 (m, 6H), 0.75 (s, 1H). MS (ESI) m/z 865.85
[M+H].sup.+.
Example EN
##STR00215##
[0587] Methyl [(1S)-2-[(2S,5S)-2-(9-{2-[(2S,5S)-5-ethyl-1-{(2S)-2
[(methoxycarbonyl)amino]-3-methylbutanoyl}pyrrolidin-2-yl]-1H-imidazol-5--
yl}-1,11dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methyl-
pyrrolidin-1-yl]-2-oxo-1(tetrahydro-2H-pyran-4-yl)ethyl]carbamate
[0588] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with
(2S,5S)-1-(tert-butoxycarbonyl)-5-ethylpyrrolidine-2-carboxylic
acid (2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methyl
butanoyl)-5-methylpyrrolidine-2-carboxylic acid with
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-2-(tetrahydro-2H-pyran-4-yl)acety-
l)-5-methyl pyrrolidine-2-carboxylic acid and
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid with
(S)-2-(methoxycarbonylamino)-3-methyl butanoic acid. .sup.1H NMR
(400 MHz, dmso) .delta. 8.63 (s, 1H), 8.22-8.11 (m, 1H), 7.68 (m,
8H), 5.26 (s, 2H), 5.13 (s, 1H), 4.99 (s, 1H), 4.77-4.64 (m, 1H),
4.38-4.25 (m, 1H), 4.03 (s, 1H), 3.85 (d, 2H), 3.60-2.92 (m, 9H),
2.63 (s, 1H), 2.29 (s, 4H), 1.90 (m, 6H), 1.58 (s, 1H), 1.49 (d,
4H), 1.15 (s, 4H), 0.95 (d, 4H), 0.84 (d, 4H), 0.71 (d, 4H). MS
(ESI) m/z 875.67 [M+H].sup.+.
Example EO
##STR00216##
[0589] methyl [(1S)-2-[(2S,5S)-2-ethyl-5-(9-{2-[(2S,5S)-1-{(2S)-2
[(methoxycarbonyl)amino]-3-methylbutanoyl}-5-methylpyrrolidin-2-yl]-1H-im-
idazol-5-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl-
)pyrrolidin-1-yl]-2-oxo-1-(tetrahydro-2H-pyran-4-yl)ethyl]carbamate
[0590] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with
(2S,5S)-1-((2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoyl)-5-met-
hyl pyrrolidine-2 carboxylic acid;
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid with
(2S,5S)-1-(tert-butoxycarbonyl)-5-ethylpyrrolidine-2-carboxylic
acid and (2S,3R)-3-methoxy-2-(methoxycarbonyl amino)butanoic acid
with (S)-2-(methoxycarbonylamino)-2-(tetra
hydro-2H-pyran-4-yl)acetic acid. .sup.1H NMR (400 MHz, dmso)
.delta. 8.66 (s, 1H), 8.20 (d, 1H), 8.02 (d, 1H), 7.81 (m, 3H),
7.58 (m, 3H), 5.27 (d, 2H), 5.15 (s, 1H), 5.04-4.93 (m, 1H), 4.62
(s, 1H), 4.39 (s, 1H), 4.03 (s, 2H), 3.94-3.34 (m, 9H), 3.26-2.96
(m, 4H), 2.43-2.06 (m, 4H), 2.00 (s, 2H), 1.84 (s, 4H), 1.59 (d,
1H), 1.44 (d, 3H), 1.28 (d, 4H), 0.97 (m, 2H), 0.84 (d, 4H), 0.69
(m, 4H). MS (ESI) m/z 875.74 [M+H].sup.+.
Example EP
##STR00217##
[0591] methyl
{(2S,3R)-1-[(2S,5S)-2-ethyl-5-(9-{2-[(2S,5S)-1-{(2S)-[(methoxycarbonyl)
amino]-3-methylbutanoyl}-5-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11--
dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)pyrrolidin-1-yl]--
3-methoxy-1-oxobutan-2-yl}carbamate
[0592] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with
(2S,5S)-1-((2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoyl)-5-met-
hylpyrrolidine-2 carboxylic acid and
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid with
(2S,5S)-1-(tert-butoxycarbonyl)-5-ethylpyrrolidine-2-carboxylic
acid. .sup.1H NMR (400 MHz, dmso) .delta. 8.69 (s, 1H), 8.21 (d,
1H), 8.07 (s, 1H), 8.01-7.48 (m, 6H), 5.28 (s, 2H), 5.14 (m, 1H),
5.06-4.94 (m, 1H), 4.70-4.35 (m, 2H), 4.23-3.82 (m, 3H), 3.52 (m,
6H), 3.41 (s, 3H), 3.25 (s, 1H), 3.15 (s, 2H), 2.42-2.06 (m, 4H),
1.90 (m, 4H), 1.44 (d, 3H), 1.08 (d, 1H), 1.02-0.76 (m, 10H), 0.71
(d, 4H). MS (ESI) m/z 849.79 [M+H].sup.+.
Example EQ
##STR00218##
[0593]
methyl{(2S,3R)-1-[(2S,5S)-2-(9-{2-[(2S,5S)-5-ethyl-1-{(2S)-2-[(meth-
oxycarbonyl)
amino]-3-methylbutanoyl}pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydrois-
ochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidin-1-yl]--
3-methoxy-1-oxobutan-2-yl}carbamate
[0594] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with with
(2S,5S)-5-ethyl-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoy-
l)pyrrolidine-2-carboxylic acid and
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid with
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid. .sup.1H NMR (400 MHz, dmso) .delta. 8.68 (s, 1H), 8.19 (m,
1H), 8.05 (s, 1H), 8.00-7.70 (m, 4H), 7.60 (m, 2H), 5.28 (s, 2H),
5.19-5.08 (m, 1H), 5.05-4.94 (m, 1H), 4.71 (s, 1H), 4.29 (s, 1H),
4.22-4.06 (m, 2H), 3.94-3.82 (m, 3H), 3.75-3.19 (m, 9H), 3.14 (s,
2H), 2.36 (m, 2H), 2.14 (m, 2H), 1.87 (m, 3H), 1.50 (d, 3H), 1.25
(d, 1H), 1.15-1.01 (m, 1H), 1.01-0.76 (m, 10H), 0.71 (d, 3H). MS
(ESI) m/z 849.83 [M+H].sup.+.
Example ER
##STR00219##
[0595] methyl
{(2S)-1-[(2S,4S)-2-(9-{2-[(2S,5S)-5-ethyl-1-{(2S)-2-[(methoxycarbonyl)ami-
no]-3-methylbutanoyl}pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydroisochr-
omeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-(methoxymethyl)pyrrolidin-1-
-yl]-3-methyl-1-oxobutan-2-yl}carbamate
[0596] Was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with
(2S,5S)-5-ethyl-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)pyr-
rolidine-2-carboxylic acid;
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid with
(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrrolidine-2-carboxylic
acid and (2S,3R)-3-methoxy-2-(methoxycarbonyl amino)butanoic acid
with (S)-2-(methoxycarbonylamino)-3-methylbutanoic acid. .sup.1H
NMR (400 MHz, dmso) .delta. 8.72 (s, 1H), 8.25-8.11 (m, 1H),
8.07-7.84 (m, 3H), 7.67 (m, 3H), 7.26 (d, 1H), 5.30 (s, 2H),
5.25-5.15 (m, 1H), 5.06-4.91 (m, 1H), 4.36-4.00 (m, 3H), 3.94-3.81
(m, 2H), 3.65-3.35 (m, 10H), 3.27 (s, 3H), 2.69 (s, 2H), 2.51 (m,
1H), 2.33 (s, 1H), 2.19 (s, 2H), 2.05-1.63 (m, 7H), 0.99-0.63 (m,
12H). MS (ESI) m/z 863.88 [M+H].sup.+.
Example ES
##STR00220##
[0597]
methyl{(2R,3R)-1-[(2S,4S)-2-(9-{2-[(2S,5S)-5-ethyl-1-{(2S)-2-[(meth-
oxycarbonyl)
amino]-3-methylbutanoyl}pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydrois-
ochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-(methoxymethyl)pyrrolid-
in-1-yl]-3-methoxy-1-oxobutan-2-yl}carbamate
[0598] Was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with
(2S,5S)-5-ethyl-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)pyr-
rolidine-2-carboxylic acid;
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methyl
pyrrolidine-2-carboxylic acid with
(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxy methyl)
pyrrolidine-2-carboxylic acid. .sup.1H NMR (400 MHz, dmso) .delta.
8.71 (s, 1H), 8.19 (m, 1H), 7.94 (m, 3H), 7.76 (m, 1H), 7.65 (d,
1H), 7.57 (d, 1H), 7.12 (d, 1H), 5.29 (s, 1H), 5.25-5.16 (m, 1H),
5.06-4.93 (m, 1H), 4.37-4.10 (m, 3H), 3.95-3.82 (m, 2H), 3.51 (m,
8H), 3.25 (m, 3H), 3.11 (s, 3H), 2.60 (m, 3H), 2.25 (m, 3H),
2.06-1.65 (m, 6H), 1.11-0.77 (m, 8H), 0.71 (d, 3H). MS (ESI) m/z
879.81 [M+H].sup.+.
Example ET
##STR00221##
[0599]
(2S,5S)-1-((2S,3S)-2-(methoxycarbonylamino)-3-methylpentanoyl)-5
methylpyrrolidine-2-carboxylic acid
[0600] Was synthesized in a similar manner as Example BN
substituting (S)-2-(methoxycarbonylamino)-3-methylbutanoic acid
with (2S,3S)-2-(methoxycarbonyl-amino)-3-methylpentanoic acid MS
(ESI) m/z 301.19 [M+H].sup.+.
Example EU
##STR00222##
[0601]
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-2-(tetrahydro-2H-pyran-4-yl-
)acetyl)-5-methyl pyrrolidine-2-carboxylic acid
[0602] Was synthesized in a similar manner as Example BN
substituting (S)-2-(methoxycarbonylamino)-3-methylbutanoic acid
with (S)-2-(methoxycarbonylamino)-2-(tetrahydro-2H-pyran-4-yl)
acetic acid. MS (ESI) m/z 329.36 [M+H].sup.+.
Example EV
##STR00223##
[0603]
(2S,5S)-1-((2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoyl)-5-me-
thylpyrrolidine-2-carboxylic acid
[0604] Was synthesized in a similar manner as Example BN
substituting (S)-2-(methoxycarbonylamino)-3-methylbutanoic acid
with (2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid. MS
(ESI) m/z 303.19 [M+H].sup.+.
Example EW
##STR00224##
[0605]
(2S,5S)-5-ethyl-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)py-
rrolidine-2-carboxylic acid
[0606] Was synthesized in a similar manner as Example BN
substituting (2S,5S)-ethyl 5-methylpyrrolidine-2-carboxylate-TFA
with (2S,5S)-methyl 5-ethylpyrrolidine-2-carboxylate-HCl. MS (ESI)
m/z 301.15 [M+H].sup.+.
Example EX
##STR00225##
[0607] methyl
{(2S,3R)-3-methoxy-1-[(2S,4S)-2-(9-{2-[(2S,4S)-1-[N-(methoxycarbonyl)-O-m-
ethyl-L-threonyl]-4-(methoxymethyl)pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-
-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-(methoxymethy-
l)pyrrolidin-1-yl]-1-oxobutan-2-yl}carbamate
[0608] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid and
(2S,5S)-1-(2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrrolidine-
-2-carboxylic acid with
(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrrolidine-2-carboxylic
acid. (0.083g) LCMS-ESI.sup.+: calculated for
C.sub.47H.sub.58N.sub.8O.sub.11: 910.42; observed [M+1].sup.+:
911.78. .sup.1H NMR (400 MHz, cd.sub.3od) .delta. 8.63 (s, 1H),
8.19 (d, 1H), 8.00 (d, 1H), 7.91 (d, 2H), 7.83 (d, 1H), 7.68 (s,
1H), 7.63 (d, 1H), 5.45-5.37 (m, 1H), 5.32 (s, 2H), 5.30-5.24 (m,
1H), 4.55-4.44 (m, 2H), 4.37-4.23 (m, 3H), 3.78-3.65 (m, 10H),
3.65-3.54 (m, 5H), 3.41 (s, 7H), 3.28 (s, 3H), 2.90-2.59 (m, 6H),
2.12 (dq, 3H), 1.12 (q, 6H).
Example EY
##STR00226##
[0609] methyl
{(1R)-2-[(2S,4S)-2-(5-{2-[(2S,4S)-1-{(2R)-2-[(methoxycarbonyl)amino]-2-ph-
enylacetyl}-4-(methoxymethyl)pyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3-
':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)pyrr-
olidin-1-yl]-2-oxo-1-phenylethyl}carbamate
[0610] was synthesized in a similar manner as methyl
{(2S,3R)-3-methoxy-1-[(2S,4S)-2-(9-{2-[(2S,4S)-1-[N-(methoxycarbonyl)-O-m-
ethyl-L-threonyl]-4-(methoxymethyl)pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-
-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-(methoxymethy-
l)pyrrolidin-1-yl]-1-oxobutan-2-yl}carbamate, substituting
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid with
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid and substituting
HATU with COMU. (0.068g) LCMS-ESI.sup.+: calculated for
C.sub.53H.sub.54N.sub.8O.sub.9: 946.40; observed [M+1].sup.+:
947.83. .sup.1H NMR (400 MHz, acetone) .delta. 8.21 (s, 1H), 7.95
(s, 1H), 7.88-7.71 (m, 3H), 7.59 (d, 3H), 7.51 (d, 2H), 7.48-7.32
(m, 7H), 7.27-7.18 (m, 1H), 5.74 (t, 1H), 5.63 (dd, 2H), 5.52 (t,
1H), 5.11 (s, 3H), 3.98-3.87 (m, 2H), 3.83 (d, 2H), 3.78 (s, 3H),
3.60 (s, 3H), 3.51-3.37 (m, 4H), 3.25 (d, 3H), 3.19 (s, 3H),
2.86-2.75 (m, 1H), 2.73-2.54 (m, 4H), 2.25 (dd, 1H), 2.18-2.10 (m,
1H).
Example EZ
##STR00227##
[0611] methyl
[(2S,3R)-3-methoxy-1-{(2S,4S)-2-[9-(2-{(2S,4S)-1-[N-(methoxycarbonyl)-O-m-
ethyl-L-threonyl]-4-methylpyrrolidin-2-yl}-1H-imidazol-5-yl)-1,11-dihydroi-
sochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]-4-methylpyrrolidin-1-yl}-
-1-oxobutan-2-yl]carbamate
[0612] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid and
(2S,5S)-1-(2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrrolidine-
-2-carboxylic acid with
(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidine-2-carboxylic
acid. (0.068g) LCMS-ESI.sup.+: calculated for
C.sub.45H.sub.54N.sub.8O.sub.9: 850.40; observed [M+1].sup.+:
851.78. .sup.1H NMR (400 MHz, cd.sub.3od) .delta. 8.65 (s, 1H),
8.20 (d, 1H), 8.04 (d, 1H), 7.93 (s, 1H), 7.90 (s, 1H), 7.87-7.81
(m, 1H), 7.69 (s, 1H), 7.64 (d, 1H), 5.39 (q, 1H), 5.33 (s, 2H),
5.25 (q, 1H), 4.51 (dd, 2H), 4.43-4.23 (m, 3H), 3.73-3.62 (m, 8H),
3.57-3.46 (m, 2H), 3.45-3.35 (m, 2H), 3.27 (s, 3H), 2.83-2.63 (m,
3H), 2.61-2.47 (m, 2H), 1.93 (dq, 3H), 1.26 (dd, 6H), 1.22-1.14 (m,
2H), 1.11 (t, 6H).
Example FA
##STR00228##
[0613] methyl
[(2S)-1-{(2S,5S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-O-methyl-L-threo-
nyl]-5-methylpyrrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,-
2-d]imidazol-9-yl)-1H-imidazol-2-yl]-5-methylpyrrolidin-1-yl}-3-methyl-1-o-
xobutan-2-yl]carbamate
[0614] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpy-
rrolidine-2-carboxylic acid, and substituting
(2S,5S)-1-(2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrrolidine-
-2-carboxylic acid with
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid. (0.102g) LCMS-ESI.sup.+: calculated for
C.sub.4hH.sub.54N.sub.8O.sub.8: 834.41; observed [M+1].sup.+:
835.77. .sup.1H NMR (400 MHz, cd.sub.3od) .delta. 8.68-8.61 (m,
1H), 8.25-8.17 (m, 1H), 8.09-7.97 (m, 2H), 7.96-7.91 (m, 1H),
7.88-7.82 (m, 1H), 7.73-7.63 (m, 2H), 6.10-6.01 (m, 1H), 5.75-5.66
(m, 1H), 5.33 (d, 3H), 5.22-5.11 (m, 1H), 4.84-4.75 (m, 2H),
4.68-4.58 (m, 1H), 4.42 (d, 1H), 4.35-4.25 (m, 1H), 4.18-4.07 (m,
1H), 3.76 (d, 2H), 3.67 (d, 4H), 3.62-3.55 (m, 1H), 3.40 (s, 1H),
3.28 (s, 2H), 2.67-2.46 (m, 3H), 2.44-2.26 (m, 4H), 2.10-1.90 (m,
3H), 1.61 (d, 2H), 1.56 (d, 3H), 1.34-1.22 (m, 4H), 1.14-1.06 (m,
2H), 1.03 (d, 1H), 0.98 (d, 2H), 0.87 (d, 3H).
Example FB
##STR00229##
[0615] methyl
{(1R)-2-[(2S,5S)-2-(9-{2-[(2S,5S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-me-
thylbutanoyl}-5-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydroisoch-
romeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidin-1-yl]-2-o-
xo-1-phenylethyl}carbamate
[0616] was synthesized in a similar manner as methyl
[(2S)-1-{(2S,5S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-O-methyl-L-threo-
nyl]-5-methylpyrrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,-
2-d]imidazol-9-yl)-1H-imidazol-2-yl]-5-methylpyrrolidin-1-yl}-3-methyl-1-o-
xobutan-2-yl]carbamate by substituting
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid with
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid, and substituting
HATU with COMU. (0.033g) LCMS-ESI.sup.+: calculated for
C.sub.48H.sub.52N.sub.8O.sub.7: 852.40; observed [M+1].sup.+:
853.77. .sup.1H NMR (400 MHz, cd.sub.3od) .delta. 8.67 (s, 1H),
8.27-8.17 (m, 1H), 8.14-8.03 (m, 2H), 8.02-7.96 (m, 1H), 7.93 (s,
1H), 7.89-7.78 (m, 1H), 7.72-7.65 (m, 2H), 7.57-7.51 (m, 2H),
7.51-7.42 (m, 2H), 5.62 (s, 1H), 5.50 (t, 1H), 5.33 (s, 2H),
5.22-5.13 (m, 1H), 4.84-4.78 (m, 1H), 4.35-4.24 (m, 1H), 4.21-4.07
(m, 1H), 3.82-3.72 (m, 3H), 3.67 (s, 3H), 2.75-2.49 (m, 3H),
2.47-2.25 (m, 4H), 2.10-1.95 (m, 3H), 1.92-1.83 (m, 1H), 1.59 (dd,
6H), 1.33-1.27 (m, 1H), 1.06 (dd, 2H), 0.99 (d, 2H), 0.88 (d,
3H).
Example FC
##STR00230##
[0617] methyl
[(1S)-2-[(2S,5S)-2-(9-{2-[(2S,5S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-me-
thylbutanoyl}-5-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydroisoch-
romeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidin-1-yl]-2-o-
xo-1-(tetrahydro-2H-pyran-4-yl)ethyl]carbamate
[0618] was synthesized in a similar manner as methyl
[(2S)-1-{(2S,5S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-O-methyl-L-threo-
nyl]-5-methylpyrrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,-
2-d]imidazol-9-yl)-1H-imidazol-2-yl]-5-methylpyrrolidin-1-yl}-3-methyl-1-o-
xobutan-2-yl]carbamate by substituting
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid with
(S)-2-(methoxycarbonylamino)-2-(tetrahydro-2H-pyran-4-yl)acetic
acid. (0.116g) LCMS-ESI.sup.+: calculated for
C.sub.47H.sub.56N.sub.8O.sub.8: 860.42; observed [M+1].sup.+:
861.42. .sup.1H NMR (400 MHz, cd.sub.3od) .delta. 8.65 (s, 1H),
8.27-8.17 (m, 1H), 8.08-7.97 (m, 1H), 7.93 (s, 1H), 7.88-7.83 (m,
1H), 7.73-7.62 (m, 2H), 5.41-5.26 (m, 3H), 5.21-5.12 (m, 1H),
4.85-4.76 (m, 1H), 4.39-4.21 (m, 2H), 4.12 (d, 1H), 4.04-3.90 (m,
2H), 3.87-3.81 (m, 1H), 3.76 (d, 2H), 3.67 (d, 4H), 3.50-3.38 (m,
1H), 3.25-3.10 (m, 2H), 2.68-2.21 (m, 7H), 2.12-1.87 (m, 4H),
1.85-1.70 (m, 1H), 1.64 (d, 2H), 1.56 (d, 3H), 1.51-1.33 (m, 2H),
1.32-1.25 (m, 2H), 1.25-1.18 (m, 1H), 1.06 (dd, 2H), 0.99 (d, 2H),
0.88 (d, 2H).
Example FD
##STR00231##
[0619] (S)-3-methoxy-2-(methoxycarbonylamino)propanoic acid
[0620] To a solution of (S)-2-amino-3-methoxypropanoic acid
hydrochloride (2.5g, 16.17 mmol) in THF (40 mL) was added aqueous
NaOH (6M, 6.47 mL, 38.82 mmol) and Methyl Chloroformate (1.50 mL,
19.41 mmol). The solution was stirred for 18 h. Aqueous HCl (1M, 40
mL) was slowly added. The solution was extracted with ethyl acetate
(3 times) and the combined organic layers were dried over sodium
sulfate and concentrated to provide
(S)-3-methoxy-2-(methoxycarbonylamino)propanoic acid (1.60g, 56%).
H NMR (400 MHz, cdcl.sub.3) .delta. 5.61 (d, 1H), 4.52 (d, 1H),
3.88 (d, 1H), 3.72 (s, 3H), 3.65 (dd, 1H), 3.43-3.35 (s, 3H).
Example FE
##STR00232##
[0621] methyl
[(2S)-1-{(2S,5S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-O-methyl-L-seryl-
]-5-methylpyrrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d-
]imidazol-9-yl)-1H-imidazol-2-yl]-5-methylpyrrolidin-1-yl}-3-methyl-1-oxob-
utan-2-yl]carbamate
[0622] was synthesized in a similar manner as methyl
[(2S)-1-{(2S,5S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-O-methyl-L-threo-
nyl]-5-methylpyrrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,-
2-d]imidazol-9-yl)-1H-imidazol-2-yl]-5-methylpyrrolidin-1-yl}-3-methyl-1-o-
xobutan-2-yl]carbamate substituting
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid with
(S)-3-methoxy-2-(methoxycarbonylamino)propanoic acid. (0.059g)
LCMS-ESI.sup.+: calculated for C.sub.44H.sub.52N.sub.8O.sub.8:
820.39; observed [M+1].sup.+: 821.76. .sup.1H NMR (400 MHz,
cd.sub.3od) .delta. 8.66-8.57 (m, 1H), 8.24-8.14 (m, 2H), 8.06-7.94
(m, 2H), 7.93-7.88 (m, 1H), 7.85-7.80 (m, 1H), 7.79-7.74 (m, 1H),
7.69-7.60 (m, 2H), 6.01-5.59 (m, 2H), 5.38-5.24 (m, 3H), 5.21-5.07
(m, 1H), 4.82-4.63 (m, 3H), 4.34-4.21 (m, 1H), 4.09 (d, 1H), 3.81
(s, 2H), 3.72 (s, 1H), 3.62-3.44 (m, 2H), 3.37 (s, 1H), 3.31 (s,
1H), 2.86-2.74 (m, 1H), 2.69-2.45 (m, 3H), 2.42-2.24 (m, 4H),
2.07-1.88 (m, 3H), 1.55 (dd, 5H), 1.27 (d, 2H), 1.05 (dd, 2H), 0.96
(d, 2H), 0.85 (d, 3H).
Example FF
##STR00233##
[0623] (2S,3R)-3-tert-butoxy-2-(methoxycarbonylamino)butanoic
acid
[0624] was synthesized in a similar manner as
(S)-3-methoxy-2-(methoxycarbonylamino)propanoic acid substituting
(S)-2-amino-3-methoxypropanoic acid hydrochloride with
(2S,3R)-2-amino-3-tert-butoxybutanoic acid. (1.33g, 99%).sup.1H NMR
(400 MHz, cdcl.sub.3) .delta. 5.65 (s, 1H), 4.41-4.25 (m, 2H), 3.71
(s, 3H), 1.29 (d, 9H), 1.16 (d, 3H).
Example FG
##STR00234##
[0625] methyl
{(2S,3R)-3-tert-butoxy-1-[(2S,5S)-2-(9-{2-[(2S,5S)-1-{(2S)-2-[(methoxycar-
bonyl)amino]-3-methylbutanoyl}-5-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}--
1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyr-
rolidin-1-yl]-1-oxobutan-2-yl}carbamate
[0626] was synthesized in a similar manner as methyl
[(2S)-1-{(2S,5S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-O-methyl-L-threo-
nyl]-5-methylpyrrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,-
2-d]imidazol-9-yl)-1H-imidazol-2-yl]-5-methylpyrrolidin-1-yl}-3-methyl-1-o-
xobutan-2-yl]carbamate substituting
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid with
(2S,3R)-3-tert-butoxy-2-(methoxycarbonylamino)butanoic acid.
(0.133g) LCMS-ESI.sup.+: calculated for
C.sub.48H.sub.60N.sub.8O.sub.8: 876.45; observed [M+1].sup.+:
877.73. .sup.1H NMR (400 MHz, cd.sub.3od) .delta. 8.62 (d, 1H),
8.24-8.13 (m, 1H), 8.07-7.76 (m, 4H), 7.73-7.59 (m, 2H), 5.32 (d,
2H), 5.20-5.11 (m, 1H), 4.82-4.75 (m, 2H), 4.70-4.62 (m, 1H),
4.47-4.22 (m, 3H), 4.19-3.98 (m, 2H), 3.94-3.85 (m, 1H), 3.80-3.61
(m, 6H), 2.85-2.46 (m, 4H), 2.43-2.25 (m, 4H), 2.11-1.91 (m, 3H),
1.64 (d, 2H), 1.56 (d, 3H), 1.31 (dd, 2H), 1.25-1.17 (m, 6H),
1.14-1.07 (m, 2H), 1.04 (s, 4H), 0.98 (d, 2H), 0.88 (d, 2H).
Example FH
##STR00235##
[0627] (2S,3R)-3-hydroxy-2-(methoxycarbonylamino)butanoic acid
[0628] was synthesized in a similar manner as
(S)-3-methoxy-2-(methoxycarbonylamino)propanoic acid substituting
(S)-2-amino-3-methoxypropanoic acid hydrochloride with
(2S,3R)-2-amino-3-tert-butoxybutanoic acid. (0.59g, 39%).sup.1H NMR
(400 MHz, cdcl.sub.3) .delta. 5.95 (d, 1H), 4.52-4.29 (m, 2H), 4.08
(d, 1H), 3.75 (d, 4H), 1.57 (t, 3H).
Example FI
##STR00236##
[0629] methyl
{(2S,3R)-3-hydroxy-1-[(2S,5S)-2-(9-{2-[(2S,5S)-1-{(2S)-2-[(methoxycarbony-
l)amino]-3-methylbutanoyl}-5-methylpyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-
-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrroli-
din-1-yl]-1-oxobutan-2-yl}carbamate
[0630] was synthesized in a similar manner as methyl
[(2S)-1-{(2S,5S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-O-methyl-L-threo-
nyl]-5-methylpyrrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,-
2-d]imidazol-9-yl)-1H-imidazol-2-yl]-5-methylpyrrolidin-1-yl}-3-methyl-1-o-
xobutan-2-yl]carbamate substituting
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid with
(2S,3R)-3-hydroxy-2-(methoxycarbonylamino)butanoic acid. (0.013g)
LCMS-ESI.sup.+: calculated for C.sub.44H.sub.52N.sub.8O.sub.8:
820.39; observed [M+1].sup.+: 821.73. .sup.1H NMR (400 MHz,
cd.sub.3od) .delta. 8.63 (s, 1H), 8.19 (d, 1H), 8.09-7.76 (m, 4H),
7.71-7.62 (m, 2H), 5.47-5.26 (m, 3H), 5.20-5.12 (m, 1H), 4.83-4.71
(m, 3H), 4.58-4.40 (m, 2H), 4.32 (s, 1H), 4.19-3.97 (m, 3H),
3.80-3.64 (m, 6H), 2.71-2.44 (m, 4H), 2.41-2.27 (m, 3H), 2.08-1.92
(m, 3H), 1.67-1.47 (m, 5H), 1.33-1.24 (m, 3H), 1.17 (d, 2H), 1.05
(dd, 2H), 0.98 (d, 2H), 0.87 (d, 2H).
Example FJ
##STR00237##
[0632] To a solution of compound 1 (7 g, 0.053 mol) in water (260
mL) was added Na.sub.2CO.sub.3 (11.2 g, 0.106 mol) in portions, and
the resultant mixture was cooled to 0.degree. C. Then methyl
chloroformate (5.5 g, 0.058 mol) was added dropwise over 5 minutes.
The reaction was allowed to stir at room temperature for 18 hours.
TLC showed the reaction was completed. The mixture was then
partitioned between 1N HCl and EtOAc, separated. The organic layer
was collected and the aqueous layer was further extracted with
additional EtOAc. The combined organic layers were washed with
brine, dried over magnesium sulfate, concentrated, purified by
chromatography (PE/EA=5/1 to 1/1) to give G-01431-1 (5.6 g, 55%) as
pure yellow oil. .sup.1HNMR: (400 M CDCl.sub.3) .delta. 8.88 (br,
1H), 5.51-5.49 (m, 1H), 4.56-4.53 (m, 1H), 3.73 (s, 3H), 3.73 (br,
1H), 3.41 (s, 3H), 1.29 (d, 3H).
Example FK
##STR00238##
[0633] methyl
[(2S)-1-{(2S,5S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-O-methyl-L-allot-
hreonyl]-5-methylpyrrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphth-
o[1,2-d]imidazol-9-yl)-1H-imidazol-2-yl]-5-methylpyrrolidin-1-yl}-3-methyl-
-1-oxobutan-2-yl]carbamate
[0634] was synthesized in a similar manner as methyl
[(2S)-1-{(2S,5S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-O-methyl-L-threo-
nyl]-5-methylpyrrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,-
2-d]imidazol-9-yl)-1H-imidazol-2-yl]-5-methylpyrrolidin-1-yl}-3-methyl-1-o-
xobutan-2-yl]carbamate substituting
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid with
(2S,3S)-3-methoxy-2-(methoxycarbonylamino)butanoic acid. (0.150g)
LCMS-ESI.sup.+: calculated for C.sub.45H.sub.54N.sub.8O.sub.8:
834.41; observed [M+1].sup.+: 835.76. .sup.1H NMR (400 MHz,
cd.sub.3od) .delta. 8.61 (s, 1H), 8.23 (s, 1H), 8.18 (d, 1H),
8.07-7.87 (m, 3H), 7.83 (d, 1H), 7.77 (s, 1H), 7.66 (t, 2H), 6.00
(d, 1H), 5.74-5.65 (m, 1H), 5.30 (d, 2H), 5.21-5.11 (m, 1H),
4.82-4.75 (m, 1H), 4.36 (t, 1H), 4.32-4.25 (m, 1H), 4.11 (d, 1H),
3.85 (s, 2H), 3.73 (s, 1H), 3.66 (d, 3H), 3.63-3.56 (m, 1H),
3.51-3.41 (m, 1H), 3.36 (s, 2H), 3.09 (s, 1H), 2.86-2.77 (m, 1H),
2.71-2.58 (m, 1H), 2.57-2.47 (m, 1H), 2.44-2.21 (m, 4H), 2.09-1.91
(m, 3H), 1.63 (d, 2H), 1.55 (d, 3H), 1.27 (t, 4H), 1.20 (d, 1H),
1.04 (dd, 2H), 0.97 (d, 2H), 0.87 (d, 2H).
Example FL
##STR00239##
[0635] 2-tert-Butoxycarbonylamino-3-difluoromethoxy-butyric acid
methyl ester
[0636] To a mixture of 2-tert-butoxycarbonylamino-3-hydroxy-butyric
acid methyl ester (630 mg, 2.70 mmol) and copper(I) iodide (105 mg,
0.55 mmol) in acetonitrile at 45.degree. C. was added a solution of
2-(fluorosulfonyl)difluoroacetic acid (0.560 mL, 5.42 mmol) in
acetonitrile (2 mL) by syringe pump over 45 minutes. The reaction
was then stirred at 45.degree. C. for 30 minutes. Another solution
of 2-(fluorosulfonyl)difluoroacetic acid (0.560 mL, 5.42 mmol) in
acetonitrile (2 mL) was added by syringe pump over 45 minutes at
45.degree. C. The reaction was stirred for 30 minutes at 45.degree.
C. after the second syringe pump addition was complete. Water was
carefully added to quench the reaction, and the mixture was diluted
with ethyl acetate. The organic layer was separated, washed with
water and brine, dried (MgSO.sub.4) and concentrated. The crude
material was purified by flash chromatography (10% ethyl
acetate/hexanes) to yield
2-tert-butoxycarbonylamino-3-difluoromethoxy-butyric acid methyl
ester (276 mg, 36%). .sup.1H-NMR: 400 MHz, (CDCl.sub.3): 6.16 (t,
J.sub.HF=74.0 Hz, 1H), 5.23-5.16 (br, 1H), 4.86-4.80 (m, 1H), 4.40
(br d, J=9.8 Hz, 1H), 3.76 (s, 3H), 1.46 (br s, 9H), 1.36 (d, J=6.4
Hz, 3H) ppm.
(2S,3R)-methyl-3-(difluoromethoxy)-2-(methoxycarbonylamino)butanoate
[0637] To a solution of
2-tert-Butoxycarbonylamino-3-difluoromethoxy-butyric acid methyl
ester (3 g, 10.6 mmol) in methanol (40 mL) was added concentrated
HCl solution (10 mL) and the reaction was stirred at 50.degree. C.
for 1 hour. The reaction was concentrated on a rotary evaporator
and the resulting residue was basified with saturated NaHCO.sub.3
solution. The aqueous layer was extracted twice with ethyl acetate.
The organic layer was separated, washed with brine, dried (MgSO4)
and concentrated.
[0638] To a solution of the crude material in dichloromethane (50
mL) was added diisopropylethylamine (4.2 mL, 24.2 mmol), followed
by methyl chloroformate (0.95 mL, 12.3 mmol). The reaction was
stirred at room temperature for 2 hours, quenched by the careful
addition of saturated NH.sub.4Cl solution and diluted with ethyl
acetate. The organic layer was separated, washed with water and
brine, dried (MgSO.sub.4) and concentrated. The crude material was
purified by flash chromatography to yield
(2S,3R)-methyl-3-(difluoromethoxy)-2-(methoxycarbonylamino)butanoat-
e (1.2 g, 47%).
(2S,3R)-3-(difluoromethoxy)-2-(methoxycarbonylamino)butanoic
acid
[0639] To a solution of
(2S,3R)-methyl-3-(difluoromethoxy)-2-(methoxycarbonylamino)butanoate
(265 mg, 1.1 mmol) in dichloroethane (10 mL) was added trimethyltin
hydroxide (1 g, 5.5 mmol) and the resulting mixture was heated to
80.degree. C. for 1 hour. The reaction was cooled to room
temperature, diluted with ethyl acetate, washed twice with 5%
aqueous HCl solution and brine, dried (MgSO.sub.4) and
concentrated. The resulting crude material (209 mg, 84%) was used
without further purification.
Example FM
##STR00240##
[0640] methyl
{(2S)-1-[(2S,5S)-2-(5-{2-[(2S,5S)-1-{(2S,3R)-3-(difluoromethoxy)-2-[(meth-
oxycarbonyl)amino]butanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroisochrome-
no[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-5-methylpyrrol-
idin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate
[0641] was synthesized in a similar manner as methyl
[(2S)-1-{(2S,5S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-O-methyl-L-threo-
nyl]-5-methylpyrrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,-
2-d]imidazol-9-yl)-1H-imidazol-2-yl]-5-methylpyrrolidin-1-yl}-3-methyl-1-o-
xobutan-2-yl]carbamate substituting
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid with
(2S,3R)-3-(difluoromethoxy)-2-(methoxycarbonylamino)butanoic acid.
(0.092g) LCMS-ESI.sup.+: calculated for
C.sub.45H.sub.52F.sub.2N.sub.8O.sub.8: 870.39; observed
[M+1].sup.+: 871.78. .sup.1H NMR (400 MHz, cd.sub.3od) .delta. 8.64
(s, 1H), 8.18 (d, 1H), 8.12-7.96 (m, 2H), 7.92 (s, 1H), 7.87-7.77
(m, 1H), 7.71-7.61 (m, 2H), 6.31 (t, 2H), 5.92-5.70 (m, 1H),
5.38-5.26 (m, 3H), 5.22-5.11 (m, 1H), 4.83-4.75 (m, 1H), 4.73-4.64
(m, 1H), 4.62-4.52 (m, 1H), 4.50-4.40 (m, 1H), 4.29 (s, 1H), 4.13
(d, 1H), 3.78-3.62 (m, 5H), 3.40 (s, 1H), 2.72-2.58 (m, 2H),
2.56-2.44 (m, 2H), 2.42-2.24 (m, 3H), 2.12-1.90 (m, 3H), 1.76 (d,
1H), 1.62 (d, 2H), 1.55 (d, 2H), 1.40 (d, 1H), 1.35 (d, 1H), 1.29
(d, 1H), 1.25 (d, 2H), 1.07 (d, 1H), 1.02 (d, 1H), 0.98 (d, 2H),
0.87 (d, 2H).
Example FN
##STR00241##
[0642] methyl
[(2S)-1-{(2S,4S)-2-[5-(2-{(2S,5S)-1-[(2S)-2-[(methoxycarbonyl)amino]-2-(t-
etrahydro-2H-pyran-4-yl)acetyl]-5-methylpyrrolidin-2-yl}-1,11-dihydroisoch-
romeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imidazol-2-yl]-4-methylpy-
rrolidin-1-yl}-3-methyl-1-oxobutan-2-yl]carbamate
[0643] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with
(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidine-2-carboxylic
acid, and substituting
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid with
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-2-(tetrahydro-2H-pyran-4-yl)acety-
l)-5-methylpyrrolidine-2-carboxylic acid, and substituting
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid with
(S)-2-(methoxycarbonylamino)-3-methylbutanoic acid. (0.022g)
LCMS-ESI.sup.+: calculated for C.sub.47H.sub.56N.sub.8O.sub.8:
860.42; observed [M+1].sup.+: 861.91. .sup.1H NMR (400 MHz,
cd.sub.3od) .delta. 8.62 (s, 1H), 8.27-8.13 (m, 1H), 7.92 (s, 2H),
7.85-7.77 (m, 1H), 7.73-7.60 (m, 2H), 5.37-5.13 (m, 4H), 4.43-4.12
(m, 4H), 4.04-3.78 (m, 3H), 3.76-3.60 (m, 5H), 3.50-3.37 (m, 2H),
3.20-3.09 (m, 1H), 2.92-2.20 (m, 9H), 2.14-1.75 (m, 6H), 1.63 (d,
3H), 1.24 (d, 5H), 0.89 (dd, 6H).
Example FO
##STR00242##
[0644] methyl
[(2S,3R)-1-{(2S,4S)-4-[(difluoromethoxy)methyl]-2-[9-(2-{(2S,5S)-1-[N-(me-
thoxycarbonyl)-L-valyl]-5-methylpyrrolidin-2-yl}-1H-imidazol-5-yl)-1,11-di-
hydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]pyrrolidin-1-yl}-3--
methoxy-1-oxobutan-2-yl]carbamate
[0645] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpy-
rrolidine-2-carboxylic acid, and substituting
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid with
(2S,4S)-1-(tert-butoxycarbonyl)-4-((difluoromethoxy)methyl)pyrrolidine-2--
carboxylic acid. (0.079g) LCMS-ESI.sup.+: calculated for
C.sub.46H.sub.54F.sub.2N.sub.8O.sub.9: 900.40; observed
[M+1].sup.+: 901.78. .sup.1H NMR (400 MHz, cd.sub.3od) .delta. 8.61
(s, 1H), 8.17 (d, 1H), 8.06-7.95 (m, 2H), 7.89 (d, 1H), 7.84-7.75
(m, 1H), 7.71-7.57 (m, 2H), 6.47 (t, 2H), 5.50-5.39 (m, 1H), 5.30
(s, 2H), 5.22-5.12 (m, 1H), 4.83-4.75 (m, 1H), 4.52 (d, 1H),
4.42-4.24 (m, 2H), 4.19-4.03 (m, 3H), 3.86-3.72 (m, 2H), 3.68 (s,
4H), 3.28 (s, 2H), 2.98-2.85 (m, 2H), 2.82-2.72 (m, 1H), 2.71-2.65
(m, 1H), 2.59-2.48 (m, 1H), 2.44-2.14 (m, 4H), 2.08-1.94 (m, 2H),
1.56 (d, 2H), 1.30 (d, 1H), 1.12 (d, 2H), 1.06 (dd, 2H), 0.99 (d,
2H), 0.89 (d, 2H).
Example FP
##STR00243##
[0646] methyl
[(2S)-1-{(2S,4S)-2-[9-(2-{(2S,5S)-1-[(2S)-2-[(methoxycarbonyl)amino]-2-(t-
etrahydro-2H-pyran-4-yl)acetyl]-5-methylpyrrolidin-2-yl}-1H-imidazol-5-yl)-
-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]-4-methylpy-
rrolidin-1-yl}-3-methyl-1-oxobutan-2-yl]carbamate
[0647] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-2-(tetrahydro-2H-pyran-4-yl)-
acetyl)-5-methylpyrrolidine-2-carboxylic acid, and substituting
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid with
(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidine-2-carboxylic
acid, and substituting
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid with
(S)-2-(methoxycarbonylamino)-3-methylbutanoic acid. (0.005g)
LCMS-ESI.sup.+: calculated for C.sub.47H.sub.56N.sub.8O.sub.8:
860.42; observed [M+1].sup.+: 861.90. .sup.1H NMR (400 MHz,
cd.sub.3od) .delta. 8.62 (s, 1H), 8.18 (d, 1H), 8.06-7.93 (m, 1H),
7.90-7.73 (m, 3H), 7.68-7.58 (m, 2H), 5.40-5.26 (m, 2H), 5.18-5.09
(m, 1H), 4.44-4.33 (m, 1H), 4.31-4.15 (m, 3H), 4.04-3.83 (m, 3H),
3.79-3.60 (m, 6H), 3.56-3.42 (m, 2H), 2.80-2.45 (m, 5H), 2.42-2.19
(m, 3H), 2.08-1.86 (m, 4H), 1.74 (d, 2H), 1.55 (d, 3H), 1.48-1.33
(m, 3H), 1.30-1.17 (m, 4H), 1.05-0.75 (m, 7H).
Example FQ
##STR00244##
[0648] methyl
[(1S)-2-[(2S,5S)-2-(5-{2-[(2S,5S)-1-{(2S,3S)-2-[(methoxycarbonyl)amino]-3-
-methylpentanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6-
,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-5-methylpyrrolidin-1-yl]-
-2-oxo-1-(tetrahydro-2H-pyran-4-yl)ethyl]carbamate
[0649] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid with (2S,5S)-1-((2S,3
S)-2-(methoxycarbonylamino)-3-methylpentanoyl)-5-methylpyrrolidine-2-carb-
oxylic acid, and substituting
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid with
(S)-2-(methoxycarbonylamino)-2-(tetrahydro-2H-pyran-4-yl)acetic
acid. (0.094g) LCMS-ESI.sup.+: calculated for
C.sub.48H.sub.58N.sub.8O.sub.8: 874.44; observed [M+1].sup.+:
875.81. .sup.1H NMR (400 MHz, cd.sub.3od) .delta. 8.39 (t, 1H),
8.21-7.24 (m, 8H), 5.71-5.33 (m, 2H), 5.30-5.01 (m, 3H), 4.85-4.70
(m, 2H), 4.45-4.13 (m, 3H), 4.06-3.71 (m, 4H), 3.67 (s, 4H),
3.51-3.38 (m, 1H), 3.26-3.18 (m, 1H), 3.08-2.94 (m, 1H), 2.91-2.55
(m, 2H), 2.53-2.07 (m, 5H), 2.05-1.88 (m, 2H), 1.87-1.66 (m, 3H),
1.56 (dd, 5H), 1.43-1.22 (m, 3H), 1.19-1.08 (m, 2H), 1.06-0.92 (m,
3H), 0.90-0.72 (m, 3H).
Example FR
##STR00245##
[0650] methyl
[(1S)-2-[(2S,5S)-2-(5-{2-[(2S,5S)-1-{(2S,3R)-3-methoxy-2-[(methoxycarbony-
l)amino]butanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6-
,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-5-methylpyrrolidin-1-yl]-
-2-oxo-1-(tetrahydro-2H-pyran-4-yl)ethyl]carbamate
[0651] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid with
(2S,5S)-1-((2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoyl)-5-methylpy-
rrolidine-2-carboxylic acid, and substituting
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid with
(S)-2-(methoxycarbonylamino)-2-(tetrahydro-2H-pyran-4-yl)acetic
acid. (0.089g) LCMS-ESI.sup.+: calculated for
C.sub.47H.sub.56N.sub.8O.sub.9: 876.42; observed [M+1].sup.+:
877.81. .sup.1H NMR (400 MHz, cd.sub.3od) .delta. 8.52-8.28 (m,
1H), 8.21-7.82 (m, 3H), 7.81-7.28 (m, 6H), 5.88-5.67 (m, 1H),
5.51-5.02 (m, 4H), 4.82-4.71 (m, 1H), 4.69-4.58 (m, 1H), 4.55-4.33
(m, 2H), 4.31-4.13 (m, 2H), 4.04-3.77 (m, 4H), 3.75-3.54 (m, 5H),
3.40 (s, 2H), 3.28-3.21 (m, 1H), 2.98-2.67 (m, 2H), 2.64-2.44 (m,
2H), 2.40-2.09 (m, 4H), 2.06-1.87 (m, 2H), 1.84-1.70 (m, 1H), 1.56
(dd, 5H), 1.43-1.00 (m, 8H).
Example FS
##STR00246##
[0652] methyl
{(2S,3S)-1-[(2S,5S)-2-(9-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-
-methylbutanoyl}-4-(methoxymethyl)pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11--
dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolid-
in-1-yl]-3-methyl-1-oxopentan-2-yl}carbamate
[0653] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with
(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrrolidine-2-carbo-
xylic acid, and substituting
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid with
(2S,5S)-1-((2S,3S)-2-(methoxycarbonylamino)-3-methylpentanoyl)-5-methylpy-
rrolidine-2-carboxylic acid, and substituting
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid with
(S)-2-(methoxycarbonylamino)-3-methylbutanoic acid. (0.119g)
LCMS-ESI.sup.+: calculated for C.sub.47H.sub.58N.sub.8O.sub.8:
862.44; observed [M+1].sup.+: 863.87. .sup.1H NMR (400 MHz,
cd.sub.3od) .delta. 8.60 (s, 1H), 8.31-8.13 (m, 2H), 8.00 (d, 1H),
7.90 (d, 2H), 7.83-7.78 (m, 1H), 7.70-7.60 (m, 2H), 5.38-5.15 (m,
4H), 4.41-4.15 (m, 4H), 3.78 (s, 1H), 3.72-3.48 (m, 7H), 3.41 (s,
3H), 2.92-2.72 (m, 2H), 2.69-2.55 (m, 2H), 2.52-2.29 (m, 3H),
2.13-1.96 (m, 3H), 1.91-1.69 (m, 2H), 1.64 (d, 3H), 1.32-1.13 (m,
3H), 1.07-0.75 (m, 12H).
Example FT
##STR00247##
[0654] methyl
{(2S,3S)-1-[(2S,4S)-2-(5-{2-[(2S,5S)-1-{(2S,3R)-3-methoxy-2-[(methoxycarb-
onyl)amino]butanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3-
':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)pyrr-
olidin-1-yl]-3-methyl-1-oxopentan-2-yl}carbamate
[0655] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with
(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrrolidine-2-carbo-
xylic acid, and substituting
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid with
(2S,5S)-1-((2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoyl)-5-methylpy-
rrolidine-2-carboxylic acid, and substituting
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid with
(2S,3S)-2-(methoxycarbonylamino)-3-methylpentanoic acid. (0.118g)
LCMS-ESI.sup.+: calculated for C.sub.47H.sub.58N.sub.8O.sub.9:
878.43; observed [M+1].sup.+: 879.86. .sup.1H NMR (400 MHz,
cd.sub.3od) .delta. 8.52 (s, 1H), 8.23-8.07 (m, 1H), 7.99-7.72 (m,
2H), 7.68-7.55 (m, 1H), 5.30-5.24 (m, 1H), 4.81 (s, 8H), 4.61-4.18
(m, 3H), 4.14-4.00 (m, 6H), 3.95-3.76 (m, 1H), 3.72-3.47 (m, 3H),
3.37 (d, 1H), 3.33 (s, 3H), 3.29 (s, 2H), 3.26 (s, 1H), 2.86-2.68
(m, 1H), 2.66-2.54 (m, 1H), 2.50-2.27 (m, 2H), 2.11-2.03 (m, 1H),
1.99 (s, 9H), 1.80-1.69 (m, 1H), 1.57 (d, 1H), 1.49-1.33 (m, 1H),
1.21 (t, 10H), 1.16-1.02 (m, 2H), 0.92-0.78 (m, 2H).
Example FU
##STR00248##
[0656] methyl
{(2S)-1-[(2S,5S)-2-(5-{2-[(2S,4S)-1-{(2S,3S)-3-methoxy-2-[(methoxycarbony-
l)amino]butanoyl}-4-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6-
,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-5-methylpyrrolidin-1-yl]-
-3-methyl-1-oxobutan-2-yl}carbamate
[0657] was synthesized in a similar manner as Example DX
substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpy-
rrolidine-2-carboxylic acid, and substituting
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid with
(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidine-2-carboxylic
acid, and substituting
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid with
(2S,3S)-3-methoxy-2-(methoxycarbonylamino)butanoic acid. (0.065g)
LCMS-ESI.sup.+: calculated for C.sub.45H.sub.54N.sub.8O.sub.8:
834.41; observed [M+1].sup.+: 835.89. .sup.1H NMR (400 MHz,
cd.sub.3od) .delta. 8.62 (s, 1H), 8.16 (d, 1H), 8.09-7.92 (m, 2H),
7.91-7.86 (m, 1H), 7.84-7.76 (m, 1H), 7.69-7.58 (m, 2H), 5.41-5.27
(m, 3H), 5.21-5.13 (m, 1H), 4.80 (t, 1H), 4.49-4.35 (m, 2H),
4.33-4.21 (m, 1H), 4.19-4.06 (m, 1H), 3.72 (s, 1H), 3.66 (s, 4H),
3.55 (t, 1H), 3.49-3.41 (m, 1H), 3.38-3.33 (m, 1H), 3.24-3.14 (m,
1H), 3.10 (s, 2H), 2.81-2.70 (m, 1H), 2.66-2.46 (m, 2H), 2.44-2.23
(m, 3H), 2.08-1.88 (m, 3H), 1.55 (d, 2H), 1.27 (d, 3H), 1.22-1.17
(m, 1H), 1.14 (d, 2H), 1.07 (d, 1H), 1.02 (d, 1H), 0.98 (d, 2H),
0.87 (d, 2H).
Example FV
##STR00249##
[0658] methyl
{(1R)-2-[(2S,4S)-2-(4-bromo-5-{2-[(2S,5S)-1-{(2S)-2-(methoxycarbonyl)amin-
o]-3-methylbutanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3-
':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)pyrr-
olidin-1-yl]-2-oxo-1-phenylethyl}carbamate
[0659] To a solution of methyl {(2S,3
S)-1-[(2S,5S)-2-(9-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-methy-
lbutanoyl}-4-(methoxymethyl)pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihydr-
oisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidin-1-y-
l]-3-methyl-1-oxobutan-2-yl}carbamate (0.06 g, 0.07 mmol) in AcOH
(1.0 mL) was added bromine (0.004 mL, 0.08 mmol) in AcOH (0.4 mL).
The solution was stirred at room temperature for 1 h and
concentrated in vacuo. The crude oil was purified by reverse phase
HPLC (Gemini, 10.fwdarw.65% MeCN/H.sub.2O (0.1% TFA)). The desired
fractions were combined, basified with aqueous sodium bicarbonate,
and extracted with CH.sub.2Cl.sub.2. The combined organic layers
were dried over Na.sub.2SO.sub.4 and concentrated in vacuo to
afford methyl
{(1R)-2-[(2S,4S)-2-(4-bromo-5-{2-[(2S,5S)-1-{(2S)-2-[(methoxycarbonyl)ami-
no]-3-methylbutanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',-
3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)pyr-
rolidin-1-yl]-2-oxo-1-phenylethyl}carbamate (0.04 g, 54%).
LCMS-ESI.sup.+: calc'd for C.sub.46H.sub.55BrN.sub.8O.sub.8: 926.33
(M.sup.+); Found: 927.17 (M+H.sup.+).
methyl
{(1R)-2-[(2S,4S)-2-(4-cyclopropyl-5-{2-[(2S,5S)-1-{(2S)-2-[(methoxy-
carbonyl)amino]-3-methylbutanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroiso-
chromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(metho-
xymethyl)pyrrolidin-1-yl]-2-oxo-1-phenylethyl}carbamate
[0660] To a solution of methyl
{(1R)-2-[(2S,4S)-2-(4-bromo-5-{2-[(2S,5S)-1-{(2S)-2-[(methoxycarbonyl)ami-
no]-3-methylbutanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',-
3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)pyr-
rolidin-1-yl]-2-oxo-1-phenylethyl}carbamate (0.04 g, 0.036 mmol) in
toluene (0.75 mL) was added c-propylboronic acid (0.006 g, 0.08
mmol), palladium acetate (0.005 g, 0.007 mmol),
tricyclohexylphosphine tetrafluoroborate (0.005 g, 0.014 mmol), and
potassium phosphate (aqueous, 2 M, 0.075 mL, 0.15 mmol). The
solution was degassed with argon for 5 minutes and heated to
100.degree. C. (external, oil bath) for 20 h. The solution was
cooled to room temperature, diluted with CH.sub.2Cl.sub.2, and
washed with water. The aqueous layer was back extracted with
CH.sub.2Cl.sub.2/MeOH (2.times.). The combined organic layers were
dried over Na.sub.2SO.sub.4 and concentrated in vacuo. The crude
oil was purified by reverse phase HPLC (Gemini, 10.fwdarw.50%
MeCN/H.sub.2O (0.1% TFA)). The desired fractions were combined and
concentrated under reduced pressure to remove volatile organics.
The addition of aqueous sodium bicarbonate with stirring resulted
in precipitation of a white solid. The precipitate was filtered
through a membrane filter and washed with water. Drying under
reduced pressure afforded methyl
{(1R)-2-[(2S,4S)-2-(4-cyclopropyl-5-{2-[(2S,5S)-1-{(2S)-2-[(methoxycarbon-
yl)amino]-3-methylbutanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroisochrome-
no[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymeth-
yl)pyrrolidin-1-yl]-2-oxo-1-phenylethyl}carbamate (0.01 g, 42%).
LCMS-ESI.sup.+: calc'd for C.sub.49H.sub.60N.sub.8O.sub.8: 888.45
(M.sup.+); Found: 889.86 (M+H.sup.+). .sup.1H NMR (400 MHz, cd3od)
.delta. (Mixture of rotomers) 8.38 (d, 1H), 8.01 (d, 1H), 7.85 (d,
2H), 7.73-7.60 (m, 2H), 7.53-7.42 (m, 1H), 5.33-5.16 (m, 3H),
4.38-4.27 (m, 1H), 4.26-4.14 (m, 2H), 4.14-4.00 (m, 2H), 3.69 (s,
3H), 3.63 (s, 3H), 3.60-3.51 (m, 2H), 3.38 (s, 3H), 2.85-2.65 (m,
2H), 2.65-2.47 (m, 2H), 2.37-2.16 (m, 2H), 2.16-1.91 (m, 5H), 1.48
(d, 3H), 1.18 (d, 2H), 1.09-0.94 (m, 5H), 0.91 (d, 3H), 0.89-0.84
(m, 2H), 0.82 (d, 3H), 0.65 (s, 1H).
Example FW
##STR00250##
[0661] methyl
{(2S,3R)-3-methoxy-1-[(2S,4S)-2-(9-{2-[(2S,4S)-1-[N-(methoxycarbonyl)-O-m-
ethyl-L-threonyl]-4-(methoxymethyl)pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-
-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-methylpyrroli-
din-1-yl]-1-oxobutan-2-yl}carbamate
[0662] Following Example DX, substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with
(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrrolidine-2-carbo-
xylic acid,
(1R,3S)-2-(2-(methoxycarbonylamino)-3-methylbutanoyl)-3-methylcyclopen
tanecarboxylic acid with
(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidine-2-carboxylic
acid, and using 2 equivalents of
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid, provided
methyl
{(2S,3R)-3-methoxy-1-[(2S,4S)-2-(9-{2-[(2S,4S)-1-[N-(methoxycarbonyl)-O-m-
ethyl-L-threonyl]-4-(methoxymethyl)pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-
-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-4-methylpyrroli-
din-1-yl]-1-oxobutan-2-yl}carbamate (0.08 g). LCMS-ESI.sup.+:
calc'd for C.sub.46H.sub.56N.sub.8O.sub.10: 880.41 (M.sup.+);
Found: 882.11 (M+H.sup.+). .sup.1H NMR (400 MHz, cd.sub.3od)
.delta. (Mixture of rotomers) 8.21 (d, 1H), 7.91-7.72 (m, 2H),
7.70-7.33 (m, 4H), 7.33-7.11 (m, 2H), 5.24-5.13 (m, 1H), 5.13-4.91
(m, 3H), 4.45-4.29 (m, 2H), 4.26-3.97 (m, 3H), 3.57 (s, 6H),
3.50-3.37 (m, 3H), 3.28 (s, 3H), 3.19-3.10 (m, 7H), 2.62-2.45 (m,
2H), 2.45-2.30 (m, 2H), 2.09-1.74 (m, 4H), 1.14 (d, 3H), 1.11-0.97
(m, 6H).
Example FX
##STR00251##
[0663] methyl
{(2S,3R)-3-methoxy-1-[(2S,5S)-2-(9-{2-[(2S,4S)-1-[N-(methoxycarbonyl)-O-m-
ethyl-L-threonyl]-4-(methoxymethyl)pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-
-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrroli-
din-1-yl]-1-oxobutan-2-yl}carbamate
[0664] Following Example DX, substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with
(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrrolidine-2-carbo-
xylic acid,
(1R,3S)-2-(2-(methoxycarbonylamino)-3-methylbutanoyl)-3-methylcyclopen
tanecarboxylic acid with
(2S,4S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid, and using 2 equivalents of
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid, provided
methyl
{(2S,3R)-3-methoxy-1-[(2S,5S)-2-(9-{2-[(2S,4S)-1-[N-(methoxycarbonyl)-O-m-
ethyl-L-threonyl]-4-(methoxymethyl)pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-
-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrroli-
din-1-yl]-1-oxobutan-2-yl}carbamate (0.14 g). LCMS-ESI.sup.+:
calc'd for C.sub.46H.sub.56N.sub.8O.sub.10: 880.41 (M.sup.+);
Found: 881.85 (M+H.sup.+). .sup.1H NMR (400 MHz, cd.sub.3od)
.delta. (mixture of rotomers) 8.40-8.22 (m, 2H), 8.07-7.84 (m, 2H),
7.83-7.25 (m, 6H), 5.75 (s, 1H), 5.29-5.07 (m, 4H), 4.42 (d, 2H),
4.32-4.12 (m, 2H), 3.86 (s, 1H), 3.75-3.44 (m, 9H), 3.41-3.32 (m,
4H), 3.26-3.19 (m, 4H), 2.72-2.35 (m, 4H), 2.35-1.87 (m, 5H), 1.55
(d, 3H), 1.23 (s, 2H), 1.13 (d, 5H).
Example FY
##STR00252##
[0665] tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-4-chloroimidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
[0666] To a solution of tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate (0.1 g,
0.12 mmol) in DMF (1 mL) was added N-chlorosuccinimide (0.02 g,
0.16 mmol). The resulting solution was stirred at room temperature
for 1 h, and then heated to 45.degree. C. for 4 h. The solution was
purified by reverse phase HPLC (Gemini, 10.fwdarw.68% MeCN/H.sub.2O
(0.1% TFA)). The desired fractions were diluted with EtOAc and
washed with a 1:1 mixture of aqueous sodium bicarbonate and brine.
The aqueous layers were backextracted with EtOAc (2.times.). The
combined organic layers were dried over Na.sub.2SO.sub.4 and
concentrated in vacuo to provide tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-4-chloroimidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
(0.09 g, 87%). LCMS-ESI.sup.+: calc'd for
C.sub.44H.sub.52ClN.sub.7O.sub.7: 825.36 (M.sup.+); Found: 827.13
(M+H.sup.+).
methyl
{(1R)-2-[(2S,4S)-2-(4-chloro-5-{2-[(2S,5S)-1-{(2S)-2-[(methoxycarbo-
nyl)amino]-3-methylbutanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroisochrom-
eno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymet-
hyl)pyrrolidin-1-yl]-2-oxo-1-phenylethyl}carbamate
[0667] To a solution of tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-4-chloroimidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
(0.09g, 0.11 mmol) in a mixture of CH.sub.2Cl.sub.2 (1.5 mL) and
methanol (0.25 mL) was added HCl (in dioxanes, 4M, 0.8 mL, 3.20
mmol). The resulting solution was stirred at 40.degree. C. for 1 h,
and concentrated in vacuo. The resulting solid was slurried in
CH.sub.2Cl.sub.2 (1.5 mL), and
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid (0.04 g, 0.17
mmol) and diisopropylethylamine (0.07 mL, 0.40 mmol) were added.
The reaction was cooled to -40.degree. C. (MeCN/CO.sub.2 bath) and
COMU (0.07 g, 0.18 mmol) was added. The resulting solution was
allowed to warm to room temperature over 30 min, and stirred at
room temperature for 1.5 h. The reaction was diluted with
CH.sub.2Cl.sub.2 and washed with aqueous sodium bicarbonate. The
aqueous layer was backextracted with CH.sub.2Cl.sub.2, and the
combined organic layers were dried (Na.sub.2SO.sub.4) and
concentrated. The crude oil was purified by reverse phase HPLC
(Gemini, 10.fwdarw.58% MeCN/H.sub.2O (0.1% TFA)). The desired
fractions were diluted with EtOAc and washed with brine. The
aqueous layer was backextracted with EtOAc (2.times.). The combined
organic layers were dried over Na.sub.2SO.sub.4 and concentrated in
vacuo. The resulting material was lyophilized from MeCN and water
to provide methyl
{(1R)-2-[(2S,4S)-2-(4-chloro-5-{2-[(2S,5S)-1-{(2S)-2-[(methoxycarbonyl)am-
ino]-3-methylbutanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4'-
,3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)py-
rrolidin-1-yl]-2-oxo-1-phenylethyl}carbamate (0.09 g, 90%).
LCMS-ESI.sup.+: calc'd for C.sub.49H.sub.53ClN.sub.8O.sub.8: 916.37
(M.sup.+); Found: 918.28 (M+H.sup.+). .sup.1H NMR (400 MHz,
cd.sub.3od) .delta. (Mixture of rotomers) 8.43 (s, 1H), 8.18-7.94
(m, 2H), 7.90-7.78 (m, 1H), 7.77-7.55 (m, 3H), 7.53-7.29 (m, 4H),
7.13-6.95 (m, 1H), 5.49-5.30 (m, 2H), 5.31-5.13 (m, 2H), 5.12-5.00
(m, 1H), 4.40-4.08 (m, 3H), 3.89 (s, 1H), 3.72-3.61 (m, 3H), 3.58
(s, 2H), 3.26 (s, 3H), 2.57 (s, 2H), 2.50-2.00 (m, 7H), 2.00-1.84
(m, 3H), 1.56 (d, 3H), 1.10 (d, 2H), 1.07-0.73 (m, 7H).
Example FZ
##STR00253##
[0668] tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-4-bromoimidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
[0669] To a solution of tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate (0.3 g,
0.38 mmol) in DMF (3.8 mL) at 0.degree. C. was added
N-bromosuccinimide (0.067 g, 0.38 mmol). The resulting solution was
stirred at 0.degree. C. for 1 h. The solution was purified by
reverse phase HPLC (Gemini, 10.fwdarw.65% MeCN/H.sub.2O (0.1%
TFA)). The desired fractions were diluted with EtOAc and washed
with a 1:1 mixture of aqueous sodium bicarbonate and brine. The
aqueous layers were backextracted with EtOAc (2.times.). The
combined organic layers were dried over Na.sub.2SO.sub.4 and
concentrated in vacuo to provide tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-4-bromoimidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
(0.33 g, 99%). LCMS-ESI.sup.+: calc'd for
C.sub.44H.sub.52BrN.sub.7O.sub.7: 869.31 (M.sup.+); Found: 871.61
(M+H.sup.+).
tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-meth-
ylpyrrolidin-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazo-
l-9-yl)-1H-4-cyclopropyl-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-car-
boxylate
[0670] To a solution of tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-4-bromoimidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
(0.20 g, 0.23 mmol) in toluene (2.5 mL) was added
cyclopropylboronic acid (0.04 g, 0.47 mmol), Pd(OAc).sub.2 (0.03 g,
0.05 mmol), tricyclohexylphosphine tetrafluoroborate (0.04 g, 0.12
mmol), and potassium phosphate (aqueous, 2M, 0.40 mL, 0.80 mmol).
The slurry was degassed with argon for 5 min and heated to
100.degree. C. (external, oil bath) for 20 h. The reaction was
cooled to room temperature, diluted with EtOAc, and filtered
through celite. The filtrate was concentrated and purified by
column chromatography (SiO.sub.2, 0 to 30% MeOH/EtOAc) to provide
tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-4-cyclopropyl-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
(0.13 g, 67%). LCMS-ESI.sup.+: calc'd for
C.sub.47H.sub.57N.sub.7O.sub.7: 831.43 (M.sup.+); Found: 832.62
(M+H.sup.+).
methyl
{(1R)-2-[(2S,4S)-2-(4-cyclopropyl-5-{2-[(2S,5S)-1-{(2S)-2-[(methoxy-
carbonyl)amino]-3-methylbutanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroiso-
chromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(metho-
xymethyl)pyrrolidin-1-yl]-2-oxo-1-phenylethyl}carbamate
[0671] To a solution of tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-4-cyclopropyl-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate
(0.13 g, 0.15 mmol) in a mixture of CH.sub.2Cl.sub.2 (3.0 mL) and
methanol (0.25 mL) was added HCl (in dioxanes, 4M, 1.1 mL, 4.40
mmol). The resulting solution was stirred at 40.degree. C. for 1 h,
and concentrated in vacuo. The resulting solid was slurried in
CH.sub.2Cl.sub.2 (3.0 mL), and
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid (0.05 g, 0.23
mmol) and diisopropylethylamine (0.1 mL, 0.57 mmol) were added. The
reaction was cooled to -40.degree. C. (MeCN/CO.sub.2 bath) and COMU
(0.11 g, 0.25 mmol) was added. The resulting solution was allowed
to warm to room temperature over 30 min, and stirred at room
temperature for 1.5 h. The reaction was diluted with
CH.sub.2Cl.sub.2 and washed with aqueous sodium bicarbonate. The
aqueous layer was backextracted with CH.sub.2Cl.sub.2, and the
combined organic layers were dried (Na.sub.2SO.sub.4) and
concentrated. The crude oil was purified by reverse phase HPLC
(Gemini, 10.fwdarw.58% MeCN/H.sub.2O (0.1% TFA)). The desired
fractions were combined with MeOH and concentrated to remove
volitiles. The resulting solution was basified with aqueous sodium
bicarbonate (sat.). The resulting slurry was stirred at room
temperature for 30 min, filtered (nylon membrane filter (0.45 um)),
and washed with water. The solid was dried in vacuo to provide
methyl
{(1R)-2-[(2S,4S)-2-(4-cyclopropyl-5-{2-[(2S,5S)-1-{(2S)-2-[(methoxycarbon-
yl)amino]-3-methylbutanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroisochrome-
no[4',3':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymeth-
yl)pyrrolidin-1-yl]-2-oxo-1-phenylethyl}carbamate (0.05 g, 38%).
LCMS-ESI.sup.+: calc'd for C.sub.52H.sub.58N.sub.8O.sub.8: 922.44
(M.sup.+); Found: 923.69 (M+H.sup.+).
[0672] .sup.1H NMR (400 MHz, cd.sub.3od) .delta. (Mixture of
rotomers) 8.28 (s, 2H), 7.93 (s, 2H), 7.74-7.52 (m, 3H), 7.52-7.32
(m, 3H), 7.27-7.07 (m, 4H), 5.48-5.38 (m, 2H), 4.10-3.98 (m, 2H),
3.67-3.48 (m, 4H), 3.42-3.34 (m, 6H), 3.06 (s, 3H), 2.43-2.16 (m,
4H), 2.16-1.61 (m, 8H), 1.55-1.32 (m, 3H), 1.02-0.50 (m, 11H).
Example GA
##STR00254##
[0673] methyl
[(2S)-1-{(2S,4S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-O-methyl-L-threo-
nyl]-5-methylpyrrolidin-2-yl}-1H-imidazol-5-yl)-1,1-dihydroisochromeno[4',-
3':6,7]naphtho[1,2-d]imidazol-2-yl]-4-methylpyrrolidin-1-yl}-3-methyl-1-ox-
obutan-2-yl]carbamate
[0674] Following Example DX, substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with
(2S,5S)-1-((2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoyl)-5-met-
hylpyrrolidine-2-carboxylic acid,
(1R,3S)-2-(2-(methoxycarbonylamino)-3-methylbutanoyl)-3-methylcyclopen
tanecarboxylic acid with
(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidine-2-carboxylic
acid, and (2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid
with (S)-2-(methoxycarbonylamino)-3-methylbutanoic acid, provided
methyl
[(2S)-1-{(2S,4S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-O-methyl-L-threo-
nyl]-5-methylpyrrolidin-2-yl}-1H-imidazol-5-yl)-1,11-dihydroisochromeno[4'-
,3':6,7]naphtho[1,2-d]imidazol-2-yl]-4-methylpyrrolidin-1-yl}-3-methyl-1-o-
xobutan-2-yl]carbamate (0.12 g). LCMS-ESI.sup.+: calc'd for
C.sub.45H.sub.54N.sub.8O.sub.8: 834.41 (M.sup.+); Found: 835.47
(M+H.sup.+). .sup.1H NMR (400 MHz, cd.sub.3od) .delta. (Mixture of
rotomers) 8.29 (s, 2H), 8.02-7.71 (m, 3H), 7.71-7.20 (m, 5H), 5.52
(s, 1H), 5.31-4.98 (m, 4H), 4.74-4.62 (m, 1H), 4.56-4.04 (m, 5H),
3.74 (s, 1H), 3.65 (s, 2H), 3.63 (s, 2H), 3.59-3.44 (m, 2H), 3.35
(s, 2H), 2.65-2.28 (m, 4H), 2.27-1.82 (m, 5H), 1.53-1.44 (m, 2H),
1.26 (s, 1H), 1.21 (d, 3H), 1.18-1.06 (m, 3H), 1.03-0.77 (m,
6H).
Example GB
##STR00255##
[0675] tert-butyl
(2S,4S)-2-(9-{2-[(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidin-2-yl]-
-1H-imidazol-5-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]-
imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate
[0676] Following Example DX, substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid and
(1R,3S)-2-(2-(methoxycarbonylamino)-3-methylbutanoyl)-3-methylcyclopen
tanecarboxylic acid with
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid, and omitting the final step, provided tert-butyl
(2S,4S)-2-(9-{2-[(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidin-2-yl]-
-1H-imidazol-5-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]-
imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate (0.83 g).
LCMS-ESI.sup.+: calc'd for C.sub.41H.sub.48N.sub.6O.sub.5: 704.37
(M.sup.+); Found: 705.52 (M+H.sup.+).
tert-butyl
(2S,4S)-2-(9-{2-[(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrol-
idin-2-yl]-1H-4-chloroimidazol-5-yl}-1,4,5,11-tetrahydroisochromeno[4',3':-
6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate
[0677] To a solution of tert-butyl
(2S,4S)-2-(9-{2-[(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidin-2-yl]-
-1H-imidazol-5-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]-
imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate (0.15 g, 0.21
mmol) in DMF (2.2 mL) was added N-chlorosuccinimide (0.04 g, 0.28
mmol). The resulting solution was heated to 45.degree. C. for 3 h.
The solution cooled to room temperature, diluted with EtOAc, and
washed with aqueous LiCl (5%, 2.times.). The aqueous layers were
backextracted with EtOAc. The combined organic layers were dried
over (Na.sub.2SO.sub.4) an concentrated in vacuo. The crude oil was
purified by column chromatography (SiO.sub.2, 50 to 100% EtOAc (5%
MeOH)/Hexanes) to provide tert-butyl
(2S,4S)-2-(9-{2-[(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidin-2-yl]-
-1H-4-chloroimidazol-5-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphth-
o[1,2-d]imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate (0.13 g,
86%). LCMS-ESI.sup.+: calc'd for C.sub.41H.sub.47ClN.sub.6O.sub.5:
738.33 (M.sup.+); Found: 739.84 (M+H.sup.+).
methyl
[(2S,3R)-1-{(2S,5S)-2-[9-(4-chloro-2-{(2S,5S)-1-[N-(methoxycarbonyl-
)-O-methyl-L-threonyl]-5-methylpyrrolidin-2-yl}-1H-imidazol-5-yl)-1,11-dih-
ydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]-5-methylpyrrolidin--
1-yl}-3-methoxy-1-oxobutan-2-yl]carbamate
[0678] To a solution of tert-butyl
(2S,4S)-2-(9-{2-[(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidin-2-yl]-
-1H-4-chloroimidazol-5-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphth-
o[1,2-d]imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate (0.14 g,
0.19 mmol) in a mixture of CH.sub.2Cl.sub.2 (2.0 mL) and methanol
(0.5 mL) was added HCl (in dioxanes, 4M, 1.3 mL, 5.20 mmol). The
resulting solution was stirred at 40.degree. C. for 1 h, and
concentrated in vacuo. The resulting solid was slurried in
CH.sub.2Cl.sub.2 (2.0 mL), and
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid (0.04 g,
0.23 mmol), HATU (0.08 g, 0.22 mmol), and diisopropylethylamine
(0.1 mL, 0.57 mmol) were added. The resulting solution was stirred
at room temperature over 2 h. The reaction was diluted with DMF and
concentrated. The crude oil was purified by reverse phase HPLC
(Gemini, 10.fwdarw.60% MeCN/H.sub.2O (0.1% TFA)). The desired
fractions were combined with MeOH and concentrated to remove
volitiles. The resulting solution was basified with aqueous sodium
bicarbonate (sat.). The resulting slurry was stirred at room
temperature for 30 min, filtered (nylon membrane filter (0.45 um)),
and washed with water. The solid was dried in vacuo to provide
methyl
[(2S,3R)-1-{(2S,5S)-2-[9-(4-chloro-2-{(2S,5S)-1-[N-(methoxycarbony-
l)-O-methyl-L-threonyl]-5-methylpyrrolidin-2-yl}-1H-imidazol-5-yl)-1,11-di-
hydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]-5-methylpyrrolidin-
-1-yl}-3-methoxy-1-oxobutan-2-yl]carbamate (0.05 g, 62%).
LCMS-ESI.sup.+: calc'd for C.sub.45H.sub.53ClN.sub.8O.sub.9: 884.36
(M.sup.+); Found: 886.33 (M+H.sup.+). .sup.1H NMR (400 MHz,
cd.sub.3od) .delta. (Mixture of rotomers) 8.35 (s, 1H), 8.10-7.87
(m, 2H), 7.88-7.82 (m, 1H), 7.77-7.57 (m, 2H), 7.57-7.45 (m, 1H),
5.77-5.63 (m, 1H), 5.51-5.42 (m, 1H), 5.24-5.06 (m, 2H), 4.98-4.86
(m, 1H), 4.70-4.51 (m, 2H), 4.43 (d, 1H), 4.24 (d, 1H), 4.21-4.06
(m, 2H), 3.81 (s, 1H), 3.63 (s, 2H), 3.58 (s, 2H), 3.57 (s, 2H),
3.48 (s, 2H), 3.32-3.27 (m, 3H), 2.90-2.77 (m, 1H), 2.60 (s, 2H),
2.27 (d, 6H), 1.84 (s, 1H), 1.48 (d, 2H), 1.42 (d, 2H), 1.29-0.89
(m, J=31.3, 29.3, 19.7 Hz, 9H).
Example GC
##STR00256##
[0679] tert-butyl
(2S,4S)-2-(9-{2-[(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidin-2-yl]-
-1H-4-cyclopropyl-imidazol-5-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]-
naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate
[0680] Following Example FZ, substituting tert-butyl
(2S,4S)-2-[5-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-L-valyl]-5-methylpyrrolid-
in-2-yl}-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-
-imidazol-2-yl]-4-(methoxymethyl)pyrrolidine-1-carboxylate with
tert-butyl
(2S,4S)-2-(9-{2-[(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidin-2-yl]-
-1H-imidazol-5-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphtho[1,2-d]-
imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate, provided
tert-butyl
(2S,4S)-2-(9-{2-[(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidin-2-yl]-
-1H-4-cyclopropyl-imidazol-5-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]-
naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate
(0.27 g). LCMS-ESI.sup.+: calc'd for
C.sub.44H.sub.52N.sub.6O.sub.5: 744.40 (M.sup.+); Found: 745.46
(M+H.sup.+).
methyl
[(2S,3R)-1-{(2S,5S)-2-[9-(4-cyclopropyl-2-{(2S,5S)-1-[N-(methoxycar-
bonyl)-O-methyl-L-threonyl]-5-methylpyrrolidin-2-yl}-1H-imidazol-5-yl)-1,1-
1-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]-5-methylpyrrol-
idin-1-yl}-3-methoxy-1-oxobutan-2-yl]carbamate
[0681] To a solution of tert-butyl
(2S,4S)-2-(9-{2-[(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidin-2-yl]-
-1H-4-chloroimidazol-5-yl}-1,4,5,11-tetrahydroisochromeno[4',3':6,7]naphth-
o[1,2-d]imidazol-2-yl)-5-methylpyrrolidine-1-carboxylate (0.27 g,
0.36 mmol) in a mixture of CH.sub.2Cl.sub.2 (3.5 mL) and methanol
(0.5 mL) was added HCl (in dioxanes, 4M, 2.7 mL, 10.80 mmol). The
resulting solution was stirred at 40.degree. C. for 1 h, and
concentrated in vacuo. The resulting solid was slurried in
CH.sub.2Cl.sub.2 (2.0 mL), and
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid (0.17 g,
0.91 mmol), HATU (0.35 g, 0.91 mmol), and diisopropylethylamine
(0.5 mL, 2.86 mmol) were added. The resulting solution was stirred
at room temperature over 2 h. The reaction was diluted with DMF and
concentrated. The crude oil was purified by reverse phase HPLC
(Gemini, 10.fwdarw.45% MeCN/H.sub.2O (0.1% TFA)). The desired
fractions were diluted with EtOAc and washed with brine. The
aqueous layer was backextracted with EtOAc (2.times.). The combined
organic layers were dried over Na.sub.2SO.sub.4 and concentrated in
vacuo. The resulting material was lyophilized from MeCN and water
to provide methyl
[(2S,3R)-1-{(2S,5S)-2-[9-(4-cyclopropyl-2-{(2S,5S)-1-[N-(methoxycarbonyl)-
-O-methyl-L-threonyl]-5-methylpyrrolidin-2-yl}-1H-imidazol-5-yl)-1,11-dihy-
droisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]-5-methylpyrrolidin-1-
-yl}-3-methoxy-1-oxobutan-2-yl]carbamate (0.16 g, 48%).
LCMS-ESI.sup.+: calc'd for C.sub.48H.sub.58N.sub.8O.sub.9: 890.43
(M.sup.+); Found: 891.88 (M+H.sup.+). .sup.1H NMR (400 MHz,
cd.sub.3od) .delta. (Mixture of rotomers) 8.41 (s, 1H), 8.13-7.93
(m, 2H), 7.91-7.79 (m, 1H), 7.78-7.40 (m, 3H), 5.85-5.68 (m, 1H),
5.46 (d, 1H), 5.33-5.14 (m, 3H), 5.09-4.92 (m, 1H), 4.78-4.59 (m,
1H), 4.44-4.32 (m, 2H), 4.31-4.11 (m, 2H), 3.88 (s, 1H), 3.74-3.48
(m, 6H), 3.41-3.32 (m, 3H), 2.75-2.39 (m, 3H), 2.38-1.79 (m, 7H),
1.55 (d, 2H), 1.47 (d, 2H), 1.33-1.03 (m, 9H), 0.98 (s, 3H), 0.81
(s, 2H), 0.66 (s, 1H).
Example GD
##STR00257##
[0682] methyl
[(2S,3R)-3-methoxy-1-{(2S,5S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-O-m-
ethyl-L-threonyl]-5-methylpyrrolidin-2-yl}-4-methyl-1H-imidazol-5-yl)-1,11-
-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]-5-methylpyrroli-
din-1-yl}-1-oxobutan-2-yl]carbamate
[0683] Following Example GC, substituting methylboronic acid for
cyclopropylboronic acid, provided methyl
[(2S,3R)-3-methoxy-1-{(2S,5S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-O-m-
ethyl-L-threonyl]-5-methylpyrrolidin-2-yl}-4-methyl-1H-imidazol-5-yl)-1,11-
-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]-5-methylpyrroli-
din-1-yl}-1-oxobutan-2-yl]carbamate (0.08 g). LCMS-ESI.sup.+:
calc'd for C.sub.46H.sub.56N.sub.8O.sub.9: 864.42 (M.sup.+); Found:
865.91 (M+H.sup.+). .sup.1H NMR (400 MHz, cd.sub.3od) .delta.
(Mixture of rotomers) 8.40 (s, 1H), 8.14-7.85 (m, 2H), 7.78-7.34
(m, 4H), 5.78 (s, 1H), 5.47 (s, 1H), 5.30-5.13 (m, 3H), 5.11-4.96
(m, 1H), 4.79-4.58 (m, 2H), 4.48-4.30 (m, 2H), 4.30-4.13 (m, 2H),
3.88 (s, 1H), 3.73-3.50 (m, 6H), 3.42-3.32 (m, 4H), 2.57-2.03 (m,
9H), 2.03-1.76 (m, 2H), 1.55 (d, 3H), 1.47 (d, 2H), 1.39-0.99 (m,
10H).
Example GE
##STR00258##
[0684] methyl
[(2S,3S)-3-methoxy-1-{(2S,5S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-O-m-
ethyl-L-allothreonyl]-5-methylpyrrolidin-2-yl}-1H-imidazol-5-yl)-1,11-dihy-
droisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]-5-methylpyrrolidin-1-
-yl}-1-oxobutan-2-yl]carbamate
[0685] Following Example DX, substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid and
(1R,3S)-2-(2-(methoxycarbonylamino)-3-methylbutanoyl)-3-methylcyclopen
tanecarboxylic acid with
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid, and substituting
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid with 2
equivalents of (2S,3S)-3-methoxy-2-(methoxycarbonylamino)butanoic
acid, provided methyl
[(2S,3S)-3-methoxy-1-{(2S,5S)-2-[9-(2-{(2S,5S)-1-[N-(methoxycarbonyl)-O-m-
ethyl-L-allothreonyl]-5-methylpyrrolidin-2-yl}-1H-imidazol-5-yl)-1,11-dihy-
droisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]-5-methylpyrrolidin-1-
-yl}-1-oxobutan-2-yl]carbamate (0.27 g). LCMS-ESI.sup.+: calc'd for
C.sub.45H.sub.54N.sub.8O.sub.9: 850.40 (M.sup.+); Found: 851.80
(M+H.sup.+). .sup.1H NMR (400 MHz, cd.sub.3od) .delta. (Mixture of
rotomers) 8.43-8.29 (m, 1H), 8.12-7.90 (m, 2H), 7.87-7.61 (m, 3H),
7.61-7.32 (m, 3H), 5.74 (d, 1H), 5.54 (d, 1H), 5.24-5.09 (m, 2H),
4.76-4.60 (m, 1H), 4.46-4.30 (m, 2H), 4.31-4.12 (m, 2H), 3.89 (s,
2H), 3.80-3.60 (m, 4H), 3.60-3.44 (m, 2H), 3.34 (s, 2H), 3.32 (s,
2H), 2.97-2.63 (m, 2H), 2.62-2.35 (m, 2H), 2.35-1.78 (m, 6H),
1.65-1.52 (m, 2H), 1.50 (d, 1H), 1.42 (d, 1H), 1.35-1.04 (m,
10H).
Example GF
##STR00259##
[0686] methyl
{(2S,3S)-1-[(2S,5S)-2-(5-{2-[(2S,5S)-1-{(2S,3R)-3-methoxy-2-[(methoxycarb-
onyl)amino]butanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3-
':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-5-methylpyrrolidin-1--
yl]-3-methyl-1-oxopentan-2-yl}carbamate
[0687] Following Example DX, substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with (2S,5S)-1-((2S,3
S)-2-(methoxycarbonylamino)-3-methylpentanoyl)-5-methylpyrrolidine-2-carb-
oxylic acid and
(1R,3S)-2-(2-(methoxycarbonylamino)-3-methylbutanoyl)-3-methylcyclopen
tanecarboxylic acid with
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid, provided methyl
{(2S,3S)-1-[(2S,5S)-2-(5-{2-[(2S,5S)-1-{(2S,3R)-3-methoxy-2-[(methoxycarb-
onyl)amino]butanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3-
':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-5-methylpyrrolidin-1--
yl]-3-methyl-1-oxopentan-2-yl}carbamate (0.14 g). LCMS-ESI.sup.+:
calc'd for C.sub.46H.sub.56N.sub.8O.sub.8: 848.42 (M.sup.+); Found:
849.80 (M+H.sup.+). .sup.1H NMR (400 MHz, cd.sub.3od) .delta.
(Mixture of rotomers) 8.43-8.14 (m, J=14.6 Hz, 2H), 8.09-7.75 (m,
3H), 7.75-7.24 (m, 5H), 5.80-5.64 (m, 1H), 5.38-4.95 (m, 4H),
4.80-4.67 (m, 1H), 4.31-4.09 (m, J=20.2, 7.7 Hz, 2H), 3.85 (s, 1H),
3.72-3.54 (m, J=20.5 Hz, 4H), 3.37 (s, 2H), 2.94-2.64 (m, J=51.0
Hz, 2H), 2.63-2.37 (m, J=35.2 Hz, 2H), 2.37-2.01 (m, 4H), 2.00-1.83
(m, 1H), 1.83-1.69 (m, 1H), 1.67-1.51 (m, J=6.6 Hz, 3H), 1.47 (d,
J=6.6 Hz, 2H), 1.35-1.00 (m, 7H), 1.00-0.69 (m, 7H).
Example GG
##STR00260##
[0688] methyl
[(2S,3S)-1-{(2S,5S)-2-[5-(2-{(2S,5S)-1-[(2S)-2-[(methoxycarbonyl)amino]-2-
-(tetrahydro-2H-pyran-4-yl)acetyl]-5-methylpyrrolidin-2-yl}-1,11-dihydrois-
ochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imidazol-2-yl]-5-methy-
lpyrrolidin-1-yl}-3-methyl-1-oxopentan-2-yl]carbamate
[0689] Following Example DX, substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with (2S,5S)-1-((2S,3
S)-2-(methoxycarbonylamino)-3-methylpentanoyl)-5-methylpyrrolidine-2-carb-
oxylic acid,
(1R,3S)-2-(2-(methoxycarbonylamino)-3-methylbutanoyl)-3-methylcyclopentan-
ecarboxylic acid with
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid, and (2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid
with
(S)-2-(methoxycarbonylamino)-2-(tetrahydro-2H-pyran-4-yl)acetic
acid provided methyl
[(2S,3S)-1-{(2S,5S)-2-[5-(2-{(2S,5S)-1-[(2S)-2-[(methoxycarbonyl)amino]-2-
-(tetrahydro-2H-pyran-4-yl)acetyl]-5-methylpyrrolidin-2-yl}-1,11-dihydrois-
ochromeno[4',3':6,7]naphtho[1,2-d]imidazol-9-yl)-1H-imidazol-2-yl]-5-methy-
lpyrrolidin-1-yl}-3-methyl-1-oxopentan-2-yl]carbamate (0.07 g).
LCMS-ESI.sup.+: calc'd for C.sub.48H.sub.58N.sub.8O.sub.8: 874.44
(M.sup.+); Found: 876.07 (M+H.sup.+). .sup.1H NMR (400 MHz,
cd.sub.3od) .delta. (Mixture of rotomers) 8.33-8.10 (m, 2H),
8.04-7.68 (m, 3H), 7.68-7.16 (m, 5H), 5.49 (s, 1H), 5.35-5.20 (m,
1H), 5.20-4.91 (m, 3H), 4.73-4.61 (m, 1H), 4.25-4.01 (m, 3H),
3.98-3.65 (m, 4H), 3.57 (d, 3H), 3.36-3.24 (m, 1H), 3.17-2.97 (m,
1H), 2.91-2.58 (m, 2H), 2.57-1.76 (m, 9H), 1.52 (d, 3H), 1.41 (d,
3H), 1.28-0.93 (m, 5H), 0.93-0.56 (m, 7H).
Example GH
##STR00261##
[0690] methyl
{(2S)-1-[(2S,4S)-2-(5-{2-[(2S,5S)-1-{(2S,3R)-3-methoxy-2-[(methoxycarbony-
l)amino]butanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6-
,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-methylpyrrolidin-1-yl]-
-3-methyl-1-oxobutan-2-yl}carbamate
[0691] Following Example DX, substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with
(2S,4S)-1-(tert-butoxycarbonyl)-4-methylpyrrolidine-2-carboxylic
acid,
(1R,3S)-2-(2-(methoxycarbonylamino)-3-methylbutanoyl)-3-methylcyclo-
pen tanecarboxylic acid with
(2S,5S)-1-((2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoyl)-5-methylpy-
rrolidine-2-carboxylic acid, and
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid with
(S)-2-(methoxycarbonylamino)-3-methylbutanoic acid, provided methyl
{(2S)-1-[(2S,4S)-2-(5-{2-[(2S,5S)-1-{(2S,3R)-3-methoxy-2-[(methoxycarbony-
l)amino]butanoyl}-5-methylpyrrolidin-2-yl]-1,11-dihydroisochromeno[4',3':6-
,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-methylpyrrolidin-1-yl]-
-3-methyl-1-oxobutan-2-yl)}carbamate (0.16 g). LCMS-ESI.sup.+:
calc'd for C.sub.45H.sub.54N.sub.8O.sub.8: 834.41 (M.sup.+); Found:
835.86 (M+H.sup.+). .sup.1H NMR (400 MHz, cd.sub.3od) .delta.
(Mixture of rotomers) 8.23-8.09 (m, 1H), 7.94-7.68 (m, 3H),
7.67-7.13 (m, 6H), 5.70-5.56 (m, 1H), 5.23-5.13 (m, 1H), 5.12-4.91
(m, 4H), 4.25-4.08 (m, 3H), 3.76 (s, 2H), 3.66-3.52 (m, 5H),
3.39-3.25 (m, 3H), 3.18 (s, 1H), 2.45-2.07 (m, 4H), 2.03-1.73 (m,
3H), 1.47 (d, 2H), 1.25-0.98 (m, 8H), 0.94-0.81 (m, 4H), 0.79 (d,
3H).
Example GI
##STR00262##
[0692] methyl
[(2S)-1-{(2S,4S)-2-[9-(2-{(2S,5S)-1-[(2S)-2-[(methoxycarbonyl)amino]-2-(t-
etrahydro-2H-pyran-4-yl)acetyl]-4-(methoxymethyl)pyrrolidin-2-yl}-1H-imida-
zol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]-5-
-methylpyrrolidin-1-yl}-3-methyl-1-oxobutan-2-yl]carbamate
[0693] Following Example DX, substituting
(2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic
acid with
(2S,4S)-1-(tert-butoxycarbonyl)-4-(methoxymethyl)pyrrolidine-2-carbo-
xylic acid,
(1R,3S)-2-(2-(methoxycarbonylamino)-3-methylbutanoyl)-3-methylcyclopen
tanecarboxylic acid with
(2S,5S)-1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-5-methylpyrroli-
dine-2-carboxylic acid, and
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid with
(S)-2-(methoxycarbonylamino)-2-(tetrahydro-2H-pyran-4-yl)acetic
acid, provided methyl
[(2S)-1-{(2S,4S)-2-[9-(2-{(2S,5S)-1-[(2S)-2-[(methoxycarbonyl)amino]-2-(t-
etrahydro-2H-pyran-4-yl)acetyl]-4-(methoxymethyl)pyrrolidin-2-yl}-1H-imida-
zol-5-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]-5-
-methylpyrrolidin-1-yl}-3-methyl-1-oxobutan-2-yl]carbamate (0.06
g). LCMS-ESI.sup.+: calc'd for C.sub.48H.sub.58N.sub.8O.sub.9:
890.43 (M.sup.+); Found: 891.81 (M+H.sup.+). .sup.1H NMR (400 MHz,
cd.sub.3od) .delta. (Mixture of rotomers) 8.50 (s, 1H), 8.17-8.01
(m, 2H), 7.88 (t, 1H), 7.83-7.74 (m, 2H), 7.74-7.63 (m, 1H),
7.62-7.48 (m, 2H), 5.72 (d, 1H), 5.26-5.08 (m, 4H), 4.33-4.12 (m,
3H), 4.05 (d, 1H), 3.90-3.76 (m, 2H), 3.67 (d, 1H), 3.58 (s, 2H),
3.56 (s, 2H), 3.54-3.39 (m, 3H), 3.29 (s, 3H), 2.75-2.60 (m, 2H),
2.60-2.17 (m, 5H), 2.06-1.76 (m, 5H), 1.53 (d, 2H), 1.48-1.17 (m,
5H), 1.15 (d, 1H), 0.98 (dd, 2H), 0.86 (d, 2H), 0.77 (d, 2H).
Example GJ
##STR00263##
[0694] Methyl
{(2S)-1-[(2S,5S)-2-(9-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino]-2-ph-
enylacetyl}-4-(methoxymethyl)pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihyd-
roisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidin-1--
yl]-3-methyl-1-oxobutan-2-yl}carbamate
[0695] Following Example CY, substituting
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid with
(S)-2-(methoxycarbonylamino)-2-phenylacetic acid, COMU with DMTMM,
and diisopropylethylamine with N-methylmorpholine, provided methyl
{(2S)-1-[(2S,5S)-2-(9-{2-[(2S,4S)-1-{(2S)-2-[(methoxycarbonyl)amino]-2-ph-
enylacetyl}-4-(methoxymethyl)pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihyd-
roisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidin-1--
yl]-3-methyl-1-oxobutan-2-yl}carbamate (0.16 g). LCMS-ESI.sup.+:
calculated for C.sub.49H.sub.54N.sub.8O.sub.8: 882.41; observed
[M+1].sup.+: 883.77.
Example GK
##STR00264##
[0696] methyl
{(1R)-2-[(2S,4S)-2-(5-{2-[(2S,5S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-me-
thylbutanoyl}-5-methylpyrrolidin-2-yl]-11-oxo-1,11-dihydroisochromeno[4',3-
':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)pyrr-
olidin-1-yl]-2-oxo-1-phenylethyl}carbamate
[0697] To a solution of methyl
{(2S)-1-[(2S,5S)-2-(9-{2-[(2S,4S)-1-{(2R)-2-[(methoxycarbonyl)amino]-2-ph-
enylacetyl}-4-(methoxymethyl)pyrrolidin-2-yl]-1H-imidazol-5-yl}-1,11-dihyd-
roisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidin-1--
yl]-3-methyl-1-oxobutan-2-yl}carbamate (0.19 g, 0.22 mmol) in
CH.sub.2Cl.sub.2 (3 mL) was added pyridinium chlorochromate (0.48
g, 2.21 mmol). The resulting slurry was stirred at room temperature
for 5 days. The reaction was diluted with MeOH and filtered. The
filtrate was diluted with CH.sub.2Cl.sub.2 and washed with water
and aqueous sodium bicarbonate (saturated). The aqueous layers were
backextracted with CH.sub.2Cl.sub.2. The combined organic layers
were dried over Na.sub.2SO.sub.4 and concentrated in vacuo. The
crude oil was purified by reverse phase HPLC (Gemini, 10.fwdarw.55%
MeCN/H.sub.2O (0.1% TFA)). The desired fractions were combined and
concentrated under reduced pressure to remove volatile organics.
The addition of aqueous sodium bicarbonate with stirring resulted
in precipitation of a white solid. The precipitate was filtered
through a membrane filter and washed with water. Drying under
reduced pressure afforded methyl
{(1R)-2-[(2S,4S)-2-(5-{2-[(2S,5S)-1-{(2S)-2-[(methoxycarbonyl)amino]-3-me-
thylbutanoyl}-5-methylpyrrolidin-2-yl]-11-oxo-1,11-dihydroisochromeno[4',3-
':6,7]naphtho[1,2-d]imidazol-9-yl}-1H-imidazol-2-yl)-4-(methoxymethyl)pyrr-
olidin-1-yl]-2-oxo-1-phenylethyl}carbamate (0.08 g, 39%).
LCMS-ESI.sup.+: calc'd for C.sub.49H.sub.52N.sub.8O.sub.9: 896.39
(M.sup.+); Found: 897.72 (M+H.sup.+).
Examples GL-IY
[0698] Using procedures similar to those described herein, the
following compounds of the invention were prepared.
TABLE-US-00003 LCMS (observed Ex. Structure (M + H).sup.+) GL
##STR00265## 833.79 GM ##STR00266## 833.86 GN ##STR00267## 887.798
GO ##STR00268## 849.9 GP ##STR00269## 821.81 GQ ##STR00270##
889.727 GR ##STR00271## 833.86 GS ##STR00272## 835.77 GT
##STR00273## 833.83 GU ##STR00274## 849.83 GV ##STR00275## 875.85
GW ##STR00276## 833.84 GX ##STR00277## 849.82 GY ##STR00278##
821.72 GZ ##STR00279## 807.87 HA ##STR00280## 819.786 HB
##STR00281## 835.754 HC ##STR00282## 791.843 HD ##STR00283##
817.718 HE ##STR00284## 859.876 HF ##STR00285## 763.698 HG
##STR00286## 823.71 HH ##STR00287## 819.77 HI ##STR00288## 875.78
HJ ##STR00289## 875.76 HK ##STR00290## 805.82 HL ##STR00291## 791.8
HM ##STR00292## 827.725 HN ##STR00293## 834.196 HO ##STR00294##
859.977 HP ##STR00295## 833.81 HQ ##STR00296## 875.76 HR
##STR00297## 817.822 HS ##STR00298## 823.867 HT ##STR00299##
865.924 HU ##STR00300## 839.832 HV ##STR00301## 877.751 HW
##STR00302## 821.898 HX ##STR00303## 833.84 HY ##STR00304## 891.84
HZ ##STR00305## 875.97 IA ##STR00306## 887.991 IB ##STR00307##
887.891 IC ##STR00308## 875.937 ID ##STR00309## 889.862 IE
##STR00310## 931.96 IF ##STR00311## 833.65 IG ##STR00312## 889.48
IH ##STR00313## 867.52 II ##STR00314## 889.861 IJ ##STR00315##
889.514 IK ##STR00316## 889.38 IL ##STR00317## 901.351 IM
##STR00318## 889.443 IN ##STR00319## 901.81 IO ##STR00320## 901.328
IP ##STR00321## 901.544 IQ ##STR00322## 901.951 IR ##STR00323##
875.87 IS ##STR00324## 876.035 IT ##STR00325## 913.97 IU
##STR00326## 901.94 IV ##STR00327## 889.958 IW ##STR00328## 919.96
IX ##STR00329## 915.539 IY ##STR00330## 887.985
BIOLOGICAL ASSAYS
[0699] Effect of Serum Proteins on Replicon Potency:
[0700] Replicon assays are conducted in normal cell culture medium
(DMEM+10% FBS) supplemented with physiologic concentrations of
human serum albumin (40 mg/mL) or .alpha.-acid glycoprotein (1
mg/mL). EC.sub.50s in the presence of human serum proteins are
compared to the EC.sub.50 in normal medium to determine the fold
shift in potency.
[0701] MT-4 Cell Cytotoxicity:
[0702] MT4 cells are treated with serial dilutions of compounds for
a five day period. Cell viability is measured at the end of the
treatment period using the Promega CellTiter-Glo assay and
non-linear regression is performed to calculate CC.sub.50.
[0703] Compound Concentration Associated with Cells at
EC.sub.50:
[0704] Huh-luc cultures are incubated with compound at
concentrations equal to EC.sub.50. At multiple time points (0-72
hours), cells are washed 2.times. with cold medium and extracted
with 85% acetonitrile; a sample of the media at each time-point
will also be extracted. Cell and media extracts are analyzed by
LC/MS/MS to determine the Molar concentration of compounds in each
fraction. Representative compounds of the disclosure have shown
activity.
[0705] Solubility and Stability:
[0706] Solubility is determined by taking an aliquot of 10 mM DMSO
stock solution and preparing the compound at a final concentration
of 100 .mu.M in the test media solutions (PBS, pH 7.4 and 0.1 N
HCl, pH 1.5) with a total DMSO concentration of 1%. The test media
solutions are incubated at room temperature with shaking for 1 hr.
The solutions will then be centrifuged and the recovered
supernatants are assayed on the HPLC/UV. Solubility will be
calculated by comparing the amount of compound detected in the
defined test solution compared to the amount detected in DMSO at
the same concentration. Stability of compounds after an 1 hour
incubation with PBS at 37.degree. C. will also be determined.
[0707] Stability in Cryopreserved Human, Dog, and Rat
Hepatocytes:
[0708] Each compound is incubated for up to 1 hour in hepatocyte
suspensions (100 .mu.l, 80,000.degree. Cells per well) at
37.degree. C. Cryopreserved hepatocytes are reconstituted in the
serum-free incubation medium. The suspension is transferred into
96-well plates (50 .mu.L/well). The compounds are diluted to 2
.mu.M in incubation medium and then are added to hepatocyte
suspensions to start the incubation. Samples are taken at 0, 10, 30
and 60 minutes after the start of incubation and reaction will be
quenched with a mixture consisting of 0.3% formic acid in 90%
acetonitrile/10% water. The concentration of the compound in each
sample is analyzed using LC/MS/MS. The disappearance half-life of
the compound in hepatocyte suspension is determined by fitting the
concentration-time data with a monophasic exponential equation. The
data will also be scaled up to represent intrinsic hepatic
clearance and/or total hepatic clearance.
[0709] Stability in Hepatic S9 Fraction from Human, Dog, and
Rat:
[0710] Each compound is incubated for up to 1 hour in S9 suspension
(500 .mu.l, 3 mg protein/mL) at 37.degree. C. (n=3). The compounds
are added to the S9 suspension to start the incubation. Samples are
taken at 0, 10, 30, and 60 minutes after the start of incubation.
The concentration of the compound in each sample is analyzed using
LC/MS/MS. The disappearance half-life of the compound in S9
suspension is determined by fitting the concentration-time data
with a monophasic exponential equation.
[0711] Caco-2 Permeability:
[0712] Compounds are assayed via a contract service (Absorption
Systems, Exton, Pa.). Compounds are provided to the contractor in a
blinded manner. Both forward (A-to-B) and reverse (B-to-A)
permeability will be measured. Caco-2 monolayers are grown to
confluence on collagen-coated, microporous, polycarbonate membranes
in 12-well Costar TRANSWELL.RTM. plates. The compounds are dosed on
the apical side for forward permeability (A-to-B), and are dosed on
the basolateral side for reverse permeability (B-to-A). The cells
are incubated at 37.degree. C. with 5% CO.sub.2 in a humidified
incubator. At the beginning of incubation and at 1 hr and 2 hr
after incubation, a 200-.mu.L aliquot is taken from the receiver
chamber and replaced with fresh assay buffer. The concentration of
the compound in each sample is determined with LC/MS/MS. The
apparent permeability, Papp, is calculated.
[0713] Plasma Protein Binding:
[0714] Plasma protein binding is measured by equilibrium dialysis.
Each compound is spiked into blank plasma at a final concentration
of 2 .mu.M. The spiked plasma and phosphate buffer is placed into
opposite sides of the assembled dialysis cells, which will then be
rotated slowly in a 37.degree. C. water bath. At the end of the
incubation, the concentration of the compound in plasma and
phosphate buffer is determined. The percent unbound is calculated
using the following equation:
% Unbound = 100 ( C f C b + C f ) ##EQU00001##
[0715] Where C.sub.f and C.sub.b are free and bound concentrations
determined as the post-dialysis buffer and plasma concentrations,
respectively.
[0716] CYP450 Profiling:
[0717] Each compound is incubated with each of 5 recombinant human
CYP450 enzymes, including CYP1A2, CYP2C9, CYP3A4, CYP2D6 and
CYP2C19 in the presence and absence of NADPH. Serial samples will
be taken from the incubation mixture at the beginning of the
incubation and at 5, 15, 30, 45 and 60 minutes after the start of
the incubation. The concentration of the compound in the incubation
mixture is determined by LC/MS/MS. The percentage of the compound
remaining after incubation at each time point is calculated by
comparing with the sampling at the start of incubation.
[0718] Stability in Rat, Dog, Monkey and Human Plasma:
[0719] Compounds will be incubated for up to 2 hours in plasma
(rat, dog, monkey, or human) at 37.degree. C. Compounds are added
to the plasma at final concentrations of 1 and 10 .mu.g/mL.
Aliquots are taken at 0, 5, 15, 30, 60, and 120 minutes after
adding the compound. Concentration of compounds and major
metabolites at each time point are measured by LC/MS/MS.
[0720] Evaluation of Cell-Based Anti-HCV Activity:
[0721] Antiviral potency (EC.sub.50) was determined using a Renilla
luciferase (RLuc)-based HCV replicon reporter assay. To perform the
assay for genotype 1 and 2a JFH-1, stable HCV 1a RLuc replicon
cells (harboring a dicistronic genotype 1a H77 replicon that
encodes a RLuc reporter), stable HCV 1b RLuc replicon cells
(harboring a dicistronic genotype 1b Con1 replicon that encodes a
RLuc reporter), or stable HCV 2a JFH-1 Rluc replicon cells
(harboring a dicistronic genotype 2a JFH-1 replicon that encodes a
RLuc reporter; with L31 present in NS5A) were dispensed into
384-well plates for EC.sub.50 assays. To perform the assay for
genotype 2a (with M31 present in NS5A) or 2b, NS5A chimeric
genotype 2a JFH-1 replicons that encodes a RLuc-Neo reporter and
either genotype 2a J6 strain NS5A gene or genotype 2b MD2b-1 strain
NS5A gene (both with M31 present) respectively, were either
transiently transfected (t) into Huh-Lunet cells or were
established as stably replicating replicon cells (s) is provided.
Either cells were dispensed into 384-well plates for EC.sub.50
assays. To perform the assay for genotype 3 and 4, NS5A chimeric
genotype 1b Con1 replicons that encodes a Pi-RLuc reporter and
either genotype 3a S52 strain NS5A gene or genotype 4a ED43 strain
NS5A gene respectively, were transiently transfected (t) into
Huh-Lunet cells, which were subsequently dispensed into 384-well
plates. Compounds were dissolved in DMSO at a concentration of 10
mM and diluted in DMSO either manually or using an automated
pipeting instrument. Serially 3-fold diluted compounds were either
manually mixed with cell culture media and added to the seeded
cells or directly added to the cells using an automated instrument.
DMSO was used as a negative (solvent; no inhibition) control, and
the protease inhibitor ITMN-191 was included at a concentration
>100.times. EC.sub.50 as a positive control. 72 hours later,
cells were lysed and Renilla luciferase activity quantified as
recommended by the manufacturer (Promega-Madison, Wis.). Non-linear
regression was performed to calculate EC.sub.50 values.
[0722] To determine the antiviral potency (EC.sub.50) against
resistance mutants, resistance mutations, including M28T, Q30R,
Q30H, Q30E, L31M, Y93C, Y93H, and Y93N in genotype 1a NS5A, Y93H
and L31V/Y93H in genotype 1b NS5A, and Y93H for in genotype 3a
NS5A, were introduced individually into either 1a Pi-Rluc or 1b
Pi-Rluc replicons by site directed mutagenesis. Replicon RNA of
each resistant mutant was transiently transfected into
Huh-7-derived cured-51 cells and antiviral potency was determined
on these transfected cells as described above.
[0723] IV and PO Single Dose Pharmacokinetic Studies in SD
Rats:
[0724] The pharmacokinetics of selected compounds was characterized
in male Sprague-Dawley (SD) rats (250-300g). In this study, two
groups of naive purebred SD rats (N=3 per group, fasted over night)
received the selected compound either as an intravenous (IV)
infusion (1 mg/kg over 30 minutes) via the jugular vein or by oral
gavage (2 mg/kg). The intravenous (IV) dosing vehicle was 5%
ethanol, 35% polyethylene glycol 400 (PEG 400) and 60% water pH
2.0. The oral dosing vehicle was 5% ethanol, 55% PEG 400 and 40%
citrate buffer pH 2.2.
[0725] Serial blood samples (approximately 0.3 mL each) were
collected from jugular vein or other suitable vein at specified
time points. For the IV infusion group, the blood samples were
collected predose and at 0.25, 0.48, 0.58, 0.75, 1.5, 3, 6, 8, 12
and 24 hours after the start of infusion. For the oral group, the
blood samples were collected predose and at 0.25, 0.50, 1, 2, 4, 6,
8, 12 and 24 hours after dosing. The blood samples were collected
into Vacutainer.TM. tubes containing EDTA-K.sub.3 as the
anti-coagulant and were centrifuged at approximately 4.degree. C.
to obtain plasma. The plasma samples were stored at -20.degree. C.
until analysis by LC/MS/MS.
[0726] A bioanalytical method utilizing high performance liquid
chromatography coupled to tandem mass spectrometry (LC/MS/MS) was
developed for analysis of the selected compound in rat plasma.
Detection was performed using selected reaction monitoring (SRM);
Ions representing the precursor (M+H).sup.+ species was selected in
quadrupole 1 (Q1) and collided with argon gas in the collision cell
(Q2) to generate specific product ion, which was subsequently
monitored by quadrupole 3 (Q3). Standard curve and quality control
samples were prepared in male rat plasma and processed in the same
way as the test samples to generate quantitative data.
[0727] Pharmacokinetic parameters were generated using
non-compartmental pharmacokinetic analysis (Phoenix WinNonlin,
version 6.3). Values below the lower limit of quantification (LLOQ)
were assigned a value of zero if predose and treated as missing
thereafter. Area under the curve (AUC) was calculated using the
linear trapezoidal rule. The oral bioavailability (% F) was
determined by comparison of the area under the curve (AUC) of the
compound and/or a metabolite generated in plasma following oral
administration to that generated following intravenous
administration.
TABLE-US-00004 TABLE 1A 2a 2a 1a Ex. 1b 1a 2a J6 J6 2b 2b 3a 3a 4a
1a Q30R No. No. (nM) 1a Q30R JFH (t) (s) (t) (s) (t) (s) (s) (nM)
(nM) 97 GK 0.036 D C D D D C C D 0.031 0.111 98 DZ 0.035 D D D D C
D D 0.021 99 DY 0.065 D D D D C C D 0.044 100 FV 0.036 D C B C B B
D 0.023 101 FW 0.187 C D C C C B D 0.121 102 GJ 103 EA 0.028 D D D
D D D D 0.018 104 DX 0.031 D C D C D C D D 0.021 0.138 105 FX 0.060
D D D C C C D 0.041 106 EB 0.051 D D D D D D D D 0.024 0.042 107 EC
0.017 D D C C D D 0.008 108 FY 0.017 D D D D D D D 0.010 0.017 109
FZ 0.031 D D D D C D D 0.019 0.048 110 ED 0.029 D D D C D D 0.015
111 EX 0.197 D D D C B D 0.079 112 EZ 0.084 D D D C C D 0.028 113
FA 0.014 D D D D D C D D 0.011 0.046 114 FC 0.021 D D D D D D D D
0.014 0.031 115 FB 0.014 D D D C D D D 0.009 0.077 116 FE 0.015 D C
D C C D D 0.012 0.253 117 EE 0.025 D D D C D C D 0.019 118 EF 0.053
D D D D C C D 0.039 119 GA 0.035 D D D C D D 0.019 120 EG 0.045 D D
D D C D D 0.036 121 EH 0.015 D D D D C D D D 0.011 0.082 122 GB
0.019 D D D D D D D D 0.016 0.075 123 EI 0.048 D D D D D D D 0.025
124 EJ 0.039 D D D C D D D 0.016 125 GC 0.022 D D C C D C D 0.013
126 GD 0.027 D C D D D D D D 0.019 0.105 127 EY 0.049 D D D D D C D
D 0.029 0.057 128 EK 0.050 D D C C C D 0.034 129 GE 0.062 D C C C C
D 0.043 130 FG 0.040 D C D B B C D 0.024 0.577 131 FK 0.037 D C D C
C C D 0.024 0.498 132 EL 0.030 D D C C C D 0.021 133 EM 0.020 D D D
D D D 0.013 134 FN 0.053 D D D C D D 0.035 135 GF 0.015 D D C D D
0.007 136 GG 0.022 D D D D D D D 0.015 0.032 137 FO 0.009 D C D C D
D 0.010 0.112 138 FP 0.024 D D D D D 0.016 139 FI 0.022 D C D C D D
0.010 0.115 140 EN 0.034 D D D D D D 0.018 0.043 141 EO 0.040 D D D
D D D 0.024 0.052 142 EP 0.024 D D C C 0.014 143 FQ 0.019 D D D D D
0.012 0.097 144 FR 0.050 D D D D D 0.026 0.071 145 GH 0.027 D D C D
0.020 146 FT 0.045 D D C C D 0.040 147 FS 0.025 D D C C D 0.024 148
FU 0.032 D D C C D 0.028 149 EQ 0.036 D D C C D 0.034 150 ER 0.020
D D C B D 0.016 151 ES 0.029 D D C B D 0.021 152 GI 0.064 D D C C D
0.055 153 FM 0.018 D D C D D 0.009 154 GL 0.021 D D C C D D 0.015
155 GM 0.016 D D C C D D 0.012 156 GN 0.023 D D D C D D 0.013 157
GO 0.028 D D C C B D 0.021 158 GP 0.027 D D B B C D 0.018 159 GQ
160 GR 0.022 D D C C C D 0.016 161 GS 0.021 D D C C C D 0.018 162
GT 0.021 D D C B C D 0.017 163 GU 0.022 D D D C C D 0.014 164 GV
0.027 D D D D C D D 0.018 0.061 165 GW 0.015 D D C B C D 0.017 166
GX 0.016 D D C B C D 0.016 167 GY 0.032 D D D C D D 0.023 168 GZ
0.045 D D C B C D 0.042 169 HA 0.019 D D B B C D 0.018 170 HB 0.012
D D C C D D 0.012 171 HC 0.016 D D B B C D 0.012 172 HD 0.017 D D B
B C D 0.015 173 HE 0.020 D D C B D D 0.011 174 HF 0.066 D D B B C C
0.043 175 HG 0.109 D D C C C D 0.060 176 HH 0.020 D D B B D D 0.011
177 HI 0.416 C D C C C C 0.203 178 HJ 0.020 D D B B D D 0.016 179
HK 0.026 D D C B C D 0.017 180 HL 0.021 D D B B C D 0.017 181 HM
0.018 D D C C D D 0.011 182 HN 0.012 D D B B C D 0.010 183 HO 0.074
D D C C C D 0.059 184 HP 0.026 D D C B D D 0.019 185 HQ 0.027 D D D
D D C D D D 0.022 0.031 186 HR 0.024 D D B B D D 0.015 187 HS 0.023
D D B B D D 0.011 188 HT 0.110 D D C B D D 0.070 189 HU 0.055 D D B
B D D 0.016 190 HV 0.091 B B A A B B 3.654 191 HW 0.066 D D B B D D
0.056 192 HX 0.020 D D B B C D 0.011 193 HY 0.028 D D D D D D D D D
0.015 0.046 194 HZ 0.025 D D D D C D 0.012 195 IA 0.024 D D D D D D
D D D 0.015 0.024 196 IB 0.032 D D D C D D 0.021 197 IC 0.027 D D D
C C D 0.024 198 ID 0.038 D D C B C D 0.035 199 IE 0.054 D D D D C D
0.042 200 IF 0.021 D D C C C D 0.016 201 IG 0.035 D D C C C D 0.027
202 IH 0.021 D D C C D D 0.020 203 II 0.033 D D C C C D 0.024 204
IJ 0.029 D D C C D 0.027 205 IK 0.038 D D C C D 0.039 206 IL 0.034
D D D C D D 0.028 207 IM 0.040 D D C C D 0.033 208 IN 0.028 D D D C
C D 0.021 209 IO 0.043 D D D C C D 0.027 210 IP 0.029 D D D D D D
0.025 211 IQ 0.019 D D D D D D 0.018 212 IR 0.021 D D D D D D 0.018
213 IS 0.021 D D D D C D 0.017 214 IT 0.017 D D D D D D 0.012 215
IU 0.022 D D D C D D 0.016 216 IV 0.053 D D D C C D 0.045 217 IW
218 IX 0.052 D D C C D 0.035 219 IY 0.030 D D D D D D 0.023
Activity Ranges: A .gtoreq.44 nM, B = 1 nM-43.999 nM, C = 0.1
nM-0.999 nM, D <0.1 nM.
TABLE-US-00005 TABLE 1B 2a 2a J6 2a J6 Ex. JFH (t) (s) 2b (t) 2b
(s) 3a (t) 3a (s) 4a (s) Rat No. No. (nM) (nM) (nM) (nM) (nM) (nM)
(nM) (nM) % F 97 GK 0.024 0.071 0.087 0.187 0.156 0.028 98 DZ 0.016
0.054 0.072 0.173 0.089 0.020 99 DY 0.028 0.047 0.083 0.199 0.130
0.035 8.3 100 FV 0.111 3.783 0.772 2.554 5.247 0.029 101 FW 0.054
0.104 0.399 0.773 1.171 0.080 102 GJ 103 EA 0.015 0.035 0.037 0.088
0.035 0.019 10.2 104 DX 0.019 0.109 0.060 0.201 0.048 0.018 21.3
105 FX 0.024 0.064 0.122 0.288 0.243 0.031 106 EB 0.012 0.012 0.092
0.038 0.075 0.014 4.2 107 EC 0.015 0.429 0.400 0.029 0.004 108 FY
0.007 0.005 0.034 0.029 0.005 13.5 109 FZ 0.025 0.041 0.101 0.098
0.025 18.5 110 ED 0.011 0.021 0.241 0.099 0.025 111 EX 0.027 0.052
0.393 1.685 0.072 112 EZ 0.016 0.036 0.262 0.263 0.025 113 FA 0.014
0.033 0.036 0.130 0.034 0.011 13.5 114 FC 0.011 0.015 0.024 0.048
0.031 0.011 0 115 FB 0.013 0.105 0.081 0.026 0.010 116 FE 0.016
0.122 0.463 0.072 0.012 117 EE 0.014 0.033 0.265 0.057 0.188 0.009
118 EF 0.014 0.023 0.091 0.102 0.120 0.020 119 GA 0.018 0.064 0.245
0.063 0.016 3.2 120 EG 0.022 0.023 0.072 0.103 0.076 0.016 121 EH
0.013 0.086 0.153 0.024 0.022 0.006 15.8 122 GB 0.011 0.023 0.089
0.034 0.029 0.007 123 EI 0.033 0.022 0.048 0.074 0.077 0.020 4.4
124 EJ 0.028 0.041 0.112 0.046 0.081 0.017 125 GC 0.063 0.181 0.117
0.032 0.140 0.013 126 GD 0.035 0.040 0.090 0.042 0.070 0.018 127 EY
0.029 0.008 0.035 0.118 0.087 0.025 128 EK 0.030 0.116 0.238 0.173
0.025 129 GE 0.104 0.508 0.772 0.445 0.026 130 FG 0.047 1.447 1.527
0.298 0.044 131 FK 0.038 0.400 0.476 0.137 0.018 132 EL 0.024 0.107
0.247 0.838 0.018 133 EM 0.012 0.043 0.082 0.061 0.008 134 FN 0.028
0.068 0.142 0.084 0.020 135 GF 0.018 0.203 0.027 0.011 15.6 136 GG
0.020 0.044 0.083 0.038 0.013 22.1 137 FO 0.008 0.164 0.055 0.007
17.2 138 FP 0.016 0.085 0.052 0.017 139 FI 0.015 0.152 0.040 0.012
140 EN 0.015 0.052 0.095 0.061 29.9 141 EO 0.017 0.038 0.091 0.054
46.6 142 EP 0.013 0.213 0.115 17.5 143 FQ 0.010 0.066 0.020 17.7
144 FR 0.015 0.054 0.031 145 GH 0.011 0.247 0.070 146 FT 0.029
0.395 0.283 0.028 147 FS 0.025 0.784 0.411 0.017 148 FU 0.021 0.347
0.337 0.018 149 EQ 0.022 0.279 0.475 0.025 150 ER 0.021 0.852 2.798
0.011 151 ES 0.018 0.536 2.950 0.013 152 GI 0.025 0.193 0.126 0.022
153 FM 0.019 0.259 0.061 0.007 22.7 154 GL 0.024 0.364 0.577 0.054
0.022 155 GM 0.016 0.222 0.658 0.048 0.015 156 GN 0.017 0.033 0.247
0.072 0.016 157 GO 0.025 0.112 0.775 1.285 0.029 158 GP 0.027 1.073
2.332 0.571 0.031 159 GQ 160 GR 0.025 0.198 0.794 0.159 0.025 161
GS 0.017 0.116 0.372 0.271 0.017 162 GT 0.028 0.257 1.725 0.187
0.031 163 GU 0.014 0.075 0.728 0.152 0.026 164 GV 0.008 0.012 0.112
0.042 0.016 9.9 165 GW 0.018 0.771 2.412 0.127 0.010 166 GX 0.013
0.135 1.181 0.106 0.010 167 GY 0.013 0.060 0.311 0.048 0.015 168 GZ
0.019 0.534 1.145 0.158 0.031 169 HA 0.033 4.115 5.422 0.132 0.028
170 HB 0.011 0.155 0.490 0.038 0.011 171 HC 0.014 1.428 1.817 0.105
0.014 172 HD 0.017 1.391 1.903 0.102 0.016 173 HE 0.017 0.677 1.589
0.074 0.014 174 HF 0.060 19.483 16.256 0.556 0.111 175 HG 0.021
0.185 0.733 0.129 0.033 176 HH 0.012 3.001 2.246 0.060 0.011 177 HI
0.041 0.200 0.203 0.447 0.111 178 HJ 0.020 2.143 2.428 0.095 0.021
179 HK 0.034 0.878 11.466 0.705 0.020 180 HL 0.019 1.428 3.716
0.127 0.020 181 HM 0.019 0.234 0.709 0.077 0.020 182 HN 0.018 1.099
2.862 0.282 0.018 183 HO 0.022 0.207 0.639 0.136 0.040 184 HP 0.014
0.220 1.023 0.079 0.023 185 HQ 0.024 0.088 0.079 0.233 0.049 0.076
0.020 34.3 186 HR 0.022 1.125 2.177 0.047 0.015 187 HS 0.022 4.140
3.374 0.082 0.008 188 HT 0.051 0.778 1.351 0.075 0.030 189 HU 0.026
3.167 3.564 0.083 0.012 190 HV 1.874 44.444 44.444 12.626 1.271 191
HW 0.047 1.098 1.786 0.085 0.021 192 HX 0.027 3.283 2.917 0.266
0.014 193 HY 0.015 0.026 0.031 0.049 0.055 0.052 0.017 194 HZ 0.014
0.023 0.073 0.140 0.012 195 IA 0.021 0.024 0.033 0.062 0.055 0.052
0.019 21.8 196 IB 0.027 0.050 0.129 0.077 0.026 197 IC 0.020 0.052
0.122 0.116 0.012 198 ID 0.051 0.953 1.807 0.801 0.026 199 IE 0.035
0.042 0.065 0.198 0.039 2.2 200 IF 0.026 0.840 0.691 0.350 0.017
201 IG 0.034 0.122 0.250 0.787 0.025 28.2 202 IH 0.024 0.514 0.194
0.052 0.016 203 II 0.029 0.209 0.197 0.701 0.016 204 IJ 0.012 0.212
0.127 0.036 205 IK 0.015 0.181 0.155 0.042 27.4 206 IL 0.019 0.025
0.143 0.083 0.040 40.9 207 IM 0.016 0.212 0.150 0.043 208 IN 0.030
0.044 0.109 0.212 0.023 209 IO 0.033 0.070 0.118 0.293 0.030 210 IP
0.033 0.041 0.074 0.067 0.027 18.9 211 IQ 0.023 0.046 0.069 0.045
0.021 212 IR 0.018 0.084 0.081 0.091 0.017 213 IS 0.018 0.052 0.083
0.174 0.015 214 IT 0.017 0.007 0.064 0.032 0.004 16.2 215 IU 0.020
0.028 0.119 0.098 0.004 26.5 216 IV 0.055 0.068 0.426 0.236 0.018
217 IW 218 IX 0.024 0.236 0.246 0.057 219 IY 0.012 0.047 0.069
0.045 0.019 Activity Ranges: A .gtoreq.44 nM, B = 1 nM-43.999 nM, C
= 0.1 nM-0.999 nM, D <0.1 nM.
* * * * *