US2007167621A1PendingUtilityA1
Substituted pyrimidinones
Est. expiryApr 3, 2023(expired)· nominal 20-yr term from priority
Inventors:Richard C. Durley
C07D 403/06C07D 403/12C07D 403/10C07D 401/06C07D 239/52C07D 405/12C07D 239/47A61P 29/00C07D 405/04
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Claims
Abstract
Disclosed are compounds Formula I and pharmaceutically acceptable salts thereof, wherein R 1 , R 2 , R 4 , and R 5 are defined herein. These compounds are useful for treating diseases and conditions caused or exacerbated by unregulated p38 MAP Kinase and/or TNF activity. Pharmaceutical compositions containing the compounds, methods of preparing the compounds and methods of treatment using the compounds are also disclosed.
Claims
exact text as granted — not AI-modified1 . A compound of the formula:
or a pharmaceutically acceptable salt thereof, wherein
R 1 is H, halogen, NO 2 , alkyl, carboxaldehyde, hydroxyalkyl, dihydroxyalkyl, arylalkoxy, arylalkyl, alkenyl, alkynyl, arylalkynyl, —CN, aryl, alkanoyl, alkoxy, alkoxyalkyl, haloalkyl, haloalkoxy, carboxyl, or arylalkanoyl,
wherein the aryl portion of arylalkoxy, arylalkyl, and arylalkanoyl is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, nitro, CN, haloalkyl, haloalkoxy or CO 2 R;
wherein the alkyl portion of the alkyl, hydroxyalkyl, dihydroxyalkyl, arylalkoxy, arylalkyl, alkanoyl, alkoxy, alkoxyalkyl and arylalkanoyl groups is unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, C 1 -C 4 alkoxy, C 1 -C 4 alkoxycarbonyl, or C 3 -C 7 cycloalkyl;
R 2 is H, OH, halogen, —OSO 2 —(C 1 -C 6 ) alkyl, —OSO 2 -aryl, arylalkoxy, aryloxy, arylthio, arylthioalkoxy, arylalkynyl, alkoxy, aryloxy(C 1 -C 6 )alkyl, alkyl, alkynyl, —OC(O)NH(CH 2 ) n aryl, —OC(O)N(alkyl)(CH 2 ) n aryl, alkoxyalkoxy, dialkylamino, alkyl, alkoxy, aryl, arylalkyl, heteroaryl, heteroarylalkyl, arylalkenyl, heterocycloalkyl, heterocycloalkylalkyl, alkoxyalkoxy, NR 8 R 9 , dialkylamino, or CO 2 R, wherein
n is 0, 1, 2, 3, 4, 5 or 6;
each of which groups is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, —(C 1 -C 6 )alkyl-N(R)—CO 2 R 30 , haloalkyl, heteroaryl, heteroarylalkyl, —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, —C(O)NR 6 R 7 , —(C 1 -C 4 )alkyl-C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-NRC(O)NR 16 R 17 , haloalkoxy, alkyl, CN, hydroxyalkyl, dihydroxyalkyl, alkoxy, alkoxycarbonyl, phenyl, —SO 2 -phenyl wherein the phenyl and —SO 2 -phenyl groups are optionally substituted with 1, 2, or 3 groups that are independently halogen or NO 2 , or —OC(O)NR 6 R 7 , wherein
R 16 and R 17 are independently H or C 1 -C 6 alkyl; or
R 16 , R 17 and the nitrogen to which they are attached form a morpholinyl ring;
R 6 and R 7 are independently at each occurrence H, alkyl, hydroxyalkyl, dihydroxyalkyl, alkoxy, alkanoyl, arylalkyl, arylalkoxy, alkoxycarbonyl, —SO 2 -alkyl, OH, alkoxy, alkoxyalkyl, arylalkoxycarbonyl, —(C 1 -C 4 )alkyl-CO 2 -alkyl, heteroarylalkyl, or arylalkanoyl, wherein each is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, OH, SH, heterocycloalkyl, heterocycloalkylalkyl, C 3 -C 7 cycloalkyl, alkoxy, NH 2 , NH(alkyl), N(alkyl)(alkyl), —O-alkanoyl, alkyl, haloalkyl, carboxaldehyde, or haloalkoxy; or
R 6 , R 7 , and the nitrogen to which they are attached form a morpholinyl, pyrrolidinyl, thiomorpholinyl, thiomorpholinyl S-oxide, thiomorpholinyl S,S-dioxide, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C 1 -C 4 alkyl, alkoxycarbonyl, C 1 -C 4 alkoxy, hydroxyl, hydroxyalkyl, dihydroxyalkyl, or halogen;
R at each occurrence is independently hydrogen or C 1 -C 6 alkyl optionally substituted with 1 or 2 groups that are independently OH, SH, halogen, amino, monoalkylamino, dialkylamino or C 3 -C 6 cycloalkyl;
R 30 is C 1 -C 6 alkyl optionally substituted with 1 or 2 groups that are independently OH, SH, halogen, amino, monoalkylamino, dialkylamino or C 3 -C 6 cycloalkyl;
each R 8 is independently hydrogen, alkyl, alkanoyl, arylalkyl and arylalkanoyl, wherein each of the above is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, alkoxy, alkoxycarbonyl, halogen, or haloalkyl;
each R 9 is hydrogen, alkyl, alkanoyl, arylalkyl, cycloalkyl, cycloalkylalkyl, alkenyl, heteroaryl, aminoalkyl, monoalkylaminoalkyl, dialkylaminoalkyl, arylalkanoyl, —SO 2 -phenyl, and aryl wherein each of the above is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, alkoxy, alkoxycarbonyl, halogen, or haloalkyl;
R 4 is hydrogen or R 4 is alkyl unsubstituted or substituted with one or two groups that are independently CO 2 R, —CO 2 —(C 1 -C 6 )alkyl, —C(O)NR 6 R 7 , —C(O)R 6 , —N(R 30 )C(O)NR 16 R 17 , —N(R 30 )C(O)—(C 1 -C 6 )alkoxy, or —NR 6 R 7 , arylalkoxy, arylalkyl, heteroaryl, heteroarylalkyl, hydroxyalkyl, dihydroxyalkyl, haloalkyl, R 6 R 7 N—(C 1 -C 6 alkyl)-, —NR 6 R 7 , alkoxy, hydroxyalkoxy-, (R 6 R 7 N)-alkoxy-, R 6 R 7 NC(O)-alkoxy-, R 6 C(O)N(R 7 )alkoxy-, carboxaldehyde, —C(O)NR 6 R 7 , CO 2 R, alkoxyalkyl, or alkoxyalkoxy, wherein the heteroaryl or aryl portions of is the above are unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, hydroxy, alkoxy, alkyl, —CO 2 —(C 1 -C 6 )alkyl, —CONR 6 R 7 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 )alkyl-, nitro, haloalkyl, or haloalkoxy; and
R 5 is H, aryl, arylalkyl, arylthioalkyl, alkyl optionally substituted with 1, 2, or 3 groups that are independently arylalkoxycarbonyl, —NR 8 R 9 , halogen, —C(O)NR 8 R 9 , alkoxycarbonyl, C 3 -C 7 cycloalkyl, or alkanoyl, alkoxy, alkoxyalkyl optionally substituted with one trimethylsilyl group, amino, alkoxycarbonyl, hydroxyalkyl, dihydroxyalkyl, alkynyl, —SO 2 -alkyl, alkoxy optionally substituted with one trimethylsilyl group, heterocycloalkylalkyl, cycloalkyl, cycloalkylalkyl, -alkyl-S-aryl, -alkyl-SO 2 -aryl, heteroarylalkyl, heterocycloalkyl, heteroaryl, or alkenyl optionally substituted with alkoxycarbonyl, wherein
each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, halogen, alkoxy, hydroxyalkyl, dihydroxyalkyl, arylalkoxy, thioalkoxy, alkoxycarbonyl, arylalkoxycarbonyl, CO 2 R, CN, OH, hydroxyalkyl, dihydroxyalkyl, amidinooxime, —NR 6 R 7 , —NR 8 R 9 , R 6 R 7 N—(C 1 -C 6 alkyl)-, carboxaldehyde, SO 2 alkyl, —SO 2 H, —SO 2 NR 6 R 7 , alkanoyl wherein the alkyl portion is optionally substituted with OH, halogen or alkoxy, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , amidino, haloalkyl, —(C 1 -C 4 alkyl)-NR 15 C(O)NR 16 R 17 , —(C 1 -C 4 alkyl)-NR 15 C(O)R 18 , —O—CH 2 —O, —O—CH 2 CH 2 —O—, or haloalkoxy; wherein
R 15 is H or C 1 -C 6 alkyl; and
R 18 is C 1 -C 6 alkyl optionally substituted with —O—(C 2 -C 6 alkanoyl, C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl,
C 1 -C 6 alkoxy, C 1 -C 6 alkoxy C 1 -C 6 alkyl; amino C 1 -C 6 alkyl, mono or dialkylamino C 1 -C 6 alkyl.
2 . A compound according to claim 1 , of the formula:
or a pharmaceutically acceptable salt thereof, wherein
R 1 is H, halogen, alkyl, carboxaldehyde, hydroxyalkyl, dihydroxyalkyl, arylalkoxy, arylalkyl, alkenyl, alkynyl, arylalkynyl, CN, alkanoyl, alkoxy, alkoxyalkyl, haloalkyl, carboxyl, or arylalkanoyl,
wherein the aryl portion of arylalkoxy, arylalkyl, and arylalkanoyl is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, nitro, CN, haloalkyl, haloalkoxy or CO 2 R;
wherein the alkyl portion of the alkyl, hydroxyalkyl, dihydroxyalkyl, arylalkoxy, arylalkyl, alkanoyl, alkoxy, alkoxyalkyl and arylalkanoyl groups is unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, C 1 -C 4 alkoxy, C 1 -C 4 alkoxycarbonyl, or cyclopropyl;
R 2 is H, OH, halogen, —OSO 2 —(C 1 -C 6 ) alkyl, —OSO 2 -aryl, arylalkoxy, aryloxy, arylthioalkoxy, arylalkynyl, alkoxy, phenyloxy(C 1 -C 6 )alkyl, —OC(O)NH(CH 2 ) n aryl, —OC(O)N(alkyl)(CH 2 ) n aryl, alkyl, alkynyl, alkoxyalkoxy, dialkylamino, heteroaryl, heterocycloalkyl, aryloxyalkyl, or CO 2 R, wherein
each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, —NR 6 R 7 , haloalkyl, haloalkoxy, alkyl, heteroaryl, heteroarylalkyl, —(C 1 -C 4 )alkyl-C(O)NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-NRC(O)NR 16 R 17 , CN, hydroxyalkyl, dihydroxyalkyl, —OC(O)NR 6 R 7 , or —(C 1 -C 6 )alkyl-N(R)—CO 2 R 30 , wherein
R 16 and R 17 are independently H or C 1 -C 6 alkyl; or
R 16 , R 17 and the nitrogen to which they are attached form a morpholinyl ring;
R 6 and R 7 are independently at each occurrence H, alkyl, hydroxyalkyl, dihydroxyalkyl, alkoxy, alkoxyalkyl, alkanoyl, arylalkyl, arylalkoxy, arylalkoxycarbonyl, or arylalkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, alkoxy, alkyl, OH, SH, carboxaldehyde, haloalkyl, or haloalkoxy; or
R 6 , R 7 , and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, thiomorpholinyl S-oxide, thiomorpholinyl S,S-dioxide, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C 1 -C 4 alkyl, alkoxycarbonyl, hydroxyl, hydroxyalkyl, dihydroxyalkyl, or halogen;
n is 0, 1, 2, 3, 4, 5 or 6;
R at each occurrence is independently H or C 1 -C 6 alkyl optionally substituted with 1 or 2 groups that are independently OH, SH, halogen, amino, monoalkylamino, dialkylamino or C 3 -C 6 cycloalkyl;
R 30 is C 1 -C 6 alkyl optionally substituted with 1 or 2 groups that are independently OH, SH, halogen, amino, monoalkylamino, dialkylamino or C 3 -C 6 cycloalkyl;
R 4 is H, alkyl optionally substituted with one or two groups that are independently CO 2 R, —CO 2 alkyl, —C(O)NR 6 R 7 , —C(O)R 6 , —N(R 30 )C(O)NR 16 R 17 , —N(R 30 )C(O)—(C 1 -C 6 )alkoxy, or —NR 6 R 7 , arylalkoxy, heteroaryl, arylalkyl, hydroxyalkyl, dihydroxyalkyl, haloalkyl, —NR 6 R 7 , —C(O)NR 6 R 7 , alkoxy, hydroxyalkoxy-, (R 6 R 7 N)-alkoxy-, R 6 R 7 NC(O)-alkoxy-, R 6 C(O)N(R 7 )alkoxy-, alkoxyalkyl, or alkoxyalkoxy, wherein
the heteroaryl or aryl portions of the above are unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, hydroxy, alkoxy, alkyl, —CO 2 —(C 1 -C 6 )alkyl, —CONR 6 R 7 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 )alkyl-, nitro, haloalkyl, or haloalkoxy; and
R 5 is H, arylalkyl, alkyl optionally substituted with 1, 2, or 3 groups that are independently arylalkoxycarbonyl, —NR 8 R 9 , halogen, —C(O)NR 8 R 9 , alkoxycarbonyl, or alkanoyl, alkoxyalkyl optionally substituted with one trimethylsilyl group, alkoxycarbonyl, amino, hydroxyalkyl, dihydroxyalkyl, alkenyl optionally substituted with alkoxycarbonyl, alkynyl, —SO 2 -alkyl, aryl, alkoxy optionally substituted with one trimethylsilyl group, heterocycloalkylalkyl, heteroarylalkyl, heterocycloalkyl, or heteroaryl, wherein
each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, halogen, alkoxy, arylalkoxy, hydroxyalkyl, dihydroxyalkyl, thioalkoxy, —SO 2 alkyl, alkoxycarbonyl, arylalkoxycarbonyl, CO 2 R, CN, OH, amidinooxime, NR 8 R 9 , R 6 R 7 N—(C 1 -C 6 alkyl)-, —C(O)NR 6 R 7 , amidino, hydroxyalkyl, dihydroxyalkyl, carboxaldehyde, —NR 6 R 7 , haloalkyl, —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-CO 2 R, —(C 1 -C 4 alkyl)-C 1 -C 6 alkoxycarbonyl, —(C 1 -C 4 alkyl)-CN, —(C 1 -C 4 alkyl)-NR 15 C(O)R 18 , —O—CH 2 —O—, —O—CH 2 CH 2 —O—, phenyl or haloalkoxy;
R 8 is hydrogen, alkyl, alkanoyl, arylalkyl and arylalkanoyl;
R 9 is alkyl, alkanoyl, arylalkyl, heteroaryl, aminoalkyl, monoalkylaminoalkyl, dialkylaminoalkyl, and arylalkanoyl.
3 . A compound according to claim 2 wherein
R 1 is H, halogen, alkyl optionally substituted with C 1 -C 4 alkoxycarbonyl, carboxaldehyde, hydroxyalkyl, dihydroxyalkyl, phenyl(C 1 -C 6 )alkoxy, phenyl(C 1 -C 6 )alkyl, CN, alkanoyl, alkoxy, C 2 -C 4 alkynyl, C 2 -C 6 alkenyl optionally substituted with C 1 -C 4 alkoxycarbonyl, alkoxyalkyl, haloalkyl, or phenyl(C 1 -C 6 )alkanoyl,
wherein the phenyl groups are unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, nitro, CN, CF 3 , OCF 3 or CO 2 R;
wherein the alkyl groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, methoxy, or ethoxy;
R 2 is OH, phenyl(C 1 -C 6 )alkoxy, phenyloxy, phenyloxy(C 1 -C 6 )alkyl, phenyl (C 1 -C 4 ) thioalkoxy, C 1 -C 8 alkoxy, alkoxyalkoxy, —O—SO 2 phenyl, alkynyl, phenyl (C 2 -C 4 ) alkynyl, alkyl, —OC(O)NH(CH 2 ) n phenyl, —OC(O)N(alkyl)(CH 2 ) n phenyl, dialkylamino, pyridyl, pyrimidyl, pyridazyl, pyrazolyl, imidazolyl, pyrrolyl, tetrahydroquinolinyl, tetrahydroisoquinolinyl, tetrazolyl, pyrazinyl, benzimidazolyl, triazinyl, tetrahydrofuryl, piperidinyl, hexahydropyrimidinyl, thiazolyl, thienyl, or CO 2 R, wherein
n is 0, 1, 2, 3, 4, 5 or 6;
each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, NR 6 R 7 , haloalkyl, haloalkoxy, hydroxyalkyl, dihydroxyalkyl, alkyl, phenyl, pyridyl, piperidinyl, piperazinyl, —(C 1 -C 6 )alkyl-N(R)—CO 2 R 30 , R 6 R 7 N—(C 1 -C 6 alkyl)-, —C(O)NR 6 R 7 , —(C 1 -C 4 )alkyl-C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-NRC(O)NR 16 R 17 , or —OC(O)NR 6 R 7 , wherein
R 6 and R 7 are independently at each occurrence H, alkyl, (C 1 -C 4 ) hydroxyalkyl, (C 1 -C 4 ) dihydroxyalkyl, (C 1 -C 4 ) alkoxy, (C 1 -C 4 ) alkoxy (C 1 -C 4 ) alkyl, (C 1 -C 4 ) alkanoyl, phenyl (C 1 -C 4 ) alkyl, phenyl (C 1 -C 4 ) alkoxy, phenyl (C 1 -C 4 ) alkoxycarbonyl, or phenyl (C 1 -C 4 ) alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, OH, SH, C 3 -C 6 cycloalkyl, (C 1 -C 4 ) alkoxy, (C 1 -C 4 ) alkyl, CF 3 , carboxaldehyde, NH 2 , NH(C 1 -C 6 )alkyl, N(C 1 -C 6 )alkyl (C 1 -C 6 )alkyl, OCF 3 ; or
R 6 , R 7 , and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C 1 -C 4 alkyl, hydroxy, hydroxy C 1 -C 4 alkyl, C 1 -C 4 dihydroxyalkyl, C 1 -C 4 alkoxycarbonyl, or halogen; and
R 4 is H, alkyl optionally substituted with one or two groups that are independently CO 2 R, —CO 2 alkyl, —C(O)NR 6 R 7 , —C(O)R 6 , —N(R 30 )C(O)NR 16 R 17 , —N(R 30 )C(O)—(C 1 -C 6 )alkoxy, or —NR 6 R 7 , arylalkoxy, heteroaryl, arylalkyl, hydroxyalkyl, dihydroxyalkyl, haloalkyl, —NR 6 R 7 , —C(O)NR 6 R 7 , alkoxy, hydroxyalkoxy-, (R 6 R 7 N)-alkoxy-, R 6 R 7 NC(O)-alkoxy-, R 6 C(O)N(R 7 )alkoxy-, alkoxyalkyl, or alkoxyalkoxy, wherein
the heteroaryl or aryl portions of the above are unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, hydroxy, alkoxy, alkyl, —CO 2 —(C 1 -C 6 )alkyl, —CONR 6 R 7 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 )alkyl-, nitro, haloalkyl, or haloalkoxy; and
R 5 is phenyl(C 1 -C 6 )alkyl, (C 1 -C 6 )alkyl optionally substituted with 1, 2, 3, 4, or 5 groups that are independently phenyl C 1 -C 4 alkoxycarbonyl, —NR 8 R 9 , halogen, —C(O)NR 8 R 9 , alkoxycarbonyl, or alkanoyl, phenyl, alkoxy, C 2 -C 6 alkynyl, C 2 -C 6 alkenyl optionally substituted with alkoxycarbonyl, indolyl, quinolinyl, isoquinolinyl, isoindolyl, dihydroindolyl, pyrazolyl, imidazolyl, dihydroisoindolyl, indolon-2-yl, indazolyl, benzimidazolyl, pyridyl, imidazolidine dione, pyrazolyl(C 1 -C 6 alkyl), imidazolyl(C 1 -C 6 alkyl), piperidinyl(C 1 -C 6 )alkyl, pyrrolidinyl(C 1 -C 6 )alkyl, imidazolidinyl(C 1 -C 6 )alkyl, tetrahydroisoquinolinyl(C 1 -C 6 )alkyl, 1H-indazolyl(C 1 -C 6 )alkyl, dihydroindolon-2-yl(C 1 -C 6 alkyl), indolinyl(C 1 -C 6 alkyl), dihydrobenzimidazolyl(C 1 -C 6 alkyl), or dihydrobenzoimidazolonyl(C 1 -C 6 alkyl), pyridyl (C 1 -C 6 ) alkyl, pyridazinyl (C 1 -C 6 ) alkyl, pyrimidinyl (C 1 -C 6 ) alkyl, pyrazinyl (C 1 -C 6 ) alkyl, tetrahydrofuryl(C 1 -C 6 )alkyl, naphthyl(C 1 -C 6 )alkyl, morpholinyl (C 1 -C 6 ) alkyl, tetrahydrofuryl (C 1 -C 6 ) alkyl, thienyl (C 1 -C 6 ) alkyl, piperazinyl (C 1 -C 6 ) alkyl, indolyl (C 1 -C 6 ) alkyl, quinolinyl(C 1 -C 6 ) alkyl, isoquinolinyl(C 1 -C 6 ) alkyl, isoindolyl(C 1 -C 6 ) alkyl, dihydroindolyl(C 1 -C 6 ) alkyl, pyrazolyl(C 1 -C 4 ) alkyl, imidazolyl(C 1 -C 4 ) alkyl, dihydroisoindolyl(C 1 -C 6 ) alkyl, indoon-2-yl(C 1 -C 6 ) alkyl, indolon-2-yl(C 1 -C 6 ) alkyl, or morpholinyl C 1 -C 6 alkyl,
wherein
each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently C 1 -C 6 alkyl, halogen, C 1 -C 6 alkoxy, phenyl C 1 -C 6 alkoxy, C 1 -C 6 thioalkoxy, C 1 -C 6 alkoxycarbonyl, CO 2 R, CN, —SO 2 (C 1 -C 6 )alkyl, amidinooxime, NR 8 R 9 , —NR 6 R 7 , NR 6 R 7 C 1 -C 6 alkyl, —C(O)NR 6 R 7 , —(C 1 -C 4 )alkyl-C(O)NR 6 R 7 , amidino, C 1 -C 4 haloalkyl, hydroxy C 1 -C 6 alkyl, C 1 -C 6 dihydroxyalkyl, or C 1 -C 4 haloalkoxy; wherein
R 8 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 alkanoyl, phenyl C 1 -C 6 alkyl and phenyl C 1 -C 6 alkanoyl; and
R 9 is aminoalkyl, mono C 1 -C 6 alkylamino C 1 -C 6 alkyl, di C 1 -C 6 alkylamino C 1 -C 6 alkyl, C 1 -C 6 alkyl, C 1 -C 6 alkanoyl, phenyl C 1 -C 6 alkyl, indazolyl, and phenyl C 1 -C 6 alkanoyl.
4 . A compound according to claim 3 , wherein
R 1 is H, halogen, C 1 -C 4 alkyl optionally substituted with C 1 -C 4 alkoxycarbonyl, C 2 -C 4 alkenyl optionally substituted with C 1 -C 4 alkoxycarbonyl, C 2 -C 4 alkynyl, or carboxaldehyde; R 2 is benzyloxy, OH, phenyloxy, phenyloxy(C 1 -C 6 )alkyl, phenyl (C 1 -C 4 ) thioalkoxy, or pyridyl; wherein each of the above is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, —(C 1 -C 6 )alkyl-N(R)—CO 2 R 30 , NR 6 R 7 , (C 1 -C 4 )alkyl-C(O)NR 6 R 7 , (C 1 -C 4 ) haloalkyl, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-NRC(O)NR 16 R 17 , (C 1 -C 4 ) haloalkoxy, hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, (C 1 -C 6 ) alkyl, pyridyl, or R 6 R 7 N—(C 1 -C 6 alkyl)-.
5 . A compound according to claim 4 , wherein
R 5 is indolyl, pyridyl, pyridazinyl, pyrimidinyl, indazolyl, tetrahydroquinolyl, tetrahydroisoquinolyl, pyrazolyl, imidazolyl, furanyl, quinolinyl, isoquinolinyl, isoindolyl, dihydroindolyl, dihydroisoindolyl, indolon-2-yl, or pyrazinyl, each of which is unsubstituted or substituted with 1, 2, 3, 4 or 5 groups that are independently C 1 -C 4 alkyl, halogen, CF 3 , OCF 3 , —CO 2 CH 3 , C 1 -C 4 hydroxyalkyl, dihydroxyalkyl, C 1 -C 4 alkoxy, —CO 2 (C 1 -C 5 alkyl), benzyloxy, —NR 6 R 7 , —(C 1 -C 4 )alkyl-C(O)NR 6 R 7 , —NR 8 R 9 , NR 6 R 7 —(C 1 -C 4 alkyl), —C(O)NR 6 R 7 , or amidinooxime; wherein
R 6 and R 7 are independently at each occurrence H, C 1 -C 4 alkyl, C 1 -C 4 hydroxyalkyl, C 1 -C 4 dihydroxyalkyl, C 1 -C 4 alkoxy, C 1 -C 4 alkoxy C 1 -C 4 alkyl, C 1 -C 4 alkanoyl, phenyl C 1 -C 4 alkyl, phenyl C 1 -C 4 alkoxy, or phenyl C 1 -C 4 alkanoyl, wherein each is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, OH, SH, C 3 -C 6 cycloalkyl, aryl, C 1 -C 4 alkoxy, C 1 -C 4 alkyl, OH, CF 3 , or OCF 3 ; or
R 6 , R 7 , and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C 1 -C 4 alkyl, hydroxy, hydroxy C 1 -C 4 alkyl, C 1 -C 4 dihydroxyalkyl, or halogen.
6 . A compound according to claim 5 , wherein
R 5 is indolyl, pyridyl, pyrimidinyl, pyrazolyl, furanyl, indazolyl, dihydroindolyl, dihydroisoindolyl, indolon-2-yl, or pyrazinyl, each of which is unsubstituted or substituted with 1, 2, 3, or 4 groups that are independently C 1 -C 4 alkyl, halogen, CF 3 , OCF 3 , —CO 2 CH 3 , C 1 -C 4 hydroxyalkyl, C 1 -C 4 dihydroxyalkyl, C 1 -C 4 alkoxy, —CO 2 (C 1 -C 5 alkyl), benzyloxy, —C(O)NR 6 R 7 , —NR 8 R 9 , —(C 1 -C 4 )alkyl-C(O)NR 6 R 7 , —NR 6 R 7 , NR 6 R 7 —(C 1 -C 4 alkyl)-, and amidinooxime.
7 . A compound according to claim 6 , wherein
R 5 is indolyl, pyridyl, pyrimidinyl, dihydroindolyl, dihydroisoindolyl, pyrazolyl, or pyrazinyl, each of which is unsubstituted or substituted with 1, 2, 3, or 4 groups that are independently C 1 -C 4 alkyl, halogen, CF 3 , OCF 3 , —CO 2 CH 3 , C 1 -C 4 hydroxyalkyl, C 1 -C 4 dihydroxyalkyl, C 1 -C 4 alkoxy, —CO 2 (C 1 -C 5 alkyl), benzyloxy, —C(O)NR 6 R 7 , NR 8 R 9 , —(C 1 -C 4 )alkyl-C(O)NR 6 R 7 , —NR 6 R 7 , NR 6 R 7 —(C 1 -C 4 alkyl)-, or amidinooxime; wherein
R 6 and R 7 are independently at each occurrence H, C 1 -C 4 alkyl, C 1 -C 4 hydroxyalkyl, C 1 -C 4 dihydroxyalkyl, C 1 -C 4 alkoxy, C 1 -C 4 alkanoyl, C 1 -C 4 alkoxy C 1 -C 4 alkyl, each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, OH, SH, C 3 -C 6 cycloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 alkyl, OH, CF 3 , or OCF 3 .
8 . A compound according to claim 7 , wherein
R 5 is indolyl, pyridyl, pyrimidinyl, dihydroindolyl, dihydroisoindolyl, pyrazolyl, or pyrazinyl, each of which is unsubstituted or substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkyl, halogen, CF 3 , OCF 3 , C 1 -C 4 hydroxyalkyl, C 1 -C 4 dihydroxyalkyl, C 1 -C 4 alkoxy, —C(O)NR 6 R 7 , —(C 1 -C 4 )alkyl-C(O)NR 6 R 7 , NR 8 R 9 , —NR 6 R 7 , or NR 6 R 7 —(C 1 -C 4 alkyl)-; wherein
R 6 and R 7 are independently at each occurrence H, C 1 -C 4 alkyl, C 1 -C 4 hydroxyalkyl, C 1 -C 4 dihydroxyalkyl, C 1 -C 4 alkanoyl, or C 1 -C 4 alkoxy, each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, OH, SH, C 3 -C 6 cycloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 alkyl, OH, CF 3 , or OCF 3 .
9 . A compound according to claim 4 , wherein
R 5 is phenyl, phenyl(C 1 -C 6 )alkyl, or (C 1 -C 6 )alkyl, wherein
each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, halogen, alkoxy, benzyloxy, hydroxyalkyl, dihydroxyalkyl, thioalkoxy, —CO 2 (C 1 -C 5 alkyl), CO 2 R, CN, amidinooxime, —NR 8 R 9 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, —C(O)NR 6 R 7 , —(C 1 -C 4 ).alkyl-C(O)NR 6 R 7 , amidino, CF 3 , or OCF 3 ;
R 8 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 alkanoyl, phenyl C 1 -C 6 alkyl and phenyl C 1 -C 6 alkanoyl; and R 9 is aminoalkyl, mono C 1 -C 6 alkylamino C 1 -C 6 alkyl, di C 1 -C 6 alkylamino C 1 -C 6 alkyl, C 1 -C 6 alkyl, C 1 -C 6 alkanoyl, phenyl C 1 -C 4 alkyl, indazolyl, and phenyl C 1 -C 4 alkanoyl.
10 . A compound according to claim 4 , wherein
R 5 is phenyl or phenyl(C 1 -C 6 )alkyl, each of which is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, halogen, alkoxy, benzyloxy, thioalkoxy, —CO 2 (C 1 -C 5 alkyl), CO 2 R, CN, amidinooxime, —NR 8 R 9 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, —C(O)NR 6 R 7 , —(C 1 -C 4 )—C(O)NR 6 R 7 , amidino, CF 3 , or OCF 3 ; wherein
R 6 and R 7 are independently at each occurrence H, C 1 -C 4 alkyl, C 1 -C 4 hydroxyalkyl, C 1 -C 4 .dihydroxyalkyl, C 1 -C 4 alkoxy, C 1 -C 4 alkoxy C 1 -C 4 alkyl, C 1 -C 4 alkanoyl, phenyl C 1 -C 4 alkyl, phenyl C 1 -C 4 alkoxy, or phenyl C 1 -C 4 alkanoyl, wherein each is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, OH, SH, C 3 -C 6 cycloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 alkyl, CF 3 , or OCF 3 ; or
R 6 , R 7 , and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C 1 -C 4 alkyl, hydroxy, hydroxy C 1 -C 4 alkyl, C 1 -C 4 dihydroxyalkyl, or halogen;
R 8 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 alkanoyl, phenyl C 1 -C 6 alkyl and phenyl C 1 -C 6 alkanoyl; and
R 9 is aminoalkyl, mono C 1 -C 6 alkylamino C 1 -C 6 alkyl, di C 1 -C 6 alkylamino C 1 -C 6 alkyl, C 1 -C 6 alkyl, C 1 -C 6 alkanoyl, phenyl C 1 -C 4 alkyl, indazolyl, and phenyl C 1 -C 4 alkanoyl.
11 . A compound according to claim 10 , wherein
R 5 is phenyl, benzyl or phenethyl, wherein each is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently C 1 -C 6 alkyl, —NR 6 R 7 , —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , —NR 8 R 9 , halogen, C 1 -C 6 alkoxy, CO 2 R, —(C 1 -C 4 alkyl)-CO 2 R, C 1 -C 6 thioalkoxy, amidinooxime, C 1 -C 6 alkoxycarbonyl, —(C 1 -C 4 alkyl)-C 1 -C 6 alkoxycarbonyl, C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, —(C 1 -C 4 alkyl)-CN, CN, phenyl C 1 -C 6 alkoxy, OH, C 1 -C 4 haloalkyl, C 1 -C 4 haloalkoxy, R 6 R 7 N—(C 1 -C 6 alkyl)-, —(C 1 -C 4 alkyl)-NR 15 C(O)R 18 , amidinooxime, —SO 2 (C 1 -C 6 alkyl), —O—CH 2 —O—, —O—CH 2 CH 2 —O—, phenyl C 1 -C 4 alkoxy, or phenyl; wherein
R 6 and R 7 are independently at each occurrence H, C 1 -C 4 alkyl, C 1 -C 4 hydroxyalkyl, C 1 -C 4 dihydroxyalkyl, C 1 -C 4 alkanoyl, or C 1 -C 4 alkoxy, each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, OH, SH, C 3 -C 6 cycloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 alkyl, OH, CF 3 , or OCF 3 .
12 . A compound according to claim 11 , wherein
R 5 is phenyl, benzyl or phenethyl, each of which is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently CN, halogen, C 1 -C 4 alkoxy, CF 3 , OCF 3 , C 1 -C 4 alkyl, —NR 8 R 9 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, or —C(O)NR 6 R 7 , wherein
R 6 and R 7 are independently at each occurrence H, C 1 -C 4 alkyl, C 1 -C 4 hydroxyalkyl, C 1 -C 4 dihydroxyalkyl, C 1 -C 4 alkanoyl, or C 1 -C 4 alkoxy, each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, OH, SH, C 3 -C 6 cycloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 alkyl, OH, CF 3 , or OCF 3 .
13 . A compound according to claim 4 , wherein the R 5 group is of the formula:
wherein
Z 1 and Z 2 are independently H, halogen, C 1 -C 4 alkyl, or CO 2 R; and
Z is —C(O)NR 6 R 7 , —(C 1 -C 4 )alkyl-C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-NR 15 C(O)R 18 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, —NR 8 R 9 , C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, C 1 -C 6 alkyl, CO 2 R, or halogen; wherein
R 6 and R 7 at each occurrence are independently H, OH, C 1 -C 6 alkyl, amino C 1 -C 4 alkyl, NH(C 1 -C 6 alkyl)alkyl, N(C 1 -C 6 alkyl)(C 1 -C 6 alkyl) C 1 -C 6 alkyl, C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, C 1 -C 6 alkoxy C 1 -C 6 alkyl, or —SO 2 (C 1 -C 6 alkyl) each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, OH, SH, C 3 -C 6 cycloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 alkyl, OH, CF 3 , or OCF 3 ;
or
R 6 , R 7 , and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl, thiomorpholinyl, ring optionally substituted with 1 or 2 groups that are independently alkyl, hydroxy, hydroxy C 1 -C 4 alkyl, C 1 -C 4 dihydroxyalkyl, or halogen; and
R 18 is C 1 -C 6 alkyl optionally substituted with —O—(C 2 -C 6 alkanoyl, C 1 -C 6 hydroxyalkyl, C 1 -C 4 dihydroxyalkyl, C 1 -C 6 alkoxy, C 1 -C 6 alkoxy C 1 -C 6 alkyl; amino C 1 -C 6 alkyl, mono or dialkylamino C 1 -C 6 alkyl.
14 . A compound according to claim 4 , wherein
R 5 is pyrazolyl(C 1 -C 6 alkyl), imidazolyl(C 1 -C 6 alkyl), thienyl(C 1 -C 6 alkyl), furanyl(C 1 -C 6 alkyl), piperidinyl(C 1 -C 6 )alkyl, pyrrolidinyl(C 1 -C 6 )alkyl, imidazolidinyl(C 1 -C 6 )alkyl, piperazinyl(C 1 -C 6 )alkyl, pyridyl(C 1 -C 6 )alkyl, pyrimidyl(C 1 -C 6 )alkyl, pyridazyl(C 1 -C 6 )alkyl, pyrazinyl(C 1 -C 6 )alkyl, isoquinolinyl(C 1 -C 6 )alkyl, tetrahydroisoquinolinyl(C 1 -C 6 )alkyl, indolyl(C 1 -C 6 )alkyl, 1H-indazolyl(C 1 -C 6 )alkyl, dihydroindolyl(C 1 -C 6 alkyl), dihydroindolon-2-yl(C 1 -C 6 alkyl), indolinyl(C 1 -C 6 alkyl), dihydroisoindolyl(C 1 -C 6 alkyl), dihydrobenzimdazolyl(C 1 -C 6 alkyl), or dihydrobenzoimidazolonyl(C 1 -C 6 alkyl), wherein
each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently (C 1 -C 6 )alkyl, halogen, (C 1 -C 6 )alkoxy, (C 1 -C 6 )hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, phenyl(C 1 -C 6 )alkoxy, (C 1 -C 6 )thioalkoxy, (C 1 -C 6 )alkoxycarbonyl, phenyl(C 1 -C 6 )alkoxycarbonyl, OH, CO 2 R, CN, amidinooxime, —NR 8 R 9 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , amidino, piperazinyl, morpholinyl, —SO 2 (C 1 -C 6 ) alkyl, —SO 2 NH 2 , —SO 2 NH(C 1 -C 6 )alkyl, —SO 2 N(C 1 -C 6 )alkyl (C 1 -C 6 )alkyl, (C 1 -C 4 )haloalkyl, —(C 1 -C 4 alkyl)-NR 15 C(O)NR 16 R 17 , —(C 1 -C 4 alkyl)-NR 15 C(O)R 18 , —O—CH 2 —O, —O—CH 2 CH 2 —O—, or (C 1 -C 4 )haloalkoxy; wherein
R 6 and R 7 are independently at each occurrence H, (C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy, (C 1 -C 6 )alkoxy(C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxycarbonyl, (C 1 -C 6 )hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, —(C 1 -C 4 )alkyl-CO 2 —(C 1 -C 6 )alkyl, (C 1 -C 6 )alkanoyl, phenyl(C 1 -C 6 )alkyl, phenyl(C 1 -C 6 )alkoxy, or phenyl(C 1 -C 6 )alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, (C 1 -C 4 )alkoxy, OH, SH, C 3 -C 6 cycloalkyl, NH 2 , NH(C 1 -C 6 alkyl), N(C 1 -C 6 alkyl)(C 1 -C 6 alkyl), (C 1 -C 4 )alkyl, CF 3 or OCF 3 ; or
R 6 , R 7 , and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C 1 -C 4 alkyl, hydroxy, hydroxy C 1 -C 4 alkyl, C 1 -C 4 dihydroxyalkyl, or halogen; and
R 18 is C 1 -C 6 alkyl optionally substituted with —O—(C 2 -C 6 alkanoyl, C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, C 1 -C 6 alkoxy, C 1 -C 6 alkoxy C 1 -C 6 alkyl; amino C 1 -C 6 alkyl, mono or dialkylamino C 1 -C 6 alkyl,
15 . A compound according to claim 14 , wherein
R 5 is pyrazolyl(C 1 -C 6 alkyl), imidazolyl(C 1 -C 6 alkyl), benzimidazolyl(C 1 -C 6 alkyl), thienyl(C 1 -C 6 alkyl), pyrimidyl(C 1 -C 6 )alkyl, indolyl(C 1 -C 6 alkyl), dihydroindolyl(C 1 -C 6 alkyl), dihydroisoindolyl(C 1 -C 6 alkyl), dihydroindolon-2-yl(C 1 -C 6 alkyl), pyridinyl(C 1 -C 6 alkyl), piperazinyl(C 1 -C 6 alkyl), or pyrazinyl(C 1 -C 6 alkyl) each of which is optionally substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkyl, C 1 -C 4 hydroxyalkyl, C 1 -C 4 dihydroxyalkyl, halogen, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , C 1 -C 6 alkoxycarbonyl, —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, haloalkyl, C 1 -C 6 alkanoyl,
R 6 and R 7 at each occurrence are independently H, C 1 -C 6 alkyl optionally substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkoxycarbonyl, halogen, C 3 -C 6 cycloalkyl, OH, SH, or C 1 -C 4 alkoxy;
or
R 6 , R 7 , and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl ring optionally substituted with 1 or 2 groups that are independently alkyl, hydroxy, hydroxy C 1 -C 4 alkyl, C 1 -C 4 dihydroxyalkyl, or halogen.
16 . A compound according to claim 15 , wherein
R 5 is of the formula: wherein Z 5 is C 1 -C 4 alkyl, C 1 -C 4 hydroxyalkyl, C 1 -C 4 dihydroxyalkyl, halogen, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , C 1 -C 6 alkoxycarbonyl, R 6 R 7 N—(C 1 -C 6 alkyl)-, —NR 6 R 7 , CF 3 , or C 1 -C 6 alkanoyl, wherein
R 6 and R 7 at each occurrence are independently H, C 1 -C 6 alkyl optionally substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkoxycarbonyl, halogen, C 3 -C 6 cycloalkyl, OH, SH, or C 1 -C 4 alkoxy;
or
R 6 , R 7 , and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl ring optionally substituted with 1 or 2 groups that are independently alkyl, hydroxy, hydroxy C 1 -C 4 alkyl, C 1 -C 4 dihydroxyalkyl, or halogen.
17 . A compound according to claim 15 , wherein
R 5 is of the formula: wherein Z 5 is C 1 -C 4 alkyl, C 1 -C 4 hydroxyalkyl, C 1 -C 4 dihydroxyalkyl, halogen, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , C 1 -C 6 alkoxycarbonyl, R 6 R 7 N—(C 1 -C 6 alkyl)-, —NR 6 R 7 , CF 3 , or C 1 -C 6 alkanoyl, wherein
R 6 and R 7 at each occurrence are independently H, C 1 -C 6 alkyl optionally substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkoxycarbonyl, halogen, C 3 -C 6 cycloalkyl, OH, SH, or C 1 -C 4 alkoxy;
or
R 6 , R 7 , and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl ring optionally substituted with 1 or 2 groups that are independently alkyl, hydroxy, hydroxy C 1 -C 4 alkyl, C 1 -C 4 dihydroxyalkyl, or halogen.
18 . A compound according to claim 16 , wherein
Z 5 is C 1 -C 4 alkyl, C 1 -C 4 hydroxyalkyl, C 1 -C 4 dihydroxyalkyl, halogen, C 1 -C 6 alkoxycarbonyl, CF 3 , or C 1 -C 6 alkanoyl.
19 . A compound according to claim 16 , wherein
Z 5 is C 1 -C 4 alkyl, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, or —NR 6 R 7 , CF 3 , or C 1 -C 4 alkanoyl, wherein
R 6 and R 7 at each occurrence are independently H, C 1 -C 6 alkyl optionally substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkoxycarbonyl, halogen, C 3 -C 6 cycloalkyl, OH, SH, or C 1 -C 4 alkoxy;
or
R 6 , R 7 , and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl ring optionally substituted with 1 or 2 groups that are independently alkyl, hydroxy, hydroxy C 1 -C 4 alkyl, C 1 -C 4 dihydroxyalkyl, or halogen.
20 . A compound according to claim 19 , wherein
Z 5 is —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-,
or —NR 6 R 7 , wherein
R 6 and R 7 at each occurrence are independently H, C 1 -C 6 alkyl optionally substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkoxycarbonyl, halogen, cyclopropyl, OH, SH, or C 1 -C 4 alkoxy.
21 . A compound according to claim 15 , wherein
R 5 is of the formula: wherein Z 10 is H or methyl; and Z 20 is hydroxy(C 1 -C 4 )alkyl, C 1 -C 4 dihydroxyalkyl, OH, halogen, haloalkyl, (C 1 -C 4 )alkyl, OCF 3 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , or —C(O)NR 6 R 7 , wherein R 6 and R 7 at each occurrence are independently H, C 1 -C 6 alkyl optionally substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkoxycarbonyl, halogen, C 3 -C 6 cycloalkyl, OH, SH, or C 1 -C 4 alkoxy.
22 . A compound according to claim 15 , wherein
R 5 is of the formula: wherein Z 10 is H or methyl; and Z 20 is hydroxy(C 1 -C 4 )alkyl, C 1 -C 4 dihydroxyalkyl, OH, halogen, CF 3 , (C 1 -C 4 )alkyl, OCF 3 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , or —C(O)NR 6 R 7 , wherein R 6 and R 7 at each occurrence are independently H, C 1 -C 6 alkyl optionally substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkoxycarbonyl, halogen, C 3 -C 6 cycloalkyl, OH, SH, or C 1 -C 4 alkoxy.
23 . A compound according to claim 15 , wherein
R 5 is of the formula: wherein Z 10 is H or methyl; and Z 20 is hydroxy(C 1 -C 4 )alkyl, C 3 -C 4 dihydroxyalkyl, OH, halogen, haloalkyl, (C 1 -C 4 )alkyl, OCF 3 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , or —C(O)NR 6 R 7 , wherein R 6 and R 7 at each occurrence are independently H, C 1 -C 6 alkyl optionally substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkoxycarbonyl, halogen, C 3 -C 6 cycloalkyl, OH, SH, or C 1 -C 4 alkoxy.
24 . A compound according to claim 15 , wherein
R 5 is of the formula: wherein Z 10 is H or methyl; and Z 20 is hydroxy(C 1 -C 4 )alkyl, C 1 -C 4 dihydroxyalkyl, OH, halogen, CF 3 , (C 1 -C 4 )alkyl, OCF 3 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , or —C(O)NR 6 R 7 , wherein R 6 and R 7 at each occurrence are independently H, C 1 -C 6 alkyl optionally substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkoxycarbonyl, halogen, C 3 -C 6 cycloalkyl, OH, SH, or C 1 -C 4 alkoxy.
25 . A compound according to claim 15 , wherein
R 5 is of the formula: wherein Z 10 is H or methyl; and Z 20 is hydroxy(C 1 -C 4 )alkyl, C 1 -C 4 dihydroxyalkyl, OH, halogen, haloalkyl, (C 1 -C 4 )alkyl, OCF 3 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , or —C(O)NR 6 R 7 , wherein R 6 and R 7 at each occurrence are independently H, C 1 -C 6 alkyl optionally substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkoxycarbonyl, halogen, C 3 -C 6 cycloalkyl, OH, SH, or C 1 -C 4 alkoxy.
26 . A compound according to claim 15 , wherein
R 5 is of the formula: wherein Z 10 is H or methyl; and Z 20 is hydroxy(C 1 -C 4 )alkyl, C 1 -C 4 dihydroxyalkyl, OH, halogen, CF 3 , (C 1 -C 4 )alkyl, OCF 3 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , or —C(O)NR 6 R 7 , wherein R 6 and R 7 at each occurrence are independently H, C 1 -C 6 alkyl optionally substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkoxycarbonyl, halogen, C 3 -C 6 cycloalkyl, OH, SH, or C 1 -C 4 alkoxy.
27 . A compound according to claim 15 , wherein
R 5 is of the formula: wherein Z 10 is H or methyl; and Z 20 is hydroxy(C 1 -C 4 )alkyl, C 1 -C 4 dihydroxyalkyl, OH, halogen, haloalkyl, (C 1 -C 4 )alkyl, OCF 3 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , or —C(O)NR 6 R 7 , wherein R 6 and R 7 at each occurrence are independently H, C 1 -C 6 alkyl optionally substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkoxycarbonyl, halogen, C 3 -C 6 cycloalkyl, OH, SH, or C 1 -C 4 alkoxy.
28 . A compound according to claim 15 , wherein
R 5 is of the formula: wherein Z 10 is H or methyl; and Z 20 is hydroxy(C 1 -C 4 )alkyl, C 1 -C 4 dihydroxyalkyl, OH, halogen, CF 3 , (C 1 -C 4 )alkyl, OCF 3 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , or —C(O)NR 6 R 7 , wherein R 6 and R 7 at each occurrence are independently H, C 1 -C 6 alkyl optionally substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkoxycarbonyl, halogen, C 3 -C 6 cycloalkyl, OH, SH, or C 1 -C 4 alkoxy.
29 . A compound according to claim 4 , wherein
R 5 is phenyl, which is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently C 1 -C 4 alkyl, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , —NR 6 R 7 , NR 6 R 7 (C 1 -C 6 alkyl), C 1 -C 6 hydroxyalkyl, dihydroxyalkyl, halogen, C 1 -C 4 alkoxy, CO 2 R, OH, C 1 -C 6 alkoxycarbonyl, CF 3 , —(C 1 -C 4 alkyl)-NR 15 C(O)NR 16 R 17 , —(C 1 -C 4 alkyl)-NR 15 C(O)R 18 ; wherein
R 15 is H or C 1 -C 6 alkyl;
R 16 and R 17 are independently H or C 1 -C 6 alkyl; or
R 16 , R 17 , and the nitrogen to which they are attached form a morpholinyl ring; and
R 18 is C 1 -C 6 alkyl optionally substituted with —O—(C 2 -C 6 alkanoyl, C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, C 1 -C 6 alkoxy, C 1 -C 6 alkoxy C 1 -C 6 alkyl; amino C 1 -C 6 alkyl, mono or dialkylamino C 1 -C 6 alkyl.
30 . A compound according to claim 29 , wherein
R 5 is of the formula: Z 1 is H, halogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 1 -C 4 hydroxyalkyl, C 1 -C 4 dihydroxyalkyl, or C 1 -C 4 alkoxy; and Z 2 is C 1 -C 4 alkyl, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , —NR 6 R 7 , NR 6 R 7 (C 1 -C 6 alkyl), C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, halogen, C 1 -C 4 alkoxy, CO 2 R, OH, C 1 -C 6 alkoxycarbonyl, or C 1 -C 4 haloalkyl; Z 3 is H, C 1 -C 4 alkyl, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , —NR 6 R 7 , NR 6 R 7 (C 1 -C 6 alkyl), C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, halogen, C 1 -C 4 alkoxy, CO 2 R, OH, C 1 -C 6 alkoxycarbonyl, or C 1 -C 4 haloalkyl; wherein R 6 and R 7 at each occurrence are independently H, OH, C 1 -C 6 alkyl, amino C 1 -C 4 alkyl, NH(C 1 -C 6 alkyl)alkyl, N(C 1 -C 6 alkyl)(C 1 -C 6 alkyl) C 1 -C 6 alkyl, C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, C 1 -C 6 alkoxy C 1 -C 6 alkyl, —SO 2 (C 1 -C 6 alkyl), —SO 2 NH 2 , —SO 2 NH(C 1 -C 6 alkyl), —SO 2 N(C 1 -C 6 alkyl)(C 1 -C 6 alkyl), or C 1 -C 6 alkanoyl, each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, OH, SH, C 3 -C 6 cycloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 alkyl, OH, CF 3 , or OCF 3 .
31 . A compound according to claim 30 , wherein
R 5 is of the formula: wherein Z 1 is H, halogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 1 -C 4 hydroxyalkyl, C 1 -C 4 dihydroxyalkyl, or C 1 -C 4 alkoxy; and Z 2 is C 1 -C 4 alkyl, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , —NR 6 R 7 , NR 6 R 7 (C 1 -C 6 alkyl), C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, halogen, C 1 -C 4 alkoxy, CO 2 R, OH, C 1 -C 6 alkoxycarbonyl, or C 1 -C 4 haloalkyl; Z 3 is H, C 1 -C 4 alkyl, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , —NR 6 R 7 , NR 6 R 7 (C 1 -C 6 alkyl), C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, halogen, C 1 -C 4 alkoxy, CO 2 R, OH, C 1 -C 6 alkoxycarbonyl, or C 1 -C 4 haloalkyl, wherein R 6 and R 7 at each occurrence are independently H, OH, C 1 -C 6 alkyl, amino C 1 -C 4 alkyl, NH(C 1 -C 6 alkyl)alkyl, N(C 1 -C 6 alkyl)(C 1 -C 6 alkyl) C 1 -C 6 alkyl, C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, C 1 -C 6 alkoxy C 1 -C 6 alkyl, —SO 2 (C 1 -C 6 alkyl), —SO 2 NH 2 , —SO 2 NH(C 1 -C 6 alkyl), —SO 2 N(C 1 -C 6 alkyl)(C 1 -C 6 alkyl), or C 1 -C 6 alkanoyl, each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, OH, SH, C 3 -C 6 cycloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 alkyl, OH, CF 3 , or OCF 3 .
32 . A compound according to claim 30 , wherein
R 5 is of the formula: wherein Z 1 is H, halogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 1 -C 4 hydroxyalkyl, C 1 -C 4 dihydroxyalkyl, or C 1 -C 4 alkoxy; and Z 2 is C 1 -C 4 alkyl, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , —NR 6 R 7 , NR 6 R 7 (C 1 -C 6 alkyl), C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, halogen, C 1 -C 4 alkoxy, CO 2 R, OH, C 1 -C 6 alkoxycarbonyl, or C 1 -C 4 haloalkyl; Z 3 is H, C 1 -C 4 alkyl, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , —NR 6 R 7 , NR 6 R 7 (C 1 -C 6 alkyl), C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, halogen, C 1 -C 4 alkoxy, CO 2 R, OH, C 1 -C 6 alkoxycarbonyl, or C 1 -C 4 haloalkyl, wherein R 6 and R 7 at each occurrence are independently H, OH, C 1 -C 6 alkyl, amino C 1 -C 4 alkyl, NH(C 1 -C 6 alkyl)alkyl, N(C 1 -C 6 alkyl)(C 1 -C 6 alkyl) C 1 -C 6 alkyl, C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, C 1 -C 6 alkoxy C 1 -C 6 alkyl, —SO 2 (C 1 -C 6 alkyl), —SO 2 NH 2 , —SO 2 NH(C 1 -C 6 alkyl), —SO 2 N(C 1 -C 6 alkyl)(C 1 -C 6 alkyl), or C 1 -C 6 alkanoyl, each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, OH, SH, C 3 -C 6 cycloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 alkyl, OH, CF 3 , or OCF 3 .
33 . A compound according to claim 29 , wherein
R 5 is either wherein Z 1 is H, halogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 1 -C 4 hydroxyalkyl, C 1 -C 4 dihydroxyalkyl, or C 1 -C 4 alkoxy; and Z 2 is C 1 -C 4 alkyl, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , —NR 6 R 7 , NR 6 R 7 (C 1 -C 6 alkyl), C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, halogen, C 1 -C 4 alkoxy, CO 2 R, C 1 -C 6 alkoxycarbonyl, —(C 1 -C 4 alkyl)-NR 15 C(O)NR 16 R 17 , or —(C 1 -C 4 alkyl)-NR 15 C(O)R 18 ; Z 3 is H, C 1 -C 4 alkyl, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , —NR 6 R 7 , NR 6 R 7 (C 1 -C 6 alkyl), C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, halogen, C 1 -C 4 alkoxy, CO 2 R, C 1 -C 6 alkoxycarbonyl, —(C 1 -C 4 alkyl)-NR 15 C(O)NR 16 R 17 , or —(C 1 -C 4 alkyl)-NR 15 C(O)R 18 ;
R 6 , R 7 , and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl ring optionally substituted with 1 or 2 groups that are independently alkyl, hydroxy, hydroxy C 1 -C 4 alkyl, C 1 -C 4 dihydroxyalkyl, or halogen;
R 15 is H or C 1 -C 6 alkyl;
R 16 and R 17 are independently H or C 1 -C 6 alkyl; or
R 16 , R 17 , and the nitrogen to which they are attached form a morpholinyl ring;
R 18 is C 1 -C 6 alkyl optionally substituted with —O—(C 2 -C 6 alkanoyl, C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, C 1 -C 6 alkoxy, C 1 -C 6 alkoxy C 1 -C 6 alkyl; amino C 1 -C 6 alkyl, mono or dialkylamino C 1 -C 6 alkyl.
34 . A compound according to claim 33 , wherein
R 5 is of the formula: Z 1 is H, halogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 1 -C 4 hydroxyalkyl, C 1 -C 4 dihydroxyalkyl, or C 1 -C 4 alkoxy; and Z 2 is C 1 -C 4 alkyl, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , —NR 6 R 7 , NR 6 R 7 (C 1 -C 6 alkyl), C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, halogen, C 1 -C 4 alkoxy, CO 2 R, C 1 -C 6 alkoxycarbonyl, —(C 1 -C 4 alkyl)-NR 15 C(O)NR 16 R 17 , or —(C 1 -C 4 alkyl)-NR 15 C(O)R 18 ; Z 3 is H, C 1 -C 4 alkyl, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , —NR 6 R 7 , NR 6 R 7 (C 1 -C 6 alkyl), C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, halogen, C 1 -C 4 alkoxy, CO 2 R, C 1 -C 6 alkoxycarbonyl, —(C 1 -C 4 alkyl)-NR 15 C(O)NR 16 R 17 , or —(C 1 -C 4 alkyl)-NR 15 C(O)R 18 ;
R 6 , R 7 , and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl ring optionally substituted with 1 or 2 groups that are independently alkyl, hydroxy, hydroxy C 1 -C 4 alkyl, C 1 -C 4 dihydroxyalkyl, or halogen;
R 15 is H or C 1 -C 6 alkyl;
R 16 and R 17 are independently H or C 1 -C 6 alkyl; or
R 16 , R 17 , and the nitrogen to which they are attached form a morpholinyl ring;
R 18 is C 1 -C 6 alkyl optionally substituted with —O—(C 2 -C 6 alkanoyl, C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, C 1 -C 6 alkoxy, C 1 -C 6 alkoxy C 1 -C 6 alkyl; amino C 1 -C 6 alkyl, mono or dialkylamino C 1 -C 6 alkyl.
35 . A compound according to claim 33 , wherein
R 5 is of the formula: wherein Z 1 is H, halogen, C 1 -C 4 alkyl C 1 -C 4 haloalkyl, C 1 -C 4 hydroxyalkyl, C 1 -C 4 dihydroxyalkyl, or C 1 -C 4 alkoxy; and Z 2 is C 1 -C 4 alkyl, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , —NR 6 R 7 , NR 6 R 7 (C 1 -C 6 alkyl), C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, halogen, C 1 -C 4 alkoxy, CO 2 R, C 1 -C 6 alkoxycarbonyl, —(C 1 -C 4 alkyl)-NR 15 C(O)NR 16 R 17 , or —(C 1 -C 4 alkyl)-NR 15 C(O)R 18 ; Z 3 is H, C 1 -C 4 alkyl, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , —NR 6 R 7 , NR 6 R 7 (C 1 -C 6 alkyl), C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, halogen, C 1 -C 4 alkoxy, CO 2 R, C 1 -C 6 alkoxycarbonyl, —(C 1 -C 4 alkyl)-NR 15 C(O)NR 16 R 17 , or —(C 1 -C 4 alkyl)-NR 15 C(O)R 18 ;
R 6 , R 7 , and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl ring, each of which is optionally substituted with 1 or 2 groups that are independently alkyl, hydroxy, hydroxy C 1 -C 4 alkyl, C 1 -C 4 dihydroxyalkyl, or halogen;
R 15 is H or C 1 -C 6 alkyl;
R 16 and R 17 are independently H or C 1 -C 6 alkyl; or
R 16 , R 17 , and the nitrogen to which they are attached form a morpholinyl ring;
R 18 is C 1 -C 6 alkyl optionally substituted with —O—(C 2 -C 6 alkanoyl, C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, C 1 -C 6 alkoxy, C 1 -C 6 alkoxy C 1 -C 6 alkyl; amino C 1 -C 6 alkyl, mono or dialkylamino C 1 -C 6 alkyl.
36 . A compound of the formula
or a pharmaceutically acceptable salt thereof, wherein
L and M are independently selected from —O—, —CH 2 —, —S—, —NR—, —N(R)—N(R)—, C(═O)—, —SO 2 —;
R 5 is
wherein
X 1 , X 2 , X a , X b , X c , X d , and X e at are independently selected from —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , —NR 6 R 7 , hydroxy(C 1 -C 4 )alkyl, C 1 -C 4 dihydroxyalkyl, H, OH, halogen, haloalkyl, alkyl, haloalkoxy, heteroaryl, heterocycloalkyl, C 3 -C 7 cycloalkyl, R 6 R 7 N—(C 1 -C 6 alkyl)-, —CO 2 —(C 1 -C 6 )alkyl, —N(R)C(O)NR 6 R 7 , —N(R)C(O)—(C 1 -C 6 )alkoxy, CO 2 R—(C 1 -C 6 alkyl)-, or —SO 2 NR 6 R 7 ; wherein the heteroaryl and heterocycloalkyl groups are optionally substituted with —NR 6 R 7 , —C(O)NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, or halogen; or
R 5 is heteroaryl or heteroarylalkyl, wherein the heteroaryl and heteroaryl groups are optionally substituted with 1, 2, 3, or 4 groups that are independently —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , —NR 6 R 7 , hydroxy(C 1 -C 4 )alkyl, C 1 -C 4 dihydroxyalkyl, H, OH, halogen, haloalkyl, alkyl, haloalkoxy, R 6 R 7 N—(C 1 -C 6 alkyl)-, —CO 2 —(C 1 -C 6 )alkyl, —N(R)C(O)NR 6 R 7 , or —N(R)C(O)—(C 1 -C 6 )alkoxy; wherein
R 6 and R 7 are independently at each occurrence H, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 1 -C 6 alkoxy C 1 -C 6 alkyl, C 1 -C 6 alkoxycarbonyl, OH, C 1 -C 6 hydroxyalkyl, C 1 -C 4 dihydroxyalkyl, C 1 -C 6 thiohydroxyalkyl, —(C 1 -C 4 )alkyl-CO 2 -alkyl, pyridyl C 1 -C 6 alkyl, C 1 -C 6 alkanoyl, benzyl, phenyl C 1 -C 6 alkoxy, or phenyl C 1 -C 6 alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C 3 -C 6 cycloalkyl, C 1 -C 6 alkoxy, piperidinyl C 1 -C 6 alkyl, morpholinyl C 1 -C 6 alkyl, piperazinyl C 1 -C 6 alkyl, OH, SH, NH 2 , NH(alkyl), N(alkyl)(alkyl), —O—C 1 -C 4 alkanoyl, C 1 -C 4 alkyl, CF 3 , or OCF 3 ; or
R 6 , R 7 , and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C 1 -C 4 alkyl, C 1 -C 4 alkoxy, hydroxy, hydroxy C 1 -C 4 alkyl, C 1 -C 4 dihydroxyalkyl, or halogen;
R at each occurrence is independently H or C 1 -C 6 alkyl; and
Y, Y 1 , Y 2 , Y 3 , and Y 4 are independently selected from H, halogen, alkyl, carboxaldehyde, hydroxyalkyl, dihydroxyalkyl, alkenyl, alkynyl, CN, alkanoyl, alkoxy, alkoxyalkyl, haloalkyl, and carboxyl.
37 . A compound according to claim 36 of the formula
or a pharmaceutically acceptable salt thereof.
38 . A compound according to claim 37 , wherein
R 5 is
39 . A compound according to claim 31 , wherein
Y 2 , Y 4 , and Y are independently halogen; and Y 1 and Y 3 are both hydrogen.
40 . A compound according to claim 39 , wherein
R 5 is X 1 and X 2 are independently H, methyl, NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, —C(O)NR 6 R 7 , C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, or —(C 1 -C 4 alkyl)-morpholinyl; and X a and X e are independently halogen, NH 2 , NH(C 1 -C 6 alkyl), N(C 1 -C 6 alkyl)(C 1 -C 6 alkyl), methyl, or hydrogen.
41 . A compound according to claim 40 , wherein
one of X b and X c is hydrogen and the other is —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, —C(O)NR 6 R 7 , —SO 2 NR 6 R 7 , or halogen; where
R 6 and R 7 are independently at each occurrence H, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 1 -C 6 alkoxy C 1 -C 6 alkyl, C 1 -C 6 alkoxycarbonyl, OH, C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, —(C 1 -C 4 )alkyl-CO 2 -alkyl, pyridyl C 1 -C 6 alkyl, C 1 -C 6 alkanoyl, benzyl, phenyl C 1 -C 6 alkoxy, or phenyl C 1 -C 6 alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C 3 -C 6 cycloalkyl, C 1 -C 6 alkoxy, piperidinyl C 1 -C 6 alkyl, morpholinyl C 1 -C 6 alkyl, piperazinyl C 1 -C 6 alkyl, OH, SH, NH 2 , NH (alkyl), N(alkyl)(alkyl), —O—C 1 -C 4 alkanoyl, C 1 -C 4 alkyl, CF 3 , or OCF 3 ; or
R 6 , R 7 , and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C 1 -C 4 alkyl, C 1 -C 4 alkoxy, hydroxy, hydroxy C 1 -C 4 alkyl, C 1 -C 4 dihydroxyalkyl, or halogen.
42 . A compound according to claim 41 , wherein
R 6 and R 7 are independently at each occurrence H, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 1 -C 6 alkoxy C 1 -C 6 alkyl, C 1 -C 6 alkoxycarbonyl, OH, C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, —(C 1 -C 4 )alkyl-CO 2 -alkyl, pyridyl C 1 -C 6 alkyl, C 1 -C 6 alkanoyl, benzyl, phenyl C 1 -C 6 alkoxy, or phenyl C 1 -C 6 alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C 3 -C 6 cycloalkyl, C 1 -C 6 alkoxy, piperidinyl C 1 -C 6 alkyl, morpholinyl C 1 -C 6 alkyl, piperazinyl C 1 -C 6 alkyl, OH, NH 2 , NH(alkyl), N(alkyl)(alkyl), —O—C 1 -C 4 alkanoyl, C 1 -C 4 alkyl, CF 3 , or OCF 3 .
43 . A compound according to claim 42 , wherein
X a is hydrogen, methyl, fluorine, or chlorine; X c and X d are both hydrogen; X b is —NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, —C(O)NR 6 R 7 ; wherein R 6 and R 7 are independently at each occurrence H, C 1 -C 6 alkyl, C 1 -C 6 hydroxyalkyl, C 1 -C 4 dihydroxyalkyl, C 1 -C 6 alkoxy, C 1 -C 6 alkoxy C 1 -C 6 alkyl, or C 1 -C 6 alkanoyl, wherein each of the above is optionally substituted with 1, 2, or 3 groups that are independently OH, SH, halogen, or C 3 -C 6 cycloalkyl.
44 . A compound according to claim 39 , wherein
R 5 is X a is H, fluoro, chloro, or methyl; X e is hydrogen, halogen, or methyl; and X b is H; X d is H or halogen;
45 . A compound according to claim 44 , wherein
X c is —SO 2 NR 6 R 7 , or halogen; wherein
R 6 and R 7 are independently at each occurrence H, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 1 -C 6 alkoxy C 1 -C 6 alkyl, C 1 -C 6 alkoxycarbonyl, OH, C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, —(C 1 -C 4 )alkyl-CO 2 -alkyl, pyridyl C 1 -C 6 alkyl, C 1 -C 6 alkanoyl, benzyl, phenyl C 1 -C 6 alkoxy, or phenyl C 1 -C 6 alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C 3 -C 6 cycloalkyl, C 1 -C 6 alkoxy, piperidinyl C 1 -C 6 alkyl, morpholinyl C 1 -C 6 alkyl, piperazinyl C 1 -C 6 alkyl, OH, SH, NH 2 , NH(alkyl), N(alkyl)(alkyl), —O—C 1 -C 4 alkanoyl, C 1 -C 4 alkyl, CF 3 , or OCF 3 ; or
R 6 , R 7 , and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C 1 -C 4 alkyl, C 1 -C 4 alkoxy, hydroxy, hydroxy C 1 -C 4 alkyl, C 1 -C 4 dihydroxyalkyl, or halogen; or
X c is fluoro, chloro, —NH 2 , —NH(C 1 -C 6 alkyl), —N(C 1 -C 6 alkyl)(C 1 -C 6 alkyl), —SO 2 NH 2 , —SO 2 NH(C 1 -C 6 alkyl), —SO 2 N(C 1 -C 6 alkyl)(C 1 -C 6 alkyl), or piperazinyl, wherein the piperazinyl group is optionally substituted with 1 or 2 groups that are independently C 1 -C 4 alkyl, C 1 -C 4 alkoxy, hydroxy, hydroxy C 1 -C 4 alkyl, C 1 -C 4 dihydroxyalkyl, or halogen.
46 . A compound according to claim 44 , wherein
X c is —C(O)NR 6 R 7 , —(C 1 -C 6 alkyl)-C(O)NR 6 R 7 , —NR 6 R 7 , or R 6 R 7 N—(C 1 -C 6 alkyl)-; wherein
R 6 and R 7 are independently at each occurrence H, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 1 -C 6 alkoxy C 1 -C 6 alkyl, C 1 -C 6 alkoxycarbonyl, OH, C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, C 1 -C 6 dihydroxyalkyl, —(C 1 -C 4 )alkyl-CO 2 -alkyl, pyridyl C 1 -C 6 alkyl, C 1 -C 6 alkanoyl, benzyl, phenyl C 1 -C 6 alkoxy, or phenyl C 1 -C 6 alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C 3 -C 6 cycloalkyl, C 1 -C 6 alkoxy, piperidinyl C 1 -C 6 alkyl, morpholinyl C 1 -C 6 alkyl, piperazinyl C 1 -C 6 alkyl, OH, —NH 2 , —NH(alkyl), —N(alkyl)(alkyl), —O—C 1 -C 4 alkanoyl, C 1 -C 4 alkyl, CF 3 , or OCF 3 ; or
R 6 , R 7 , and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C 1 -C 4 alkyl, C 1 -C 4 alkoxy, hydroxy, hydroxy C 1 -C 4 alkyl, C 1 -C 4 dihydroxyalkyl, or halogen.
47 . A compound according to claim 46 , wherein
R 6 is hydrogen; and R 7 is C 1 -C 6 alkyl or C 1 -C 6 alkanoyl, each of which is optionally substituted with 1, 2, or 3 groups that are independently NH 2 , NH(C 1 -C 6 alkyl), N(C 1 -C 6 alkyl)(C 1 -C 6 alkyl), OH, SH, cyclopropyl, or C 1 -C 4 alkoxy;
48 . A compound according to claim 47 , wherein
X c is —C(O)NR 6 R 7 .
49 . A compound according to claim 47 , wherein
X c is NR 6 R 7 , or R 6 R 7 N—(C 1 -C 6 alkyl)-.
50 . A compound according to claim 38 , wherein
X a is hydrogen; two of X b , X c , and X d are hydrogen and the other is —C(O)NR 6 R 7 , —(C 1 -C 6 alkyl)-C(O)NR 6 R 7 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)- or —CO 2 —(C 1 -C 6 )alkyl; wherein
R 6 and R 7 are independently at each occurrence H, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 1 -C 6 alkoxy C 1 -C 6 alkyl, C 1 -C 6 alkoxycarbonyl, OH, C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, —(C 1 -C 4 )alkyl-CO 2 -alkyl, pyridyl C 1 -C 6 alkyl, C 1 -C 6 alkanoyl, benzyl, phenyl C 1 -C 6 alkoxy, or phenyl C 1 -C 6 alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C 3 -C 6 cycloalkyl, C 1 -C 6 alkoxy, piperidinyl C 1 -C 6 alkyl, morpholinyl C 1 -C 6 alkyl, piperazinyl C 1 -C 6 alkyl, OH, NH 2 , NH(alkyl), N(alkyl)(alkyl), —O—C 1 -C 4 alkanoyl, C 1 -C 4 alkyl, CF 3 , or OCF 3 ; or
R 6 , R 7 , and the nitrogen to which they are attached form a morpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C 1 -C 4 alkyl, C 1 -C 4 alkoxy, hydroxy, hydroxy C 1 -C 4 alkyl, C 1 -C 4 dihydroxyalkyl, or halogen; and
X e is hydrogen, methyl, C 1 -C 2 alkoxy, or halogen.
51 . A compound according to claim 50 , wherein
X b is —C(O)NR 6 R 7 , —(C 1 -C 6 alkyl)-C(O)NR 6 R 7 , —NR 6 R 7 , or R 6 R 7 N—(C 1 -C 6 alkyl)- wherein R 6 is hydrogen or C 1 -C 4 alkyl; R 7 is OH, C 1 -C 6 alkyl or C 1 -C 6 alkanoyl, wherein the alkyl and alkanoyl groups substituted with 1, 2, or 3 groups that are independently NH 2 , NH(C 1 -C 6 alkyl), N(C 1 -C 6 alkyl)(C 1 -C 6 alkyl), C 3 -C 6 cycloalkyl, OH, or C 1 -C 4 alkoxy.
52 . A compound according to claim 38 , wherein
X a is halogen or methyl; X b is H, —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, —C(O)NR 6 R 7 , or —CO 2 —(C 1 -C 6 )alkyl; X c is —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, —C(O)NR 6 R 7 , halogen, —CO 2 —(C 1 -C 6 )alkyl, NH 2 , NH(C 1 -C 6 alkyl), N(C 1 -C 6 alkyl)(C 1 -C 6 alkyl), —SO 2 NH 2 , —SO 2 NH(C 1 -C 6 alkyl), —SO 2 N(C 1 -C 6 alkyl)(C 1 -C 6 alkyl), or piperazinyl, wherein the piperazinyl group is optionally substituted with 1 or 2 groups that are independently C 1 -C 4 alkyl, C 1 -C 4 alkoxy, hydroxy, hydroxy C 1 -C 4 alkyl, C 1 -C 4 dihydroxyalkyl, or halogen; X d is hydrogen; X e is H, methyl, NH 2 , NH(C 1 -C 6 alkyl) or N(C 1 -C 6 alkyl)(C 1 -C 6 alkyl).
53 . A compound according to claim 38 , wherein
X 1 , X 2 , X a , X b , X c , X d , and X e are independently selected from H, OH, halogen, CF 3 , alkyl, OCF 3 , pyridyl, pyridazinyl, pyrimidyl, pyrazinyl, thienyl, furyl, pyrrolyl, piperidinyl, piperazinyl, or C 3 -C 7 cycloalkyl, wherein each of the above is optionally substituted with —NR 6 R 7 , —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, or halogen.
54 . A compound according to claim 37 , wherein
R 5 is a heteroaryl or heteroarylalkyl group, where each heteroaryl is pyrazolyl, imidazolyl, furanyl, pyridyl, pyridazinyl, pyrimidinyl, pyrazinyl, pyrazolyl, imidazolyl, dihydroindolyl, dihydroisoindolyl, indolon-2-yl, quinolinyl, isoquinolinyl, tetrahydroisoquinolinyl, dihydroisoquinolinyl, or indolyl, each of which is optionally substituted with 1, 2, 3, or 4 groups that are independently —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , —NR 6 R 7 , hydroxy(C 1 -C 4 )alkyl, C 1 -C 4 dihydroxyalkyl, hydrogen, hydroxy, halogen, haloalkyl, alkyl, haloalkoxy, R 6 R 7 N—(C 1 -C 6 alkyl)-, —CO 2 —(C 1 -C 6 )alkyl, —N(R)C(O)NR 6 R 7 , or —N(R)C(O)—(C 1 -C 6 )alkoxy; wherein
R 6 and R 7 are independently at each occurrence H, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 1 -C 6 alkoxy C 1 -C 6 alkyl, C 1 -C 6 alkoxycarbonyl, OH, C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, C 1 -C 6 thiohydroxyalkyl, —(C 1 -C 4 )alkyl-CO 2 -alkyl, pyridyl C 1 -C 6 alkyl, C 1 -C 6 alkanoyl, benzyl, phenyl C 1 -C 6 alkoxy, or phenyl C 1 -C 6 alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C 3 -C 6 cycloalkyl, C 1 -C 6 alkoxy, piperidinyl C 1 -C 6 alkyl, morpholinyl C 1 -C 6 alkyl, piperazinyl C 1 -C 6 alkyl, OH, SH, NH 2 , NH(alkyl), N(alkyl)(alkyl), —O—C 1 -C 4 alkanoyl, C 1 -C 4 alkyl, CF 3 , or OCF
55 . A compound according to claim 54 , wherein
Y 2 , Y 4 , and Y are independently halogen; and Y 1 and Y 3 are both hydrogen.
56 . A compound according to claim 55 , wherein
X 1 and X 2 are independently H, methyl, —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, or —(C 1 -C 4 alkyl)-morpholinyl.
57 . A compound according to claim 56 , wherein
R 5 is pyridyl C 1 -C 6 alkyl, pyrimidinyl C 1 -C 6 alkyl, or pyrazinyl C 1 -C 6 alkyl, each of which is optionally substituted with 1, 2, or 3 groups that are independently hydroxy(C 1 -C 4 )alkyl, C 1 -C 4 dihydroxyalkyl, OH, halogen, CF 3 , (C 1 -C 4 )alkyl, OCF 3 , —NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, or —C(O)NR 6 R 7 .
58 . A compound according to claim 57 , wherein
R 5 is of the formula: wherein Z 5 is hydroxy(C 1 -C 4 )alkyl, C 1 -C 4 dihydroxyalkyl, OH, halogen, CF 3 , (C 1 -C 4 )alkyl, OCF 3 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , or —C(O)NR 6 R 7 , wherein
R 6 and R 7 at each occurrence are independently H, C 1 -C 6 alkyl optionally substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkoxycarbonyl, halogen, C 3 -C 6 cycloalkyl, OH, SH, or C 1 -C 4 alkoxy.
59 . A compound according to claim 57 , wherein
R 5 is of the formula: wherein Z 5 is hydroxy(C 1 -C 4 )alkyl, C 1 -C 4 dihydroxyalkyl, OH, halogen, CF 3 , (C 1 -C 4 )alkyl, OCF 3 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , or —C(O)NR 6 R 7 , wherein
R 6 and R 7 at each occurrence are independently H, C 1 -C 6 alkyl optionally substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkoxycarbonyl, halogen, C 3 -C 6 cycloalkyl, OH, SH, or C 1 -C 4 alkoxy.
60 . A compound according to claim 57 , wherein
R 5 is of the formula: wherein Z 10 is H or methyl; and Z 20 is —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , hydroxy(C 1 -C 4 )alkyl, C 1 -C 4 dihydroxyalkyl, OH, halogen, CF 3 , (C 1 -C 4 )alkyl, OCF 3 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, or —C(O)NR 6 R 7 , wherein R 6 and R 7 at each occurrence are independently H, C 1 -C 6 alkyl optionally substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkoxycarbonyl, halogen, C 3 -C 6 cycloalkyl, OH, SH, or C 1 -C 4 alkoxy.
61 . A compound according to claim 57 , wherein
R 5 is of the formula: wherein Z 10 is H or methyl; and Z 20 is —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , hydroxy(C 1 -C 4 )alkyl, C 1 -C 4 dihydroxyalkyl, OH, halogen, CF 3 , (C 1 -C 4 )alkyl, OCF 3 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, or —C(O)NR 6 R 7 , wherein R 6 and R 7 at each occurrence are independently H, C 1 -C 6 alkyl optionally substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkoxycarbonyl, halogen, C 3 -C 6 cycloalkyl, OH, SH, or C 1 -C 4 alkoxy.
62 . A compound according to claim 57 , wherein
R 5 is of the formula: wherein Z 10 is H or methyl; and Z 20 is —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , hydroxy(C 1 -C 4 )alkyl, C 1 -C 4 dihydroxyalkyl, OH, halogen, CF 3 , (C 1 -C 4 )alkyl, OCF 3 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, or —C(O)NR 6 R 7 , wherein R 6 and R 7 at each occurrence are independently H, C 1 -C 6 alkyl optionally substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkoxycarbonyl, halogen, C 3 -C 6 cycloalkyl, OH, SH, or C 1 -C 4 alkoxy.
63 . A compound according to claim 57 , wherein
R 5 is of the formula: wherein Z 10 is H or methyl; and Z 20 is —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , hydroxy(C 1 -C 4 )alkyl, C 1 -C 4 dihydroxyalkyl, OH, halogen, CF 3 , (C 1 -C 4 )alkyl, OCF 3 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, or —C(O)NR 6 R 7 , wherein R 6 and R 7 at each occurrence are independently H, C 1 -C 6 alkyl optionally substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkoxycarbonyl, halogen, C 3 -C 6 cycloalkyl, OH, SH, or C 1 -C 4 alkoxy.
64 . A compound according to claim 57 , wherein
R 5 is of the formula: wherein Z 10 is H or methyl; and Z 20 is —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , hydroxy(C 1 -C 4 )alkyl, C 1 -C 4 dihydroxyalkyl, OH, halogen, CF 3 , (C 1 -C 4 )alkyl, OCF 3 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, or —C(O)NR 6 R 7 , wherein R 6 and R 7 at each occurrence are independently H, C 1 -C 6 alkyl optionally substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkoxycarbonyl, halogen, C 3 -C 6 cycloalkyl, OH, SH, or C 1 -C 4 alkoxy.
65 . A compound according to claim 57 , wherein
R 5 is of the formula: wherein Z 10 is H or methyl; and Z 20 is —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , hydroxy(C 1 -C 4 )alkyl, C 1 -C 4 dihydroxyalkyl, OH, halogen, CF 3 , (C 1 -C 4 )alkyl, OCF 3 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, or —C(O)NR 6 R 7 , wherein R 6 and R 7 at each occurrence are independently H, C 1 -C 6 alkyl optionally substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkoxycarbonyl, halogen, C 3 -C 6 cycloalkyl, OH, SH, or C 1 -C 4 alkoxy.
66 . A compound according to claim 57 , wherein
R 5 is of the formula: wherein Z 10 is H or methyl; and Z 20 is —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , hydroxy(C 1 -C 4 )alkyl, C 1 -C 4 dihydroxyalkyl, OH, halogen, CF 3 , (C 1 -C 4 )alkyl, OCF 3 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, or —C(O)NR 6 R 7 , wherein R 6 and R 7 at each occurrence are independently H, C 1 -C 6 alkyl optionally substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkoxycarbonyl, halogen, C 3 -C 6 cycloalkyl, OH, SH, or C 1 -C 4 alkoxy.
67 . A compound according to claim 57 , wherein
R 5 is of the formula: wherein Z 10 is H or methyl; and Z 20 is —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , hydroxy(C 1 -C 4 )alkyl, C 1 -C 4 dihydroxyalkyl, OH, halogen, CF 3 , (C 1 -C 4 )alkyl, OCF 3 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, or —C(O)NR 6 R 7 , wherein R 6 and R 7 at each occurrence are independently H, C 1 -C 6 alkyl optionally substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkoxycarbonyl, halogen, C 3 -C 6 cycloalkyl, OH, SH, or C 1 -C 4 alkoxy.
68 . A method of treating a TNF mediated disorder, a p38 kinase mediated disorder, inflammation and/or arthritis in a subject, the method comprising treating a subject having or susceptible to such disorder or condition with a compound of the formula:
or a pharmaceutically acceptable salt thereof, wherein
R 1 is H, halogen, NO 2 , alkyl, carboxaldehyde, hydroxyalkyl, dihydroxyalkyl, arylalkoxy, arylalkyl, alkenyl, alkynyl, arylalkynyl, —CN, aryl, alkanoyl, alkoxy, alkoxyalkyl, haloalkyl, haloalkoxy, carboxyl, or arylalkanoyl,
wherein the aryl portion of arylalkoxy, arylalkyl, and arylalkanoyl is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, nitro, CN, haloalkyl, haloalkoxy or CO 2 R;
wherein the alkyl portion of the alkyl, hydroxyalkyl, dihydroxyalkyl, arylalkoxy, arylalkyl, alkanoyl, alkoxy, alkoxyalkyl and arylalkanoyl groups is unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, C 1 -C 4 alkoxy, C 1 -C 4 alkoxycarbonyl, or C 3 -C 7 cycloalkyl;
R 2 is H, OH, halogen, —OSO 2 —(C 1 -C 6 ) alkyl, —OSO 2 -aryl, arylalkoxy, aryloxy, arylthio, arylthioalkoxy, arylalkynyl, alkoxy, aryloxy(C 1 -C 6 )alkyl, alkyl, alkynyl, —OC(O)NH(CH 2 ) n aryl, —OC(O)N(alkyl)(CH 2 ) n aryl, alkoxyalkoxy, dialkylamino, alkyl, alkoxy, aryl, arylalkyl, heteroaryl, heteroarylalkyl, arylalkenyl, heterocycloalkyl, heterocycloalkylalkyl, alkoxyalkoxy, NR 8 R 9 , dialkylamino, or CO 2 R, wherein
n is 0, 1, 2, 3, 4, 5 or 6;
each of which groups is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, —(C 1 -C 6 )alkyl-N(R)—CO 2 R 30 , haloalkyl, heteroaryl, heteroarylalkyl, —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-NRC(O)NR 16 R 17 , haloalkoxy, alkyl, CN, alkoxy, alkoxycarbonyl, phenyl, —SO 2 -phenyl wherein the phenyl and —SO 2 -phenyl groups are optionally substituted with 1, 2, or 3 groups that are independently halogen or NO 2 , or —OC(O)NR 6 R 7 , wherein
R 16 and R 17 are independently H or C 1 -C 6 alkyl; or
R 16 , R 17 and the nitrogen to which they are attached form a morpholinyl ring;
R 6 and R 7 are independently at each occurrence H, alkyl, hydroxyalkyl, dihydroxyalkyl, alkoxy, alkanoyl, arylalkyl, arylalkoxy, alkoxycarbonyl, —SO 2 -alkyl, OH, alkoxy, alkoxyalkyl, arylalkoxycarbonyl, —(C 1 -C 4 )alkyl-CO 2 -alkyl, heteroarylalkyl, or arylalkanoyl, wherein each is unsubstituted or substituted with 1, 2, or 2 groups that are independently, halogen, OH, SH, heterocycloalkyl, heterocycloalkylalkyl, C 3 -C 7 cycloalkyl, alkoxy, NH 2 , NH(alkyl), N(alkyl)(alkyl), —O-alkanoyl, alkyl, haloalkyl, carboxaldehyde, or haloalkoxy; or
R 6 , R 7 , and the nitrogen to which they are attached form a morpholinyl, pyrrolidinyl, thiomorpholinyl, thiomorpholinyl S-oxide, thiomorpholinyl S,S-dioxide, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C 1 -C 4 alkyl, alkoxycarbonyl, C 1 -C 4 alkoxy, hydroxyl, hydroxyalkyl, dihydroxyalkyl, or halogen;
R at each occurrence is independently hydrogen or C 1 -C 6 alkyl optionally substituted with optionally substituted with 1 or 2 groups that are independently OH, SH, halogen, amino, monoalkylamino, dialkylamino or C 3 -C 6 cycloalkyl;
R 30 is C 1 -C 6 alkyl optionally substituted with 1 or 2 groups that are independently OH, SH, halogen, amino, monoalkylamino, dialkylamino or C 3 -C 6 cycloalkyl;
each R 8 is independently hydrogen, alkyl, alkanoyl, arylalkyl and arylalkanoyl, wherein each of the above is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, alkoxy, alkoxycarbonyl, halogen, or haloalkyl;
each R 9 is hydrogen, alkyl, alkanoyl, arylalkyl, cycloalkyl, cycloalkylalkyl, alkenyl, heteroaryl, aminoalkyl, monoalkylaminoalkyl, dialkylaminoalkyl, arylalkanoyl, —SO 2 -phenyl, and aryl wherein each of the above is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, alkoxy, alkoxycarbonyl, halogen, or haloalkyl;
R 4 is hydrogen or R 4 is alkyl unsubstituted or substituted with one or two groups that are independently CO 2 R, —CO 2 —(C 1 -C 6 )alkyl, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , —N(R 30 )C(O)NR 16 R 17 , —N(R 30 )C(O)—(C 1 -C 6 )alkoxy, or —NR 6 R 7 , arylalkoxy, arylalkyl, heteroaryl, hydroxyalkyl, dihydroxyalkyl, haloalkyl, R 6 R 7 N—(C 1 -C 6 alkyl)-, —NR 6 R 7 , alkoxy, carboxaldehyde, CO 2 R, alkoxyalkyl, or alkoxyalkoxy, wherein the aryl portion of arylalkoxy and arylalkyl is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, hydroxy, alkoxy, alkyl, —CO 2 —(C 1 -C 6 )alkyl, —CONR 6 R 7 , —NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 )alkyl-, nitro, haloalkyl, or haloalkoxy; and
R 5 is H, aryl, arylalkyl, arylthioalkyl, alkyl optionally substituted with 1, 2, or 3 groups that are independently arylalkoxycarbonyl, —NR 8 R 9 , halogen, —C(O)NR 8 R 9 , alkoxycarbonyl, C 3 -C 7 cycloalkyl, or alkanoyl, alkoxy, alkoxyalkyl optionally substituted with one trimethylsilyl group, amino, alkoxycarbonyl, hydroxyalkyl, dihydroxyalkyl, alkynyl, —SO 2 -alkyl, alkoxy optionally substituted with one trimethylsilyl group, heterocycloalkylalkyl, cycloalkyl, cycloalkylalkyl, -alkyl-S-aryl, -alkyl-SO 2 -aryl, heteroarylalkyl, heterocycloalkyl, heteroaryl, or alkenyl optionally substituted with alkoxycarbonyl, wherein
each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, halogen, alkoxy, hydroxyalkyl, dihydroxyalkyl, arylalkoxy, thioalkoxy, alkoxycarbonyl, arylalkoxycarbonyl, CO 2 R, CN, OH, hydroxyalkyl, dihydroxyalkyl, amidinooxime, —NR 6 R 7 , —NR 8 R 9 , R 6 R 7 N—(C 1 -C 6 alkyl)-, carboxaldehyde, SO 2 alkyl, —SO 2 H, —SO 2 NR 6 R 7 , alkanoyl wherein the alkyl portion is optionally substituted with OH, halogen or alkoxy, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , amidino, haloalkyl, —(C 1 -C 4 alkyl)-NR 15 C(O)NR 16 R 17 , —(C 1 -C 4 alkyl)-NR 15 C(O)R 18 , —O—CH 2 —O, —O—CH 2 CH 2 —O—, or haloalkoxy; wherein
R 15 is H or C 1 -C 6 alkyl;
R 18 is C 1 -C 6 alkyl optionally substituted with —O—(C 2 -C 6 alkanoyl, C 1 -C 6 hydroxyalkyl, C 1 -C 6 dihydroxyalkyl, C 1 -C 6 alkoxy, C 1 -C 6 alkoxy C 1 -C 6 alkyl; amino C 1 -C 6 alkyl, mono or dialkylamino C 1 -C 6 alkyl.
69 . A compound according to claim 17 , wherein Z 5 is C 1 -C 4 alkyl, C 1 -C 4 hydroxyalkyl, C 1 -C 4 dihydroxyalkyl, halogen, C 1 -C 6 alkoxycarbonyl, CF 3 , or C 1 -C 6 alkanoyl.
70 . A compound according to claim 17 , wherein
Z 5 is C 1 -C 4 alkyl, —C(O)NR 6 R 7 , —(C 1 -C 4 alkyl)-C(O)NR 6 R 7 , R 6 R 7 N—(C 1 -C 6 alkyl)-, or —NR 6 R 7 , CF 3 , or C 1 -C 4 alkanoyl, wherein R 6 and R 7 at each occurrence are independently H, C 1 -C 6 alkyl optionally substituted with 1, 2, or 3 groups that are independently C 1 -C 4 alkoxycarbonyl, halogen, C 3 -C 6 cycloalkyl, OH, SH, or C 1 -C 4 alkoxy.Join the waitlist — get patent alerts
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