IP Library Granted Patent US 11,208,407
Granted Patent B2
US 11,208,407 · App. 16/631,191 · Granted Dec 28, 2021

Substituted phenyl compounds as indoleamine 2,3-dioxygenase (IDO) inhibitors

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Quick Facts
Patent No.
US 11,208,407
App. No.
16/631,191
Granted
Dec 28, 2021
Kind
B2
Abstract

Disclosed herein is a compound of formula (I), or a pharmaceutically acceptable salt thereof: (I) Also disclosed herein are uses of the compounds disclosed herein in the potential treatment or prevention of an IDO-associated disease or disorder. Also disclosed herein are compositions comprising a compound disclosed herein. Further disclosed herein are uses of the compositions in the potential treatment or prevention of an IDO-associated disease or disorder.

Claims (100)

1. A compound of formula (I), or a pharmaceutically acceptable salt thereof:

wherein:

L is selected from (1) —NHC(O)—, (2) —C(O)NH—, (3) —NH— and (4) —NHC(O)O—;

one M is —N═ and the other M is selected from (1) —CR a ═ and (2) —N═; wherein R a is selected from (a) H, (b) halogen and (c) C 1-6 alkyl;

V is selected from (1) —CR b R b , (2) —NR c — and (3) —O—; wherein each occurrence of R b is independently selected from (a) H, (b) —OH, (c) halogen and (d) C 1-6 alkyl; and R c is selected from (a) H and (b) C 1-6 alkyl;

R 1 is selected from (1) C 1-6 alkyl, (2) C 3-6 cycloalkyl, (3) aryl and (4) 5- or 6-membered heteroaryl;

wherein:

the C 1-6 alkyl of (1) is optionally substituted with —NH 2 ; and

each of the aryl of (3) and the heteroaryl of (4) is optionally substituted with 1 to 3 substituents independently selected from: (a) halogen, (b) —CN, (c) —NH 2 , (d) C 1-6 alkyl optionally substituted with 1 to 3 substituents independently selected from halogen and —OH, (e) —O—C 1-6 alkyl optionally substituted with 1 to 3 halogens and (f) C 3-6 cycloalkyl;

each occurrence of R 2 is independently selected from (1) H, (2) —OH, (3) halogen, (4) —CN and (5) C 1-6 alkyl; wherein the C 1-6 alkyl of (5) is optionally substituted with 1 to 3 substituents independently selected from (a) —OH and (b) halogen;

R 3 is selected from (1) H and (2) C 1-6 alkyl optionally substituted with (a) halogen or (b) —OH; and

R 4 is selected from (1) H, (2) halogen, (3) —CN, (4) alkenyl and (5) C 1-6 alkyl optionally substituted with —OH.

2. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein:

L is selected from (1) —NHC(O)— and (2) —C(O)NH—;

V is selected from (1) —CR b R b — and (2) —O—; wherein each occurrence of R b is independently selected from (a) H, (b) —OH and (c) halogen;

R 1 is selected from (1) C 1-6 alkyl, (2) C 3-6 cycloalkyl, (3) aryl and (4) 5- or 6-membered heteroaryl; wherein the aryl of (3) and the heteroaryl of (4) is optionally substituted with 1 to 3 substituents independently selected from (a) halogen, (b) —CN, (c) —CF 3 , (d) —NH 2 , (e) C 1-6 alkyl optionally substituted with —OH, (f) —O—C 1-6 alkyl optionally substituted with 1 to 3 halogens and (g) C 3-6 cycloalkyl;

each occurrence of R 2 is independently selected from (1) H, (2) halogen, (3) —CN and (4) C 1-6 alkyl; wherein the C 1-6 alkyl is optionally substituted with 1 to 3 halogens;

R 3 is selected from (1) H and (2) C 1-6 alkyl; and

R 4 is selected from (1) H, (2) halogen, (3) —CN and (4) C 1-6 alkyl optionally substituted with —OH.

3. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein:

one M is —N═ and the other M is selected from (1) —CH═ and (2) —N═;

V is selected from (1) —CR b R b — and (2) —O—, wherein each occurrence of R b is independently selected from (a) H, (b) —OH and (c) halogen;

R 1 is selected from (1) C 1-6 alkyl, (2) C 3-6 cycloalkyl, (3) aryl and (4) 5- or 6-membered heteroaryl; wherein the aryl of (3) and the heteroaryl of (4) is optionally substituted with 1 to 3 substituents independently selected from (a) halogen, (b) —CN, (c) —CF 3 , (d) —NH 2 , (e) C 1-6 alkyl optionally substituted with —OH, (f) —O—CHF 2 and (g) C 3-6 cycloalkyl;

each occurrence of R 2 is independently selected from (1) H, (2) halogen, (3) —CN and (4) C 1-6 alkyl; wherein the C 1-6 alkyl is optionally substituted with 1 to 3 halogens;

R 3 is H; and

R 4 is selected from (1) H, (2) halogen, (3) —CN and (4) C 1-4 alkyl optionally substituted with —OH.

4. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein:

L is selected from (1) —NHC(O)— and (2) —C(O)NH—;

V is selected from (1) —CH 2 —, (2) —CHF—, (3) —CF 2 — and (4) —O—;

R 1 is selected from (1) C 1-4 alkyl, (2) C 3-6 cycloalkyl, (3) phenyl and (4) 5- or 6-membered heteroaryl selected from isoxazolyl, oxadiazolyl, oxazolyl, oxoimidazolidinyl, pyranyl, pyrazinyl, pyrazolyl, pyridazinyl, pyridinyl, pyrimidinyl and pyrrolyl; wherein the phenyl of (3) and the heteroaryl of (4) is optionally substituted with 1 to 3 substituents independently selected from (a) halogen, (b) —CN, (c) —CF 3 , (d) —NH 2 , (e) C 1-6 alkyl optionally substituted with —OH, (f) —O—CHF 2 and (g) C 3-6 cycloalkyl; and

each occurrence of R 2 is independently selected from (1) H, (2) halogen, (3) —CN, (4) —CH 3 (5) ethyl and (6) —CF 3 .

5. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein:

L is selected from (1) —NHC(O)— and (2) —C(O)NH—;

V is selected from (1) —CH 2 —, (2) —CHF—, (3) —CF 2 — and (4) —O—;

R 1 is selected from (1) C 1-4 alkyl, (2) cyclopropyl, (3) phenyl and (4) 5- or 6-membered heteroaryl selected from pyrazinyl, pyrazolyl, pyridazinyl, pyridinyl and pyrimidinyl; wherein the phenyl of (3) and the heteroaryl of (4) is optionally substituted with 1 to 3 substituents independently selected from (a) halogen, (b) —CN, (c) —CF 3 , (d) —NH 2 , (e) —CH 3 , (f) —CH 2 OH, (g) —O—CHF 2 and (h) cyclopropyl; and

each occurrence of R 2 is independently selected from (1) H, (2) halogen, (3) —CN, (4) —CH 3 and (5) —CF 3 , and

R 4 is selected from (1) H, (2) halogen, (3) —CN, (4) —CH 3 and (5) —CH 2 OH.

6. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, of formula (Ia):

wherein:

L is selected from (1) —NHC(O)—, (2) —C(O)NH— and (3) —NHC(O)O—;

V is selected from (1) —CR b R b — and (2) —O—, wherein each occurrence of R b is independently selected from (a) H, (b) —OH and (c) halogen;

R 1 is selected from (1) C 1-6 alkyl, (2) C 3-6 cycloalkyl, (3) aryl and (4) 5- or 6-membered heteroaryl; wherein the aryl of (3) and the heteroaryl of (4) is optionally substituted with 1 to 3 substituents independently selected from (a) halogen, (b) —CN, (c) —NH 2 , (d) C 1-6 alkyl optionally substituted with 1 to 3 substituents independently selected from halogen and —OH, (e) —O—C 1-6 alkyl optionally substituted with 1 to 3 halogens and (f) C 3-6 cycloalkyl;

each occurrence of R 2 is independently selected from (1) H, (2) halogen, (3) —CN and (4) C 1-6 alkyl; wherein the C 1-6 alkyl is optionally substituted with 1 to 3 halogens; and

R 4 is selected from (1) H, (2) halogen, (3) —CN and (4) C 1-4 alkyl optionally substituted with —OH.

7. The compound of claim 6 , or a pharmaceutically acceptable salt thereof, wherein:

L is selected from (1) —NHC(O)— and (2) —C(O)NH—;

V is selected from (1) —CR b R b — and (2) —O—; wherein each occurrence of R b is independently selected from (a) H and (b) halogen;

R 1 is selected from (1) C 3-6 cycloalkyl, (2) phenyl and (3) 5- or 6-membered heteroaryl selected from isoxazolyl, oxadiazolyl, oxazolyl, oxoimidazolidinyl, pyranyl, pyrazinyl, pyrazolyl, pyridazinyl, pyridinyl, pyrimidinyl and pyrrolyl; wherein each of the phenyl of (2) and the heteroaryl of (3) is optionally substituted with 1 to 3 substituents independently selected from (a) halogen, (b) —CN, (c) —CF 3 , (d) C 1-6 alkyl optionally substituted with —OH, (e) —O—CHF 2 and (f) cyclopropyl;

each occurrence of R 2 is independently selected from (1) H, (2) halogen, (3) —CN, (4) —CH 3 and (5) —CF 3 ; and

R 4 is selected from (1) H, (2) halogen, (3) —CN, (4) —CH 3 and (5) —CH 2 OH.

8. The compound of claim 6 , or a pharmaceutically acceptable salt thereof, wherein:

V is selected from (1) —CH 2 —, (2) —CHF—, (3) —CF 2 — and (4) —O—;

R 1 is selected from (1) C 3-6 cycloalkyl, (2) phenyl and (3) 5- or 6-membered heteroaryl selected from pyrazinyl, pyrazolyl, pyridazinyl, pyridinyl and pyrimidinyl; wherein the phenyl of (2) and the heteroaryl of (3) is optionally substituted with 1 to 3 substituents independently selected from (a) halogen, (b) —CN, (c) —CF 3 , (d) —CH 3 (e) —CH 2 OH, (f) —O—CHF 2 and (g) cyclopropyl;

each occurrence of R 2 is independently selected from (1) H, (2) halogen, (3) —CN and (4) —CF 3 ; and

R 4 is selected from (1) H, (2) halogen, (3) —CN and (4) —CH 2 OH.

9. The compound of claim 6 , or a pharmaceutically acceptable salt thereof, wherein R 1 is selected from (1) C 3-6 cycloalkyl, (2) phenyl and (3) 5- or 6-membered heteroaryl selected from pyrazolyl, pyridinyl and pyrimidinyl; wherein the phenyl of (2) and the heteroaryl of (3) is optionally substituted with 1 to 3 substituents independently selected from (a) halogen, (b) —CN, (c) —CF 3 , (d) —CH 3 , (e) —CH 2 OH, (f) —O—CHF 2 and (g) cyclopropyl.

10. A compound of formula (Ib), or a pharmaceutically acceptable salt thereof:

wherein:

V is selected from (1) —CR b R b — and (2) —O—; wherein each occurrence of R b is independently selected from (a) H, (b) —OH and (c) halogen;

R 1 is selected from (1) C 3-6 cycloakyl, and (2) aryl; wherein the aryl of (2) is optionally substituted with 1 to 3 substituents independently selected from (a) halogen, (b) —CN, (c) C 1-6 alkyl optionally substituted with 1 to 3 substituents independently selected from halogen and —OH, (d) —O—C 1-6 alkyl optionally substituted with 1 to 3 halogens and (e) C 3-6 cycloakyl;

each occurrence of R 2 is independently selected from (1) H, (2) halogen, (3) —CN and (4) C 1-6 alkyl; wherein the C 1-6 alkyl is optionally substituted with 1 to 3 halogens; and

R 4 is selected from (1) H, (2) halogen, (3) —CN and (4) —CH 2 OH.

11. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, selected from the group consisting of:

3-cyano-N-(4-(1-(6-(trifluoromethyl)-3H-imidazo[4,5-b]pyridin-2-yl)cyclobutyl)phenyl)benzamide,

3-cyano-N-(4-{1-[6-(trifluoromethyl)-1H-benzimidazol-2-yl]cyclobutyl}phenyl)benzamide,

N-{4-[1-(7-chloro-1H-benzimidazol-2-yl)cyclobutyl]phenyl}-3-cyanobenzamide,

3-cyano-N-{4-[1-(7-cyano-1H-benzimidazol-2-yl)cyclobutyl]phenyl}benzamide,

N-{4-[1-(6-chloro-1H-imidazo[4,5-b]pyridin-2-yl)cyclobutyl]phenyl}-3-cyanobenzamide,

N-(4-(3-(6-chloro-1H-benzo[d]imidazol-2-yl)oxetan-3-yl)phenyl)-3-cyanobenzamide,

3-bromo-N-(4-(1-(6-bromo-3H-imidazo[4,5-b]pyridin-2-yl)cyclobutyl)-2-chlorophenyl)benzamide,

N-(2-chloro-4-(1-(6-cyano-3H-imidazo[4,5-b]pyridin-2-yl)cyclobutyl)phenyl)-3-cyanobenzamide,

3-cyano-N-(4-(1-(6-cyano-3H-imidazo[4,5-b]pyridin-2-yl)cyclobutyl)-2-methylphenyl)benzamide,

N-(4-(1-(6-bromo-3H-imidazo[4,5-b]pyridin-2-yl)cyclobutyl)-2-fluorophenyl)-3-cyanobenzamide,

3-cyano-N-(4-(1-(6-cyano-3H-imidazo[4,5-b]pyridin-2-yl)cyclobutyl)-2-fluorophenyl)benzamide,

N-{4-[1-(6-chloro-3H-imidazo[4,5-b]pyridin-2-yl)cyclobutyl]-2-fluorophenyl}-3-cyanobenzamide,

3-cyano-N-(2-fluoro-4-{1-[6-(trifluoromethyl)-3H-imidazo[4,5-b]pyridin-2-yl]cyclobutyl}phenyl)benzamide,

2-(1-(4-((1-Methyl-1H-pyrazol-3-yl)amino)-3-vinylphenyl)cyclobutyl)-3H-imidazo[4,5-b]pyridine-6-carbonitrile,

2-(1-(3-(Hydroxymethyl)-4-((1-methyl-1H-pyrazol-3-yl)amino)phenyl)cyclobutyl)-3H-imidazo[4,5-b]pyridine-6-carbonitrile,

cyclopropyl (4-(1-(6-cyano-3H-imidazo[4,5-b]pyridin-2-yl)cyclobutyl)phenyl)carbamate,

N-(4-(1-(6-chloro-1H-benzo[d]imidazol-2-yl)-3-hydroxycyclobutyl)phenyl)-3-cyanobenzamide,

3-chloro-N-(4-(1-(6-chloro-1H-imidazo[4,5-b]pyridin-2-yl)-3,3-difluorocyclobutyl)phenyl)benzamide,

N-(4-(1-(6-chloro-1H-benzo[d]imidazol-2-yl)-3-fluorocyclobutyl)phenyl)-3-cyanobenzamide,

3-cyano-N-(4-(1-(6-cyano-1H-benzo[d]imidazol-2-yl)-3-fluorocyclobutyl)phenyl)benzamide,

N-(3-chlorophenyl)-4-(1-(6-(trifluoromethyl)-1H-imidazo[4,5-b]pyridin-2-yl)cyclobutyl)benzamide,

4-(1-(6-cyano-1H-imidazo[4,5-b]pyridin-2-yl)-3,3-difluorocyclobutyl)-N-cyclohexylbenzamide,

4-(1-(6-cyano-1H-imidazo[4,5-b]pyridin-2-yl)-3,3-difluorocyclobutyl)-N-(6-methylpyridin-2-yl)benzamide,

N-(3-cyanophenyl)-4-{1-[6-(trifluoromethyl)-1H-imidazo[4,5-b]pyridin-2-yl]cyclobutyl}benzamide,

N-(3-fluorophenyl)-4-{1-[6-(trifluoromethyl)-1H-imidazo[4,5-b]pyridin-2-yl]cyclobutyl}benzamidem

N-(2,4-difluorophenyl)-4-{1-[6-(trifluoromethyl)-1H-imidazo[4,5-b]pyridin-2-yl]cyclobutyl}benzamide,

N-(5-chloropyridin-3-yl)-4-{1-[6-(trifluoromethyl)-1H-imidazo[4,5-b]pyridin-2-yl]cyclobutyl}benzamide,

N-cyclohexyl-4-{1-[6-(trifluoromethyl)-1H-imidazo[4,5-b]pyridin-2-yl]cyclobutyl}benzamide,

N-(2-methylpropyl)-4-{1-[6-(trifluoromethyl)-1H-imidazo[4,5-b]pyridin-2-yl]cyclobutyl}benzamide,

N-(5-cyano-2-fluorophenyl)-4-{1-[6-(trifluoromethyl)-1H-imidazo[4,5-b]pyridin-2-yl]cyclobutyl}benzamide,

N-(5-chloro-2-fluorophenyl)-4-{1-[6-(trifluoromethyl)-1H-imidazo[4,5-b]pyridin-2-yl]cyclobutyl}benzamide, and

4-[1-(6-cyano-1H-imidazo[4,5-b]pyridin-2-yl)-3,3-difluorocyclobutyl]-N-(3-cyanophenyl)benzamide.

12. A composition which comprises an inert carrier and a compound of claim 1 or a pharmaceutically acceptable salt thereof.

13. A method for treating an IDO-associated disease or disorder in a mammalian subject which comprises administering to the subject an effective amount of a compound of claim 1 or a pharmaceutically acceptable salt thereof.

14. A method for treating an IDO-associated disease or disorder in a mammalian subject which comprises administering to the subject an effective amount of a compound of claim 1 or a pharmaceutically acceptable salt thereof in combination with another anti-cancer agent.

15. The method of claim 14 , wherein the IDO-associated disease or disorder is a cancer, viral infection, HCV infection, depression, neurodegenerative disorders, trauma, age-related cataracts, organ transplantation, and autoimmune diseases.

16. The method of claim 15 , wherein the cancer is a cancer of the colon, pancreas, breast, prostate, lung, brain, ovary, cervix, testes, renal, head and neck, lymphoma, leukemia, and melanoma.

Assignments (2)
MERGER Recorded Aug 8, 2022
From: MERCK SHARP & DOHME CORP.
To: MERCK SHARP & DOHME LLC
Reel/Frame 061102/0145 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 15, 2020
From: ZHOU, HUA; ACHAB, ABDELGHANI; FRADERA, XAVIER; HAN, YONGXIN; LI, DERUN; MCGOWAN, MEREDETH A; SCIAMMETTA, NUNZIO; SLOMAN, DAVID L; YU, WENSHENG
To: MERCK SHARP & DOHME CORP.
Reel/Frame 051518/0725 →