IP Library › Granted Patent US 11,312,712
Granted Patent B2
US 11,312,712 · App. 15/569,299 · Granted Apr 26, 2022

Azabenzimidazoles and their use as AMPA receptor modulators

Inventors: Michael K. Ameriks (San Diego, CA); Cynthia G. B. Berry (San Diego, CA); Gang Chen (San Diego, CA); Suchitra Ravula (San Diego, CA); Bradley M. Savall (San Diego, CA); Devin M. Swanson (Carlsbad, CA); Dongpei Wu (San Diego, CA); Wei Zhang (San Diego, CA)
Assignee: Janssen Pharmaceutica NV
C07D471/04A61P25/00C07D471/14C07C2601/02C07C2601/04C07C2601/08C07C2601/14C07C2601/16
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Quick Facts
Patent No.
US 11,312,712
App. No.
15/569,299
Granted
Apr 26, 2022
Kind
B2
Abstract

Provided herein are compounds of Formula (I), and pharmaceutically acceptable salts, N-oxides, or solvates thereof, Also provided herein are pharmaceutical compositions comprising compounds of Formula (I) and methods of using compounds of Formula (I).

Claims (43)

1. A compound of Formula (I):

Wherein

X is N;

R 1 is a member selected from the group consisting of:

—C 1-5 alkyl, —C 1-5 haloalkyl, —C 1-5 alkoxy, —C 3-8 cycloalkyl or phenyl, wherein the —C 3-8 cycloalkyl and phenyl are each independently optionally substituted with 1-3 substituents selected from the group consisting of: halo, —C 1-5 alkyl, —C 1-5 haloalkyl, —C 1-5 haloalkoxy, —OH, and —C(═O)OC 1-5 alkyl;

R 2 is selected from the group consisting of:

R 3 is selected from the group consisting of: H, —C 1-5 alkyl or —C 1-5 haloalkyl;

R 4 is selected from the group consisting of: H, halo, —CH 3 , and —CF 3 ;

R 5 is selected from the group consisting of: H, —OH, —C 1-5 alkyl, —C 1-5 alkoxy, —C 1-5 haloalkyl, —C 1-5 haloalkoxy, —NR 5a R 5b , azetidinyl, and morpholinyl; each R 5a and R 5b are independently selected from the group consisting of: —C 1-5 alkyl, and —C 1-5 haloalkyl;

and

R 7 is H;

or pharmaceutically acceptable salts, N-oxides, or solvates thereof.

2. A compound of claim 1 , wherein the compound is: 5-[2,5-Bis(trifluoromethyl)imidazo[4,5-b]pyridin-3-yl]indolin-2-one, and pharmaceutically acceptable salts, N-oxides or solvates thereof.

3. A compound of claim 1 , wherein the compound is: 2-(Difluoromethyl)-3-(1H-indazol-5-yl)-5-(trifluoromethyl)imidazo[4,5-b]pyridine, and pharmaceutically acceptable salts, N-oxides or solvates thereof.

4. A compound of claim 1 , wherein the compound is: 3-(1H-Indazol-5-yl)-2-isopropyl-5-(trifluoromethyl)imidazo[4,5-b]pyridine, and pharmaceutically acceptable salts, N-oxides or solvates thereof.

5. A compound of claim 1 , wherein the compound is: 6-[2,5-Bis(trifluoromethyl)imidazo[4,5-b]pyridin-3-yl]-3H-1,3-benzothiazol-2-one, and pharmaceutically acceptable salts, N-oxides or solvates thereof.

6. A compound of claim 1 , wherein the compound is: 5-(Difluoromethyl)-3-(1H-indazol-5-yl)-2-(trifluoromethyl)imidazo[4,5-b]pyridine; and pharmaceutically acceptable salts, N-oxides or solvates thereof.

7. A pharmaceutical composition comprising an effective amount of at least one compound of claim 6 and at least one pharmaceutically acceptable excipient.

8. A pharmaceutical composition comprising:

(A) an effective amount of at least one compound of Formula (I):

wherein

X is N;

R 1 is a member selected from the group consisting of:

—C 1-5 alkyl, —C 1-5 haloalkyl, —C 1-5 alkoxy, —C 3-8 cycloalkyl or phenyl, wherein the —C 3-8 cycloalkyl and phenyl are each independently optionally substituted with 1-3 substituents selected from the group consisting of: halo, —C 1-5 alkyl, —C 1-5 haloalkyl, —C 1-5 haloalkoxy, —OH, and —C(═)OC 1-5 alkyl;

R 2 is selected from the group consisting of:

R 3 is selected from the group consisting of: H, —C 1-5 alkyl, or —C 1-5 haloalkyl;

R 4 is selected from the group consisting of: H, halo, —CH 3, and —CF 3 ;

R 5 is selected from the group consisting of: H, —OH, —C 1-5 alkyl, —C 1-5 alkoxy, —C 1-5 haloalkyl, —C 1-5 haloalkoxy, —NR 5a R 5b , azetidinyl, and morpholinyl; each R 5a and R 5b are independently selected from the group consisting of: —C 1-5 alkyl, and —C 1-5 haloalkyl; and

R 7 is H;

or pharmaceutically acceptable salts, N-oxides or solvates of compounds of Formula (I) and (B) at least one pharmaceutically acceptable excipient.

9. A method of inhibiting TARP γ2 dependent AMPA receptor activity in a subject suffering from or diagnosed with a disease, disorder, or medical condition comprising administering to a subject in need of such treatment an effective amount of at least one compound of Formula (I):

wherein

X is N;

R 1 is a member selected from the group consisting of:

—C 1-5 alkyl, —C 1-5 haloalkyl, —C 1-5 alkoxy, —C 3-8 cycloalkyl or phenyl, wherein the -C 3-8 cycloalkyl and phenyl are each independently optionally substituted with 1-3 substituents selected from the group consisting of: halo, —C 1-5 alkyl, —C 1-5 haloalkyl, —C 1-5 haloalkoxy, —OH, and —C(═)OC 1-5 alkyl;

R 2 is selected from the group consisting of:

R 3 is selected from the group consisting of: H, —C 1-5 alkyl, or —C 1-5 haloalkyl;

R 4 is selected from the group consisting of: H, halo, —CH 3, and —CF 3 ;

R 5 is selected from the group consisting of: H, —OH, —C 1-5 alkyl, —C 1-5 alkoxy, —C 1-5 haloalkyl, —C 1-5 haloalkoxy, —NR 5a R 5b , azetidinyl, and morpholinyl; each R 5a and R 5b are independently selected from the group consisting of: —C 1-5 alkyl, and —C 1-5 haloalkyl; and

R 7 is H; or

pharmaceutically acceptable salts, N-oxides or solvates of compounds of Formula (I).

10. The method of claim 9 , wherein the disease, disorder, or medical condition is selected from cerebral ischemia, head injury, spinal cord injury, Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis (ALS), Huntington's chorea, AIDS nervous disturbance, epilepsy, mental disorder, mobility disturbance, pain, spasticity, nervous disturbance by toxin in food, various neurodegenerative diseases, various mental diseases, chronic pain, migraine, cancer pain, diabetic neuropathy, encephalitis, acute disseminated encephalomyelitis, acute demyelinating polyneuropathy, Guillain Barre syndrome, chronic inflammatory demyelinating polyneuropathy, multiple sclerosis, Marchifava-Bignami disease, central pontine myelinolysis, Devic syndrome, Balo disease, HV- or HTLV-myelopathy, progressive multifocal leucoencephalopathy, a secondary demyelinating disorder, CNS lupus erythematodes, polyarteritis nodosa, Sjogren syndrome, sarcoidosis, isolated cerebral vasculitis, schizophrenia, prodromal schizophrenia, cognitive disorder, depression, anxiety disorders, anxious depression, and bipolar disorder.

11. The method of claim 9 , wherein the disease, disorder or condition is depression, post traumatic stress disorder, epilepsy, schizophrenia, prodromal schizophrenia, or a cognitive disorder.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 20, 2017
From: AMERIKS, MICHAEL K.; BERRY, CYNTHIA G. B.; CHEN, GANG; LEBOLD, TERRY PATRICK; LIN, DAVID WEI; RAVULA, SUCHITRA; SAVALL, BRADLEY M.; SWANSON, DEVIN M.; WU, DONGPEI; ZHANG, WEI
To: JANSSEN PHARMACEUTICA NV
Reel/Frame 044452/0052 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 20, 2017
From: JOURDAN, FABRICE LOIC; PENA PINON, MIGUEL ANGEL
To: NOVALIX SAS
Reel/Frame 044452/0334 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 20, 2017
From: NOVALIX SAS
To: JANSSEN PHARMACEUTICA NV
Reel/Frame 044452/0440 →
Continuity (2)
Provisional Application 62154313 · Apr 29, 2015
Related Publication 20180118740A1 · May 3, 2018
Cited By (1)
US 12,304,908