IP Library Granted Patent US 9,845,308
Granted Patent B2
US 9,845,308 · App. 14/933,468 · Granted Dec 19, 2017

Isoindoline inhibitors of ROR-gamma

Inventors: David A. Claremon (Maple Glen, PA); Lawrence Wayne Dillard (Yardley, PA); Chengguo Dong (Staten Island, NY); Yi Fan (Doylestown, PA); Lanqi Jia (Horsham, PA); Stephen D. Lotesta (Burlington, NJ); Andrew Marcus (Media, PA); Suresh B. Singh (Kendall Park, NJ); Colin M. Tice (Maple Glen, PA); Jing Yuan (Lansdale, PA); Wei Zhao (Germantown, MD); Yajun Zheng (Hockessin, DE); Linghang Zhuang (Chalfont, PA)
Assignee: Vitae Pharmaceuticals, Inc.
C07D401/12C07D209/44C07D403/12C07D405/14C07D413/14
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Quick Facts
Patent No.
US 9,845,308
App. No.
14/933,468
Granted
Dec 19, 2017
Kind
B2
Abstract

Provided are novel compounds of Formula (I): pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are useful in the treatment of diseases and disorders mediated by RORγ. Also provided are pharmaceutical compositions comprising the novel compounds of Formula (I) and methods for their use in treating one or more inflammatory, metabolic, autoimmune and other diseases or disorders.

Claims (28)

1. A compound of the Formula:

or a pharmaceutically acceptable salt thereof, wherein

R 2 is (C 1 -C 3 )alkyl;

R 3 is hydrogen, monocyclic cycloalkyl, monocyclic heterocyclyl, or (C 1 -C 6 )alkyl, wherein the (C 1 -C 6 )alkyl is optionally substituted with 1 to 2 groups independently selected from hydroxy, halo, and cyano;

R 4 is hydrogen, (C 1 -C 3 )alkyl, or ═O;

X is —C(O)NH— or —NHC(O)—;

m is 0, 1, or 2;

n is 0, 1, 2, or 3;

Cy 1 is phenyl or pyridinyl, each of which is optionally substituted with 1 to 2 groups independently selected from R 5 ;

Cy 2 is cyclohexyl or phenyl, each of which is optionally substituted with 1 to 2 groups independently selected from R 6 ;

R 5 is (C 1 -C 3 )alkylsulfonyl;

R 6 is selected from (C 1 -C 3 )alkyl, halo(C 1 -C 3 )alkyl, hydroxy, and (C 1 -C 3 )alkoxy; and

R 7 and R 8 are each independently hydrogen, hydroxy, (C 1 -C 3 )alkyl, hydroxy(C 1 -C 3 )alkyl, (C 1 -C 3 )alkoxy(C 1 -C 3 )alkyl, aminocarbonyl-O(C 1 -C 3 )alkyl, hydroxycarbonyl(C 1 -C 3 )alkoxy(C 1 -C 3 )alkyl, (C 1 -C 3 )alkylcarbonylamino(C 1 -C 3 )alkyl, (C 1 -C 3 )alkoxycarbonylamino(C 1 -C 3 )alkyl, di(C 1 -C 3 )alkylamino(C 1 -C 3 )alkyl, di(C 1 -C 3 )alkylaminocarbonyl(C 1 -C 3 )alkyl, (C 1 -C 3 )alkylaminocarbonyl(C 1 -C 3 )alkyl, aminocarbonyl(C 1 -C 3 )alkyl, aminocarbonyl, mono(C 1 -C 3 )alkylamino, di(C 1 -C 3 )alkylamino, CO 2 H, (CH 2 ) 1-3 COOH, moncyclic heterocyclyl, (C 1 -C 3 )alkoxycarbonyl, halophenyl, halophenyl(C 1 -C 3 )alkyl, or quinolin-2(1H)one-4yl-methyl; or

R 7 and R 8 , together with the carbon atom to which they are attached, form a 3- to 6-membered cycloalkyl or heterocyclyl.

2. The compound of claim 1 , wherein the compound is of the Formula:

or a pharmaceutically acceptable salt thereof.

3. The compound of claim 2 , wherein the compound is of the Formula:

or a pharmaceutically acceptable salt thereof.

4. The compound of claim 3 , wherein R 7 is hydrogen; and R 8 is hydrogen, hydroxy(C 1 -C 3 )alkyl, (C 1 -C 3 )alkoxy(C 1 -C 3 )alkyl, aminocarbonyl-O(C 1 -C 3 )alkyl, hydroxycarbonyl(C 1 -C 3 )alkoxy(C 1 -C 3 )alkyl, (C 1 -C 3 )alkylcarbonylamino(C 1 -C 3 )alkyl, (C 1 -C 3 )alkoxycarbonylamino(C 1 -C 3 )alkyl, di(C 1 -C 3 )alkylamino(C 1 -C 3 )alkyl, di(C 1 -C 3 )alkylaminocarbonyl(C 1 -C 3 )alkyl, (C 1 -C 3 )alkylaminocarbonyl(C 1 -C 3 )alkyl, aminocarbonyl(C 1 -C 3 )alkyl, or aminocarbonyl.

5. The compound of claim 4 , wherein R 7 is hydrogen; and R 8 is hydrogen, —CH 2 OH, —(CH 2 ) 2 OH, —CH 2 OCH 3 , —CH 2 OC(O)NH 2 , —CH 2 OCH 2 COOH, —CH 2 NHC(O)CH 3 , —CH 2 NHC(O)OCH 3 , —(CH 2 ) 2 N(CH 3 ) 2 , —CH 2 C(O)N(CH 3 ) 2 , —CH 2 C(O)NHCH 3 , —CH 2 C(O)NH 2 , or CONH 2 .

6. The compound of claim 5 , wherein R 7 is hydrogen; and R 8 is hydrogen, —CH 2 OH, —(CH 2 ) 2 OH, or —CH 2 OCH 3 .

7. The compound of claim 6 , wherein R 5 is —SO 2 CH 2 CH 3 or —SO 2 CH 3 .

8. The compound of claim 7 , wherein R 6 is CF 3 .

9. The compound of claim 8 , wherein R 2 is ethyl or isopropyl.

10. A compound selected from:

or a pharmaceutically acceptable salt thereof.

11. A pharmaceutical composition comprising a compound of claim 1 , or a pharmaceutically acceptable salt thereof; and a pharmaceutically acceptable carrier.

12. A method of treating one or more diseases or disorders selected from asthma, chronic obstructive pulmonary disease (COPD), allergic rhinitis, atopic dermatitis, contact dermatitis, acne, urticaria, cystic fibrosis, allograft rejection, multiple sclerosis, scleroderma, arthritis, rheumatoid arthritis, juvenile rheumatoid arthritis, osteoarthritis, ankylosing spondylitis, systemic lupus erythematosus (SLE), psoriasis, Hashimoto's disease, pancreatitis, autoimmune diabetes, type I diabetes, autoimmune ocular disease, ulcerative colitis, Crohn's disease, regional enteritis, inflammatory bowel disease (IBD), inflammatory bowel syndrome (IBS), Sjögren's syndrome, obesity, hepatosteatosis, adipose tissue-associated inflammation, insulin resistance, type II diabetes, neuromyelitis optica, myasthenia gravis, dry eye, uveitis, Guillain-Barré syndrome, psoriasis, psoriatic arthritis (PsA), steroid resistant asthma, Graves' disease, scleritis, major depression, seasonal affective disorder, bipolar disorder, autism, epilepsy, Alzheimer's, endometriosis, obstructive sleep apnea syndrome (OSAS), Behçet's disease, dermatomyositis, polymyocitis, graft versus host disease, primary biliary cirrhosis, liver fibrosis, non-alcoholic fatty liver disease (NAFLD), sarcoidosis, primary sclerosing cholangitis, autoimmune thyroid disease, autoimmune polyendocrine syndrome type I, autoimmune polyendocrine syndrome type II, celiac disease, neuromyelitis, juvenile idiopathic arthritis, systemic sclerosis, myocardial infarction, pulmonary hypertension, osteoarthritis, cutaneous leishmaniasis, sinonasal polyposis, and cancer in a subject, comprising administering to the subject a therapeutically effective amount of a compound according to claim 1 , or a pharmaceutically acceptable salt thereof.

Assignments (2)
CHANGE OF NAME Recorded Mar 20, 2019
From: VITAE PHARMACEUTICALS, INC.
To: VITAE PHARMACEUTICALS, LLC
Reel/Frame 050150/0044 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 8, 2015
From: CLAREMON, DAVID A.; DILLARD, LAWRENCE WAYNE; DONG, CHENGGUO; FAN, YI; JIA, LANQI; LOTESTA, STEPHEN D.; MARCUS, ANDREW; SINGH, SURESH B.; TICE, COLIN M.; YUAN, JING; ZHAO, WEI; ZHENG, YAJUN; ZHUANG, LINGHANG
To: VITAE PHARMACEUTICALS, INC.
Reel/Frame 037232/0863 →
Continuity (2)
Provisional Application 62075612 · Nov 5, 2014
Related Publication 20160122318A1 · May 5, 2016