IP Library Granted Patent US 7,893,102
Granted Patent B2
US 7,893,102 · App. 12/363,664 · Granted Feb 22, 2011

Fluoroalkoxy-substituted 1,3-dihydro-isoindolyl compounds and their pharmaceutical uses

Assignee: Celgene Corporation
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Quick Facts
Patent No.
US 7,893,102
App. No.
12/363,664
Granted
Feb 22, 2011
Kind
B2
Abstract

The invention encompasses novel compounds, pharmaceutically acceptable salts, hydrates, solvates, clathrates, enantiomers, diastereomers, racemates, or mixtures of stereoisomers thereof, pharmaceutical compositions of these compounds, and methods of using these compounds and compositions in mammals for treatment or prevention of diseases associated with PDE4.

Claims (17)

1. A method of treating myelodysplastic syndrome, complex regional pain syndrome, arthritis, rheumatoid arthritis, inflammatory bowel disease, sepsis, Crohn's disease, aphthous ulcer, cachexia, graft versus host disease, asthma, adult respiratory distress syndrome, acquired immune deficiency syndrome, inflammation of the lungs, depression, chronic obstructive pulmonary disorder, atopic dermatitis, psoriasis, multiple sclerosis, congestive heart failure, cardiomyopathy, pulmonary edema, endotoxin-mediated septic shock, acute viral myocarditis, cardiac allograft rejection or myocardial infarction in a mammal which comprises administering thereto a therapeutically effective amount of a compound having the formula (I):

wherein:

Y is —C(O)—, —CH 2 , —CH 2 C(O)—, —C(O)CH 2 —, or SO 2 ,

Z is —H, —C(O)R 3 , —(C 0-1 -alkyl)-SO 2 —(C 1-4 -alkyl), —C 1-8 -alkyl, —CH 2 OH, CH 2 (O)(C 1-8 -alkyl) or —CN;

R 1 and R 2 are each independently —CHF 2 , —C 1-8 -alkyl, —C 3-18 -cycloalkyl, or —(C 1-10 -alkyl)(C 3-18 -cycloalkyl), and at least one of R 1 and R 2 is CHF 2 ;

R 3 is —NR 4 R 5 , -alkyl, —OH, —O-alkyl, phenyl, benzyl, substituted phenyl, or substituted benzyl;

R 4 and R 5 are each independently —H, —C 1-8 -alkyl, —OH, —OC(O)R 6 ;

R 6 is —C 1-8 -alkyl, -amino(C 1-8 -alkyl), -phenyl, -benzyl, or -aryl;

X 1 , X 2 , X 3 , and X 4 are each independent —H, -halogen, -nitro, —NH 2 , —CF 3 , —C 1-6 -alkyl, —(C 0-4 -alkyl)-(C 3-6 -cycloalkyl), (C 0-4 -alkyl)-NR 7 R 8 , (C 0-4 -alkyl)-N(H)C(O)—(R 8 ), (C 0-4 -alkyl)-N(H)C(O)N(R 7 R 8 ), (C 0-4 -alkyl)-N(H)C(O)O(R 7 R 8 ), (C 0-4 -alkyl)-OR 8 , (C 0-4 -alkyl)-imidazolyl, (C 0-4 -alkyl)-pyrrolyl, (C 0-4 -alkyl)-oxadiazolyl, or (C 0-4 -alkyl)-triazolyl triazolyl or X 1 and X 2 or X 2 and X 3 or X 3 and X 4 are taken together with the atoms that join them to form a cycloalkyl or heterocycloalkyl ring of 3, 4, 5, 6 or 7 atoms; and

R 7 and R 8 are each independently H, C 1-9 -alkyl, (C 1-6 -alkyl)-(C 3-6 -cycloalkyl), (C 1-6 -alkyl)-N(R 7 R 8 ), (C 1-6 -alkyl)-OR 8 , phenyl, benzyl, or aryl;

or a pharmaceutically acceptable salt, stereoisomer, or prodrug thereof.

2. The method of claim 1 , wherein the therapeutically effective amount of the compound of the formula (I) is administered before, during or after surgery or physical therapy directed at reducing or avoiding a symptom of complex regional pain syndrome in the patient.

3. The method of claim 1 , wherein the effective amount of the compound of the formula (I) is from about 0.1 mg to about 300 mg per day.

4. The method of claim 3 , wherein the effective amount is from about 1 mg to about 250 mg per day.

5. The method of claim 1 , wherein the compound of the formula (I) is administered orally, parenterally, topically or mucosally.

6. The method of claim 1 , wherein the mammal is human.

7. The method of claim 1 , wherein the compound is 3-(3,4-bis-difluoromethoxy-phenyl)-3-[7-(cyclopropanecarbonyl-amino)-1-oxo-1,3-dihydro-isoindol-2-yl]-propionic acid.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 4, 2019
From: CELGENE CORPORATION
To: AMGEN INC.
Reel/Frame 051181/0038 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 28, 2010
From: MULLER, GEORGE W.; MAN, HON WAH; ZHANG, WEIHONG
To: CELGENE CORPORATION
Reel/Frame 025055/0498 →
Continuity (4)
Division 11601355 · Nov 16, 2006
Division 10748085 · Dec 29, 2003
Provisional Application 60436975 · Dec 30, 2002
Related Publication 20090143382A1 · Jun 4, 2009