IP Library Granted Patent US 7,173,058
Granted Patent B2
US 7,173,058 · App. 10/748,085 · Granted Feb 6, 2007

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

Assignee: Celgene Corporation
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Quick Facts
Patent No.
US 7,173,058
App. No.
10/748,085
Granted
Feb 6, 2007
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 (60)

1. 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 or X1 and X2 or X2 and X3 or X3 and X4 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 3-6 -cycloalkyl, (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, solvate, hydrate, stereoisomer, clathrate, or prodrug thereof.

2. The compound of claim 1 wherein, one of X 1 , X 2 , X 3 , and X 4 is (C 0-4 -alkyl)-NR 7 R 8 .

3. The compound of claim 1 wherein, one of X 1 , X 2 , X 3 , and X 4 is (C 0-4 -alkyl)-NHC(O)(R 8 ).

4. The compound of claim 1 wherein, one of X 1 , X 2 , X 3 , and X 4 is (C 0-4 -alkyl)-NHC(O)(R 8 ) and one of X 1 , X 2 , X 3 , and X 4 is halogen.

5. The compound of claim 1 wherein one of X 1 , X 2 , X 3 , and X 4 is (C 0-4 -alkyl)-NHC(O)NR 7 R 8 .

6. The compound of claim 1 wherein, one of X 1 , X 2 , X 3 , and X 4 is (C 0-4 -alkyl)-NHC(O)O(R 7 R 8 ).

7. The compound of claim 1 wherein, one of X 1 , X 2 , X 3 , and X 4 is (C 0-4 -alkyl)-OR 8 .

8. The compound of claim 1 wherein, one of X 1 , X 2 , X 3 , and X 4 is (C 0-4 -alkyl)-imidazolyl, (C 0-4 -alkyl)-pyrrolyl, (C 0-4 -alkyl)-oxadiazolyl, or (C 0-4 -alkyl)-triazolyl.

9. The compound of claim 1 wherein, one of X 1 , X 2 , X 3 , and X 4 is (C 0-4 -alkyl)-cyclopropyl.

10. The compound of claim 1 wherein, one of X 1 , X 2 , X 3 , and X 4 is NH 2 .

11. The compound of claim 1 wherein, three of X 1 , X 2 , X 3 , and X 4 are H.

12. The compound of claim 1 wherein X 1 and X 2 are H or X 3 and X 4 are H.

13. An enantiomerically pure S isomer of a compound of claim 1 , substantially free of its R isomer, or a pharmaceutically acceptable salt, solvate, hydrate, stereoisomer, clathrate, or prodrug thereof.

14. An enantiomerically pure R isomer of a compound of claim 1 , substantially free of its S isomer, or a pharmaceutically acceptable salt, solvate, hydrate, stereoisomer, clathrate, or prodrug thereof.

15. A compound selected from the group consisting of:

3-(4-Acetylamino-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-(3-cyclopropylmethoxy-4-difluoromethoxy-phenyl)-propionic acid;

3-(4-Acetylamino-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-(3-cyclopropylmethoxy-4-difluoromethoxy-phenyl)-N,N-dimethyl-propionamide;

3-(4-Acetylamino-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-(3 cyclopropylmethoxy-4-difluoromethoxy-phenyl)-propionamide;

3-(3-Cyclopropylmethoxy-4-difluoromethoxy-phenyl)-3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propionic acid;

3-(3-Cyclopropylmethoxy-4-difluoromethoxy-phenyl)-3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-N-hydroxy-propionamide;

3-(3-Cyclopropylmethoxy-4-difluoromethoxy-phenyl)-3-(7-nitro-1-oxo-1,3-dihydro-isoindol-2-yl)-propionic acid methyl ester;

3-(3-Cyclopropylmethoxy-4-difluoromethoxy-phenyl)-3-(7-nitro-1-oxo-1,3-dihydro-isoindol-2-yl)-propionic acid;

3-(3-Cyclopropylmethoxy-4-difluoromethoxy-phenyl)-3-(7-nitro-1-oxo-1,3-dihydro-isoindol-2-yl)-)-N,N-dimethyl-propionamide;

3-(7-Amino-1-oxo-1,3-dihydro-isoindol-2-yl)-3-(3-cyclopropylmethoxy-4-difluoromethoxy-phenyl)-N,N-dimethyl-propionamide;

3-(4-Difluoromethoxy-3-ethoxy-phenyl)-3-(7-nitro-1-oxo-1,3-dihydro-isoindol-2-yl)-propionic acid methyl ester;

3-(7-Amino-1-oxo-1,3-dihydro-isoindol-2-yl)-3-(4-difluoromethoxy-3-ethoxy-phenyl)-propionic acid methyl ester;

3-[7-(Cyclopropanecarbonyl-amino)-1-oxo-1,3-dihydro-isoindol-2-yl]-3-(4-difluoromethoxy-3-ethoxy-phenyl)-propionic acid methyl ester;

3-(7-Acetylamino-1-oxo-1,3-dihydro-isoindol-2-yl)-3-(4-difluoromethoxy-3-ethoxy-phenyl)-propionic acid methyl ester;

3-(7-Acetylamino-1-oxo-1,3-dihydro-isoindol-2-yl)-3-(4-difluoromethoxy-3-ethoxy-phenyl)-propionic acid;

3-[7-(Cyclopropanecarbonyl-amino)-1-oxo-1,3-dihydro-isoindol-2-yl]-3-(4-difluoromethoxy-3-ethoxy-phenyl)-propionic acid;

Cyclopropanecarboxylic acid {2-[2-carbamoyl-1-(4-difluoromethoxy-3-ethoxy-phenyl)-ethyl]-3-oxo-2,3-dihydro-1H-isoindol-4-yl}-amide;

Cyclopropanecarboxylic acid {2-[1-(4-difluoromethoxy-3-ethoxy-phenyl)-2-dimethylcarbamoyl-ethyl]-3-oxo-2,3-dihydro-1H-isoindol-4-yl}-;

Cyclopropanecarboxylic acid {2-[1-(4-difluoromethoxy-3-ethoxy-phenyl)-2-hydroxycarbamoyl-ethyl]-3-oxo-2,3-dihydro-1H-isoindol-4-yl}-amide;

3-(7-Acetylamino-1-oxo-1,3-dihydro-isoindol-2-yl)-3-(4-difluoromethoxy-3-ethoxy-phenyl)-propionamide;

3-(7-Acetylamino-1-oxo-1,3-dihydro-isoindol-2-yl)-3-(4-difluoromethoxy-3-ethoxy-phenyl)-N,N-dimethyl-propionamide;

3-(7-Acetylamino-1-oxo-1,3-dihydro-isoindol-2-yl)-3-(4-difluoromethoxy-3-ethoxy-phenyl)-N-hydroxy-propionamide;

3-(4-Acetylamino-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-(4-difluoromethoxy-3-ethoxy-phenyl)-propionic acid;

3-(4-Acetylamino-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-(4-difluoromethoxy-3-ethoxy-phenyl)-propionamide;

3-(4-Acetylamino-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-(4-difluoromethoxy-3-ethoxy-phenyl)-N,N-dimethyl-propionamide;

3-(4-Acetylamino-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-(4-difluoromethoxy-3-ethoxy-phenyl)-N-hydroxy-propionamide;

Cyclopropanecarboxylic acid {2-[1-(4-difluoromethoxy-3-ethoxy-phenyl)-2-methanesulfonyl-ethyl]-3-oxo-2,3-dihydro-1H-isoindol-4-yl}-amide;

N-{2-[1-(4-Difluoromethoxy-3-ethoxy-phenyl)-2-methanesulfonyl-ethyl]-1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl}-acetamide;

Cyclopropanecarboxylic acid {2-[2-carbamoyl-1-(4-difluoromethoxy-3-ethoxy-phenyl)-ethyl]-7-chloro-3-oxo-2,3-dihydro-1H-isoindol-4-yl}-amide;

N-{2-[1-(4-Difluoromethoxy-3-ethoxy-phenyl)-3-morpholin-4-yl-3-oxo-propyl]-1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl}-acetamide;

N-{2-[1-(4-Difluoromethoxy-3-ethoxy-phenyl)-3-morpholin-4-yl-3-oxo-propyl]-3-oxo-2,3-dihydro-1H-isoindol-4-yl}-acetamide;

3-(4-Acetylamino-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-(3,4-bis-difluoromethoxy-phenyl)-N,N-dimethyl-propionamide;

3-(3,4-Bis-difluoromethoxy-phenyl)-3-[4-chloro-7-(cyclopropanecarbonyl-amino)-1-oxo-1,3-dihydro-isoindol-2-yl]-propionic acid methyl ester;

Cyclopropanecarboxylic acid {2-[1-(3,4-bis-difluoromethoxy-phenyl)-2-dimethylcarbamoyl-ethyl]-3-oxo-2,3-dihydro-1H-isoindol-4-yl}-amide;

Cyclopropanecarboxylic acid {2-[1-(3,4-bis-difluoromethoxy-phenyl)-2-carbamoyl-ethyl]-3-oxo-2,3-dihydro-1H-isoindol-4-yl}-amide;

Cyclopropanecarboxylic acid {2-[1-(3,4-bis-difluoromethoxy-phenyl)-2-hydroxycarbamoyl-ethyl]-3-oxo-2,3-dihydro-1H-isoindol-4-yl}-amide; and

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 Jun 11, 2004
From: MULLER, GEORG W.; MAN, HON WAH; ZHANG, WEIHONG
To: CELGENE CORPORATION
Reel/Frame 015455/0808 →
Continuity (2)
Provisional Application 6043697500 · Dec 30, 2002
Related Publication 20040204448A1 · Oct 14, 2004