IP Library Granted Patent US 6,911,464
Granted Patent B2
US 6,911,464 · App. 10/798,372 · Granted Jun 28, 2005

N-alkyl-hydroxamic acid-isoindolyl compounds and their pharmaceutical uses

Assignee: Celgene Corporation
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Quick Facts
Patent No.
US 6,911,464
App. No.
10/798,372
Granted
Jun 28, 2005
Kind
B2
Abstract

The invention encompasses novel N-alkyl-hydroxamic acid-isoindolyl compounds, pharmaceutical compositions of these compounds, and methods of using these compounds and compositions for treatment or prevention of various diseases and disorders, for example, diseases associated with PDE4.

Claims (57)

1. A compound of formula (I):

wherein:

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

R 1 and R 2 are each independently C 1-8 -alkyl, CF 2 H, CF 3 , CH 2 CHF 2 , cycloalkyl, or (C 1-8 -alkyl)cycloalkyl;

Z 1 is H, C 1-6 -alkyl, NH 2 , NR 3 R 4 or OR 5 ;

Z 2 is H or C(O)R 5 ;

X 1 , X 2 , X 3 and X 4 are each independently H, halogen, NO 2 , OR 3 , CF 3 , C 1-6 -alkyl, (C 0-4 alkyl)-(C 3-6 -cycloalkyl), (C 0-4 -alkyl)-N—(R 8 R 9 ), (C 0-4 -alkyl)-NHC(O)—(R 8 ), (C 0-4 -alkyl)-NHC(O)CH(R 8 )(R 9 ), (C 0-4 -alkyl)-NHC(O)N(R 8 R 9 ), (C 0-4 -alkyl)-NHC(O)O(R 8 ), (C 0-4 -alkyl)-O—R 8 , (C 0-4 -alkyl)-imidazolyl, (C 0-4 -alkyl)-pyrrolyl, (C 0-4 -alkyl)-oxadiazolyl, (C 0-4 -alkyl)-triazolyl (C 0-4 -alkyl)-heterocycle or NHCOCH(R 8 )N(R 7 R 8 );

R 3 , R 4 , and R 5 are each independently H, C 1-6 -alkyl, O—C 1-6 -alkyl, phenyl, benzyl, or aryl;

R 6 and R 7 are independently H or C 1-6 -alkyl;

R 8 and R 9 are each independently H, C 1-9 -alkyl, C 3-6 -cycloalkyl, (C 1-6 -alkyl)-(C 3-6 -cycloalkyl), (C 0-6 -alkyl)-N(R 4 R 5 ), (C 1-6 -alkyl)-OR 5 , phenyl, benzyl, aryl, piperidinyl, piperizinyl, pyrolidinyl, morpholino, or C 3-7 -heterocycloalkyl;

or a pharmaceutically acceptable salt or solvate thereof.

2. The compound of claim 1 wherein Y is —CH 2 — or —C(O)—.

3. The compound of claim 1 wherein Z 1 is H.

4. The compound of claim 3 wherein R 6 is C 1-6 -alkyl and R 7 is H.

5. The compound of claim 1 wherein Z 2 is H, —C(O)CH 3 or —C(O)CH 2 CH 3 .

6. The compound of claim 5 wherein X 4 is NHC(O)R 8 .

7. The compound of claim 5 wherein R 1 is CH 3 or CF 2 H and R 2 is C 1-8 -alkyl.

8. The compound of claim 5 wherein Z 2 is H.

9. The compound of claim 1 wherein R 1 is CH 3 or CF 2 H.

10. The compound of claim 1 wherein R 2 is CH 2 CH 3 , CH 3 , CF 2 H, CH 2 -cyclopropyl, or cyclopentyl.

11. The compound of claim 1 wherein R 6 and R 7 are both H or one of R 6 and R 7 is H and the other is CH 3 .

12. The compound of claim 1 wherein X 4 is —NHC(O)R 8 and X 1 is H or halogen.

13. The compound of claim 1 wherein one of X 1 , X 2 , X 3 , and X 4 is NHCOCH 2 N(CH 3 ) 2 , NHCON(CH 3 ) 2 , NHCONH 2 , NHCOCH 3 , NHCOCH(R 8 )N(R 7 R 8 ) or OCH 3 , and the rest of X 1 , X 2 , X 3 , and X 4 are H.

14. The compound of claim 1 , wherein the configuration of stereocenter a is (S).

15. The compound of claim 1 , wherein the configuration of stereocenter a is (R).

16. The compound of claim 1 , wherein R 6 and R 7 are not the same, and the configuration of stereocenter b is (S).

17. The compound of claim 1 , wherein R 6 and R 7 are not the same, and the configuration of stereocenter b is (R).

18. A diastereomerically pure SS isomer of a compound of claim 1 , substantially free of other diasteriomers, or a pharmaceutically acceptable salt, or solvate.

19. A diastereomerically pure RS isomer of a compound of claim 1 , substantially free of other diasteriomers, or a pharmaceutically acceptable salt, solvate, hydrate, stereoisomer, clathrate, or prodrug thereof.

20. A diastereomerically pure SR isomer of a compound of claim 1 , substantially free of other diasteriomers, or a pharmaceutically acceptable salt, solvate, hydrate, stereoisomer, clathrate, or prodrug thereof.

21. A diastereomerically pure RR isomer of a compound of claim 1 , substantially free of other diasteriomers, or a pharmaceutically acceptable salt, solvate, hydrate, stereoisomer, clathrate, or prodrug thereof.

22. A compound, where the compound is:

(3R)-(tert-Butoxy)-N-{3-[7-(cyclopropylcarbonylamino)-1-oxoisoindolin-2-yl]-3-(3-ethoxy-4-methoxyphenyl)propyl}carbonylamino (tert-butoxy)formate;

N-[3-(7-Amino-1-oxoisoindolin-2-yl)-3-(3-ethoxy-4-methoxyphenyl)propyl](tert-butoxy)carbonylamino (tert-butoxy)formate;

(1R)-Cyclopropanecarboxylic acid {2-[1-(3-ethoxy-4-methoxy-phenyl)-3-(N-formyl-N-hydroxy-amino)-propyl]-3-oxo-2,3-dihydro-1H-isoindol-4-yl}-amide;

(1R)-N-{2-[1-(3-Ethoxy-4-methoxy-phenyl)-3-(N-formyl-N-hydroxy-amino)-propyl]-3-oxo-2,3-dihydro-1H-isoindol-4-yl}-acetamide;

(1R)-N-{2-[1-(3-Ethoxy-4-methoxy-phenyl)-3-(N-formyl-N-hydroxy-amino)-propyl]-3-oxo-2,3-dihydro-1H-isoindol-4-yl}-isobutyramide;

(1R)-N-{2-[1-(3-Ethoxy-4-methoxy-phenyl)-3-(N-formyl-N-hydroxy-amino)-propyl]-1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl}-acetamide;

(1R)-N-{2-[3-(N-Acetoxy-N-formyl-amino)-1-(3-ethoxy-4-methoxy-phenyl)-propyl]-3-oxo-2,3-dihydro-1H-isoindol-4-yl}-isobutyramide;

(1R)-N-{2-[3-(N-Aminocarbonyl-N-hydroxy-amino)-1-(3-ethoxy-4-methoxy-phenyl)-propyl]-3-oxo-2,3-dihydro-1H-isoindol-4-yl}-isobutyramide;

(1R)-Cyclopropanecarboxylic acid {2-[1-(3-ethoxy-4-methoxy-phenyl)-3-(N-formyl-N-hydroxy-amino)-propyl]-3-oxo-2,3-dihydro-1H-isoindol-4-yl}-amide;

(N-{3-[7-(Cyclopropylcarbonylamino)-1-oxoisoindolin-2-yl]-3-(3-ethoxy-4-methoxyphenyl)propyl}acetylamino) acetate; or

(1R)-Cyclopropanecarboxylic acid {2-[1-(3-ethoxy-4-methoxy-phenyl)-3-(formyl-hydroxy-amino)-butyl]-3-oxo-2,3-dihydro-1H-isoindol-4-yl}-amide.

23. A pharmaceutical composition comprising a pharmaceutically acceptable carrier, excipient, or diluent and a compound of formula (I):

wherein:

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

R 1 and R 2 are each independently C 1-8 -alkyl, CF 2 H, CF 3 , CH 2 CHF 2 , cycloalkyl, or (C 1-8 -alkyl)cycloalkyl;

Z 1 is H, C 1-6 -alkyl, NH 2 , NR 3 R 4 or OR 5 ;

Z 2 is H or C(O)R 5 ;

X 1 , X 2 , X 3 and X 4 are each independently H, halogen, NO 2 , OR 3 , CF 3 , C 1-6 -alkyl, (C 0-4 alkyl)-(C 3-6 -cycloalkyl), (C 0-4 -alkyl)-N—(R 8 R 9 ), (C 0-4 -alkyl)-NHC(O)—(R 8 ), (C 0-4 -alkyl)-NHC(O)CH(R 8 )(R 9 ), (C 0-4 -alkyl)-NHC(O)N(R 8 R 9 ), (C 0-4 -alkyl)-NHC(O)O(R 8 ), (C 0-4 -alkyl)-O—R 8 , (C 0-4 -alkyl)-imidazolyl, (C 0-4 -alkyl)-pyrrolyl, (C 0-4 -alkyl)-oxadiazolyl, (C 0-4 -alkyl)-triazolyl or (C 0-4 -alkyl)-heterocycle;

R 3 , R 4 , and R 5 are each independently H, C 1-6 -alkyl, O—C 1-6 -alkyl, phenyl, benzyl, or aryl;

R 6 and R 7 are independently H or C 1-6 -alkyl;

R 8 and R 9 are each independently H, C 1-9 -alkyl, C 3-6 -cycloalkyl, (C 1-6 -alkyl)-(C 3-6 -cycloalkyl), (C 0-6 -alkyl)-N(R 4 R 5 ), (C 1-6 -alkyl)-OR 5 , phenyl, benzyl, aryl, piperidinyl, piperizinyl, pyrolidinyl, morpholino, or C 3-7 -heterocycloalkyl;

or a pharmaceutically acceptable salt or solvate thereof.

24. The pharmaceutical composition of claim 23 further comprising an additional therapeutic agent.

25. The pharmaceutical composition of claim 24 wherein the additional therapeutic agent is an anti-cancer agent or an anti-inflammatory agent.

26. The pharmaceutical composition of claim 25 wherein the anti-cancer agent is paclitaxel, cisplatin, tamoxifen, docetaxel, pirubicin, doxorubicin, irinotecan, leuprolide, bicalutamide, a goserlin implant, gemcitabine, sargramostim or a steroid.

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 30, 2011
From: MAN, HON-WAH; MULLER, GEORGE W.
To: CELGENE CORPORATION
Reel/Frame 026533/0090 →
Continuity (2)
Provisional Application 6045414900 · Mar 12, 2003
Related Publication 20040259873A1 · Dec 23, 2004