IP Library Granted Patent US 7,371,754
Granted Patent B2
US 7,371,754 · App. 10/510,610 · Granted May 13, 2008

Tyrosine kinase inhibitors

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Quick Facts
Patent No.
US 7,371,754
App. No.
10/510,610
Granted
May 13, 2008
Kind
B2
Abstract

The present invention relates to compounds that are capable of inhibiting, modulating and/or regulating signal transduction of both receptor-type and non-receptor type tyrosine kinases. The compounds of the instant invention possess a core structure that comprises a benzazocine moiety. The present invention is also related to the pharmaceutically acceptable salts, hydrates and stereoisomers of these compounds.

Claims (46)

1. A compound of Formula II

wherein:

R 1 is independently selected from

1) H,

2) halo,

3) OR 4 ,

4) NO 2 ,

5) —S(O) m R 4 ,

6) CN

7) unsubstituted or substituted C 1 -C 10 alkyl,

8) unsubstituted or substituted aryl,

9) unsubstituted or substituted C 2 -C 6 alkenyl,

10) unsubstituted or substituted C 3 -C 10 cycloalkyl,

11) unsubstituted or substituted C 2 -C 6 alkynyl,

12) unsubstituted or substituted heterocycle,

13) —C(O)R 4 ,

14) C(O)OR 4 ,

15) C(O)N(R 4 ) 2 ,

16) S(O) m N(R 4 ) 2 , and

17) N(R 4 ) 2 ;

R 2 is selected from

1) H,

2) C 1 -C 6 alkyl, and

3) (C═O)C 1 -C 6 alkyl,

wherein said alkyl is optionally substituted with phenyl wherein said phenyl is optionally substituted with halo;

R 3 is

1) C 1 -C 6 alkyl

wherein said alkyl is optionally substituted with phenyl wherein said phenyl is optionally substituted with halo;

R 4 is independently selected from

1) H,

2) unsubstituted or substituted C 1 - 10 alkyl,

3) unsubstituted or substituted C 3 -C 10 cycloalkyl,

4) unsubstituted or substituted aryl,

5) unsubstituted or substituted heterocycle, and

6) CF 3 ;

m is independently 0, 1 or 2;

s is 1 to 4;

or a pharmaceutically acceptable salt or stereoisomer thereof.

2. A pharmaceutical composition which is comprised of a compound in accordance with claim 1 and a pharmaceutically acceptable carrier.

3. A compound that is

3-(3-bromobenzyl)-11-methyl-1,2,3,4,5,6-hexahydro-5,2-(epiminomethano)-3-benzazocine;

3-(3-bromobenzyl)-1,2,3,4,5,6-hexahydro-5,2-(epiminomethano)-3-benzazocine;

3,11-bis(3-bromobenzyl)-1,2,3,4,5,6-hexahydro-5,2-(epiminomethano)-3-benzazocine;

11-acetyl-3-(3-bromobenzyl)-1,2,3,4,5,6-hexahydro-5,2-(epiminomethano)-3benzazocine;

or a pharmaceutically acceptable salt or stereoisomer thereof.

4. A method of treating gliomas, meningomas, colon cancer, gastric cancer, pancreatic cancer, esophageal cancer, hepatocellular cancer, lung (small cell and non-small cell) cancer, thyroid cancer, breast cancer, ovarian cancer, endometrial cancer, vaginal cancer, cervical cancer, prostate cancer, testicular cancer, renal cell cancer, bladder cancer, osteosarcoma, chondrosarcoma, melanoma, basal cell carcinoma, Hodgkin's disease and retinal vascularization in a mammal in need of such treatment comprising administering to said mammal a therapeutically effective amount of a compound of claim 1 .

Assignments (2)
CHANGE OF NAME Recorded Jan 29, 2010
From: MERCK & CO., INC.
To: MERCK SHARP & DOHME CORP.
Reel/Frame 023861/0910 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 13, 2007
From: TROTTER, B. WESLEY
To: MERCK & CO., INC.
Reel/Frame 020107/0342 →