IP Library Granted Patent US 7,906,533
Granted Patent B2
US 7,906,533 · App. 11/262,953 · Granted Mar 15, 2011

Nicotinamide pyridinureas as vascular endothelial growth factor (VEGF) receptor kinase inhibitors

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Quick Facts
Patent No.
US 7,906,533
App. No.
11/262,953
Granted
Mar 15, 2011
Kind
B2
Abstract

The invention relates to novel nicotinamide pyridinureas as VEGF receptor kinase inhibitors, their production and use as pharmaceutical agents for preventing or treating diseases that are triggered by persistent angiogenesis.

Claims (41)

1. A compound of formula (I):

wherein:

A, E and Q independently of one another, are CH;

R 1 is indazolyl, which is optionally substituted in one or more places in the same way or differently with halogen, hydroxy, C 1 -C 12 -alkyl, C 3 -C 6 -cycloalkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, aralkyloxy, C 1 -C 12 -alkoxy, halo-C 1 -C 6 -alkyl, cyano-C 1 -C 6 -alkyl, ═O, —SO 2 R 6 , —OR 5 , —SOR 4 , —COR 6 , —CO 2 R 6 or —NR 7 R 8 , wherein C 1 -C 12 -alkyl may be substituted with —OR 5 or —NR 7 R 8 ;

R 2 , R 3 and R 9 independently of one another, are hydrogen or C 1 -C 12 alkyl optionally substituted with halogen, —OR 5 , or C 1 -C 12 -alkoxy;

R 4 is C 1 -C 12 -alkyl, C 3 -C 8 -cycloalkyl, or aryl;

R 5 is hydrogen, C 1 -C 12 -alkyl, C 3 -C 8 -cycloalkyl or halo-C 1 -C 6 -alkyl;

R 6 is hydrogen, C 1 -C 12 -alkyl, C 3 -C 8 -cycloalkyl, halo-C 1 -C 6 -alkyl, aryl, or —NR 7 R 8 ; and

R 7 and R 8 independently of one another, are hydrogen, —SO 2 R 6 , —COR 6 , aryl, C 3 -C 8 -cycloalkyl, C 1 -C 12 -alkyl, halo-C 1 -C 12 -alkyl, or C 1 -C 12 -alkoxy, wherein C 1 -C 12 -alkyl is optionally substituted with —OR 5 or —N(CH 3 ) 2 ,

or an isomer, diastereoisomer, enantiomer, tautomer or salt thereof.

2. A compound according to claim 1 , wherein R 1 is indazolyl substituted with C 1 -C 12 -alkyl and with a halogen atom substituent.

3. A compound according to claim 1 , wherein R 1 is indazolyl substituted once with C 1 -C 12 -alkyl.

4. A compound according to claim 1 , wherein R 1 is indazolyl substituted with C 1 -C 12 -alkyl.

5. A compound according to claim 1 , wherein R 1 is indazolyl substituted with —CH 3 .

6. A compound according to claim 1 , wherein R 1 is 2-methyl-indazolyl.

7. A compound as claimed in claim 1 , wherein R 2 , R 3 and R 9 independently of one another, are hydrogen or C 1 -C 12 alkyl.

8. A compound as claimed in claim 1 , wherein R 2 and R 3 independently of one another, are hydrogen or —CH 3 and R 9 is hydrogen.

9. A compound according to claim 1 , wherein R 4 is C 1 -C 12 -alkyl.

10. A compound according to claim 1 , wherein R 4 is —CH 3 .

11. A compound according to claim 1 , wherein R 5 is —CH 3 or hydrogen.

12. A compound according to claim 1 , wherein R 5 is hydrogen.

13. A compound according to claim 1 , wherein R 6 is C 1 -C 12 -alkyl or —NR 7 R 8 .

14. A compound according to claim 1 , wherein R 6 is C 1 -C 12 -alkyl.

15. A compound according to claim 1 , wherein R 6 is —CH 3 .

16. A compound according to claim 1 , wherein R 7 and R 8 independently of one another, are hydrogen, —COR 6 , —SO 2 R 6 , or C 1 -C 12 -alkyl.

17. A compound according to claim 1 , wherein R 7 and R 8 independently of one another, are hydrogen or —CH 3 .

18. A compound, which is selected from the group consisting of:

N-(2-methyl-2H-indazol-6-yl)-2-{[2-(3-methyl-ureido)-pyridin-4-ylmethyl]-amino}-nicotinamide,

N-(1-methyl-1H-indazol-6-yl)-2-{[2-(3-methyl-ureido)-pyridin-4-ylmethyl]-amino}-nicotinamide,

N-(1-methyl-1H-indazol-5-yl)-2-{[2-(3-methyl-ureido)-pyridin-4-ylmethyl]-amino}-nicotinamide, and

2-{[2-(3,3-dimethyl-ureido)-pyridin-4-ylmethyl]-amino}-N-(2-methyl-2H-indazol-6-yl)-nicotinamide,

and an isomer, diastereoisomer, enantiomer, tautomer and salt thereof.

19. A pharmaceutical composition comprising a compound according to claim 1 and a pharmaceutically acceptable carrier.

20. A pharmaceutical composition comprising a compound according to claim 18 and a pharmaceutically acceptable carrier.

21. A pharmaceutically acceptable salt of a compound of formula (I) according to claim 1 .

22. A compound according to claim 18 , which is selected from the group consisting of:

N-(2-methyl-2H-indazol-6-yl)-2-{[2-(3-methyl-ureido)-pyridin-4-ylmethyl]-amino}-nicotinamide,

N-(1-methyl-1H-indazol-6-yl)-2-{[2-(3-methyl-ureido)-pyridin-4-ylmethyl]-amino}-nicotinamide,

N-(1-methyl-1H-indazol-5-yl)-2-{[2-(3-methyl-ureido)-pyridin-4-ylmethyl]-amino}-nicotinamide, and

2-{[2-(3,3-dimethyl-ureido)-pyridin-4-ylmethyl]-amino}-N-(2-methyl-2H-indazol-6-yl)-nicotinamide,

and a pharmaceutically acceptable salt thereof.

Assignments (3)
CHANGE OF NAME Recorded Jul 1, 2013
From: BAYER PHARMA AKTIENGESELLSCHAFT
To: BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 030719/0474 →
CHANGE OF NAME Recorded Nov 11, 2012
From: BAYER SCHERING PHARMA AKTIENGESELLSCHAFT
To: BAYER PHARMA AKTIENGESELLSCHAFT
Reel/Frame 029277/0286 →
CHANGE OF NAME Recorded Nov 14, 2007
From: SCHERING AKTIENGESELLSCHAFT
To: BAYER SCHERING PHARMA AKTIENGESELLSCHAFT
Reel/Frame 020110/0334 →