IP Library › Granted Patent US 7,071,216
Granted Patent B2
US 7,071,216 · App. 10/405,945 · Granted Jul 4, 2006

Substituted benz-azoles and methods of their use as inhibitors of Raf kinase

Assignee: Chiron Corporation
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Quick Facts
Patent No.
US 7,071,216
App. No.
10/405,945
Granted
Jul 4, 2006
Kind
B2
Abstract

New substituted benz-azole compounds, compositions and methods of inhibition of Raf kinase activity in a human or animal subject are provided. The new compounds compositions may be used either alone or in combination with at least one additional agent for the treatment of a Raf kinase mediated disorder, such as cancer.

Claims (113)

1. A compound of the formula (I):

wherein, X 1 and X 2 are ═N— or —NR 4 —, provided that if X 1 is —NR 4 —, then X 2 is ═N—, or if X 2 is —NR 4 —, then X 1 is ═N—;

Y is O or S;

A 1 is substituted or unsubstituted alkyl, cycloalkyl, heterocycloalkyl, aryl, polycyclic aryl, polycyclic arylalkyl, heteroaryl, biaryl, heteroarylaryl, heteroarylheteroaryl, cycloalkylalkyl, heterocycloalkylalkyl, arylalkyl, heteroarylalkyl, biarylalkyl, or heteroarylarylalkyl;

A 2 is substituted or unsubstituted heteroaryl;

R 1 is O or H, and R 2 is NR 5 R 6 or hydroxyl; or R 1 is taken together with R 2 to form a substituted or unsubstituted heterocycloalkyl or heteroaryl group; wherein, the dashed line represents a single or double bond, provided that

represents a double bond when R 1 is O and

represents a single bond when R 1 is H;

R 3 is hydrogen, halogen, loweralkyl, or loweralkoxy;

R 4 is hydrogen, hydroxyl, alkylamino, dialkylamino or alkyl;

R 5 and R 6 are independently selected from hydrogen, and substituted or unsubstituted alkyl, alkoxyalkyl, aminoalkyl, amidoalkyl, acyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkyloxyalkylheterocyclo, and heteroarylalkyl; or R 5 and R 6 are taken together to form substituted or unsubstituted heterocyclo or heteroaryl; and

the pharmaceutically acceptable salts, esters and prodrugs thereof.

2. A compound of claim 1 wherein X 1 is NR 4 .

3. A compound of claim 2 wherein R 4 is hydrogen.

4. A compound of claim 2 wherein R 4 is methyl.

5. A compound of claim 1 wherein Y is O.

6. A compound of claim 1 wherein A 1 is selected from the group consisting of substituted or unsubstituted phenyl, pyridyl, pyrimidinyl, phenylalkyl, pyridylalkyl, pyrimidinylalkyl, heterocyclylcarbonylphenyl, heterocyclylphenyl, heterocyclylalkylphenyl, chlorophenyl, fluorophenyl, bromophenyl, iodophenyl, dihalophenyl, nitrophenyl, 4-bromophenyl, 4-chlorophenyl, alkylbenzoate, alkoxyphenyl, dialkoxyphenyl, dialkylphenyl, trialkylphenyl, thiophene, thiophene-2-carboxylate, alkylthiophenyl, trifluoromethylphenyl, acetylphenyl, sulfamoylphenyl, biphenyl, cyclohexylphenyl, phenyloxyphenyl, dialkylaminophenyl, alkylbromophenyl, alkylchlorophenyl, alkylflourophenyl, triflouromethylchlorophenyl, triflouromethylbromophenyl, indenyl, 2,3-dihydroindenyl, tetralinyl, trifluorophenyl, (trifluoromethyl)thiophenyl, alkoxybiphenyl, morpholinyl, N-piperazinyl, N-morpholinylalkyl, piperazinylalkyl, cyclohexylalkyl, indolyl, 2,3-dihydroindolyl, 1-aceytl-2,3-dihydroindolyl, cycloheptyl, bicyclo[2.2.1]hept-2-yl, hydroxyphenyl, hydroxyalkylphenyl, pyrrolidinyl, pyrrolidin-1-yl, pyrrolidin-1-ylalkyl, 4-amino(imino)methylphenyl, isoxazolyl, indazolyl, adamantyl, bicyclohexyl, quinuclidinyl, imidazolyl, benzimidazolyl, imidazolylphenyl, phenylimidazolyl, pthalamido, napthyl, benzophenone, anilinyl, anisolyl, quinolinyl, quinolinonyl, phenylsulfonyl, phenylalkylsulfonyl, 9H-flouren-1-yl, piperidin-1-yl, piperidin-1-ylalkyl, cyclopropyl, cyclopropylalkyl, pyrimidin-5-ylphenyl, quinolidinylphenyl, furanyl, furanylphenyl, N-methylpiperidin-4-yl, pyrrolidin-4-ylpyridinyl, 4-diazepan-1-yl, hydroxypyrrolidn-1-yl, dialkylaminopyrrolidin-1-yl, 1,4′-bipiperidin-1′-yl, and (1,4′-bipiperidin-1′-ylcarbonyl)phenyl.

7. A compound of claim 1 wherein A 2 is substituted or unsubstituted pyridyl.

8. A compound of claim 1 wherein R 1 is O and

represents a double bond.

9. A compound of claim 1 wherein R 2 is NR 5 R 6 , R 5 is hydrogen and R 6 is selected from hydrogen, and substituted or unsubstituted alkyl, alkoxyalkyl, aminoalkyl, amidoalkyl, acyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkyloxyalkylheterocyclo, and heteroarylalkyl.

10. A compound of claim 1 wherein R 1 is taken together with R 2 to form a substituted or unsubstituted heterocycloalkyl or heteroaryl group.

11. A compound of claim 1 wherein R 3 is loweralkoxy.

12. A compound of claim 11 wherein R 3 is methoxy.

13. A compound of claim 1 wherein R 4 is loweralkyl.

14. A compound of claim 13 wherein R 4 is methyl.

15. The compound of claim 1 wherein R 1 is O, R 2 is NR 5 R 6 , R 5 is H, and R 6 is methyl.

16. A compound of the formula (II):

wherein and Y is O or S;

A 1 is substituted or unsubstituted cycloalkyl, heterocycloalkyl, aryl, polycyclic aryl, polycyclic arylalkyl, heteroaryl, biaryl, heteroarylaryl, heteroarylheteroaryl, cycloalkylalkyl, heterocycloalkylalkyl, arylalkyl, heteroarylalkyl, biarylalkyl, or heteroarylarylalkyl;

A 2 is substituted or unsubstituted heteroaryl;

R 1 is O and R 2 is NR 5 R 6 ; or R 1 is taken together with R 2 to form a substituted or unsubstituted heterocycloalkyl or heteroaryl group; wherein, the dashed line represents a single or double bond, provided that R 1 is O,

represents a double bond;

R 3 is hydrogen, halogen, loweralkyl, or loweralkoxy;

R 4 is hydrogen or loweralkyl;

R 5 and R 6 are independently selected from hydrogen, and substituted or unsubstituted alkyl, alkoxyalkyl, aminoalkyl, amidoalkyl, acyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkyloxyalkylheterocyclo, and heteroarylalkyl; or R5 and R6 are taken together to form substituted or unsubstituted heterocyclo or heteroaryl; and

the pharmaceutically acceptable salts, esters, and prodrugs thereof.

17. A compound of claim 16 wherein R4 is hydrogen.

18. A compound of claim 16 wherein R4 is methyl.

19. A compound of claim 16 wherein Y is O.

20. A compound of claim 16 wherein A1 is selected from the group consisting of substituted or unsubstituted phenyl, pyridyl, pyrimidinyl, phenylalkyl, pyridylalkyl, pyrimidinylalkyl, heterocyclylcarbonylphenyl, heterocyclylphenyl, heterocyclylalkylphenyl, chlorophenyl, fluorophenyl, bromophenyl, iodophenyl, dihalophenyl, nitrophenyl, 4-bromophenyl, 4-chlorophenyl, alkylbenzoate, alkoxyphenyl, dialkoxyphenyl, dialkylphenyl, trialkylphenyl, thiophene, thiophene-2-carboxylate, alkylthiophenyl, trifluoromethylphenyl, acetylphenyl, sulfamoylphenyl, biphenyl, cyclohexylphenyl, phenyloxyphenyl, dialkylaminophenyl, alkylbromophenyl, alkylchlorophenyl, alkylflourophenyl, triflouromethylchlorophenyl, triflouromethylbromophenyl indenyl, 2,3-dihydroindenyl, tetralinyl, trifluorophenyl, (trifluoromethyl)thiophenyl, alkoxybiphenyl, morpholinyl, N-piperazinyl, N-morpholinylalkyl, piperazinylalkyl, cyclohexylalkyl, indolyl, 2,3-dihydroindolyl, 1-aceytl-2,3-dihydroindolyl, cycloheptyl, bicyclo[2.2.1-]hept-2-yl, hydroxyphenyl, hydroxyalkylphenyl, pyrrolidinyl, pyrrolidin-1-yl, pyrrolidin-1-ylalkyl, 4-amino(imino)methylphenyl, isoxazolyl, indazolyl, adamantyl, bicyclohexyl, quinuclidinyl, imidazolyl, benzimidazolyl, imidazolylphenyl, phenylimidazolyl, pthalamido, napthyl, benzophenone, anilinyl, anisolyl, quinolinyl, quinolinonyl, phenylsulfonyl, phenylalkylsulfonyl, 9H-flouren-1-yl, piperidin-1-yl, piperidin-1-ylalkyl, cyclopropyl, cyclopropylalkyl, pyrimidin-5-ylphenyl, quinolidinylphenyl, furanyl, furanylphenyl, N-methylpiperidin-4-yl, pyrrolidin-4-ylpyridinyl, 4-diazepan-1-yl, hydroxypyrrolidn-1-yl, dialkylaminopyrrolidin-1-yl, 1,4′-bipiperidin-1′-yl, and (1,4′-bipiperidin-1′-ylcarbonyl)phenyl.

21. A compound of claim 16 wherein A 2 is substituted or unsubstituted pyridyl.

22. A compound of claim 16 wherein R 2 is NR 5 R 6 , R 5 is hydrogen and R 6 is selected from hydrogen, and substituted or unsubstituted alkyl, alkoxyalkyl, aminoalkyl, amidoalkyl, acyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkyloxyalkylheterocyclo, and heteroarylalkyl.

23. A compound of claim 16 wherein R 1 is taken together with R 2 to form a substituted or unsubstituted heterocycloalkyl or heteroaryl group.

24. A compound of claim 16 wherein R 1 is O, R 2 is NR 5 R 6 , R 5 is H, and R 6 is methyl.

25. A compound of claim 16 wherein R 3 is loweralkoxy.

26. A compound of claim 25 wherein R 3 is methoxy.

27. A compound of claim 16 wherein R 4 is loweralkyl.

28. A compound of claim 27 wherein R 4 is methyl.

29. A compound of the formula (III):

wherein X is NR 4 ;

A 1 is substituted or unsubstituted cycloalkyl, heterocycloalkyl, aryl, polycyclic aryl, polycyclic arylalkyl, heteroaryl, biaryl, heteroarylaryl, heteroarylheteroaryl, cycloalkylalkyl, heterocycloalkylalkyl, arylalkyl, heteroarylalkyl, biarylalkyl, or heteroarylarylalkyl;

A 2 is substituted or unsubstituted heteroaryl;

R 1 is O and R 2 is NR 5 R 6 ; or R 1 is taken together with R 2 to form a substituted or unsubstituted heterocycloalkyl or heteroaryl group; wherein, the dashed line represents a single or double bond, provided that when R 1 is O,

represents a double bond;

R 3 is hydrogen, halogen, loweralkyl, or loweralkoxy;

R 4 is hydrogen or loweralkyl;

R 5 and R 6 are independently selected from hydrogen, and substituted or unsubstituted alkyl, alkoxyalkyl, aminoalkyl, amidoalkyl, acyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkyloxyalkylheterocyclo, and heteroarylalkyl; or R5 and R6 are taken together to form substituted or unsubstituted heterocyclo or heteroaryl; and

the pharmaceutically acceptable salts, esters and prodrugs thereof.

30. A compound of claim 29 wherein R 4 is hydrogen.

31. A compound of claim 29 wherein R 4 is methyl.

32. A compound of claim 29 wherein A 1 is selected from the group consisting of substituted or unsubstituted phenyl, pyridyl, pyrimidinyl, phenylalkyl, pyridylalkyl, pyrimidinylalkyl, heterocyclylcarbonylphenyl, heterocyclylphenyl, heterocyclylalkylphenyl, chlorophenyl, fluorophenyl, bromophenyl, iodophenyl, dihalophenyl, nitrophenyl, 4-bromophenyl, 4-chlorophenyl, alkylbenzoate, alkoxyphenyl, dialkoxyphenyl, dialkylphenyl, trialkylphenyl, thiophene, thiophene-2-carboxylate, alkylthiophenyl, trifluoromethylphenyl, acetylphenyl, sulfamoylphenyl, biphenyl, cyclohexylphenyl, phenyloxyphenyl, dialkylaminophenyl, alkylbromophenyl, alkylchlorophenyl, alkylflourophenyl, triflouromethylchlorophenyl, triflouromethylbromophenyl indenyl, 2,3-dihydroindenyl, tetralinyl, trifluorophenyl, (trifluoromethyl)thiophenyl, alkoxybiphenyl, morpholinyl, N-piperazinyl, N-morpholinylalkyl, piperazinylalkyl, cyclohexylalkyl, indolyl, 2,3-dihydroindolyl, 1-aceytl-2,3-dihydroindolyl, cycloheptyl, bicyclo[2.2.1]hept-2-yl, hydroxyphenyl, hydroxyalkylphenyl, pyrrolidinyl, pyrrolidin-1-yl, pyrrolidin-1-ylalkyl, 4-amino(imino)methylphenyl, isoxazolyl, indazolyl, adamantyl, bicyclohexyl, quinuclidinyl, imidazolyl, benzimidazolyl, imidazolylphenyl, phenylimidazolyl, pthalamido, napthyl, benzophenone, anilinyl, anisolyl, quinolinyl, quinolinonyl, phenylsulfonyl, phenylalkylsulfonyl, 9H-flouren-1-yl, piperidin-1-yl, piperidin-1-ylalkyl, cyclopropyl, cyclopropylalkyl, pyrimidin-5-ylphenyl, quinolidinylphenyl, furanyl, furanylphenyl, N-methylpiperidin-4-yl, pyrrolidin-4-ylpyridinyl, 4-diazepan-1-yl, hydroxypyrrolidn-1-yl, dialkylaminopyrrolidin-1-yl, 1,4′-bipiperidin-1′-yl, and (1,4′-bipiperidin-1′-ylcarbonyl)phenyl.

33. A compound of claim 29 wherein A 2 is substituted or unsubstituted pyridyl.

34. A compound of claim 29 wherein R 2 is NR 5 R 6 , R 5 is hydrogen and R 6 is selected from hydrogen, and substituted or unsubstituted alkyl, alkoxyalkyl, aminoalkyl, amidoalkyl, acyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkyloxyalkylheterocyclo, and heteroarylalkyl.

35. A compound of claim 29 wherein R 1 is taken together with R 2 to form a substituted or unsubstituted heterocycloalkyl or heteroaryl group.

36. A compound of claim 29 wherein R 3 is loweralkoxy.

37. A compound of claim 36 wherein R 3 is methoxy.

38. A compound of claim 29 wherein R 4 is loweralkyl.

39. A compound of claim 38 wherein R 4 is methyl.

40. A compound of claim 29 wherein R 1 is O, R 2 is NR 5 R 6 , R 5 is H, and R 6 is methyl.

41. A compound of the formula (IV):

wherein X is NR 4 ;

Y is O or S;

A 1 is substituted or unsubstituted cycloalkyl, heterocycloalkyl, aryl, polycyclic aryl, polycyclic arylalkyl, heteroaryl, biaryl, heteroarylaryl, heteroarylheteroaryl, cycloalkylalkyl, heterocycloalkylalkyl, arylalkyl, heteroarylalkyl, biarylalkyl, or heteroarylarylalkyl;

R 1 is O and R 2 is NR 5 R 6 ; or R 1 is taken together with R 2 to form a substituted or unsubstituted heterocycloalkyl or heteroaryl group; wherein, the dashed line represents a single or double bond, provided that when R 1 is O,

represents a double bond;

R 3 is hydrogen, halogen, loweralkyl, or loweralkoxy;

R 4 is hydrogen or loweralkyl;

R 5 and R 6 are independently selected from hydrogen, and substituted or unsubstituted alkyl, alkoxyalkyl, aminoalkyl, amidoalkyl, acyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkyloxyalkylheterocyclo, and heteroarylalkyl; or R5 and R6 are taken together to form substituted or unsubstituted heterocyclo or heteroaryl; and

the pharmaceutically acceptable salts, esters and prodrugs thereof.

42. A compound of claim 41 wherein R 4 is hydrogen.

43. A compound of claim 41 wherein R 4 is methyl.

44. A compound of claim 41 wherein Y is O.

45. A compound of claim 41 wherein A 1 is selected from the group consisting of substituted or unsubstituted phenyl, pyridyl, pyrimidinyl, phenylalkyl, pyridylalkyl, pyrimidinylalkyl, heterocyclylcarbonylphenyl, heterocyclylphenyl, heterocyclylalkylphenyl, chlorophenyl, fluorophenyl, bromophenyl, iodophenyl, dihalophenyl, nitrophenyl, 4-bromophenyl, 4-chlorophenyl, alkylbenzoate, alkoxyphenyl, dialkoxyphenyl, dialkylphenyl, trialkylphenyl, thiophene, thiophene-2-carboxylate, alkylthiophenyl, trifluoromethylphenyl, acetylphenyl, sulfamoylphenyl, biphenyl, cyclohexylphenyl, phenyloxyphenyl, dialkylaminophenyl, alkylbromophenyl, alkylchlorophenyl, alkylflourophenyl, triflouromethylchlorophenyl, triflouromethylbromophenyl indenyl, 2,3-dihydroindenyl, tetralinyl, trifluorophenyl, (trifluoromethyl)thiophenyl, alkoxybiphenyl, morpholinyl, N-piperazinyl, N-morpholinylalkyl, piperazinylalkyl, cyclohexylalkyl, indolyl, 2,3-dihydroindolyl, 1-aceytl-2,3-dihydroindolyl, cycloheptyl, bicyclo[2.2.1]hept-2-yl, hydroxyphenyl, hydroxyalkylphenyl, pyrrolidinyl, pyrrolidin-1-yl, pyrrolidin-1-ylalkyl, 4-amino(imino)methylphenyl, isoxazolyl, indazolyl, adamantyl, bicyclohexyl, quinuclidinyl, imidazolyl, benzimidazolyl, imidazolylphenyl, phenylimidazolyl, pthalamido, napthyl, benzophenone, anilinyl, anisolyl, quinolinyl, quinolinonyl, phenylsulfonyl, phenylalkylsulfonyl, 9H-flouren-1-yl, piperidin-1-yl, piperidin-1-ylalkyl, cyclopropyl, cyclopropylalkyl, pyrimidin-5-ylphenyl, quinolidinylphenyl, furanyl, furanylphenyl, N-methylpiperidin-4-yl, pyrrolidin-4-ylpyridinyl, 4-diazepan-1-yl, hydroxypyrrolidn-1-yl, dialkylaminopyrrolidin-1-yl, 1,4′-bipiperidin-1′-yl, and (1,4′-bipiperidin-1′-ylcarbonyl)phenyl.

46. A compound of claim 41 wherein R 2 is NR 5 R 6 , R 5 is hydrogen and R 6 is selected from hydrogen, and substituted or unsubstituted alkyl, alkoxyalkyl, aminoalkyl, amidoalkyl, acyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkyloxyalkylheterocyclo, and heteroarylalkyl.

47. A compound of claim 41 wherein R 1 is taken together with R 2 to form a substituted or unsubstituted heterocycloalkyl or heteroaryl group.

48. A compound of claim 41 wherein R 3 is loweralkoxy.

49. A compound of claim 48 wherein R 3 is methoxy.

50. A compound of claim 44 wherein R 4 is loweralkyl.

51. A compound of claim 50 wherein R 4 is methyl.

52. A compound of claim 41 wherein R 1 is O, R 2 is NR 5 R 6 , R 5 is H, and R 6 is methyl.

53. A compound of the formula (V):

wherein X is NR 4 ;

A 1 is substituted or unsubstituted cycloalkyl, heterocycloalkyl, aryl, polycyclic aryl, polycyclic arylalkyl, heteroaryl, biaryl, heteroarylaryl, heteroarylheteroaryl, cycloalkylalkyl, heterocycloalkylalkyl, arylalkyl, heteroarylalkyl, biarylalkyl, or heteroarylarylalkyl;

R 1 is O and R 2 is NR 5 R 6 ; or R 1 is taken together with R 2 to form a substituted or unsubstituted heterocycloalkyl or heteroaryl group; wherein, the dashed line represents a single or double bond, provided that when R 1 is O,

represents a double bond;

R 3 is hydrogen, halogen, loweralkyl, or loweralkoxy;

R 4 is hydrogen or loweralkyl;

R 5 and R 6 are independently selected from hydrogen, and substituted or unsubstituted alkyl, alkoxyalkyl, aminoalkyl, amidoalkyl, acyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkyloxyalkylheterocyclo, and heteroarylalkyl; or R5 and R6 are taken together to form substituted or unsubstituted heterocyclo or heteroaryl; and

the pharmaceutically acceptable salts, esters and prodrugs thereof.

54. A compound of claim 53 wherein R 4 is hydrogen.

55. A compound of claim 53 wherein R 4 is methyl.

56. A compound of claim 53 wherein A 1 is selected from the group consisting of substituted or unsubstituted phenyl, pyridyl, pyrimidinyl, phenylalkyl, pyridylalkyl, pyrimidinylalkyl, heterocyclylcarbonylphenyl, heterocyclylphenyl, heterocyclylalkylphenyl, chlorophenyl, fluorophenyl, bromophenyl, iodophenyl, dihalophenyl, nitrophenyl, 4-bromophenyl, 4-chlorophenyl, alkylbenzoate, alkoxyphenyl, dialkoxyphenyl, dialkylphenyl, trialkylphenyl, thiophene, thiophene-2-carboxylate, alkylthiophenyl, trifluoromethylphenyl, acetylphenyl, sulfamoylphenyl, biphenyl, cyclohexylphenyl, phenyloxyphenyl, dialkylaminophenyl, alkylbromophenyl, alkylchlorophenyl, alkylflourophenyl, triflouromethylchlorophenyl, triflouromethylbromophenyl indenyl, 2,3-dihydroindenyl, tetralinyl, trifluorophenyl, (trifluoromethyl)thiophenyl, alkoxybiphenyl, morpholinyl, N-piperazinyl, N-morpholinylalkyl, piperazinylalkyl, cyclohexylalkyl, indolyl, 2,3-dihydroindolyl, 1-aceytl-2,3-dihydroindolyl, cycloheptyl, bicyclo [2.2.1]hept-2-yl, hydroxyphenyl, hydroxyalkylphenyl, pyrrolidinyl, pyrrolidin-1-yl, pyrrolidin-1-ylalkyl, 4-amino(imino)methylphenyl, isoxazolyl, indazolyl, adamantyl, bicyclohexyl, quinuclidinyl, imidazolyl, benzimidazolyl, imidazolylphenyl, phenylimidazolyl, pthalamido, napthyl, benzophenone, anilinyl, anisolyl, quinolinyl, quinolinonyl, phenylsulfonyl, phenylalkylsulfonyl, 9H-flouren-1-yl, piperidin-1-yl, piperidin-1-ylalkyl, cyclopropyl, cyclopropylalkyl, pyrimidin-5-ylphenyl, quinolidinylphenyl, furanyl, furanylphenyl, N-methylpiperidin-4-yl, pyrrolidin-4-ylpyridinyl, 4-diazepan-1-yl, hydroxypyrrolidn-1-yl, dialkylaminopyrrolidin-1-yl, 1,4′-bipiperidin-1′-yl, and (1,4′-bipiperidin-1′-ylcarbonyl)phenyl.

57. A compound of claim 53 wherein R 2 is NR 5 R 6 , R 5 is hydrogen and R 6 is selected from hydrogen, and substituted or unsubstituted alkyl, alkoxyalkyl, aminoalkyl, amidoalkyl, acyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkyloxyalkylheterocyclo, and heteroarylalkyl.

58. A compound of claim 53 wherein R 1 is taken together with R 2 to form a substituted or unsubstituted heterocycloalkyl or heteroaryl group.

59. A compound of claim 53 wherein R 3 is loweralkoxy.

60. A compound of claim 59 wherein R 3 is methoxy.

61. A compound of claim 53 wherein R 4 is loweralkyl.

62. A compound of claim 61 wherein R 4 is methyl.

63. A compound of claim 53 wherein R 1 is O, R 2 is NR 5 R 6 , R 5 is H, and R 6 is methyl.

64. A composition comprising an amount of a compound of claim 1 , 16 , 29 , 41 , or 53 effective to inhibit Raf activity in a human or animal subject when administered thereto, together with a pharmaceutically acceptable carrier.

65. A composition of claim 64 which further comprises at least one additional agent for the treatment of cancer.

66. A composition of claim 65 in which the at least one additional agent for the treatment of cancer is selected from irinotecan, topotecan, gemeitabine, 5-fluorouracil, leucovorin carboplatin, cisplatin, taxanes, tezacitabine, cyclophosphamide, vinca alkaloids, imatinib, anthracyclines, rituximab and trastuzumab.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2011
From: NOVARTIS VACCINES AND DIAGNOSTICS INC.
To: NOVARTIS AG
Reel/Frame 027262/0403 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 23, 2004
From: HANSEN, TERESA; MCBRIDE, CHRISTOPHER; SHAFER, CYNTHIA M.
To: CHIRON CORPORATION
Reel/Frame 016096/0166 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 14, 2003
From: RENHOWE, PAUL A.; RAMURTHY, SAVITHRI; AMIRI, PAYMAN; LEVINE, BARRY HASKELL; POON, DANIEL J.; SUBRAMANIAN, SHARADHA; SUNG, LEONARD; FANTL, WENDY
To: CHIRON CORPORATION
Reel/Frame 014262/0011 →
Continuity (2)
Provisional Application 6036906600 · Mar 29, 2002
Related Publication 20040087626A1 · May 6, 2004