IP Library Granted Patent US 8,778,955
Granted Patent B2
US 8,778,955 · App. 11/758,978 · Granted Jul 15, 2014

Indole derivatives or benzimidazole derivatives for modulating IkB kinase

Inventors: Olaf Ritzeler (Bad Soden, DE); Gerhard Jaehne (Frankfurt, DE)
Assignee: Sanofi-Aventis Deutschland GmbH
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Quick Facts
Patent No.
US 8,778,955
App. No.
11/758,978
Granted
Jul 15, 2014
Kind
B2
Abstract

The present invention relates to indole derivatives or benzimidazole derivatives, to processes for preparing such compounds, to pharmaceutical compositions comprising such compounds, and methods for the prophylaxis and therapy of a disease associated with an increased activity of IκB kinase comprising administering such compounds.

Claims (29)

1. A method for treating a disease selected from rheumatoid arthritis, osteoarthritis, inflammatory bowel disease, a disease which is due to overexpression of tumor necrosis factor alpha (TNFα) or an increased concentration of TNFα selected from Crohn's disease and intestinal ulcers, and treatment of an acute or chronic rejection reaction on the part of the organ recipient against the transplanted organ, in a patient in need thereof, comprising administering to such patient a pharmaceutically effective amount of a compound according to formula (I):

wherein:

X is N or CH;

M is N or CH;

R1 is hydrogen,

halogen chosen from F, Cl, I and Br,

—(C 1 -C 4 )-alkyl,

—CN,

—CF 3 ,

—OR 5 , wherein R 5 is hydrogen or —(C 1 -C 4 )-alkyl,

—N(R 5 )—R 6 , wherein R 5 and R 6 are selected from hydrogen and —(C 1 -C 4 )-alkyl,

—C(O)—R 5 , wherein R 5 is hydrogen or —(C 1 -C 4 )-alkyl, or

—S(O) x —R 5 , wherein x is the integer zero, 1 or 2, and wherein R 5 is hydrogen or —(C 1 -C 4 )-alkyl;

R 2 is a heteroaryl radical, which is selected from 3-hydroxypyrro-2,4-dione, imidazole, imidazolidine, imidazoline, indazole, isothiazole, isothiazolidine, isoxazole, 2-isoxazolidine, isoxazolidine, isoxazolone, morpholine, oxazole, 1,3,4-oxadiazole, oxadiazolidinedione, oxadiazolone, 1,2,3,5-oxathiadiazole-2-oxide, 5-oxo-4,5-dihydro[1,3,4]oxadiazole, 5-oxo-1,2,4-thiadiazole, piperazine, pyrazine, pyrazole, pyrazoline, pyrazolidine, pyridazine, pyrimidine, tetrazole, thiadiazole, thiazole, thiomorpholine, triazole and triazolone, wherein the heteroaryl radical is optionally substituted one, two, or three times by —C(O)—R 5 , wherein R 5 is selected from hydrogen and —(C 1 -C 4 )-alkyl, —(C 1 -C 4 )-alkyl, —O—R 5 , wherein R 5 is selected from hydrogen and —(C 1 -C 4 )-alkyl, —N(R 5 )—R 6 , wherein R 5 and R 6 are each selected from hydrogen and —(C 1 -C 4 -alkyl), halogen, or a keto radical, —C(O)—OR 5 , wherein R 5 is hydrogen or —(C 1 -C 4 -alkyl), or —C(O)—N(R 7 )—R 8 , wherein R 7 and R 8 are each selected from hydrogen, —(C 1 -C 4 )-alkyl-OH, —O—(C 1 -C 4 )-alkyl and —(C 1 -C 4 -alkyl);

R 3 is hydrogen or —(C 1 -C 4 -alkyl);

R 4 is a heteroaryl radical, which is selected from pyrrole, furan, thiophene, imidazole, pyrazole, oxazole, isoxazole, thiazole, isothiazole, tetrazole, 1,2,3,5-oxathiadiazole-2-oxides, triazolones, oxadiazolone, isoxazolone, oxadiazolidinedione, triazole, 3-hydroxypyrro-2,4-diones, 5-oxo-1,2,4-thiadiazoles, pyridine, pyrazine, pyrimidine, indole, isoindole, indazole, phthalazine, quinoline, isoquinoline, quinoxaline, quinazoline, cinnoline, β-carboline and benzofused cyclopenta derivatives or cyclohexa derivatives of the heteroaryl radical, wherein the heteroaryl radical is optionally substituted one, two or three times by —(C 1 -C 5 )-alkyl, —(C 1 -C 5 )-alkoxy, halogen, nitro, amino, trifluoromethyl, hydroxyl, hydroxy-(C 1 -C 4 )-alkyl, methylenedioxy, ethylenedioxy, formyl, acetyl, cyano, hydroxycarbonyl, aminocarbonyl or —(C 1 -C 4 )-alkoxycarbonyl, or an aryl radical which is selected from phenyl, naphthyl, 1-naphthyl, 2-naphthyl, biphenylyl, 2-biphenylyl, 3-biphenylyl and 4-biphenylyl, anthryl and fluorenyl, wherein the aryl radical is optionally substituted one, two, or three times by —(C 1 -C 5 )-alkyl, —(C 1 -C 5 )-alkoxy, halogen, nitro, amino, trifluoromethyl, hydroxyl, hydroxy-(C 1 -C 4 )-alkyl, methylenedioxy, ethylenedioxy, formyl, acetyl, cyano, hydroxycarbonyl, aminocarbonyl or —(C 1 -C 4 )-alkoxycarbonyl; and

R 11 is hydrogen,

halogen chosen from F, Cl, I and Br,

—(C 1 -C 4 )-alkyl,

—CN,

—CF 3 ,

—OR 5 , wherein R 5 is hydrogen or —(C 1 -C 4 )-alkyl,

—N(R 5 )—R 6 , wherein R 5 and R 6 are selected from hydrogen and —(C 1 -C 4 )-alkyl,

—C(O)—R 5 , wherein R 5 is hydrogen or —(C 1 -C 4 )-alkyl, or

—S(O) x —R 5 , wherein x is the integer zero, 1 or 2, and wherein R 5 is hydrogen or —(C 1 -C 4 )-alkyl,

or a stereoisomer or a mixture of stereoisomers in any ratio of the compound, or a pharmaceutically acceptable salt of the compound.

2. The method according to claim 1 wherein the disease due to overexpression of tumor necrosis factor alpha (TNFα) or an increased concentration of TNFα is Crohn's disease or intestinal ulcers.

3. The method according to claim 1 wherein the disease is rheumatoid arthritis.

4. The method according to claim 1 wherein the disease is osteoarthritis.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 24, 2012
From: RITZELER, OLAF, DR.; JAEHNE, GERHARD, DR.
To: AVENTIS PHARMA DEUTSCHLAND GMBH
Reel/Frame 028262/0024 →
CHANGE OF NAME Recorded May 24, 2012
From: AVENTIS PHARMA DEUTSCHLAND GMBH
To: SANOFI-AVENTIS DEUTSCHLAND GMBH
Reel/Frame 028262/0048 →
Priority Claims (1)
DE 102 37 722 · Aug 17, 2002 · national
Continuity (3)
Division 10642970 · Aug 18, 2003
Provisional Application 60434749 · Dec 19, 2002
Related Publication 20070244139A1 · Oct 18, 2007