IP Library Granted Patent US 8,906,934
Granted Patent B2
US 8,906,934 · App. 13/559,762 · Granted Dec 9, 2014

Pyridyl-and pyrimidinyl-substituted pyrrole-, thiophene-and furane-derivatives as kinase inhibitors

Inventors: Ermes Vanotti (Milan, IT); Marina Caldarelli (Milan, IT); Alessandra Cirla (Varese, IT); Barbara Forte (Milan, IT); Antonella Ermoli (Buccinasco, IT); Maria Menichincheri (Milan, IT); Antonio Pillan (Milan, IT); Alessandra Scolaro (Bresso, IT)
Assignee: Nerviano Medical Science S.R.L.
C07D401/04C07D409/04C07D403/04C07D405/04C07D401/14C07D403/14C07D405/14
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Quick Facts
Patent No.
US 8,906,934
App. No.
13/559,762
Granted
Dec 9, 2014
Kind
B2
Abstract

The present invention provides compounds of the formula (I), or the pharmaceutically acceptable salts thereof, wherein G, W, R 2 , R 3 , R 4 , R 5 and R 6 are as defined in the specification. Further objects of the invention are processes and intermediates for the preparation of the compounds of the formula (I), pharmaceutical compositions comprising them and methods for treating cell proliferative disorders. As a matter of fact, the compounds of the formula (I) are useful, in therapy, in the treatment of diseases associated with a disregulated protein kinase activity, like cancer.

Claims (20)

1. A method for treating cell proliferative disorders caused by and/or associated with an altered protein kinase activity which comprises administering to a mammal in need thereof an effective amount of a compound of formula (I):

wherein

G is CH or nitrogen atom;

W is an oxygen atom, NR 1 or S(O)n; n is 0, 1 or 2;

R 1 and R 3 independently represent hydrogen atom or an optionally substituted group selected from alkyl, cycloalkyl, alkenyl, alkynyl, heterocyclyl, heterocyclylalkyl, aryl, arylalkyl, heterocyclyloxy-alkyl and alkoxycarbonyl group;

R 2 is hydrogen or halogen atom, or an optionally substituted group selected from aryl, cycloalkyl and heterocyclyl group;

R 4 is hydrogen or halogen atom, or an optionally substituted alkyl or alkenyl group;

R 5 is hydrogen or halogen atom;

R 6 is hydrogen atom or NHR 7 ;

R 7 is hydrogen atom, an optionally substituted group selected from alkyl, aryl, cycloalkyl and heterocyclyl group or —COR 1 wherein R 1 is as defined above;

or a pharmaceutically acceptable salt thereof, with the proviso that the following compounds are excluded:

2,5-di(pyridin-4-yl)-thiophene-3-carboxylic acid amide,

2,5-di(pyridin-4-yl)-thiophene-3-carboxylic acid methylamide,

2,5-di(pyridin-4-yl)-4-methyl-pyrrole-3-carboxylic acid amide,

5-pyridin-4-yl-furan-3-carboxylic acid [4-methoxy-3-(4-methyl-piperazin-1-yl)-phenyl]-amide,

5-pyridin-4-yl-furan-3-carboxylic acid (1-methyl-1,2,3,4-tetrahydro-quinolin-7-yl)-amide and

N-[2-amino-1-(2,4-dichlorobenzyl)ethyl]-5-[2-(methylamino)pyrimidin-4-yl]thiophene-3-carboxamide, wherein the cell proliferative disorder is selected from the group consisting of cervical cancer, colon cancer, ovarian cancer, pancreatic cancer, breast cancer, ductal breast cancer, epidermal cancer, lung cancer, large cell lung cancer, squamous cell lung cancer, small cell lung cancer, non-small cell lung cancer, thyroid cancer, medullary thyroid cancer, papillary thyroid cancer, astrocitoma, neuroblastoma, glioblastoma, gliosarcoma, melanoma and osteosarcoma.

2. The method according to claim 1 further comprising subjecting the mammal in need thereof to a radiation therapy or chemotherapy regimen in combination with at least one cytostatic or cytotoxic agent.

3. The method according to claim 1 wherein the mammal in need thereof is a human.

4. A method for inhibiting Cdc7 kinase activity which comprises contacting the said kinase with an effective amount of a compound of formula (I) as defined in claim 1 .

Priority Claims (1)
EP 06111766 · Mar 27, 2006 · regional
Continuity (2)
Division 12293951
Related Publication 20120295906A1 · Nov 22, 2012