Novel heteroaryl-substituted arylaminopyridine derivatives as MEK inhibitors
申请人:Goutopoulos Andreas
公开号:US20070287737A1
公开(公告)日:2007-12-13
The invention provides novel heteroaryl-substituted arylaminopyridine derivative MEK inhibitors of Formula (Ia)
Such compounds are MEK inhibitors that are useful in the treatment of hyperproliferative diseases, such as cancer and inflammation. Also disclosed is the treatment of a hyperproliferative disease in mammals, and pharmaceutical compositions containing such compounds.
NOVEL HETEROARYL-SUBSTITUTED ARYLAMINOPYRIDINE DERIVATIVES AS MEK INHIBITORS
申请人:Laboratoires Serono SA
公开号:EP2013180A1
公开(公告)日:2009-01-14
US8076486B2
申请人:——
公开号:US8076486B2
公开(公告)日:2011-12-13
[EN] NOVEL HETEROARYL-SUBSTITUTED ARYLAMINOPYRIDINE DERIVATIVES AS MEK INHIBITORS<br/>[FR] NOUVEAUX DÉRIVÉS D'ARYLAMINOPYRIDINE SUBSTITUÉS PAR UN HÉTÉROARYLE, EN TANT QU'INHIBITEURS DE MEK
申请人:APPLIED RESEARCH SYSTEMS
公开号:WO2007123936A1
公开(公告)日:2007-11-01
[EN] The invention provides novel heteroaryl-substituted arylaminopyridine derivative MEK inhibitors of Formula (Ia) Formula (Ia) Such compounds are MEK inhibitors that are useful in the treatment of hyperproliferative diseases, such as cancer and inflammation. Also disclosed is the treatment of a hyperproliferative disease in mammals, and pharmaceutical compositions containing such compounds. [FR] L'invention concerne des inhibiteurs de MEK contenant des dérivés d'arylaminopyridine substitués par un hétéroaryle de formule (1a). Ces composés sont des inhibiteurs de MEK utilisés pour traiter des maladies hyperprolifératives, comme le cancer et des inflammations. Cette invention a aussi pour objet le traitement d'une maladie hyperproliférative chez des mammifères, ainsi que des compositions contenant ces composés.
2-Pyridyl and 3-pyridylzinc bromides: direct preparation and coupling reaction
作者:Seung-Hoi Kim、Reuben D. Rieke
DOI:10.1016/j.tet.2010.02.061
日期:2010.4
A facile synthetic approach to the direct preparation of 2-pyridyl and 3-pyridylzinc bromides has been demonstrated usingRieke zinc with 2-bromopyridine and 3-bromopyridine, respectively. A variety of different electrophiles have been coupled with the resulting organozinc reagents to give the corresponding cross-coupling products in moderate to good yields.