ARYLMETHOXY ISOINDOLINE DERIVATIVES AND COMPOSITIONS COMPRISING AND METHODS OF USING THE SAME
申请人:Celgene Corporation
公开号:US20180037567A1
公开(公告)日:2018-02-08
Provided are 4′-arylmethoxy isoindoline compounds, and pharmaceutically acceptable salts, solvates, clathrates, stereoisomers, and prodrugs thereof. Methods of use, and pharmaceutical compositions of these compounds are disclosed.
Cinnoline derivatives as phosphodiesterase 10 inhibitors
申请人:Hitchcock A. Stephen
公开号:US20070265270A1
公开(公告)日:2007-11-15
The present invention is directed to certain cinnoline compounds that are PDE10 inhibitors, pharmaceutical compositions containing such compounds and process for preparing such compounds. The invention is also directed to methods of treating diseases treatable by modulation of PDE10 enzyme, such as obesity, non-insulin dependent diabetes, schizophrenia, bipolar disorder, obsessive-compulsive disorder, and the like.
Arylmethoxy isoindoline derivatives and compositions comprising and methods of using the same
申请人:Celgene Corporation
公开号:US10189814B2
公开(公告)日:2019-01-29
Provided are 4′-arylmethoxy isoindoline compounds, and pharmaceutically acceptable salts, solvates, clathrates, stereoisomers, and prodrugs thereof. Methods of use, and pharmaceutical compositions of these compounds are disclosed.
Palladium-Catalyzed C,N-Cross Coupling Reactions of 3<i>-</i>Halo-2-aminopyridines
作者:Felix Perez、Ana Minatti
DOI:10.1021/ol200371n
日期:2011.4.15
A simple approach toward N-3-substituted-2,3-diaminopyridines is presented, based on Pd-catalyzed C,N-cross coupling. The use of RuPhos- and BrettPhos-precatalysts in combination with LiHMDS allows for C,N-cross coupling reactions of unprotected 3-halo-2-aminopyridines with primary and secondary amines.