Fluorinated pyrazoles bearing additional functional groups that allow further functionalization are of considerable interest as building blocks in medicinal chemistry. The developed synthetic strategy for new 3-amino-4-fluoropyrazoles consists of a monofluorination of beta-methylthio-beta-enaminoketones using 1-(chloromethyl)-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) (Selectfluor) toward the corresponding monofluorinated enaminoketones, followed by condensation with different hydrazines.
[EN] HALOGENOPYRAZOLES AS INHIBITORS OF THROMBIN<br/>[FR] HALOGÉNOPYRAZOLES EN TANT QU'INHIBITEURS DE THROMBINE
申请人:VERSEON INC
公开号:WO2014146059A1
公开(公告)日:2014-09-18
There are provided inter alia multisubstituted aromatic compounds useful for the inhibition of thrombin, which compounds include substituted pyrazolyl. There are additionally provided pharmaceutical compositions. There are additionally provided methods of treating and preventing a disease or disorder, which disease or disorder is amenable to treatment or prevention by the inhibition of thrombin.
[EN] HALOGENOPYRAZOLES AS INHIBITORS OF THROMBIN<br/>[FR] HALOGÉNOPYRAZOLES EN TANT QU'INHIBITEURS DE LA THROMBINE
申请人:VERSEON INC
公开号:WO2014149139A2
公开(公告)日:2014-09-25
There are provided inter alia multisubstituted aromatic compounds useful for the inhibition of thrombin, which compounds include substituted pyrazolyi. There are additionally provided pharmaceutical compositions. There are additionally provided methods of treating and preventing a disease or disorder, which disease or disorder is amenable to treatment or prevention by the inhibition of thrombin.
Synthesis of 3-Amino-4-fluoropyrazoles
作者:Riccardo Surmont、Guido Verniest、Mathias De Schrijver、Jan Willem Thuring、Peter ten Holte、Frederik Deroose、Norbert De Kimpe
DOI:10.1021/jo2000989
日期:2011.5.20
Fluorinated pyrazoles bearing additional functional groups that allow further functionalization are of considerable interest as building blocks in medicinal chemistry. The developed synthetic strategy for new 3-amino-4-fluoropyrazoles consists of a monofluorination of beta-methylthio-beta-enaminoketones using 1-(chloromethyl)-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) (Selectfluor) toward the corresponding monofluorinated enaminoketones, followed by condensation with different hydrazines.