Reaktionsgleichung
[F:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[C:10]([F:13])([F:12])[F:11])[CH2:5][NH2:6].[Cl:14][C:15]1[S:19][C:18]([NH:20][S:21]([C:24]2[CH:32]=[CH:31][C:27]([C:28](O)=[O:29])=[C:26]([C:33]#[N:34])[CH:25]=2)(=[O:23])=[O:22])=[N:17][CH:16]=1>>[Cl:14][C:15]1[S:19][C:18]([NH:20][S:21]([C:24]2[CH:32]=[CH:31][C:27]([C:28]([NH:6][CH2:5][C:4]3[CH:7]=[CH:8][C:9]([C:10]([F:11])([F:12])[F:13])=[C:2]([F:1])[CH:3]=3)=[O:29])=[C:26]([C:33]#[N:34])[CH:25]=2)(=[O:23])=[O:22])=[N:17][CH:16]=1Komponenten
3
Versuchsvorschrift
The title compound was prepared from 3-fluoro-4-(trifluoromethyl)benzylamine and 4-{[(5-chloro-1,3-thiazol-2-yl)amino]sulfonyl}-2-cyanobenzoic acid of Preparation 22, following Method O described for Example 344. The reaction mixture was stirred at room temperature for 18 hours.
Quellen und Nachweise
- ORD-Eintrag
- ord-2c10def5d8c34f55a715d8b7d8294c60
- Quelldatensatz
- uspto-grants-2014_06
- Patentnummer
- US08741934B2
Verknüpfte Notizen
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