Reaktionsgleichung
[N+:1]([C:4]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:5]=1[CH:6]=[CH:7][C:8](Cl)=[N:9]2)([O-])=O.[CH3:15][C:16]1[O:17][C:18]2[C:24]([NH2:25])=[CH:23][CH:22]=[CH:21][C:19]=2[CH:20]=1.[F:26][C:27]1[CH:32]=[CH:31][C:30]([S:33](Cl)(=[O:35])=[O:34])=[CH:29][CH:28]=1>>[F:26][C:27]1[CH:32]=[CH:31][C:30]([S:33]([NH:1][C:4]2[CH:13]=[CH:12][CH:11]=[C:10]3[C:5]=2[CH:6]=[CH:7][C:8]([NH:25][C:24]2[C:18]4[O:17][C:16]([CH3:15])=[CH:20][C:19]=4[CH:21]=[CH:22][CH:23]=2)=[N:9]3)(=[O:35])=[O:34])=[CH:29][CH:28]=1Komponenten
4
Versuchsvorschrift
The title compound, MS: m/e=448.0 (M+H+), was prepared in accordance with the general method of example 58 from 5-nitro-2-chloroquinoline, (2-methyl-1-benzofuran-7-yl)amine and 4-fluorobenzenesulfonylchloride.
Quellen und Nachweise
- ORD-Eintrag
- ord-13521e2796444cbe9a600f1e3543a530
- Quelldatensatz
- uspto-grants-2010_11
- Patentnummer
- US07825253B2
Verknüpfte Notizen
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