Reaktionsgleichung
[Cl:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][C:12]=1[S:13](Cl)(=[O:15])=[O:14])[C:5]([O:7][CH2:8][CH3:9])=[O:6].[CH3:17][N:18]1[C:26]2[C:21](=[CH:22][C:23]([CH2:27][NH2:28])=[CH:24][CH:25]=2)[CH:20]=[CH:19]1>>[Cl:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][C:12]=1[S:13](=[O:15])(=[O:14])[NH:28][CH2:27][C:23]1[CH:22]=[C:21]2[C:26](=[CH:25][CH:24]=1)[N:18]([CH3:17])[CH:19]=[CH:20]2)[C:5]([O:7][CH2:8][CH3:9])=[O:6]Komponenten
3
Versuchsvorschrift
The titled compound was prepared according to the procedure described in step-1 of Example 1 from ethyl 3-chloro-4-(chlorosulfonyl)benzoate and (1-methyl-1H-indol-5-yl)methanamine.
Quellen und Nachweise
- ORD-Eintrag
- ord-f2c27c6438ee4fb1bb9e0362b52b15c8
- Quelldatensatz
- uspto-grants-2014_09
- Patentnummer
- US08829026B2
Verknüpfte Notizen
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