Reaktionsgleichung
[C:1]([C:4]1[C:5]([CH3:22])=[CH:6][C:7]([O:20][CH3:21])=[C:8]([NH:10][C:11](=[O:19])OC2C=CC=CC=2)[CH:9]=1)(=[O:3])[CH3:2].[Cl:23][C:24]1[CH:25]=[C:26]([N:31]2[CH2:36][CH2:35][NH:34][CH2:33][CH2:32]2)[CH:27]=[C:28]([Cl:30])[CH:29]=1>>[C:1]([C:4]1[C:5]([CH3:22])=[CH:6][C:7]([O:20][CH3:21])=[C:8]([NH:10][C:11]([N:34]2[CH2:33][CH2:32][N:31]([C:26]3[CH:25]=[C:24]([Cl:23])[CH:29]=[C:28]([Cl:30])[CH:27]=3)[CH2:36][CH2:35]2)=[O:19])[CH:9]=1)(=[O:3])[CH3:2]Komponenten
3
Versuchsvorschrift
Phenyl N-(5-acetyl-2-methoxy-4-methylphenyl)carbamate and 1-(3,5-dichlorophenyl)piperazine were reacted by the same way with the example 170 to obtain the titled compound.
Quellen und Nachweise
- ORD-Eintrag
- ord-b844d351e54f49d3be1738b6cdf5df83
- Quelldatensatz
- uspto-grants-2000_02
- Patentnummer
- US06028195
Verknüpfte Notizen
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