Reaktionsgleichung
[CH3:1][O:2][C:3]1[C:18]([O:19][CH3:20])=[CH:17][C:6]2[CH2:7][C:8](=[O:16])[N:9]([CH:12]([Cl:15])[CH2:13][CH3:14])[CH2:10][CH2:11][C:5]=2[CH:4]=1.[CH3:21][NH:22][CH2:23][CH2:24][C:25]1[CH:30]=[C:29]([O:31][CH3:32])[C:28]([O:33][CH3:34])=[C:27]([O:35][CH3:36])[CH:26]=1>>[ClH:15].[CH3:1][O:2][C:3]1[C:18]([O:19][CH3:20])=[CH:17][C:6]2[CH2:7][C:8](=[O:16])[N:9]([CH2:12][CH2:13][CH2:14][N:22]([CH3:21])[CH2:23][CH2:24][C:25]3[CH:26]=[C:27]([O:35][CH3:36])[C:28]([O:33][CH3:34])=[C:29]([O:31][CH3:32])[CH:30]=3)[CH2:10][CH2:11][C:5]=2[CH:4]=1Komponenten
3
Versuchsvorschrift
This compound was prepared analogous to Example 5(b) by reacting 1-(7,8-dimethoxy-1,3,4,5-tetrahydro-2H-3-benzazepin-2-on-3-yl)-chloro-propane with N-methyl-N-[2-(3,4,5-trimethoxy-phenyl)-ethyl]-amine.
Aufarbeitung
- customThis compound was prepared analogous to Example 5(b)
Quellen und Nachweise
- ORD-Eintrag
- ord-dd25870d61334851acce0e97111e600a
- Quelldatensatz
- uspto-grants-1984_12
- Patentnummer
- US04490369
Verknüpfte Notizen
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