1-(3',4',5'-Trimethoxy benzyl)-2-phenyl piperazine → 1-(3',4',5'-Trimethoxy benzyl)-2-phenyl-4-diethylamino ethyl piperazine
Reaktionsgleichung
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:19]=[C:20]([O:24][CH3:25])[C:21]=1[O:22][CH3:23])[CH2:6][N:7]1[CH2:12][CH2:11][NH:10][CH2:9][CH:8]1[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.[CH2:26](Cl)[CH3:27].[CH2:29]([NH:31][CH2:32][CH3:33])[CH3:30]>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:19]=[C:20]([O:24][CH3:25])[C:21]=1[O:22][CH3:23])[CH2:6][N:7]1[CH2:12][CH2:11][N:10]([CH2:30][CH2:29][N:31]([CH2:26][CH3:27])[CH2:32][CH3:33])[CH2:9][CH:8]1[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1Komponenten
3
Versuchsvorschrift
1-(3',4',5'-Trimethoxy benzyl)-2-phenyl piperazine prepared according to Example 17, is alkylated by means of diethylamine ethylchloride by following the procedure described in Example 3c. The resulting reaction product is obtained in the form of yellow oil boiling at 200° C./0.03 mm. Hg.
Aufarbeitung
- customThe resulting reaction product