1-(3',4',5'-Trimethoxy benzyl)-2-phenyl piperazine → 1-(3',4',5'-Trimethoxy benzyl)-2-phenyl-4-diethylamino ethyl piperazine
反応式
[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]=1参加物
3
実験手順
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.
後処理
- customThe resulting reaction product
出典と根拠
- ORDレコード
- ord-d7a3a4c7630246ac8e9a2e6a0cbfb5fa