2-(4-Chlorophenyl)-1H-indole → {[2-(4-Chlorophenyl)-1H-indol-3-yl]-phenylmethyl}-dimethylamine
反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[NH:9][C:10]3[C:15]([CH:16]=2)=[CH:14][CH:13]=[CH:12][CH:11]=3)=[CH:4][CH:3]=1.[Cl-].[CH:18](=[N+:25]([CH3:27])[CH3:26])[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[NH:9][C:10]3[C:15]([C:16]=2[CH:18]([N:25]([CH3:27])[CH3:26])[C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[CH:14][CH:13]=[CH:12][CH:11]=3)=[CH:6][CH:7]=1参加物
3
実験手順
The preparation was carried out in accordance with general synthesis instructions 4 from 2-(4-chlorophenyl)-1H-indole and benzylidene-dimethyl-ammonium chloride, which had been prepared in accordance with example 1.
後処理
- customhad been prepared in accordance with example 1
出典と根拠
- ORDレコード
- ord-3e9f91744aff4bafad71878515c662bd
- 出典データセット
- uspto-grants-2006_08