2-Phenylindole → 2-Phenyl-3-(pyrrolidin-1-yl-o-tolylmethyl)-1H-indole
反応式
[C:1]1([C:7]2[NH:8][C:9]3[C:14]([CH:15]=2)=[CH:13][CH:12]=[CH:11][CH:10]=3)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cl-].[CH3:17][C:18]1[CH:29]=[CH:28][CH:27]=[CH:26][C:19]=1[CH:20]=[N+:21]1[CH2:25][CH2:24][CH2:23][CH2:22]1>>[C:1]1([C:7]2[NH:8][C:9]3[C:14]([C:15]=2[CH:20]([N:21]2[CH2:25][CH2:24][CH2:23][CH2:22]2)[C:19]2[CH:26]=[CH:27][CH:28]=[CH:29][C:18]=2[CH3:17])=[CH:13][CH:12]=[CH:11][CH:10]=3)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1参加物
3
実験手順
The preparation was carried out in accordance with general synthesis instructions 4 from 2-phenyl-1H-indole and 1-(2-methyl-benzylidene)-pyrrolidinium chloride, which had been prepared in accordance with example 25.
後処理
- customhad been prepared in accordance with example 25
出典と根拠
- ORDレコード
- ord-0332ce0078e14a6cb5e4f7cd2e1699f0
- 出典データセット
- uspto-grants-2006_08