Indole-2-carboxylic acid → 3-(Dimethylaminophenylmethyl)-1H-indole-2-carboxylic Acid
反応式
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[C:2]1[C:10]([OH:12])=[O:11].[Cl-].[CH:14](=[N+:21]([CH3:23])[CH3:22])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>>[CH3:22][N:21]([CH:14]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[C:3]1[C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[NH:1][C:2]=1[C:10]([OH:12])=[O:11])[CH3:23]参加物
3
実験手順
The preparation was carried out in accordance with general synthesis instructions 4 from 1H-indole-2-carboxylic acid 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-4c19ce5b2ab74400bfa9da1319b50e23
- 出典データセット
- uspto-grants-2006_08
- 特許番号
- US07091220B2
反応ノート
読み込み中…