反応式
[CH2:1]([C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[C:11]=1[NH:10][CH:9]=[CH:8]2)[CH3:2].[Cl-].[O:13]([C:20]1[CH:21]=[C:22]([CH:27]=[CH:28][CH:29]=1)[CH:23]=[N+:24]([CH3:26])[CH3:25])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.O(C1C=C(C=CC=1)C=O)C1C=CC=CC=1.CNC>>[CH2:1]([C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[C:11]=1[NH:10][CH:9]=[C:8]2[CH:23]([N:24]([CH3:26])[CH3:25])[C:22]1[CH:27]=[CH:28][CH:29]=[C:20]([O:13][C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=2)[CH:21]=1)[CH3:2]参加物
5
実験手順
The preparation was carried out in accordance with general synthesis instructions 4 from 7-ethyl-1H-indole and (3-phenoxy-benzylidene)-dimethylammonium chloride, which had been prepared in accordance with example 44 from 3-phenoxy-benzaldehyde and dimethylamine.
出典と根拠
- ORDレコード
- ord-e50db9293f9e4f3f9f2530c09171c21c
- 出典データセット
- uspto-grants-2006_08
- 特許番号
- US07091220B2
関連ノート
読み込み中…