3,4-Dimethoxyaniline → N-(3,4-Dimethoxyphenyl)-2-(3,5-dimethyl-1H-pyrrol-2-yl)-2-(2-oxo-1,2-dihydroindol-3-ylidene)-acetamide
反応式
[CH3:1][C:2]1[CH:6]=[C:5]([CH3:7])[NH:4][C:3]=1[C:8](=[C:12]1[C:20]2[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=2)[NH:14][C:13]1=[O:21])[C:9](O)=[O:10].[CH3:22][O:23][C:24]1[CH:25]=[C:26]([CH:28]=[CH:29][C:30]=1[O:31][CH3:32])[NH2:27]>>[CH3:22][O:23][C:24]1[CH:25]=[C:26]([NH:27][C:9](=[O:10])[C:8]([C:3]2[NH:4][C:5]([CH3:7])=[CH:6][C:2]=2[CH3:1])=[C:12]2[C:20]3[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=3)[NH:14][C:13]2=[O:21])[CH:28]=[CH:29][C:30]=1[O:31][CH3:32]参加物
3
実験手順
(3,5-Dimethyl-1H-pyrrol-2-yl)-(2-oxo-1,2-dihydro-indol-3-ylidene)-acetic acid (90 mg) was reacted with 3,4-dimethoxyaniline (110 mg) using method B to give 50 mg (37%) of the title compound.
出典と根拠
- ORDレコード
- ord-ea7e66c5ba40404db7d2dda992083a4d
- 出典データセット
- uspto-grants-2007_05