m-Aminoacetanilide → HCID 178474196、化合物
反応式
C(O[C:4](=[C:11]1[C:19]2[C:14](=[CH:15][CH:16]=[C:17]([N+:20]([O-:22])=[O:21])[CH:18]=2)[NH:13][C:12]1=[O:23])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)C.[C:24]([NH:27][C:28]1[CH:29]=[C:30]([CH:32]=[CH:33][CH:34]=1)[NH2:31])(=[O:26])[CH3:25]>CN(C=O)C>[C:24]([NH:27][C:28]1[CH:29]=[C:30]([NH:31]/[C:4](=[C:11]2\[C:12](=[O:23])[NH:13][C:14]3[C:19]\2=[CH:18][C:17]([N+:20]([O-:22])=[O:21])=[CH:16][CH:15]=3)/[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:32]=[CH:33][CH:34]=1)(=[O:26])[CH3:25]参加物
4
実験手順
Prepared analogously to Example 82 from 3-(1-ethoxy-1-phenyl-methylidene)-5-nitro-2-indolinone and 3-acetylamino-aniline in DMF.
出典と根拠
- ORDレコード
- ord-17e90cdd70b346aab7f5d9df16ad7764
- 出典データセット
- uspto-grants-2005_02