Aniline → HCID 22909003、化合物
反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([S:31](O)(=[O:33])=[O:32])[C:6](=[CH:27][C:28]=1[O:29][CH3:30])/[CH:7]=[CH:8]/[C:9]1[N:17]([CH3:18])[C:16]2[C:15](=[O:19])[N:14]([CH2:20][CH2:21][CH3:22])[C:13](=[O:23])[N:12]([CH2:24][CH2:25][CH3:26])[C:11]=2[N:10]=1.[NH2:35][C:36]1[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=1>>[C:36]1([NH:35][S:31]([C:5]2[C:6](=[CH:27][C:28]([O:29][CH3:30])=[C:3]([O:2][CH3:1])[CH:4]=2)/[CH:7]=[CH:8]/[C:9]2[N:17]([CH3:18])[C:16]3[C:15](=[O:19])[N:14]([CH2:20][CH2:21][CH3:22])[C:13](=[O:23])[N:12]([CH2:24][CH2:25][CH3:26])[C:11]=3[N:10]=2)(=[O:32])=[O:33])[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=1参加物
3
実験手順
Substantially the same procedure as in Example 2 was repeated using 1.00 g (1.96 mmol) of Compound 1 obtained in Example 1 and 1.85 ml (20.3 mmol) of aniline. The resulting crude crystals were recrystallized from toluene to give 261 mg (yield 23%) of Compound 10 as a pale yellow powder.
後処理
- customThe resulting crude crystals were recrystallized from toluene
出典と根拠
- ORDレコード
- ord-53d1e8e00fe14f5c86091272cd893cb6
- 出典データセット
- uspto-grants-1997_09
- DOI