1-(6-Chloro-5-nitropyridin-3-yl)ethanone → 1-[6-({4-[2-Hydroxypropyl]phenyl}amino)-5-nitro-3-pyridinyl]ethanone
反応式
Cl[C:2]1[N:7]=[CH:6][C:5]([C:8](=[O:10])[CH3:9])=[CH:4][C:3]=1[N+:11]([O-:13])=[O:12].[NH2:14][C:15]1[CH:20]=[CH:19][C:18]([CH2:21][CH:22]([OH:24])[CH3:23])=[CH:17][CH:16]=1>>[OH:24][CH:22]([CH3:23])[CH2:21][C:18]1[CH:19]=[CH:20][C:15]([NH:14][C:2]2[N:7]=[CH:6][C:5]([C:8](=[O:10])[CH3:9])=[CH:4][C:3]=2[N+:11]([O-:13])=[O:12])=[CH:16][CH:17]=1参加物
3
実験手順
The title compound was prepared according to the procedure described in step 1 of Example 162 from 1-(6-chloro-5-nitro-3-pyridinyl)ethanone (Paul, B. et al. J. Med. Chem., 1990, 33, 2231-2239.) and 1-(4-aminophenyl)-2-propanol (step 1 of Example 6).
出典と根拠
- ORDレコード
- ord-15875eeee5f0487c876b0e267da2cf94
- 出典データセット
- uspto-grants-2011_04
- 特許番号
- US07928119B2
反応ノート
読み込み中…