4-Aminophenethyl alcohol → 2-[4-[(2,6-Dimethyl-3-nitro-4-pyridinyl)amino]phenyl]ethanol
反応式
Cl[C:2]1[CH:7]=[C:6]([CH3:8])[N:5]=[C:4]([CH3:9])[C:3]=1[N+:10]([O-:12])=[O:11].[NH2:13][C:14]1[CH:19]=[CH:18][C:17]([CH2:20][CH2:21][OH:22])=[CH:16][CH:15]=1>>[CH3:9][C:4]1[C:3]([N+:10]([O-:12])=[O:11])=[C:2]([NH:13][C:14]2[CH:19]=[CH:18][C:17]([CH2:20][CH2:21][OH:22])=[CH:16][CH:15]=2)[CH:7]=[C:6]([CH3:8])[N:5]=1参加物
3
実験手順
The title compound was prepared according to the procedure described in step 3 of Example 1 from 4-chloro-2,6-dimethyl-3-nitropyridine (Tanaka, A.; et al. J. Med. Chem., 1999, 41, 4408.) and 4-aminophenylethyl alcohol.
出典と根拠
- ORDレコード
- ord-b6f94abd92ae4ca099387c764237d427
- 出典データセット
- uspto-grants-2006_11
- 特許番号
- US07141580B2
反応ノート
読み込み中…