3,5-Dimethyl-1-(4-nitrophenyl)piperazine → 4-(3,5-Dimethylpiperazin-1-yl)aniline
反応式
[CH3:1][CH:2]1[NH:7][CH:6]([CH3:8])[CH2:5][N:4]([C:9]2[CH:14]=[CH:13][C:12]([N+:15]([O-])=O)=[CH:11][CH:10]=2)[CH2:3]1>CCO.[Pd]>[CH3:8][CH:6]1[NH:7][CH:2]([CH3:1])[CH2:3][N:4]([C:9]2[CH:14]=[CH:13][C:12]([NH2:15])=[CH:11][CH:10]=2)[CH2:5]1参加物
4
実験手順
An amount of 3,5-dimethyl-1-(4-nitrophenyl)piperazine (1.86 g, 7.90 mmol) in EtOH is hydrogenated with Pd/C catalyst for 4 h. The solid is removed by filtration, and solvent is evaporated under vacuum to give pinkish residue. Recrystallization of this residue from MeOH/ether gives 1.30 g (80.2% yield) of pinkish crystal: mp 124-125° C.; MS (ESI) m/z 206.1 (M+H)+1
後処理
- customThe solid is removed by filtration, and solvent
- customis evaporated under vacuum
- customto give pinkish residue
- customRecrystallization of this residue from MeOH/ether
出典と根拠
- ORDレコード
- ord-b49a1891c5d4457daba3c49498312fcf
- 出典データセット
- uspto-grants-2010_05
- 特許番号
- US07713994B2
反応ノート
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