4-(6-Nitropyridin-3-yl)piperazin-2-one → 4-(6-Aminopyridin-3-yl)piperazin-2-one
反応式
[N+:1]([C:4]1[N:9]=[CH:8][C:7]([N:10]2[CH2:15][CH2:14][NH:13][C:12](=[O:16])[CH2:11]2)=[CH:6][CH:5]=1)([O-])=O.[H][H]>[Pd].CO>[NH2:1][C:4]1[N:9]=[CH:8][C:7]([N:10]2[CH2:15][CH2:14][NH:13][C:12](=[O:16])[CH2:11]2)=[CH:6][CH:5]=1参加物
5
実験手順
To a round-bottom flask was added 4-(6-nitropyridin-3-yl)piperazin-2-one 141-3 (0.7 g, 3.1 mmol), Pd/C (0.2 g) and methanol (20 mL). The reaction was stirred for 4 hours under hydrogen atmosphere by attaching a hydrogen balloon. The reaction was flashed with nitrogen and the solid was removed by filtration. The solvent was removed by rotary evaporation to give 4-(6-aminopyridin-3-yl)piperazin-2-one 141-4 as purple solid. MS m/z 193.2 (M+1).
後処理
- customthe solid was removed by filtration
- customThe solvent was removed by rotary evaporation
出典と根拠
- ORDレコード
- ord-1a3a63fa56ed43e3944005f8dfbdf0a3
- 出典データセット
- uspto-grants-2016_01
- 特許番号
- US09238646B2
反応ノート
読み込み中…