2-(3-Nitrophenyl)pyrazine → 3-(Pyrazin-2-yl)aniline
反応式
[N+:1]([C:4]1[CH:5]=[C:6]([C:10]2[CH:15]=[N:14][CH:13]=[CH:12][N:11]=2)[CH:7]=[CH:8][CH:9]=1)([O-])=O>O1CCCC1.C(O)C.[Pd]>[N:11]1[CH:12]=[CH:13][N:14]=[CH:15][C:10]=1[C:6]1[CH:5]=[C:4]([CH:9]=[CH:8][CH:7]=1)[NH2:1]参加物
5
実験手順
A suspension of 2-(3-nitrophenyl)pyrazine (500 mg) in tetrahydrofuran (5 ml) and ethanol (5 ml) was hydrogenated over palladium on carbon (10% w/w, 50% wet, 200 mg) under hydrogen atmosphere for 6 hours. The catalyst was filtered off and the filtrate was evaporated. The residue was crystallized from dichloromethanediisopropyl ether to give 3-(pyrazin-2-yl)aniline (410 mg, 96.5%).
後処理
- filtrationThe catalyst was filtered off
- customthe filtrate was evaporated
- customThe residue was crystallized from dichloromethanediisopropyl ether
出典と根拠
- ORDレコード
- ord-205127d164f34fa3a0250f281e9474e5
- 出典データセット
- uspto-grants-2004_08
- 特許番号
- US06770667B1
反応ノート
読み込み中…