4-(3-Hydroxypropylamino)-3-nitropyridine → 3-Amino-4-(3-hydroxypropylamino)pyridine
反応式
[OH:1][CH2:2][CH2:3][CH2:4][NH:5][C:6]1[CH:11]=[CH:10][N:9]=[CH:8][C:7]=1[N+:12]([O-])=O>C(O)C.[Ni]>[NH2:12][C:7]1[CH:8]=[N:9][CH:10]=[CH:11][C:6]=1[NH:5][CH2:4][CH2:3][CH2:2][OH:1]参加物
4
実験手順
4-(3-Hydroxypropylamino)-3-nitropyridine (4.12 g, 20.9 mmol) was dissolved in ethanol (130 ml) and Raney nickel (411 mg, 7.0 mmol) added. The stirred mixture was hydrogenated for 3 days. The catalyst was removed by filtration under argon and the solvent removed under reduced pressure to give 3-amino-4-(3- hydroxypropylamino)pyridine as a brown oil which was used directly in the next step.
後処理
- customThe catalyst was removed by filtration under argon
- customthe solvent removed under reduced pressure
出典と根拠
- ORDレコード
- ord-0b245cb559a94e40b09fed9cdc42702f
- 出典データセット
- uspto-grants-1997_06
- 特許番号
- US05637595
反応ノート
読み込み中…