3,3-Diethoxypropiononitrile → 1-cyclopropyl-1H-pyrazol-5-amine
反応式
C(O[CH:4](OCC)[CH2:5][C:6]#[N:7])C.Cl.Cl.[CH:13]1([NH:16][NH2:17])[CH2:15][CH2:14]1>C(O)C>[CH:13]1([N:16]2[C:6]([NH2:7])=[CH:5][CH:4]=[N:17]2)[CH2:15][CH2:14]1参加物
4
反応条件
- 温度
- 80 °C
実験手順
A 100-mL round-bottom flask was charged with 3,3-diethoxypropanenitrile (0.600 g, 4.19 mmol), cyclopropylhydrazine di-hydrochloride (0.610 g, 4.21 mmol) and ethanol (20 mL), and the resulting solution stirred for 18 h at 80° C. The reaction mixture was cooled to room temperature and concentrated under vacuum. The residue was purified via column chromatography on silica gel (eluting with 10:1, dichloromethane/methanol) to afford 1-cyclopropyl-1H-pyrazol-5-amine (0.206 g, 36%) as light yellow oil. MS (ESI, pos. ion) m/z 124 [M+H]+.
後処理
- temperatureThe reaction mixture was cooled to room temperature
- concentrationconcentrated under vacuum
- customThe residue was purified via column chromatography on silica gel (eluting with 10:1, dichloromethane/methanol)
出典と根拠
- ORDレコード
- ord-0bad107ea3dd4eb699fe8683abcddadf
- 出典データセット
- uspto-grants-2016_07
- 特許番号
- US09388161B2
反応ノート
読み込み中…