Phenylhydrazine hydrochloride → 3-(1,3-difluoro-2-methylpropan-2-yl)-1-phenyl-1H-pyrazol-5-amine
反応式
[F:1][CH2:2][C:3]([CH2:10][F:11])([CH3:9])[C:4](=O)[CH2:5][C:6]#[N:7].Cl.[C:13]1([NH:19][NH2:20])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>CCO>[F:1][CH2:2][C:3]([C:4]1[CH:5]=[C:6]([NH2:7])[N:19]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[N:20]=1)([CH3:9])[CH2:10][F:11]参加物
4
反応条件
- 温度
- 95 °C
実験手順
According to the procedure described in Example 161B Step 2, 5-fluoro-4-(fluoromethyl)-4-methyl-3-oxopentanenitrile (0.81 g, 5 mmol) and phenylhydrazine hydrochloride (0.868 g, 14 mmol) in EtOH were heated at 95° C. for 2 hours, to afford 3-(1,3-difluoro-2-methylpropan-2-yl)-1-phenyl-1H-pyrazol-5-amine as solid (0.75 g, 52%). LC-MS (ESI) m/z 252 (M+H)+.
出典と根拠
- ORDレコード
- ord-418ce9c5b5fe415c91db4c4966e3e183
- 出典データセット
- uspto-grants-2016_04
- 特許番号
- US09320739B2
反応ノート
読み込み中…