反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:9](=O)[CH2:10][C:11]#[N:12])[CH:6]=[CH:7][CH:8]=1.[NH2:14][NH2:15]>CCO>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:9]2[CH:10]=[C:11]([NH2:12])[NH:14][N:15]=2)[CH:6]=[CH:7][CH:8]=1参加物
4
実験手順
3-(3-Methoxy-phenyl)-3-oxo-propionitrile (2.0202 gms.) is then suspended in 55 mL of anhydrous EtOH. This suspension is treated with 0.73 mL of anhydrous hydrazine and subsequently heated to refluxing temperature for 1 day. The reaction mixture is concentrated in vacuo. The residue is then triturated with isopropanol to precipitate out the 5-(3-methoxy-phenyl)-2H-pyrazol-3-ylamine as a white solid.
後処理
- temperaturesubsequently heated
- temperatureto refluxing temperature for 1 day
- concentrationThe reaction mixture is concentrated in vacuo
- customThe residue is then triturated with isopropanol
- customto precipitate out the 5-(3-methoxy-phenyl)-2H-pyrazol-3-ylamine as a white solid
出典と根拠
- ORDレコード
- ord-7a04ae81653d45c083f1248453501ccf
- 出典データセット
- uspto-grants-2003_05
- 特許番号
- US06559173B1
関連ノート
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