反応式
[Br:1][C:2]1[C:7]([F:8])=[CH:6][C:5]([C:9](=O)[CH3:10])=[C:4]([F:12])[CH:3]=1.O.[NH2:14][NH2:15]>C(O)C>[Br:1][C:2]1[C:7]([F:8])=[CH:6][C:5](/[C:9](=[N:14]/[NH2:15])/[CH3:10])=[C:4]([F:12])[CH:3]=1参加物
4
実験手順
1-(4-bromo-2,5-difluorophenyl)ethanone (500 mg, 1.042 mmol) was dissolved in ethanol (10 mL), then hydrazine hydrate (57.4 mg, 1.147 mmol) added and stirred at RT for 16 hr. A pale yellow solid was filtered off and the filtrate was concentrated under reduced pressure to obtain the crude title compound as a brown-yellow solid (249 mg, 54% yield); 1H NMR (500 MHz, CHLOROFORM-d)delta 2.13 (3H, d, J=2.99 Hz), 7.28 (1H, dd, J=9.85, 5.60 Hz), 7.34 (1H, dd, J=9.14, 6.62 Hz).
後処理
- filtrationA pale yellow solid was filtered off
- concentrationthe filtrate was concentrated under reduced pressure
出典と根拠
- ORDレコード
- ord-9d96089b1c08479e817291ccf8f5c8d0
- 出典データセット
- uspto-grants-2014_12
- 特許番号
- US08901313B2
関連ノート
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