Hydrogen Peroxide → 5-Bromopyrazine-2-carboxamide
反応式
[Br:1][C:2]1[N:3]=[CH:4][C:5]([C:8]#[N:9])=[N:6][CH:7]=1.C(=O)([O-])[O-:11].[K+].[K+].OO.O>CS(C)=O.CC(C)=O>[Br:1][C:2]1[N:3]=[CH:4][C:5]([C:8]([NH2:9])=[O:11])=[N:6][CH:7]=1参加物
6
反応条件
- 温度
- 65 °C
実験手順
A suspension of 5-bromo-pyrazine-2-carbonitrile (1.84 g, 10.0 mmol) and potassium carbonate (1.38 g, 10.0 mmol) in DMSO/acetone (16 mL, 1:3) was treated with H2O2 (2.42 mL, 25.0 mmol) at 65° C. over 15 min. The reaction was kept stirring at 65° C. 1 h. Water (2 mL) was added at 40° C. and the suspension was cooled to 0° C. The precipitate was filtered to give the title compound as a yellow solid (556 mg). 1H NMR (300 MHz, DMSO-d6) δ 9.06 (s, 1H), 8.94 (s, 1H), 8.34 (s, 1H), 7.92 (s, 1H).
後処理
- custom1 h
- temperaturethe suspension was cooled to 0° C
- filtrationThe precipitate was filtered
出典と根拠
- ORDレコード
- ord-635e9ca714c541c7abf8d297d4fcdbcb
- 出典データセット
- uspto-grants-2013_01
- 特許番号
- US08343944B2
反応ノート
読み込み中…