Imidazole → 2-Bromo-5-(1H-imidazol-1-YL)pyrazine
反応式
[H-].[Na+].[NH:3]1[CH:7]=[CH:6][N:5]=[CH:4]1.[Br:8][C:9]1[C:14](Br)=[N:13][CH:12]=[CH:11][N:10]=1>C1COCC1>[Br:8][C:9]1[CH:14]=[N:13][C:12]([N:3]2[CH:7]=[CH:6][N:5]=[CH:4]2)=[CH:11][N:10]=1参加物
5
反応条件
- 温度
- 0 °C
実験手順
To sodium hydride (0.20 g) in THF (15 ml), imidazole (0.57 g) was added and cooled to 0° C. To the above mixture 2,3-dibromopyrazine (2 g) was added and entire reaction mixture was allowed to reflux for overnight. The reaction mixture was quenched with water 5 ml volatiles were removed under vacuum. The resulting crude mass was purified by column chromatography to afford 2-bromo-5-(1H-imidazol-1-yl)pyrazine as pure product.
後処理
- temperatureto reflux for overnight
- customThe reaction mixture was quenched with water 5 ml volatiles
- customwere removed under vacuum
- customThe resulting crude mass was purified by column chromatography
出典と根拠
- ORDレコード
- ord-e621196262334376bbb218bf8a3f6e7e
- 出典データセット
- uspto-grants-2010_10
- 特許番号
- US07807676B2
反応ノート
読み込み中…