N-bromobutanimide → 5-Bromo-6-chloromethyluracil
反応式
[Cl:1][CH2:2][C:3]1[NH:8][C:7](=[O:9])[NH:6][C:5](=[O:10])[CH:4]=1.C1C(=O)N([Br:18])C(=O)C1>CN(C=O)C>[Br:18][C:4]1[C:5](=[O:10])[NH:6][C:7](=[O:9])[NH:8][C:3]=1[CH2:2][Cl:1]参加物
4
反応条件
- 温度
- 0 °C
実験手順
To a solution of 6-(chloromethyl)uracil (2.0 g, 12.5 mmol) in DMF (15 mL) at 0° C. was added NBS (recrystallized, 2.44 g, 13.7 mmol). The mixture was stirred at 0° C. for 1.5 h, and then quenched by ice water. The precipitate was collected by filtration and washed with AcOH and water to give the title compound (2.35 g, 69%) as a white solid. 1H NMR (DMSO, 500 MHz) δ 1.66 (s, 1H), δ 11.61 (s, 1H), δ 4.47 (s, 2H). MS (Multimode, M+H+) C5H5BrClN2O2, calcd. 238.9. found 238.9.
後処理
- customquenched by ice water
- filtrationThe precipitate was collected by filtration
- washwashed with AcOH and water
出典と根拠
- ORDレコード
- ord-ded63685c8c1418584cdb4fc3ad37adc
- 出典データセット
- uspto-grants-2012_12
- 特許番号
- US08334292B1
反応ノート
読み込み中…