反应 #657329
ord-cbe0b4a2536f4ac0900ca83b08c5a10a
反应方程式
N-acetyl-N-[4-(2-phenylpyrazolo[1,5-a]pyrimidin-3-yl)pyridin-2-yl]acetamide
ethanol
sodium borohydride
water
→
N-acetyl-N-[4-(4-acetyl-2-phenyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-3-yl)pyridin-2-yl]acetamide
收率 46.0%
反应物
试剂
无
反应条件
详细条件
See reaction.notes.procedure_details.
后处理
- 1温度The mixture is refluxed for 1 h
- 2萃取extracted with dichloromethane (3×50 mL)
- 3干燥dried over anhydrous magnesium sulphate
- 4过滤filtered
- 5浓缩concentrated under reduced pressure
- 6其他The crude material is purified by column chromatography
实验过程
To a mixture of N-acetyl-N-[4-(2-phenylpyrazolo[1,5-a]pyrimidin-3-yl)pyridin-2-yl]acetamide (158 mg, 0.43 mmol, 1 eq) in 3 mL of ethanol is added sodium borohydride (35 mg, 0.94 mmol, 2.2 eq). The mixture is refluxed for 1 h. The mixture is then poured into water, extracted with dichloromethane (3×50 mL), dried over anhydrous magnesium sulphate, filtered and concentrated under reduced pressure. The crude material is purified by column chromatography using silica gel in heptane and ethyl acetate (1:0 to 0:1) as eluent and 66 mg (46%) of N-acetyl-N-[4-(4-acetyl-2-phenyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-3-yl)pyridin-2-yl]acetamide are obtained as a white solid.