反应 #657328

反应方程式

water

acetyl chloride

4-(2-phenylpyrazolo[1,5-a]pyrimidin-3-yl)pyridin-2-amine

triethylamine

→

N-acetyl-N-[4-(2-phenylpyrazolo[1,5-a]pyrimidin-3-yl)pyridin-2-yl]acetamide

收率 37.0%

溶剂

tetrahydrofurane

反应条件

后处理

1. 1
   萃取extracted with dichloromethane (3×50 mL)
2. 2
   洗涤The combined organic layers are washed with a saturated solution of NaHCO3, brine
3. 3
   干燥dried over anhydrous magnesium sulphate
4. 4
   过滤filtered
5. 5
   浓缩concentrated under reduced pressure
6. 6
   其他The crude material is purified by column chromatography

实验过程

To a solution of 4-(2-phenylpyrazolo[1,5-a]pyrimidin-3-yl)pyridin-2-amine (420 mg, 1.46 mmol, 1 eq) in 20 mL of tetrahydrofurane is added triethylamine (0.82 mL, 5.85 mmol, 4 eq) and then acetyl chloride (234 mg, 2.92 mmol, 2 eq). The mixture is stirred overnight at room temperature and then poured into water and extracted with dichloromethane (3×50 mL). The combined organic layers are washed with a saturated solution of NaHCO3, brine, 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 0.23 g (37%) of N-acetyl-N-[4-(2-phenylpyrazolo[1,5-a]pyrimidin-3-yl)pyridin-2-yl]acetamide are obtained as a yellow solid.

来源