反应 #657327

反应方程式

water

4-(2-phenyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-3-yl)pyridin-2-amine

triethylamine

Triethylamine

acetyl chloride

acetyl chloride

→

N-[4-(2-phenyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-3-yl)pyridin-2-yl]acetamide

收率 12.0%

溶剂

tetrahydrofurane

反应条件

后处理

1. 1
   workup.STIRRINGThe mixture is stirred overnight at room temperature
2. 2
   萃取extracted with dichloromethane (3×50 mL)
3. 3
   洗涤The combined organic layers are washed with a saturated solution of NaHCO3, brine
4. 4
   干燥dried over anhydrous magnesium sulphate
5. 5
   过滤filtered
6. 6
   浓缩concentrated under reduced pressure
7. 7
   其他The crude material is purified by column chromatography

实验过程

To a solution of 4-(2-phenyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-3-yl)pyridin-2-amine (29 mg, 0.1 mmol, 1 eq) in 2 mL of tetrahydrofurane is added triethylamine (0.055 mL, 0.4 mmol, 4 eq) and then acetyl chloride (0.024 mL, 0.3 mmol, 3 eq). The mixture is stirred for 4 h at room temperature. Triethylamine (0.055 mL, 0.4 mmol, 4 eq) and acetyl chloride (0.024 mL, 0.3 mmol, 3 eq) are then added. 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 4 mg (8%) of N-[4-(2-phenyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-3-yl)pyridin-2-yl]acetamide are obtained as a light brown oil.

来源