HRID2260527

反应详情

EQUATION

反应方程式

HRID 2260527 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
60 °C

PROCEDURE

实验过程

A mixture of 2,3-dihydro-6-(4-fluorophenyl)-2-oxo-7-(pyridin-4-yl)-1H-imidazo[1,2-b]pyrazole (50 mg) and diborane (0.34 mmol) in anhydrous tetrahydrofuran (5 ml) was refluxed under nitrogen atmosphere for 5 hours. After cooling of the reaction mixture, to the mixture was added 1N-hydrochloric acid (2 ml). The mixture was stirred at 60° C. for 30 minutes, cooled and neutralized with an aqueous saturated sodium bicarbonate solution. The separated oil was extracted with dichloromethane and the extract was washed with brine, dried and concentrated in vacuo. The residue was purified by thin layer chromatography on silica gel and the obtained crude solid was recrystallized from a mixture of diisopropyl ether and dichloromethane to yield 2,3-dihydro-6-(4-fluorophenyl)-7-(pyridin-4-yl)-1H-imidazo[1,2-b]pyrazole (14 mg).

WORKUP

后处理

  1. temperaturewas refluxed under nitrogen atmosphere for 5 hours
  2. temperatureAfter cooling of the reaction mixture, to the mixture
  3. temperaturecooled
  4. extractionThe separated oil was extracted with dichloromethane
  5. washthe extract was washed with brine
  6. customdried
  7. concentrationconcentrated in vacuo
  8. customThe residue was purified by thin layer chromatography on silica gel
  9. customthe obtained crude solid
  10. customwas recrystallized from a mixture of diisopropyl ether and dichloromethane