HRID42567
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
To a solution of 3-amino-2H-pyrazole (60 mg, 71.8 mmol) in EtOH (2 mL) and 1 drop of 37% HCl, 1-(4-fluorophenyl)-2-(4-pyridyl)vinyl 4-fluorobenzoate (0.22 g, 65.0 mmol, obtained in reference example 4) was added under argon atmosphere. This was heated to reflux for 3 days. The mixture was diluted with CHCl3 and MeOH. It was washed with saturated NaHCO3. The aqueous phase was extracted with CHCl3 (×2). The organic phase was dried over Na2SO4 and concentrated to dryness. The crude product obtained was purified by chromatography on silica gel using hexane-EtOAc mixtures of increasing polarity as eluent, to afford 58 mg of the desired product in a solid white form (yield: 23%).
WORKUP
后处理
- temperatureThis was heated
- temperatureto reflux for 3 days
- washIt was washed with saturated NaHCO3
- extractionThe aqueous phase was extracted with CHCl3 (×2)
- dry with materialThe organic phase was dried over Na2SO4
- concentrationconcentrated to dryness
- customThe crude product obtained
- customwas purified by chromatography on silica gel
- temperatureof increasing polarity as eluent