HRID1837249
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
CONDITIONS
反应条件
- 温度
- 80 °C
PROCEDURE
实验过程
880 mg of 11β-fluoro-3-hydroxy-7α-(5-iodopentyl)-estra-1,3,5(10)-trien-17-one and 2.21 g of methyl-(3,4,4,5,5,6,6,6-octafluoro-hex-2-enyl)-amine are dissolved in 20 ml of N-methylpyrrolidone and stirred for 1 hour at a bath temperature of 80° C. After the reaction solution is cooled to room temperature, the batch is added to saturated common salt solution, extracted with diethyl ether, dried and concentrated by evaporation in a vacuum. 1.69 g of 11β-fluoro-3-hydroxy-7α-{5-[methyl-(3,4,4,5,5,6,6,6-octafluoro-hex-2-enyl)-amino]-pentyl}-estra-1,3,5(10)-trien-17-one is obtained as a crude product, which is used without purification in the next stage.
WORKUP
后处理
- temperatureAfter the reaction solution is cooled to room temperature
- additionthe batch is added to saturated common salt solution
- extractionextracted with diethyl ether
- customdried
- concentrationconcentrated by evaporation in a vacuum