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
- -25 °C
PROCEDURE
实验过程
Under an argon atmosphere, 41 mg of 2-methanesulfonyl-4-(5-methoxy-4-methylthiazol-2-yl)aniline was dissolved into a mixed solution of 3 mL of THF and 3 mL of dimethylacetamide. The solution was cooled to −25° C. and 15 mg of sodium hydride (oily, 60%) was added thereto, followed by 10 minutes of stirring at the same temperature. Further, 44 mg of 2-chlorosulfonyl-5-fluoro-3-methylbenzo[b]thiophene was added and the whole was stirred for 2 hours at the same temperature, followed by termination of the reaction with 1 mol/L hydrochloric acid. After the reaction mixture was warmed to room temperature, the mixture was extracted with ethyl acetate-toluene (2/1) and the organic layer was washed with water and saturated brine, successively. After the organic layer was dried over anhydrous sodium sulfate, the solvent was removed by evaporation under reduced pressure and the resulting residue was purified by silica gel column chromatography (ethyl acetate/hexane=1/1) to obtain 51 mg of the title compound as light yellow powder.
WORKUP
后处理
- stirringthe whole was stirred for 2 hours at the same temperature
- temperatureAfter the reaction mixture was warmed to room temperature
- extractionthe mixture was extracted with ethyl acetate-toluene (2/1)
- washthe organic layer was washed with water and saturated brine
- dry with materialAfter the organic layer was dried over anhydrous sodium sulfate
- customthe solvent was removed by evaporation under reduced pressure
- customthe resulting residue was purified by silica gel column chromatography (ethyl acetate/hexane=1/1)