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
A solution of 11.97 g (0.0519 mol) of o-nitrobenzenesulfonyl chloride in 90 ml of cyanomethane was added slowly over several minutes to a cold (7° C.) solution of 10.7 g (0.0540 mol) of N-(3-aminopropyl)-pyrazole in a 3:1 cyanomethane/water solution containing 16.6 g (0.12 mol) of potassium carbonate, under nitrogen. The resulting reaction solution was warmed to room temperature and allowed to react. When the reaction was complete, as determined by thin layer chromatography, the reaction solution was poured into approximately 450 ml of ethyl acetate. The resulting aqueous and organic layers were separated and the organic layer was washed with both an aqueous potassium carbonate solution and an aqueous sodium chloride solution and then reduced to dryness under reduced pressure to provide an oil. This oil was purified using column chromatography (8000 ml of a gradient eluent of from 0 to 5% methanol in methylene chloride). The fractions containing the desired product were combined, reduced to dryness under reduced pressure and then recrystallized from a 1:2 ethyl acetate/diethyl ether solution to provide 13.97 g of the desired subtitled intermediate (m.p. 105°109° C.).
WORKUP
后处理
- customThe resulting reaction solution
- customto react
- customThe resulting aqueous and organic layers were separated
- washthe organic layer was washed with both an aqueous potassium carbonate solution
- customto provide an oil
- customThis oil was purified
- additionThe fractions containing the desired product
- customrecrystallized from a 1:2 ethyl acetate/diethyl ether solution