HRID278240
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 1.15 g of 1-(t-butoxycarbonyl)-4-(1-bromo-2-oxoethyl)piperidine (from Procedure 23, Step C) in 15 mL ethanol was added 388 mg of 2-aminopyridine. After refluxing for 18 h, the solvent was evaporated. The mixture was partitioned between ethyl acetate and saturated sodium bicarbonate solution. Aqueous layer was extracted with ethyl acetate (3×). The combined organic phase was washed with brine, dried over magnesium sulfate and concentrated. The residue was purified by flash chromatography with 50% ethyl acetate in hexanes, followed by 100% ethyl acetate to give 401 mg of the title compound as a solid.
WORKUP
后处理
- temperatureAfter refluxing for 18 h
- customthe solvent was evaporated
- customThe mixture was partitioned between ethyl acetate and saturated sodium bicarbonate solution
- extractionAqueous layer was extracted with ethyl acetate (3×)
- washThe combined organic phase was washed with brine
- dry with materialdried over magnesium sulfate
- concentrationconcentrated
- customThe residue was purified by flash chromatography with 50% ethyl acetate in hexanes