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
4.72 g (24.6 mmol) of EDCl was added to 100 ml of THF solution of 5.00 g (16.4 mmol) of Boc-Trp-OH (manufactured by Tokyo Chemical Industry Co., Ltd), 1.50 ml (16.4 mmol) of aniline and 1.89 g (1.64 mmol) of HO-Su, followed by stirring for 16 hours at room temperature. After a reaction mixture was concentrated under reduced pressure, the concentrate was extracted by adding water and ethyl acetate. After an organic layer was washed sequentially with a diluted hydrochloric acid, an aqueous solution of sodium hydrogen carbonate and water (one time for each), the organic layer was dried over sodium sulfate. After the drying agent was separated by filtration, the filtrate was concentrated under reduced pressure, thereby obtaining crude amide. The obtained amide compound was purified by a silica gel column chromatography (hexane/ethyl acetate=5/1 to 1/1 (volume ratio)), thereby obtaining 3.10 g of the product with a yield of 49.8%.
WORKUP
后处理
- concentrationAfter a reaction mixture was concentrated under reduced pressure
- extractionthe concentrate was extracted
- additionby adding water and ethyl acetate
- washAfter an organic layer was washed sequentially with a diluted hydrochloric acid
- dry with materialan aqueous solution of sodium hydrogen carbonate and water (one time for each), the organic layer was dried over sodium sulfate
- customAfter the drying agent was separated by filtration
- concentrationthe filtrate was concentrated under reduced pressure
- customobtaining crude amide
- customThe obtained amide compound was purified by a silica gel column chromatography (hexane/ethyl acetate=5/1 to 1/1 (volume ratio))