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
3-Hexadecanoyloxyoctadecanoic acid (150 mg) prepared by the method described in Preparation 2-(3) and N-hydroxysuccinimide (38 mg) were dissolved in dioxane (3 ml). N,N-Dicyclohexylcarbodiimide (68 mg) was added thereto under ice cooling. The mixture was reached to room temperature and stirred at ambient temperature overnight. The crystallized urea was filtered off and the filtrate was concentrated to give a residue which was dissolved in N,N-dimethylformamide (7 ml). To this solution was added a solution of N-β-alanyl-L-threonine (110 mg) and triethylamine (100 μl) in water (5 ml) at 0° C. The resulting mixture was reached to room temperature and stirred at ambient temperature overnight. The reaction mixture was acidified with 1 N hydrochloric acid, extracted with ethyl acetate, washed with water and dried over magnesium sulfate. Ethyl acetate was distilled off to give a residue which was subjected to preparative thin layer chromatography (Merck, 0.25 mm×5) and eluted with a mixture of benzene, dioxane and acetic acid (10:5:1). The band containing the object compound was extracted with a mixture of methanol and chloroform (3:7) and the solvent was evaporated off under reduced pressure to afford powder of N-[N-(3-hexadecanoyloxyoctadecanoyl)-β-alanyl]-L-threonine (95 mg).
WORKUP
后处理
- customdescribed in Preparation 2-(3)
- customwas reached to room temperature
- filtrationThe crystallized urea was filtered off
- concentrationthe filtrate was concentrated
- customto give a residue which
- customwas reached to room temperature
- stirringstirred at ambient temperature overnight
- extractionextracted with ethyl acetate
- washwashed with water
- dry with materialdried over magnesium sulfate
- distillationEthyl acetate was distilled off
- customto give a residue which
- washeluted with a mixture of benzene, dioxane and acetic acid (10:5:1)
- additionThe band containing the object compound
- extractionwas extracted with a mixture of methanol and chloroform (3:7)
- customthe solvent was evaporated off under reduced pressure