HRID1088619
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 2(S)-(N-morpholinocarbonyl-L-phenylalanyl-Nα -methyl-L-histidyl)amino-1-cyclohexyl-3(S)-hydroxy-6-methylheptane (1.00 g) in ethanol (10 ml) which was cooled to 0° C., was added 4N hydrogenchloride in dioxane (0.47 ml). After the mixture was stirred at the same temperature for 10 minutes, the solvent was evaporated under reduced pressure. This residue was crystallized from ethanol (1 ml) and ethyl acetate (30 ml) to give 2(S)-(N-morpholinocarbonyl-L-phenylalanyl-Nα -methyl-L-histidyl)amino-1-cyclohexyl-3(S)-hydroxy-6-methylheptane monohydrochloride (860 mg).
WORKUP
后处理
- customthe solvent was evaporated under reduced pressure
- customThis residue was crystallized from ethanol (1 ml) and ethyl acetate (30 ml)