HRID2305224

反应详情

EQUATION

反应方程式

HRID 2305224 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

To a mixture of 3-{[2-(4,5-diphenyloxazol-2-yl)-2-cyclohexen-1-yl]methyl}benzoic acid (150 mg, 0.345 mmol), L-phenylalanine ethyl ester hydrochloride (103 mg, 0.448 mmol) and diisopropylethylamine (0.078 ml , 0.448 mmol) in DMF (5 ml) was added 1-hydroxybenzotrioxazole (70 mg, 0.518 mmol) and 1-ethyl-3-(3′-dimethylaminopropyl)carbodiimide hydrochloride (132 mg, 0.690 mmol). After stirring the mixture at room temperature for 4 hours, the reaction mixture was diluted with EtOAc (30 ml), washed with 1N hydrochloric acid, water, saturated sodium hydrogencarbonate solution, water, and brine. The resultant mixture was dried over magnesium sulfate, and evaporated in vacuo. The resultant residue was purified by silica gel column chromatography (hexane:EtOAc, 3:1 elution) to give ethyl (2S)-2-{3-{[2-(4,5-diphenyloxazol-2-yl)-2-cyclohexen-1-yl)methyl}benzoylamino}-3-phenylpropionate (197.1 mg, 94%).

WORKUP

后处理

  1. washwashed with 1N hydrochloric acid, water, saturated sodium hydrogencarbonate solution, water, and brine
  2. dry with materialThe resultant mixture was dried over magnesium sulfate
  3. customevaporated in vacuo
  4. customThe resultant residue was purified by silica gel column chromatography (hexane:EtOAc, 3:1 elution)