HRID1040540

反应详情

EQUATION

反应方程式

HRID 1040540 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

A solution of (S)-2-{[(R)-5-(4-bromo-benzyl)-7-(3,5-dichloro-phenyl)-5-methyl-6-oxo-6,7-dihydro-5H-imidazo[1,2-a]imidazole-3-carbonyl]-amino}-propionic acid tert-butyl ester (0.20 g, 0.32 mmol), 4-fluorophenyl boronic acid (0.059 g, 0.43 mmol) and K2CO3 (0.15 g, 1.1 mmol) in DME (5 mL) was degassed under N2 for 10 minutes. To this was added PdCl2(dppf) (5 mg) and the mixture heated at 80° C. for 12 h. The resulting black mixture was cooled to room temperature, diluted with saturated NH4Cl and extracted with EtOAc (3×50 mL). The combined organic extracts were washed with water, brine, dried with MgSO4 and concentrated. The residue was purified by silica gel chromatography to afford 150 mg of (S)-2-{[(R)-7-(3,5-dichloro-phenyl)-5-(4′-fluoro-biphenyl-4-ylmethyl)-5-methyl-6-oxo-6,7-dihydro-5H-imidazo[1,2-a]imidazole-3-carbonyl]-amino}-propionic acid tert-butyl ester as a white solid, m/z 637.5 [M+]+.

WORKUP

后处理

  1. temperatureThe resulting black mixture was cooled to room temperature
  2. extractionextracted with EtOAc (3×50 mL)
  3. washThe combined organic extracts were washed with water, brine
  4. dry with materialdried with MgSO4
  5. concentrationconcentrated
  6. customThe residue was purified by silica gel chromatography