HRID1363465

反应详情

EQUATION

反应方程式

HRID 1363465 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

The mixture of 98 mg of (2S)-2-[(t-butoxycarbonyl)amino]-3-[4-(dihydroxyboranyl)phenyl]propionic acid, 46 mg of 3-hydroxyisoquinoline, 43 mg of copper acetate (II), 175 μl of triethylamine and 10 ml of dichloromethane was stirred for two days and diluted with ethanol. After Celite filtration, the filtering solvent was concentrated and the obtained residue was diluted with ethyl acetate. After extraction by an aqueous solution of 1N sodium hydroxide, the water phase was acidified by hydrochloric acid. The organic phase was extracted with ethyl acetate. The residue was washed with a saturated aqueous solution of sodium chloride and dried over magnesium sulfate to remove the solvent. The obtained residue was split by HPLC to obtain the objective compound.

WORKUP

后处理

  1. filtrationAfter Celite filtration
  2. concentrationthe filtering solvent was concentrated
  3. additionthe obtained residue was diluted with ethyl acetate
  4. extractionAfter extraction by an aqueous solution of 1N sodium hydroxide
  5. extractionThe organic phase was extracted with ethyl acetate
  6. washThe residue was washed with a saturated aqueous solution of sodium chloride
  7. dry with materialdried over magnesium sulfate
  8. customto remove the solvent
  9. customThe obtained residue was split by HPLC
  10. customto obtain the objective compound