HRID1889488

反应详情

EQUATION

反应方程式

HRID 1889488 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a mixture of 6-ethyl-3-[2-(4-methoxyphenyl)-2-oxoethyl]-1-{[2′-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]methyl}thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione (0.2 g) and methanol (15 mL) was added sodium borohydride (0.025 g), and the mixture was stirred at room temperature for 2 hr. The reaction mixture was concentrated, and the residue was extracted with chloroform and saturated aqueous ammonium chloride solution. The chloroform layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The precipitated solid was collected by filtration to give the title compound as colorless crystals (0.12 g, 61%).

WORKUP

后处理

  1. concentrationThe reaction mixture was concentrated
  2. extractionthe residue was extracted with chloroform and saturated aqueous ammonium chloride solution
  3. washThe chloroform layer was washed with saturated brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customThe solvent was evaporated under reduced pressure
  6. filtrationThe precipitated solid was collected by filtration