HRID1082085

反应详情

EQUATION

反应方程式

HRID 1082085 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

0.6 g of 4-chloro-2-(4-methoxyphenyl)-6-methylpyrimidine and 0.76 g of 1-diphenylmethyl-4-(2-hydroxyethyl)piperazine were dissolved in 20 ml of dried tetrahydrofuran. After addition of 0.1 g of 60% sodium hydride, the mixture was stirred for 20 hours at room temperature. The reaction mixture was poured into ice-water and was extracted with ethyl acetate. After the extract was washed with water and was dried with anhydrous magnesium sulfate, then was evaporated in vacuo. The resulting residue was purified with column chromatography with silica gel (Wako gel C-200, elution with chloroform and then chloroform:ethyl acetate=8:1). The desired fraction was crystallized by evaporating the solvent under reduced pressure. The crystals were recrystallized with the solvent mixed with chloroform and ether, resulting to obtain 0.6 g of crystals. Melting point is 132° to 133° C.

WORKUP

后处理

  1. extractionwas extracted with ethyl acetate
  2. washAfter the extract was washed with water
  3. dry with materialwas dried with anhydrous magnesium sulfate
  4. customwas evaporated in vacuo
  5. customThe resulting residue was purified with column chromatography with silica gel (
  6. washWako gel C-200, elution with chloroform
  7. customThe desired fraction was crystallized
  8. customby evaporating the solvent under reduced pressure
  9. customThe crystals were recrystallized with the solvent
  10. additionmixed with chloroform and ether
  11. customresulting