HRID386639

反应详情

EQUATION

反应方程式

HRID 386639 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

A mixture of 4-(4-bromo-2,6-dimethylphenylthio)-2-chloro-6-methyl-5-nitropyrimidine (59 mmol), 4-aminobenzonitrile (65 mmol) and pyridine (59 mmol) in THF (300 ml) is heated to 80° C. for 10 hours. The reaction mixture is dissolved in methanol, washed with brine and extracted with ethyl acetate. The organic layer is washed twice with brine, dried over MgSO4 and concentrated to dryness. The solid is washed with a mixture of hexane:ethyl acetate (80:20) before filtration. After filtration, the solid is washed again with methanol. The filtrate may be concentrated and additional rounds of precipitation performed following the same procedure, until all product is recovered. The combined solids are recrystallized from acetone.

WORKUP

后处理

  1. washwashed with brine
  2. extractionextracted with ethyl acetate
  3. washThe organic layer is washed twice with brine
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated to dryness
  6. washThe solid is washed with a mixture of hexane:ethyl acetate (80:20) before filtration
  7. filtrationAfter filtration
  8. washthe solid is washed again with methanol
  9. concentrationThe filtrate may be concentrated
  10. customadditional rounds of precipitation
  11. customuntil all product is recovered
  12. customThe combined solids are recrystallized from acetone