HRID14511

反应详情

EQUATION

反应方程式

HRID 14511 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture of 7-amino-3-(4-chlorophenyl)-8-hydroxy-2-isopropyl-chromen-4-one (250 mg, 0.75 mmol), CDCl3 (1 ml), saturated NaHCO3 solution (1.5 ml) and bromoacetylbromide (169 mg, 0.85 mmol) is stirred vigorously at room temperature for 5 min and then passed through an Isolute™ phase separator to separate the organic phase, which is then treated with dimethylformamide (1 ml) and K2CO3 (115 mg, 0.85 mmol) and heated in a microwave at 90° C. for 15 min. The reaction mixture is partitioned between CH2Cl2 and water. The organic phase is washed with water and brine, dried (MgSO4) and concentrated in vacuo, followed by crystallisation from methanol. The product is partitioned between ethyl acetate and water to remove traces of dimethylformamide. The organic phase is dried (MgSO4), concentrated in vacuo and crystallised from methanol to yield the title compound.

WORKUP

后处理

  1. customto separate the organic phase, which
  2. temperatureheated in a microwave at 90° C. for 15 min
  3. customThe reaction mixture is partitioned between CH2Cl2 and water
  4. washThe organic phase is washed with water and brine
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated in vacuo
  7. customfollowed by crystallisation from methanol
  8. customThe product is partitioned between ethyl acetate and water
  9. customto remove traces of dimethylformamide
  10. dry with materialThe organic phase is dried (MgSO4)
  11. concentrationconcentrated in vacuo
  12. customcrystallised from methanol