HRID1111134

反应详情

EQUATION

反应方程式

HRID 1111134 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture comprising 500 mg of 4-chloro-5-(3-n-propoxy-4-methoxybenzylamino)-6-nitro-3(2H)pyridazinone (Compound No. 22) prepared in Example 2, 820 mg of allyl bromide, 937 mg of anhydrous potassium carbonate and 25 ml of methyl ethyl ketone, was refluxed under stirring for 1.5 hours. The solvent was distilled off under reduced pressure, water was added to the residue thereby obtained, the mixture was extracted with diethyl ether. The extract was washed with a saturated sodium chloride aqueous solution and dried over sodium sulfate. Then, the solvent was distilled off, and the residue was purified by silica gel column chromatography by using a solvent mixture of benzene: ethyl acetate (85:15 v/v) as the eluent, to obtain 394 mg of the above identified compound having a melting point of from 62.5° to 64° C. as yellow crystals.

WORKUP

后处理

  1. temperaturewas refluxed
  2. distillationThe solvent was distilled off under reduced pressure, water
  3. additionwas added to the residue
  4. customthereby obtained
  5. extractionthe mixture was extracted with diethyl ether
  6. washThe extract was washed with a saturated sodium chloride aqueous solution
  7. dry with materialdried over sodium sulfate
  8. distillationThen, the solvent was distilled off
  9. customthe residue was purified by silica gel column chromatography
  10. additiona solvent mixture of benzene: ethyl acetate (85:15 v/v) as the eluent
  11. customto obtain 394 mg of the
  12. customof from 62.5° to 64° C.