HRID1857270

反应详情

EQUATION

反应方程式

HRID 1857270 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

6,7-Dimethoxy-4-(4-aminophenoxy)quinoline (50 mg) was dissolved in toluene (5 ml) with heat, after the addition of triethylamine (1 ml), triphosgene (55 mg) was added, and the admixture was refluxed with heat for 3 minutes. 2,4,6-Trifluoroaniline. (75 mg) was added to the reaction mixture, and the admixture was refluxed with heat for 20 minutes. After the addition of aqueous sodium hydrogen carbonate, the reaction mixture was extracted 2 times with ethyl acetate, and the organic layer was then washed with brine and dried with anhydrous sodium sulfate. The solvent was removed by reduced-pressure distillation, and the resulting residue was purified by column chromatography on silica gel eluting with chloroform/acetone (10/1) to obtain 37 mg of the title compound (yield: 47%).

WORKUP

后处理

  1. temperaturewith heat
  2. additionwas added
  3. temperaturethe admixture was refluxed
  4. temperaturewith heat for 3 minutes
  5. addition(75 mg) was added to the reaction mixture
  6. temperaturethe admixture was refluxed
  7. temperaturewith heat for 20 minutes
  8. extractionthe reaction mixture was extracted 2 times with ethyl acetate
  9. washthe organic layer was then washed with brine
  10. dry with materialdried with anhydrous sodium sulfate
  11. customThe solvent was removed by reduced-pressure distillation
  12. customthe resulting residue was purified by column chromatography on silica gel eluting with chloroform/acetone (10/1)