HRID969718

反应详情

EQUATION

反应方程式

HRID 969718 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

2-Chloro-6-n-propylimidazo[1,2-b]pyridazine (0.8 g, 4.1 mmol) and dichloroethane (10 ml) were introduced into a 200-ml eggplant type flask and stirred at room temperature, and chlorosulfonic acid (0.54 g, 4.5 mmol) was added thereto all at once, and the mixture was stirred for 4 hours under reflux with heating. The reaction solution was cooled to about 70° C., and triethylamine (0.5 g, 5 mmol) was added thereto all at once and stirred until the solid was dissolved, and phosphorus oxychloride (0.79 g, 5 mmol) was added thereto all at once, and the mixture was stirred for 2 hours under reflux with heating. After the reaction was completed, the reaction solution was left to cool, and water (50 ml) was added thereto and the organic phase was separated. The organic phase was washed with a saturated saline, dried over magnesium sulfate and concentrated. Acetonitrile (10 ml) and 28% ammonia water (4 ml) were added to the residue and stirred at room temperature for 2 hours. After the reaction was completed, water (100 ml) was added to the reaction solution, which was then adjusted to about pH 2 with dilute hydrochloric acid, and the formed crystals were collected by filtration, washed with water and chloroform, and dried under reduced pressure to give the title compound as pale brown crystals. The yield was 0.49 g (43.5%).

WORKUP

后处理

  1. stirringall at once, and the mixture was stirred for 4 hours
  2. temperatureunder reflux
  3. temperaturewith heating
  4. temperatureThe reaction solution was cooled to about 70° C.
  5. stirringall at once and stirred until the solid
  6. dissolutionwas dissolved
  7. stirringall at once, and the mixture was stirred for 2 hours
  8. temperatureunder reflux
  9. temperaturewith heating
  10. waitthe reaction solution was left
  11. temperatureto cool
  12. customthe organic phase was separated
  13. washThe organic phase was washed with a saturated saline
  14. dry with materialdried over magnesium sulfate
  15. concentrationconcentrated
  16. additionAcetonitrile (10 ml) and 28% ammonia water (4 ml) were added to the residue
  17. stirringstirred at room temperature for 2 hours
  18. additionwater (100 ml) was added to the reaction solution, which
  19. filtrationthe formed crystals were collected by filtration
  20. washwashed with water and chloroform
  21. customdried under reduced pressure