HRID1160750

反应详情

EQUATION

反应方程式

HRID 1160750 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. 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 and cooled, and water (50 ml) was added thereto and the organic phase was separated. The organic phase was washed with a saturated saline solution, dried over magnesium sulfate and concentrated, and 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%; 3 steps).

WORKUP

后处理

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