反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
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
- stirringall at once, and the mixture was stirred for 4 hours
- temperatureunder reflux
- temperaturewith heating
- temperatureThe reaction solution was cooled to about 70° C.
- stirringall at once and stirred until the solid
- dissolutionwas dissolved
- stirringall at once, and the mixture was stirred for 2 hours
- temperatureunder reflux
- temperaturewith heating
- waitthe reaction solution was left
- temperatureto cool
- customthe organic phase was separated
- washThe organic phase was washed with a saturated saline
- dry with materialdried over magnesium sulfate
- concentrationconcentrated
- additionAcetonitrile (10 ml) and 28% ammonia water (4 ml) were added to the residue
- stirringstirred at room temperature for 2 hours
- additionwater (100 ml) was added to the reaction solution, which
- filtrationthe formed crystals were collected by filtration
- washwashed with water and chloroform
- customdried under reduced pressure