1,1-Dichloroethane → 2-Chloro-6-propylimidazo[1,2-b]pyridazine-3-sulfonamide

Beteiligte Stoffe

Reaktionsschritte

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).

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