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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274282Generated: October 26, 2026

Hydrochloric Acid → 1-Prpopanesulfonamide, 3-((1,2,4)triazolo(1,5-b)pyridazin-6-yloxy)-

https://huagongshe.com/reaction/274282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium ChlorideHCID 5234—
ReactantSodium hydrideHCID 24758—
Reactant3-Hydroxypropane-1-sulfonamideHCID 10486918—
Reactant6-Chloro-(1,2,4)triazolo(1,5-b)pyridazineHCID 11240611—
SolventDimethylformamideHCID 6228—
Product1-Prpopanesulfonamide, 3-((1,2,4)triazolo(1,5-b)pyridazin-6-yloxy)-HCID 307380152.5%

Reaction Steps

In 12 ml of dimethylformamide was suspended 0.48 g of 60% sodium hydride in oil followed by addition of 0.835 g of 3-hydroxy-1-propanesulfonamide and the mixture was stirred under reduced pressure at room temperature for 30 minutes. Then, 0.928 g of 6-chloro[1,2,4]triazolo[1,5-b]pyridazine was added and the mixture was further stirred at room temperature for 18 hours. Following addition of 40 ml of ice water, the reaction mixture was adjusted to pH6 with 1N-hydrochloric acid then saturated with sodium chloride. The aqueous layer was extracted with tetrahydrofuran and the extract was dried over magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was crystallized from ethyl ether. The washed crystals were recrystallized from hot methanol to provide 0.811 g of title compound. m.p. 145°-147° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389633
Source datasetuspto-grants-1995_02
ORD IDord-ef5441d25a9b42f7b19df8c1f2556881
Source noteuspto-grants-1995_02