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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465941Generated: October 30, 2026

Imidazo(1,2-b)pyridazine, 6-chloro- → 6-[(3-Sulfamoyl-2,2-dimethylpropyl)thio]imidazo[1,2-b]pyridazine

https://huagongshe.com/reaction/465941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazo(1,2-b)pyridazine, 6-chloro-HCID 138828—
Reactant3-Mercapto-2,2-dimethyl-1-propylsulfonamideHCID 10464982—
ReactantSodium methanolate methanolHCID 23694274—
SolventMethanolHCID 887—
Product6-[(3-Sulfamoyl-2,2-dimethylpropyl)thio]imidazo[1,2-b]pyridazineHCID 997203066%

Reaction Steps

To a solution of 0.37 g of 3-mercapto-2,2-dimethyl-1-propylsulfonamide and 0.37 g of 28% sodium methoxide-methanol solution in 50 ml of methanol was added 0.31 g of 6-chloroimidazo[1,2-b]pyridazine, followed by refluxing at 80°-85° C. for 3 hours. The reaction solution was concentrated under reduced pressure. The residue to which 30 ml of water were added was extracted with tetrahydrofuran and ethyl acetate (1:1). The extract was dried over anhydrous magnesium sulfate and distilled under reduced pressure to remove the solvent. The residue was recrystallized from ethanol to obtain 0.4 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05155108
Source datasetuspto-grants-1992_10
ORD IDord-adc395e2f36341b8a96f5d1ee8e1d9d7
Source noteuspto-grants-1992_10