Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637630Generated: November 2, 2026

6-[3-(2-Chloromethyl-3-methylpyridin-4-ylsulfanyl)propylsulfanyl]-3-nitroimidazo[1,2-b]pyridazine → 6-{3-[2-(1H-benzimidazol-2-ylsulfanylmethyl)-3-methylpyridin-4-ylsulfanyl]propylsulfanyl}-3-nitroimidazo[1,2-b]pyridazine hydrochloride

https://huagongshe.com/reaction/1637630

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-[3-(2-Chloromethyl-3-methylpyridin-4-ylsulfanyl)propylsulfanyl]-3-nitroimidazo[1,2-b]pyridazineHCID 18799383—
ReactantHCID 178527775HCID 178527775—
SolventIsopropanolHCID 3776—
Product6-{3-[2-(1H-benzimidazol-2-ylsulfanylmethyl)-3-methylpyridin-4-ylsulfanyl]propylsulfanyl}-3-nitroimidazo[1,2-b]pyridazine hydrochlorideHCID 1879942086.4%

Reaction Steps

A suspension of 6-[3-(2-chloromethyl-3-methylpyridin-4-ylsulfanyl)propylsulfanyl]-3-nitroimidazo[1,2-b]pyrid-azine (0.39 g, 0.95 mmol) and 2-mercapto-1H-benzimidazole (160 mg, 1.05 mmol) in isopropanol (50 ml) is heated under reflux for 7 h. After cooling to room temperature, the precipitate is filtered off, washed with isopropanol and dried at 40° C. in vacuo. The title compound (0.46 g, 86%) is isolated as a beige solid. M.p. 200-207° C (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06043242
Source datasetuspto-grants-2000_03
ORD IDord-2ea89ee7ae65441f99af13d320435e22
Source noteuspto-grants-2000_03