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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637631Generated: November 1, 2026

6-[3-(2-Chloromethyl-3-methylpyridin-4-ylsulfanyl)propylsulfanyl]-3-nitroimidazo[1,2-b]pyridazine → 6-{3-[3-Methyl-2-(pyridin-4-ylsulfanylmethyl)-pyridin-4-ylsulfanyl]propylsulfanyl}-3-nitro-imidazo[1,2-b]pyridazine hydrochloride

https://huagongshe.com/reaction/1637631

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-[3-(2-Chloromethyl-3-methylpyridin-4-ylsulfanyl)propylsulfanyl]-3-nitroimidazo[1,2-b]pyridazineHCID 18799383—
Reactantpyridine-4-thiolHCID 178418431—
SolventIsopropanolHCID 3776—
Product6-{3-[3-Methyl-2-(pyridin-4-ylsulfanylmethyl)-pyridin-4-ylsulfanyl]propylsulfanyl}-3-nitro-imidazo[1,2-b]pyridazine hydrochlorideHCID 7027229287.1%

Reaction Steps

0.53 g (1.3 mmol) of 6-[3-(2-chloromethyl-3-methylpyridin-4-ylsulfanyl)propylsulfanyl]-3-nitro-imidazo[1,2-b]pyridazine and 0.15 g (1.3 mmol) of 4-mercaptopyridine in 30 ml of isopropanol are reacted as described in Example 2. 0.59 g (87%) of the title compound of m.p. 174-178° C. is isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06043242
Source datasetuspto-grants-2000_03
ORD IDord-75c605af579649edb505f05da2c41d4b
Source noteuspto-grants-2000_03