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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1590053Generated: November 4, 2026

Imidazo(1,2-b)pyridazine, 6-chloro- → HCID 178527712, compound

https://huagongshe.com/reaction/1590053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazo(1,2-b)pyridazine, 6-chloro-HCID 138828—
ReactantSodium methanolate methanolHCID 23694274—
ReactantHCID 178418634HCID 178418634—
SolventMethanolHCID 887—
ProductHCID 178527712HCID 17852771227.8%

Reaction Conditions

Temperature150 °C

Reaction Steps

6-Chloroimidazo[1,2-b]pyridazine (13.5 g), 28 W/W % sodium methoxide-methanol solution (17.5 g) and thioacetic acid (7.0 g) were dissolved in 70 ml of methanol and this solution was heated at 150° C. in a sealed tube for 6 hours. The reaction mixture was cooled to room temperature and distilled to remove the organic solvent. The residue was washed three times with chloroform, and the insoluble material was extracted six times with 50 ml of chloroform-methanol (1:1) solution. The combined extracts were distilled to remove the organic solvent. The precipitated crystals were collected by filtration, thereby obtaining 3.7 g of 6-mercaptoimidazo[1,2-b]pyridazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05202324
Source datasetuspto-grants-1993_04
ORD IDord-a4ad1f80c5a548d6a64318c367fc63ef
Source noteuspto-grants-1993_04