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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2391559Generated: October 31, 2026

Potassium Carbonate → Methyl 2-(imidazo[1,2-b]pyridazin-6-ylthio)benzoate

https://huagongshe.com/reaction/2391559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBenzoic acid, 2-mercapto-, methyl esterHCID 21009—
ReactantImidazo(1,2-b)pyridazine, 6-chloro-HCID 138828—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-(imidazo[1,2-b]pyridazin-6-ylthio)benzoateHCID 5744106323%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 6-chloroimidazo[1,2-b]pyridazine (1536 mg, 10.0 mmol), methyl 2-mercaptobenzoate (1.788 mL, 13.0 mmol), potassium carbonate (4146 mg, 30.0 mmol) and N,N-dimethylformamide (20 mL) was stirred at 70° C. for 18 hr. To the reaction mixture was added methyl 2-mercaptobenzoate (0.963 mL, 7.0 mmol), and the mixture was stirred at 70° C. for 6 hr. The reaction mixture was concentrated under reduced pressure, the residue was diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and concentrated under reduced pressure. The residue was purified by NH silica gel column chromatography (hexane/ethyl acetate=90/10→20/80) and precipitated from diisopropyl ether to give the title compound (663 mg, 2.3 mmol, yield 23%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273741B2
Source datasetuspto-grants-2012_09
ORD IDord-0d388356a03c44c09ffda2fe2d54337a
Source noteuspto-grants-2012_09