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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051122Generated: October 26, 2026

Chloroacetic Acid → 2,6-Dichloroimidazo[1,2-A]pyridine

https://huagongshe.com/reaction/2051122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetic AcidHCID 300—
ReactantTriethylamineHCID 8471—
Reactant2-Amino-5-chloropyridineHCID 66174—
SolventAcetonitrileHCID 6342—
Product2,6-Dichloroimidazo[1,2-A]pyridineHCID 1176925711.2%

Reaction Steps

Chloroacetic acid (9.5 g) is dissolved in 70 ml of acetonitrile, to which 10.1 g of triethylamine is portionwise added and further 12.9 g of 2-amino-5-chloropyrdine is added. The mixture is refluxed for 3 hours. After cooling, the precipitated 2-imino-5-chloro-1,2-dihydropyridin-1-ylacetic acid as crystals is collected by filtration and dried. The crystals are added to 40 ml of phosphorus oxychoride and refluxed for 5 hours. After cooling, the reaction mixture is poured into ice water and neutralized with aqueous ammonia. The precipitate collected by filtration is purified by silica gel chromatography(eluent: ethyl acetate) to give 2.1 g of the title compound as crystals. mp. 155°-156° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05017212
Source datasetuspto-grants-1991_05
ORD IDord-6af8c646c62d43c9b79b756a3afd39ad
Source noteuspto-grants-1991_05