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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357018Generated: October 25, 2026

Bromoacetone → 5-Chloro-2-methylimidazo[1,2-a]pyridine hydrobromide

https://huagongshe.com/reaction/357018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetoneHCID 11715—
Reactant2-Amino-6-chloropyridineHCID 206246—
SolventEthanolHCID 702—
Product5-Chloro-2-methylimidazo[1,2-a]pyridine hydrobromideHCID 18936714—

Reaction Steps

To a solution of 19.28 g (150 mmol) of 2-amino-6-chloropyridine in 150 ml of ethanol, 25 g (180 mmol) of bromoacetone was added at room temperature, followed by refluxing for 64 hours. After the reaction mixture was cooled, the solvent was distilled off. The residue was purified by recrystallization (solvent: ethanol-ethyl acetate) to yield 20.22 g (54.5%, light brown crystal) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840732
Source datasetuspto-grants-1998_11
ORD IDord-4df35b6cb8814ed7a93fd8fdc541f9cf
Source noteuspto-grants-1998_11