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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231532Generated: October 26, 2026

p-Chlorophenacyl bromide → 8-Bromo-6-chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/231532

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Chlorophenacyl bromideHCID 68303—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Bromo-5-chloropyridin-2-amineHCID 2763971—
SolventEthanolHCID 702—
Product8-Bromo-6-chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridineHCID 14234917—

Reaction Steps

17 g (82 mmol) of 2-amino-3-bromo-5-chloropyridine dissolved in 150 ml of ethanol are reacted with 29 g of 2-bromo-1-(4-chlorophenyl)-1-ethanone and 14 g of sodium hydrogen carbonate. The mixture is brought to the refluxing temperature for 6 h and cooled. The precipitate is filtered off and rinsed with CH2Cl2, and the filtrate is concentrated under reduced pressure. After recrystallization of the evaporation residue in ethyl acetate, the compound melts at 178° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04847263
Source datasetuspto-grants-1989_07
ORD IDord-8a2f27f02afd4b7b85817dfa22b20cfb
Source noteuspto-grants-1989_07