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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251761Generated: November 2, 2026

p-Bromoacetophenone → 2-(4-Bromophenyl)imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/251761

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-BromoacetophenoneHCID 7466—
Reactant2-AminopyridineHCID 10439—
ReactantSodium HydroxideHCID 14798—
SolventEthanolHCID 702—
Product2-(4-Bromophenyl)imidazo[1,2-a]pyridineHCID 62341685%

Reaction Steps

Dissolving 15 g (54 mmol) of 4-bromoacetophenone and 5.2 g (55 mmol) of 2-aminopyridine into 100 milliliter of ethanol, adding 7.0 g of sodium hydroxide, the resultant suspension was refluxed under heating for 6 hours. After completion of the reaction, resultant crystals were separated with filtration, washed with water and ethanol, thereby obtaining 12.5 g of 2-(4-bromo-phenyl)-imidazo [1,2-a] pyridine (yield: 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07867629B2
Source datasetuspto-grants-2011_01
ORD IDord-51c6f98e38224fa1b37f06b79058030e
Source noteuspto-grants-2011_01