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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199472Generated: October 26, 2026

2-Aminopyridine → 2-(2-Bromophenyl)imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1199472

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
Reactant2-Bromophenacyl BromideHCID 2737522—
SolventEthanolHCID 702—
Product2-(2-Bromophenyl)imidazo[1,2-a]pyridineHCID 2862388—

Reaction Steps

A solution of 2-aminopyridine (1.63 g) and 2-bromo-1-(2-bromophenyl)-ethanone (4.8 g) in dry ethanol (40 mls) was heated under reflux for 1 hour. The mixture was concentrated in vacuo. The residue was treated with dilute sodium bicarbonate solution and extracted with ethyl acetate. The ethyl acetate was washed with water and brine then dried and evaporated. Flash chromatography produced the sub-title compound as a light grey oil. MS MW 272/274 bp 272.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04900751
Source datasetuspto-grants-1990_02
ORD IDord-5dac21755698435cbc12774be3fba360
Source noteuspto-grants-1990_02