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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601666Generated: October 29, 2026

1-Bromo-2-butanone → 6-Bromo-2-ethylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/601666

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2-butanoneHCID 13156—
Reactant2-Amino-5-bromopyridineHCID 70622—
SolventEthanolHCID 702—
Product6-Bromo-2-ethylimidazo[1,2-a]pyridineHCID 2315826564.9%

Reaction Steps

5.0 g of 1-bromo-2-butanone was dissolved in 80 ml of ethanol, 5.71 g of 2-amino-5-bromopyridine was added, and the mixture was stirred all night by heating under reflux. After cooling down to room temperature, the solvents were distilled outunder reduced pressure, and ethyl acetated followed by saturated sodium bicarbonate aqueous solution were added. After drying organic layer with anhydrous sodium sulfate, the solvents were distilled outunder reduced pressure. The obtained residues were purified by preparative thin-layer silicagel chromatography (hexane:ethyl acetate=75:25), to obtain 4.82 g of the above compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902369B2
Source datasetuspto-grants-2011_03
ORD IDord-abd7cd04bb6643c68ca00741e741bc78
Source noteuspto-grants-2011_03