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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35518Generated: October 25, 2026

2-Amino-5-methylpyridine → 6-Methyl-2-[4-(trifluoromethyl)phenyl]imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/35518

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-methylpyridineHCID 15348—
Reactant2-Bromo-4'-(trifluoromethyl)acetophenoneHCID 321979—
ReactantSodium BicarbonateHCID 516892—
SolventEthanolHCID 702—
Product6-Methyl-2-[4-(trifluoromethyl)phenyl]imidazo[1,2-a]pyridineHCID 2813810—

Reaction Steps

24 g (0.077 mole) of 1-bromo-2-(4-trifluoromethylphenyl)-2-ethanone, 8.4 g (0.077 mole) of 2-amino-5-methylpyridine and 13 g of sodium bicarbonate are mixed in 210 ml of 95% strength ethanol, and this suspension is heated under reflux until the evolution of gas has ceased. The solvent is then evaporated off under reduced pressure and the evaporation residue is taken up with water and dichloromethane. The organic phase is decanted and dried over magnesium sulphate, and the solvent is removed by evaporation under reduced pressure. The residue is purified by column chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04767755
Source datasetuspto-grants-1988_08
ORD IDord-a4f089c2a14f4280abf7024273451486
Source noteuspto-grants-1988_08