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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35516Generated: October 26, 2026

2-Bromo-4'-methylacetophenone → 2-(p-Tolyl)-6-(trifluoromethyl)imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/35516

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-4'-methylacetophenoneHCID 69272—
Reactant2-Amino-5-(trifluoromethyl)pyridineHCID 735862—
Solvent1-PropanolHCID 1031—
Product2-(p-Tolyl)-6-(trifluoromethyl)imidazo[1,2-a]pyridineHCID 1393803770.2%

Reaction Steps

10 g (0.0616 mole) of 2-amino-5-trifluoromethylpyridine and 17.5 g (0.0616 mole) of 1-bromo-2-(4-methylphenyl)-2-ethanone are mixed in 200 ml of n-propanol and the solution is heated to reflux. At the end of the reaction, the reaction mixture is concentrated under reduced pressure and the evaporation residue taken up with water and treated with an excess of ammonia solution until the pH is basic. The imidazopyridine is extracted with dichloromethane and purified by chromatography. 11.95 g (56%) of white solid are obtained. M.p. 187°-188° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04767755
Source datasetuspto-grants-1988_08
ORD IDord-20bd24ff2e884f868dd93e00939014f6
Source noteuspto-grants-1988_08