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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 35516Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/35516

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Bromo-4'-methylacetophenoneHCID 69272—
Edukt2-Amino-5-(trifluoromethyl)pyridineHCID 735862—
Lösungsmittel1-PropanolHCID 1031—
Produkt2-(p-Tolyl)-6-(trifluoromethyl)imidazo[1,2-a]pyridineHCID 1393803770,2%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04767755
Quelldatensatzuspto-grants-1988_08
ORD IDord-20bd24ff2e884f868dd93e00939014f6
Quellennotizuspto-grants-1988_08