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HRID 35518Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/35518

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Amino-5-methylpyridineHCID 15348—
Edukt2-Bromo-4'-(trifluoromethyl)acetophenoneHCID 321979—
EduktSodium BicarbonateHCID 516892—
LösungsmittelEthanolHCID 702—
Produkt6-Methyl-2-[4-(trifluoromethyl)phenyl]imidazo[1,2-a]pyridineHCID 2813810—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04767755
Quelldatensatzuspto-grants-1988_08
ORD IDord-a4f089c2a14f4280abf7024273451486
Quellennotizuspto-grants-1988_08