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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 35518생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물2-Amino-5-methylpyridineHCID 15348—
반응물2-Bromo-4'-(trifluoromethyl)acetophenoneHCID 321979—
반응물Sodium BicarbonateHCID 516892—
용매EthanolHCID 702—
생성물6-Methyl-2-[4-(trifluoromethyl)phenyl]imidazo[1,2-a]pyridineHCID 2813810—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04767755
출처 데이터셋uspto-grants-1988_08
ORD IDord-a4f089c2a14f4280abf7024273451486
출처 메모uspto-grants-1988_08