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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 339554생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/339554

반응식

참여 물질

역할이름HCID투입량
반응물2-Amino-5-methylpyridineHCID 15348—
반응물2-Bromo-4'-nitroacetophenoneHCID 66840—
반응물Sodium BicarbonateHCID 516892—
용매EthanolHCID 702—
생성물6-Methyl-2-(4-nitrophenyl)imidazo[1,2-a]pyridineHCID 74991740.5%

반응 단계

A mixture of 2-amino-5-picoline (0.88 g, 8.19 mmol) and 2-bromo-4′-nitroacetophenone (2.0 g, 8.19 mmol) in EtOH (50 ml) was heated under reflux for 17 h. The reaction mixture was allowed to cool and sodium bicarbonate (840 mg, 9.99 mmol) was added and heating was continued for 18 h. On cooling to room temperature, the solvent was removed under reduced pressure and the residue was purified by flash chromatography (1:1 Hexane/EtOAc) to give the title compound (0.84 g, 40%) as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895313B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-7b3f524f606a4c85802e103451f69231
출처 메모uspto-grants-2014_11