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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8365생성일: 2026년 10월 24일

2-Amino-4-methylpyridine → 2-(4'-Chloropropoxy-2'fluorophenyl)-7-methylimidazo[1,2-a]pyridine

https://huagongshe.com/ko/reaction/8365

반응식

참여 물질

역할이름HCID투입량
반응물2-Amino-4-methylpyridineHCID 1533—
반응물alpha-Bromo-2'-fluoro-4'-chloropropoxyacetophenoneHCID 22015593—
용매EthanolHCID 702—
생성물2-(4'-Chloropropoxy-2'fluorophenyl)-7-methylimidazo[1,2-a]pyridineHCID 22015617—

반응 단계

A solution of the product of Step B (1.0 g) and 2-amino-4-picoline (0.357 g) in ethanol (4 mL) was heated at 73° C. for 18 hours. The reaction mixture was cooled to ambient temperature and the solvent evaporated in vacuo. A portion of the residue was purified via silica gel chromatography (ethyl acetate/hexane) directly. The remainder of the residue was dissolved in methanol/dichloromethane and treated with Dowex® 550A basic resin (Aldrich, Milwaukee, Wis.) for 10 minutes. The resin was removed via filtration and the filtrate evaporated prior to silica gel chromatography (ethyl acetate/hexane). The combined material (0.42 g) containing the title compound was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087757B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-95e42f03238643bf8dd17789479a8a05
출처 메모uspto-grants-2006_08