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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 704621생성일: 2026년 10월 25일

Ethyl bromopyruvate → Ethyl 7-ethylimidazo[1,2-a]pyridine-2-carboxylate

https://huagongshe.com/reaction/704621

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl bromopyruvateHCID 66144—
반응물4-Ethylpyridin-2-amineHCID 118425—
용매EthanolHCID 702—
생성물Ethyl 7-ethylimidazo[1,2-a]pyridine-2-carboxylateHCID 2007284918.6%

반응 단계

A mixture of 2-amino-4-ethylpyridine (3.8 g), ethyl 3-bromo-2-oxopropionate (6.84 g) and ethanol (30 ml) was refluxed for 6 hours. After the reaction mixture was concentrated, water (30 ml) and ehtyl acetate (30 ml) were added to the residue. The mixture was made basic with an aqueous solution of potassium carbonate, and the separated organic layer was washed with brine and dried over magnesium sulfate. The solvent was evaporated and the residue was subjected to a column chromatography on silica gel (150 g) and eluted with 15% solution of ethyl acetate in chloroform. The fractions containing the object compound were combined and concentrated to give ethyl 7-ethylimidazo[1,2-a]pyridine-2-carboxylate (1.26 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04988698
출처 데이터셋uspto-grants-1991_01
ORD IDord-813225852fa145a39cf7ab9cac993ee1
출처 메모uspto-grants-1991_01