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HRID 5428생성일: 2026년 10월 24일

Ethyl bromopyruvate → Ethyl 5-Chloroimidazo[1,2-a]pyridine-2-carboxylate

https://huagongshe.com/ko/reaction/5428

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl bromopyruvateHCID 66144—
반응물2-Amino-6-chloropyridineHCID 206246—
용매EthanolHCID 702—
생성물Ethyl 5-Chloroimidazo[1,2-a]pyridine-2-carboxylateHCID 1242895967.7%

반응 단계

A solution of 2-amino-6-chloropyridine (6.43 g, 50 mmoles) and ethyl bromopyruvate (9.75 g, 50 mmoles) in ethanol (150 ml) was heated at reflux for 4 hours. After the solvent was removed, chloroform was added to the residue, which was washed in turn with saturated sodium bicarbonate and saturated saline, and then dried over anhydrous magnesium sulfate. After the solvent was concentrated, n-hexane was added to the mixture. Then, the crystals precipitated were filtered off and washed with n-hexane to obtain 7.60 g of the desired product (67.6%, pale yellow crystals).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05244908
출처 데이터셋uspto-grants-1993_09
ORD IDord-aac0c1f80f444f1e85571cb9c0058d96
출처 메모uspto-grants-1993_09