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HRID 231532생성일: 2026년 10월 26일

p-Chlorophenacyl bromide → 8-Bromo-6-chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/231532

반응식

참여 물질

역할이름HCID투입량
반응물p-Chlorophenacyl bromideHCID 68303—
반응물Sodium BicarbonateHCID 516892—
반응물3-Bromo-5-chloropyridin-2-amineHCID 2763971—
용매EthanolHCID 702—
생성물8-Bromo-6-chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridineHCID 14234917—

반응 단계

17 g (82 mmol) of 2-amino-3-bromo-5-chloropyridine dissolved in 150 ml of ethanol are reacted with 29 g of 2-bromo-1-(4-chlorophenyl)-1-ethanone and 14 g of sodium hydrogen carbonate. The mixture is brought to the refluxing temperature for 6 h and cooled. The precipitate is filtered off and rinsed with CH2Cl2, and the filtrate is concentrated under reduced pressure. After recrystallization of the evaporation residue in ethyl acetate, the compound melts at 178° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04847263
출처 데이터셋uspto-grants-1989_07
ORD IDord-8a2f27f02afd4b7b85817dfa22b20cfb
출처 메모uspto-grants-1989_07