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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64492생성일: 2026년 10월 24일

Citric Acid → Diethyl butyl[({8-[(2,6-difluorobenzyl)oxy]-2-methylimidazo[1,2-a]pyridin-3-yl}carbonyl)amino]malonate

https://huagongshe.com/ko/reaction/64492

반응식

참여 물질

역할이름HCID투입량
반응물Citric AcidHCID 311—
반응물Butyl iodideHCID 10962—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium ethoxideHCID 2723922—
반응물Ethanol sodium ethoxideHCID 23706232—
반응물Diethyl[({8-[(2,6-difluorobenzyl)oxy]-2-methylimidazo[1,2-a]pyridin-3-yl}carbonyl)amino]malonateHCID 86713528—
용매EthanolHCID 702—
용매ChloroformHCID 6212—
생성물Diethyl butyl[({8-[(2,6-difluorobenzyl)oxy]-2-methylimidazo[1,2-a]pyridin-3-yl}carbonyl)amino]malonateHCID 86713527—

반응 조건

온도70 °C

반응 단계

To 252 mg of diethyl[({8-[(2,6-difluorobenzyl)oxy]-2-methylimidazo[1,2-a]pyridin-3-yl}carbonyl)amino]malonate were added 4 ml of ethanol, 0.23 ml of a 20% sodium ethoxide/ethanol solution, and 0.31 ml of 1-iodobutane, followed by stirring at 70° C. for 3 hours. Subsequently, 11 mg of sodium ethoxide was added thereto, followed by stirring at 70° C. for 1 hour. To the reaction mixture were added an aqueous citric acid solution, a saturated aqueous sodium hydrogen carbonate solution, and chloroform to carry out a layer separation operation. The organic layer was dried over anhydrous sodium sulfate and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 69 mg of diethyl butyl[({8-[(2,6-difluorobenzyl)oxy]-2-methylimidazo[1,2-a]pyridin-3-yl}carbonyl)amino]malonate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447090B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-af7d2113700a453d8a8cb158194c14ec
출처 메모uspto-grants-2016_09