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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5455생성일: 2026년 10월 23일

Triethylamine → 5-[2-[2-(Hydroxy)benzoylamino]ethylthio]imidazo[1,2-a]pyridine

https://huagongshe.com/ko/reaction/5455

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물5-[2-(Amino)ethylthio]imidazo[1,2-a]pyridineHCID 15229369—
반응물2-Acetylsalicyloyl chlorideHCID 57361564—
용매DichloromethaneHCID 6344—
생성물5-[2-[2-(Hydroxy)benzoylamino]ethylthio]imidazo[1,2-a]pyridineHCID 2336297756%

반응 단계

To a solution of 5-[2-(amino)ethylthio]imidazo[1,2-a]pyridine (3.87 g, 20 mmoles) and triethylamine (5.58 ml, 40 mmoles) in methylene chloride (200 ml) was added o-acetylsalicyloyl chloride (4.77 g, 24 mmoles) under ice-cooling with stirring and the mixture was stirred at room temperature for 30 minutes. After the solvent was distilled off, ethanol (60 ml) and 1N NaOH (40 ml) were added to the residue, followed by stirring for 1 hour. 1N HCl (40 ml) was added and ethanol was distilled off, and then the residue was extracted with chloroform and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by column chromatography (eluent: ethyl acetate/ethanol=10:1) to obtain 3.51 g of the desired product (56.0%, colorless solid).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05244908
출처 데이터셋uspto-grants-1993_09
ORD IDord-d34a489740ed4a9e8f386753fe5c41ad
출처 메모uspto-grants-1993_09