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HRID 1874398생성일: 2026년 10월 26일

Trifluoroacetic anhydride → 6-(3-Nitrophenoxy)imidazo[1,2-a]pyridin-2-amine

https://huagongshe.com/reaction/1874398

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic anhydrideHCID 9845—
반응물2-[2-{[(4-methylphenyl)sulfonyl]amino}-5-(3-nitrophenoxy)pyridin-1(2H)-yl]acetamideHCID 68988952—
용매DichloromethaneHCID 6344—
생성물6-(3-Nitrophenoxy)imidazo[1,2-a]pyridin-2-amineHCID 5774928049%

반응 단계

A mixture of 2-[2-{[(4-methylphenyl)sulfonyl]amino}-5-(3-nitrophenoxy)pyridin-1(2H)-yl]acetamide (4.70 g, 10.6 mmol), trifluoroacetic anhydride (30 mL) and dichloromethane (40 mL) was stirred at room temperature for 5 hr. The reaction solution was concentrated under reduced pressure, saturated aqueous sodium hydrogen carbonate solution was added to the residue and the mixture was extracted with ethyl acetate (×3). The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and filtrated. The filtrate was concentrated under reduced pressure, 8N aqueous sodium hydroxide solution (10 mL) and ethanol (30 mL) were added to the residue and the mixture was stirred at room temperature for 15 hr. The reaction mixture was diluted with water and extracted with ethyl acetate (×3). The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and filtrated. The filtrate was concentrated under reduced pressure, and the residue was purified by column chromatography (silica gel, ethyl acetate) to give the title compound (1.40 g, 49%) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08304557B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-162bd7cba75c4d75ac8214ddc05b54b5
출처 메모uspto-grants-2012_11