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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1874399생성일: 2026년 10월 27일

Cyclopropanecarbonyl chloride → N-[6-(3-nitrophenoxy)imidazo[1,2-a]pyridin-2-yl]cyclopropanecarboxamide

https://huagongshe.com/reaction/1874399

반응식

참여 물질

역할이름HCID투입량
반응물Cyclopropanecarbonyl chlorideHCID 77637—
반응물6-(3-Nitrophenoxy)imidazo[1,2-a]pyridin-2-amineHCID 57749280—
용매WaterHCID 962—
용매PyridineHCID 1049—
생성물N-[6-(3-nitrophenoxy)imidazo[1,2-a]pyridin-2-yl]cyclopropanecarboxamideHCID 5774910135.5%

반응 단계

To a solution of 6-(3-nitrophenoxy)imidazo[1,2-a]pyridin-2-amine (1.40 g, 5.18 mmol) in pyridine (6 mL) was added with stirring under ice-cooling cyclopropanecarbonyl chloride (706 μL, 7.77 mmol), and the mixture was stirred at room temperature for 3 hr. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate and filtrated. The filtrate was concentrated under reduced pressure, and the residue was dissolved in methanol (50 mL). Sodium carbonate (1.00 g) and water (5 mL) were added, and the mixture was stirred at 60° C. for 2 hr. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with water and 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 (622 mg, 35%) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08304557B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-52760e24bd6040f2b30d003fed947550
출처 메모uspto-grants-2012_11