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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132749생성일: 2026년 10월 23일

Potassium Carbonate → 4-{4-[3-[3-(4-fluorofluorophenyl)-3-hydroxypropyl]-2-(4-methoxyphenyl)-4-oxoazetidin-1-yl]phenoxy}butane-1-sulfonic Acid

https://huagongshe.com/ko/reaction/132749

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물1,4-Butane sultoneHCID 15411—
반응물3-[3-(4-Fluorofluorophenyl)-3-hydroxypropyl]-1-(4-hydroxyphenyl)-4-(4-methoxyphenyl)azetidin-2-oneHCID 21083136—
용매DimethylformamideHCID 6228—
생성물4-{4-[3-[3-(4-fluorofluorophenyl)-3-hydroxypropyl]-2-(4-methoxyphenyl)-4-oxoazetidin-1-yl]phenoxy}butane-1-sulfonic AcidHCID 21083142—

반응 단계

160 mg of 3-[3-(4-fluorofluorophenyl)-3-hydroxypropyl]-1-(4-hydroxyphenyl)-4-(4-methoxyphenyl)azetidin-2-one (11) were dissolved in 4 ml of absolute dimethylformamide. 210 mg of powdered potassium carbonate and 42 mg of 1,4,-butanesultone were added. The mixture was stirred at room temperature overnight. The reaction solution was concentrated under oil pump vacuum, taken up in dichloromethane and washed 1× with water. The aqueous phase was acidified with 2N hydrochloric acid and extracted 2× with dichloromethane. The combined organic phases were dried over sodium sulfate and concentrated. The residue was chromatographed on a 10 g SiO2 cartridge (dichloromethane/methanol=5/1). The product (72 mg) was obtained as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07388004B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-ccb38761d9384716ae0bc28bb704fc07
출처 메모uspto-grants-2008_06