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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 603926생성일: 2026년 10월 26일

Triethylamine → {4-[(2R,3R)-3-{[2-(1,3-benzodioxol-5-yl)-2-oxoethyl]thio}-1-(4-chlorophenyl)-4-oxoazetidin-2-yl]phenoxy}acetic acid

https://huagongshe.com/reaction/603926

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물TriphenylphosphineHCID 11776—
반응물1-(1,3-Dioxaindan-5-yl)-2-bromoethan-1-oneHCID 243777—
반응물HCID 86643081HCID 86643081—
용매AcetoneHCID 180—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물{4-[(2R,3R)-3-{[2-(1,3-benzodioxol-5-yl)-2-oxoethyl]thio}-1-(4-chlorophenyl)-4-oxoazetidin-2-yl]phenoxy}acetic acidHCID 67270870—

반응 단계

tert-Butyl (4-{(2R,3R)-1-(4-chlorophenyl)-3-[(3-nitropyridin-2-yl)dithio]-4-oxoazetidin-2-yl}phenoxy)acetate (Method 27) (0.70 g, 1.22 mmol) was dissolved in acetone (30 mL) at room temperature, then water (10 mL) and triphenyl phosphine (0.32 g, 1.22 mmol) was added. The mixture was stirred at room temperature for 15 minutes and then concentrated under reduced pressure to afford the crude thiol as a brown oil. This crude thiol was immediately dissolved in CH2Cl2 (30 mL) and 1-benzo[1,3]dioxol-5-yl-2-bromo-ethanone (0.59 g, 2.44 mmol) was added, followed by Et3N (0.34 mL, 2.44 mmol). The mixture was stirred at room temperature for 18 hours, concentrated under reduced pressure and purified by flash-chromatography (Heptane:EtOAc 7:3 and then 2:1). The resulting product (0.90 g) was dissolved in 15 ml formic acid and stirred at room temperature for 3 hours. Concentration under reduced pressure and purification by flash-chromatography afforded the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07906502B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-d33d4c7d09b5497fabebe5f35fbcdc9e
출처 메모uspto-grants-2011_03