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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 34268생성일: 2026년 10월 25일

Hydrochloric Acid → (5-Methyl-2-oxo-1,3-dioxolen-4-yl)methyl 7-formamido-3-(1,2,4-thiadiazol-4-yl)thiomethyl-3-cephem-4-carboxylate

https://huagongshe.com/reaction/34268

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Propylene OxideHCID 6378—
반응물4-Bromo-methyl-5-methyl-1,3-dioxolene-2-oneHCID 70406633—
반응물7-Formamido-3-(1,2,4-thiadiazol-4-yl)thiomethyl-3-cephem-4-carboxylic acidHCID 88640731—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물(5-Methyl-2-oxo-1,3-dioxolen-4-yl)methyl 7-formamido-3-(1,2,4-thiadiazol-4-yl)thiomethyl-3-cephem-4-carboxylateHCID 131715666—

반응 조건

온도5 °C

반응 단계

A suspension of 7-formamido-3-(1,2,4-thiadiazol-4-yl)thiomethyl-3-cephem-4-carboxylic acid (1.07 g, 3 mmole), KHCO3 (1.0 g, 10 mmole) and propylene oxide (1 ml) in DMF (5 ml) was cooled to 5° C. and treated with 4-bromo-methyl-5-methyl-1,3-dioxolene-2-one (0.87 g, 4.5 mmole). After stirring at 5° C. for 5 hr, the reaction mixture was poured into a mixture of aq HCl (pH 3) (70 ml) and EtOAc (250 ml). The EtOAc layer was separated and washed successively with aq HCl (pH 3) (70 ml×2), 10% K2HPO4 buffer (pH 7) (70 ml×2) and saturated aq NaCl (50 ml). The EtOAc solution was dried (MgSO4) and concentrated in vacuo. The residue was triturated with ether (300 ml) and the resulting precipitate was filtered to give the title compound ( 0.45 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04761409
출처 데이터셋uspto-grants-1988_08
ORD IDord-be25827142204a54ba9cfb56b41c74fe
출처 메모uspto-grants-1988_08