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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 127463생성일: 2026년 10월 25일

1,5-Diazabicyclo(5,4,0)undec-5-ene → 7beta-Phenoxyacetamido-3-methoxy-ceph-2-em-4-carboxylic acid diphenylmethyl ester

https://huagongshe.com/reaction/127463

반응식

참여 물질

역할이름HCID투입량
반응물1,5-Diazabicyclo(5,4,0)undec-5-eneHCID 314112—
반응물Isocrotonic acid diphenylmethyl esterHCID 70527120—
반응물2-[4-(p-Nitrobenzenesulphonylthio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-methoxy-crotonic acid diphenylmethyl esterHCID 70557191—
용매BenzeneHCID 241—
용매TetrahydrofuranHCID 8028—
생성물7beta-Phenoxyacetamido-3-methoxy-ceph-2-em-4-carboxylic acid diphenylmethyl esterHCID 70558413—

반응 단계

A solution of 367 mg (0.5 mM) of a mixture consisting of 2-[4-(p-nitrobenzenesulphonylthio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-methoxy-crotonic acid diphenylmethyl ester and the corresponding isocrotonic acid diphenylmethyl ester, and 152 mg (1.0 mM) of 1,5-diazabicyclo[5.4.0]undec-5-ene in 10 ml of dry tetrahydrofurane is stirred for 40 minutes at room temperature. The reaction mixture is diluted with benzene, washed successively with dilute hydrochloric acid, water and dilute aqueous sodium bicarbonate solution, dried over sodium sulphate and freed from the solvent in vacuo. The residue is chromatographed on acid-washed silica gel, using toluene/ethyl acetate, 7:1, as the running agent, whereby pure 7β-phenoxyacetamido-3-methoxy-ceph-2-em-4-carboxylic acid diphenylmethyl ester is obtained. Subsequent elution with toluene/ethyl acetate, 2:1, results in the isolation of a mixture which in addition to 7β-phenoxyacetamido-3-methoxy-ceph-2-em-4-carboxylic acid diphenylmethyl ester also contains 7β-phenoxyacetamido-3-methoxy-ceph-3-em-4-carboxylic acid diphenylmethyl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04255328
출처 데이터셋uspto-grants-1981_03
ORD IDord-5822cf5cc6b349c3b60496caed142b4c
출처 메모uspto-grants-1981_03