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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 26105생성일: 2026년 10월 27일

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/26105

반응식

참여 물질

역할이름HCID투입량
반응물1,5-Diazabicyclo(5,4,0)undec-5-eneHCID 314112—
반응물Isocrotonic acidHCID 643792—
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 dihenylmethyl 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 7βphenoxyacetamido-3-methoxy-ceph-3-em-4-carboxylic acid diphenylmethyl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04147864
출처 데이터셋uspto-grants-1979_04
ORD IDord-04ad8d5045a645ef85caa4e25b79c364
출처 메모uspto-grants-1979_04