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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 127095생성일: 2026년 10월 26일

Dicyclohexylcarbodiimide → 3-Carbamoyloxymethyl-7-(2-oxo-2,3-dihydrothiazol-4-yl)acetamido-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/127095

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물N-HydroxysuccinimideHCID 80170—
반응물Acetamide, 2-(trimethylsilyl)-HCID 357676—
반응물3-Carbamoyloxymethyl-7-amino-3-cephem-4-carboxylic acidHCID 12784759—
반응물2-Oxo-2,3-dihydrothiazol-4-ylacetic acidHCID 13132598—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물3-Carbamoyloxymethyl-7-(2-oxo-2,3-dihydrothiazol-4-yl)acetamido-3-cephem-4-carboxylic acidHCID 705724005.8%

반응 단계

To a mixture of 2-oxo-2,3-dihydrothiazol-4-ylacetic acid (0.4 g.) and N-hydroxysuccinimide (0.3 g.) in tetrahydrofuran (15 ml.) was added N,N'-dicyclohexylcarbodiimide (0.52 g.) with stirring at room temperature, and the mixture was further stirred for 2 hours at the same temperature. Thus obtained solution was added to a solution of 3-carbamoyloxymethyl-7-amino-3-cephem-4-carboxylic acid (0.816 g.) and trimethylsilylacetamide (0.27 g.) in ethyl acetate (30 ml.) at room temperature, and the mixture was stirred for 16 hours at the same temperature. After the reaction, the reaction mixture was cooled to at -20° C., and then water (20 ml.) was added thereto. After stirring the mixture sufficiently, the mixture was filtered, and then the ethyl acetate layer was separated therefrom. The ethyl acetate layer was washed with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate, treated with activated carbon, and then the solvent was distilled off under reduced pressure. The residue was pulverized in diethyl ether, collected by filtration and then dried to give 3-carbamoyloxymethyl-7-(2-oxo-2,3-dihydrothiazol-4-yl)acetamido-3-cephem-4-carboxylic acid (60 mg.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04254260
출처 데이터셋uspto-grants-1981_03
ORD IDord-5c293cd717ea436daa20727f75ed10fa
출처 메모uspto-grants-1981_03