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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 34501생성일: 2026년 10월 24일

Hydrochloric Acid → 7-[2-(2-Aminothiazol-4-yl)-2-difluoromethoxyiminoacetamido]-3-(4-methoxy-1-pyridiniomethyl)-3-cephem-4-carboxylate

https://huagongshe.com/ko/reaction/34501

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium IodideHCID 5238—
반응물4-MethoxypyridineHCID 69278—
반응물7-[2-(2-Aminothiazol-4-yl)-2-difluoromethoxyiminoacetamido]-3-acetoxymethyl-3-cephem-4-carboxylic acidHCID 131715680—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물7-[2-(2-Aminothiazol-4-yl)-2-difluoromethoxyiminoacetamido]-3-(4-methoxy-1-pyridiniomethyl)-3-cephem-4-carboxylateHCID 13171567813%

반응 단계

A mixture of 7-[2-(2-aminothiazol-4-yl)-2-difluoromethoxyiminoacetamido]-3-acetoxymethyl-3-cephem-4-carboxylic acid (syn isomer) (3.0 g), 4-methoxypyridine (4.0 g), sodium iodide (8.0 g), acetonitrile (4.0 ml) and water (1.0 ml) was heated for 2.0 hours at 65° to 68° C., and then water (100 ml) was added thereto. The mixture was adjusted to pH 3.0 with 1N-hydrogen chloride and the resultant precipitates were filtered off. The aqueous layer was subjected to column chromatography on macroporus nonionic adsorption resin "Diaion HP-20" and the elution was carried out with 30% aqueous methanol. The fractions containing the object compound were collected, concentrated in vacuo and lyophilized to give 7-[2-(2-aminothiazol-4-yl)-2-difluoromethoxyiminoacetamido]-3-(4-methoxy-1-pyridiniomethyl)-3-cephem-4-carboxylate (syn isomer) (0.43 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04761410
출처 데이터셋uspto-grants-1988_08
ORD IDord-350e066b5c254a018bc79404d8d526a8
출처 메모uspto-grants-1988_08