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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18691생성일: 2026년 10월 23일

Hydrochloric Acid → (6R)-8-Oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

https://huagongshe.com/ko/reaction/18691

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium HydroxideHCID 14798—
반응물Sodium BicarbonateHCID 516892—
반응물N,N'-dicyclohexylethylenediamine diacetateHCID 85594586—
반응물7-Amino-3-(sulfomethyl-1h-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acidHCID 87506921—
용매WaterHCID 962—
용매IsopropanolHCID 3776—
생성물N,N'-Dicyclohexyl-1,2-ethanediamineHCID 273886—
생성물(6R)-8-Oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acidHCID 52921562286.7%

반응 조건

온도7.5 °C

반응 단계

7-amino-3-(sulfomethyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acid (5 g), was dissolved in water (19 ml) using 30% w/w sodium hydroxide (1.5 g in 8 ml water) and sodium bicarbonate (1 g), O-formylmandeloyl chloride (2.45 g) was added at 0-5° C. and maintained at 5-10° C. over a period of 1-2 hours. After the completion of reaction, the reaction mixture was acidified with conc. HCl (2.6 g) and maintained the reaction at 28-30° C. for about 2-3 hours. After the completion of reaction, sodium bicarbonate (˜3.5 g) was added to set the pH 5±1 and the solution was added to a solution of N,N′-dicyclohexylethylenediamine diacetate (9.26 g) in water (40 mL) and isopropyl alcohol (40 mL) and stirred well at 25-30° C. for about 2-3 hours. The reaction mixture was cooled to 5-10° C., filtered, washed with chilled water (0-5° C.) and isopropyl alcohol (0-5° C.) and dried the material under vacuum at ˜40° C. to get N,N′-dicyclohexylethylenediamine salt of 7-D-mandelamido-3-(1-sulfomethyl-1H-tetrazol-5-yl)thio)methyl)-3-cephem-4-carboxylic acid (6.5 g). Step-(ii)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741478B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-a4e3c7d5b2f8495a9dd1924f570b4cfa
출처 메모uspto-grants-2010_06