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HRID 18691生成日期:2026年10月23日

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

https://huagongshe.com/zh-CN/reaction/18691

反应方程式

参与物

角色名称HCID投料
反应物海萝胶HCID 313—
反应物二甲基对苯二胺二盐酸HCID 14798—
反应物碳酸氢钠HCID 516892—
反应物N,N'-dicyclohexylethylenediamine diacetateHCID 85594586—
反应物7-Amino-3-(sulfomethyl-1h-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acidHCID 87506921—
溶剂聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]HCID 962—
溶剂异丙醇HCID 3776—
产物1,2-双(环己基氨基)乙烷HCID 273886—
产物(6R)-8-Oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acidHCID 52921562286.7%

反应条件

温度7.5 °C

反应步骤

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)

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US07741478B2
来源数据集uspto-grants-2010_06
ORD IDord-a4e3c7d5b2f8495a9dd1924f570b4cfa
来源说明uspto-grants-2010_06