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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 18692Erstellt: 23. Oktober 2026

Hydrochloric Acid → 7-D-mandelamido-3-(((1-sulfomethyl-1H-tetrazol-5-yl)thio)methyl)-3-cephem-4-carboxylic acid

https://huagongshe.com/de/reaction/18692

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium HydroxideHCID 14798—
EduktSodium BicarbonateHCID 516892—
EduktN,N'-di-(p-anisyl)ethylenediamine diacetateHCID 86625397—
Edukt7-Amino-3-(sulfomethyl-1h-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acidHCID 87506921—
LösungsmittelWaterHCID 962—
LösungsmittelIsopropanolHCID 3776—
ProduktN,N'-di-(p-anisyl)ethylenediamineHCID 408327—
Produkt7-D-mandelamido-3-(((1-sulfomethyl-1H-tetrazol-5-yl)thio)methyl)-3-cephem-4-carboxylic acidHCID 4500614499,1%

Reaktionsbedingungen

Temperatur7.5 °C

Reaktionsschritte

7-amino-3-(1-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 under stirring at 28-30° C. over 2-3 hours. After the completion of reaction, sodium bicarbonate (˜3.5 g) was added to set the pH 5±1. The solution was added to a solution of N,N′-di-(p-anisyl)ethylenediamine diacetate (11.7 g) in water (40 mL) and isopropyl alcohol (40 mL) and stirred well at 25-30° C. After stirring for 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′-di-(p-anisyl)ethylenediamine salt of 7-D-mandelamido-3-(((1-sulfomethyl-1H-tetrazol-5-yl)thio)methyl)-3-cephem-4-carboxylic acid (6.4 g). Step-(ii)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741478B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-82464808ea184eac849c01f6e3428383
Quellennotizuspto-grants-2010_06