HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 18690Erstellt: 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/18690
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | N,N'-diisobutylethylenediamine diacetate | HCID 85588787 | — |
| Edukt | 7-Amino-3-(sulfomethyl-1h-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acid | HCID 87506921 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Isopropanol | HCID 3776 | — |
| Produkt | 1,2-Ethanediamine, N,N'-bis(2-methylpropyl)- | HCID 469900 | — |
| Produkt | 7-D-mandelamido-3-(((1-sulfomethyl-1H-tetrazol-5-yl)thio)methyl)-3-cephem-4-carboxylic acid | HCID 45006144 | 85,2% |
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 the reaction at 28-30° C. for about 2-3 hrs, sodium bicarbonate (3.5 g) was added to set the pH 5±1 and the reaction mass solution was added to a solution of N,N′-diisobutylethylenediamine diacetate (8.2 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.) followed by isopropyl alcohol (0-5° C.) and dried the material at ˜40° C. to get N,N′-diisobutylethylenediamine salt of 7-D-mandelamido-3-(((1-sulfomethyl-1H-tetrazol-5-yl)thio)methyl)-3-cephem-4-carboxylic acid (5.5 g). Step(ii)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07741478B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-990d0f90a5184a249a9729eed3fd48c2 |
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| Quellennotiz | uspto-grants-2010_06 |
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