HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 543539Erstellt: 23. Oktober 2026
Dacthal → 7-Amino-3-(1-methyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylicacid
https://huagongshe.com/de/reaction/543539
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dacthal | HCID 2943 | — |
| Edukt | HCID 70463326 | HCID 70463326 | — |
| Edukt | HCID 178482017 | HCID 178482017 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 7-Amino-3-(1-methyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylicacid | HCID 13020813 | 86,5% |
Reaktionsschritte
A 3.5 ml portion of acetonitrile was added to 0.946 g of 7-amino-3-(2-carboxybenzoyloxy)methyl-3-cephem-4-carboxylic acid and 0.32 g of 5-mercapto-1-methyl-1H-tetrazole, and the mixture was cooled over a dry-ice/ethanol bath, followed by adding through a dropping funnel 3.71 g of DCPA to it with stirring and rinsing the funnel with 1.0 ml of acetonitrile. The external bath was removed, and the reaction mixture was warmed to 0° C., whereby the starting materials dissolved. The solution was stirred at 14° to 16° C. for 40 minutes to allow the reaction to proceed, and the reaction solution was cooled with ice, and poured into ice-water, which was placed in a refrigerator overnight. The precipitate was filtered out and washed with 10 ml of water, and the filtrate and washing were combined and adjusted to pH 4.0 with 25% aqueous ammonia under ice cooling. The precipitated powder was recovered by filtration, washed with water and acetone successively, and dried, thereby affording 0.710 g (86.5% of yield) of 7-amino-3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acid. The IR and NMR values of the product were in accordance with those of the authentic sample.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04446318 |
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| Quelldatensatz | uspto-grants-1984_05 |
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| ORD ID | ord-85c49044718c4f0c915c14e5dbcdb505 |
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| Quellennotiz | uspto-grants-1984_05 |
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