CARINDACILLIN Struktur

CARINDACILLIN

Bezeichnung:CARINDACILLIN

CAS-Nr35531-88-5

Englisch Name:CARINDACILLIN

CBNumberCB01091049

SummenformelC26H26N2O6S

Molgewicht494.56

MOL-Datei35531-88-5.mol

CARINDACILLIN Chemische Eigenschaften,Einsatz,Produktion Methoden

Originator
Geocillin,Roerig,US,1972
Verwenden
Antibacterial.
Definition
ChEBI: Carindacillin is a penicillin. It is a conjugate acid of a carindacillin(1-).
Manufacturing Process
(A) Preparation of Phenylchlorocarbonyl Ketene: To phenylmalonic acid (20 g) in ethyl ether (100 ml) there is added phosphorus pentachloride (46 g). A vigorous reaction occurs. The reaction mixture is refluxed for 4 hours then the ether partially removed by heating on a steam bath. The reaction mixture becomes black when about half the ether is removed and the remaining ether is removed under reduced pressure (at 100 mm). The residue is distilled under vacuum and the fraction boiling at 75° to 90°C at 1.5 to 4 mm collected. The product, a yellow liquid, is redistilled at 74°C and 1.5 mm. It shows a strong peak in the infrared region of the spectrum at 4.69 mu. Repetition of this procedure but using 10 g of phenylmalonic acid instead of 20 g produces a less vigorous reaction on addition of the phosphorus pentachloride. The same product is obtained.
(B) Acylation of 6-Aminopenicillanic Acid: To a solution of the aryl halocarbonyl ketene (0.1 mol) in methylene chloride (sufficient to provide a clear solution and generally from about 5 to 10 ml per gram of ketene) there is added the proper alcohol R2OH (0.1 mol), in this case 5-indanyl alcohol. The reaction mixture is maintained under an atmosphere of nitrogen and stirred for a period of from 20 minutes to 3 hours, care being taken to exclude moisture. The temperature may range from about -70° to about - 20°C. The infrared spectrum of the mixture is then taken to determine and confirm the presence of the ketene ester. A solution of 6-aminopenicillanic acid-triethylamine salt (0.1 mol) in methylene chloride (50 ml) is added and the mixture stirred at -70° to -20°C for 10 minutes. The cooling bath is then removed and the reaction mixture stirred continuously and allowed to warm to room temperature.
Various isolation methods are then spelled out in US Patent 3,679,801.
Trademarks
Geocillin (Pfizer).
Therapeutic Function
Antibacterial

CARINDACILLIN Upstream-Materialien And Downstream Produkte

CARINDACILLIN Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

35531-88-5, CARINDACILLIN Verwandte Suche:

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