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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1656263Erstellt: 24. Oktober 2026

Phosphorus oxychloride → HCID 131714064, Verbindung

https://huagongshe.com/de/reaction/1656263

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhosphorus oxychlorideHCID 24813—
EduktAcetamide, 2-(trimethylsilyl)-HCID 357676—
Edukt7-Amino-3vinyl-3-cephem-4-carboxylic acidHCID 12818006—
Edukt2-(p-Nitrobenzyloxycarbonylmethoxyimino)-2-(2-formamidothiazol-4-yl)acetic acidHCID 54535272—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 131714064HCID 13171406473,4%

Reaktionsschritte

Vilsmeir reagent was prepared from N,N-dimethylformamide (1.67 ml) and phosphorus oxychloride (1.98 ml) in dry tetrahydrofuran (50.4 ml) in a conventional manner. 2-(p-Nitrobenzyloxycarbonylmethoxyimino)-2-(2-formamidothiazol-4-yl)acetic acid (syn isomer) (7.35 g) was added to the stirred suspension of Vilsmeir reagent under ice-cooling, followed by stirring for 30 minutes at the same temperature. To a solution of 7-amino-3-vinyl-3-cephem-4-carboxylic acid (3.4 g) and trimethylsilylacetamide (11.8 g) in ethyl acetate (35 ml) was added the activated acid solution obtained above at -20° C., and the reaction mixture was stirred at -20° C. to -10° C. for an hour. After water and ethyl acetate were added to the resultant solution, the separated organic layer was washed with water and then dried. A conventional work-up of the solution gave 7-[2-(p-nitrobenzyloxycarbonylmethoxyimino)-2-(2-formamidothiazol-4-yl)acetamido]-3-vinyl-3-cephem-4-carboxylic acid (syn isomer) (6.8 g) as yellowish powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05252731
Quelldatensatzuspto-grants-1993_10
ORD IDord-8c26705f6be24634ae3b0cca9ed0e382
Quellennotizuspto-grants-1993_10