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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 651212Erstellt: 25. Oktober 2026

Eperezolid → (S)-N-[[3-[3-Fluoro-4-[4-(hydroxyacetyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]-methyl]acetamide N-oxide

https://huagongshe.com/reaction/651212

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEperezolidHCID 73214—
Edukt3-Hydroperoxyphthalic acidHCID 19809706—
LösungsmittelMethanolHCID 887—
Produkt(S)-N-[[3-[3-Fluoro-4-[4-(hydroxyacetyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]-methyl]acetamide N-oxideHCID 86584035—

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

(S)-N-[[3-[3-Fluoro-4-[4-(hydroxyacetyl)-1-piperazinyl]-phenyl]-2-oxo-5-oxazolidinyl]methyl]-acetamide (VIII-A, R1=COCH3, R2=H, X1=F, X2=H) (11.8 g) is dissolved in 200 mL of methanol. Monoperoxyphthalic acid, magnesium salt hexahydrate (80% pure, 18.5 g) is added and the resulting suspension is stirred at 25° C. for two hours. The reaction is filtered and the filtrate is concentrated to afford a white solid. This solid is chromatographed on silica gel using 20% methanol in chloroform as eluent to afford the N-oxide. Lyophilization of this material affords the purified product as a hydrate (9.5 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06277985B1
Quelldatensatzuspto-grants-2001_08
ORD IDord-47f5199f7b3f42a58388f844627c18c3
Quellennotizuspto-grants-2001_08