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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 245321Erstellt: 24. Oktober 2026

Nitrogen → Linezolid

https://huagongshe.com/reaction/245321

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitrogenHCID 947—
EduktAcetic AnhydrideHCID 7918—
EduktTriethylamineHCID 8471—
Edukt(S)-5-((dibenzylamino)methyl)-3-(3-fluoro-4-morpholinophenyl)oxazolidin-2-oneHCID 11213668—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladiumHCID 23938—
LösungsmittelAcetoneHCID 180—
ProduktLinezolidHCID 44140175,6%

Reaktionsschritte

(S)-5-((dibenzylamino)methyl)-3-(3-fluoro-4-morpholinophenyl)oxazolidin-2-one (0.95 g, 2 mmol) and 0.1 g 10 wt % Pd—C were added to 20 mL acetone and the air was replaced with N2. The reaction went on under 5 Mpa hydrogen at room temperature for 5 hours. After filtered, acetic anhydrid (0.24 g, 2.4 mmol) and triethylamine (2.0 g, 20 mmol) were added and reacted for 2 hours at room temperature. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, filtered, most part of the solvent was evaporated, frozen crystallized and filtered to provide the crude product. The crude product was recrystallized with ethyl acetate to provide 0.51 g of linezolid in 75% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08658789B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-7d088d57876841848e04e42cad2c39d7
Quellennotizuspto-grants-2014_02