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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1804163Erstellt: 27. Oktober 2026

Hydrochloric Acid → 3-{4-[4-(2,4,6-Trimethylphenyl)piperazine-1-carbonyl]phenyl}oxazolidin-2-one

https://huagongshe.com/reaction/1804163

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium HydroxideHCID 14798—
EduktEthyl p-(2-oxo-1,3-oxazolidin-3-yl)benzoateHCID 616604—
Edukt1-(2,4,6-Trimethylphenyl)piperazineHCID 2760822—
Edukt4-(4,6-Dimethoxy[1.3.5]triazin-2-yl)-4-methylmorpholinium chloride hydrateHCID 23149411—
LösungsmittelEthanolHCID 702—
Produkt3-{4-[4-(2,4,6-Trimethylphenyl)piperazine-1-carbonyl]phenyl}oxazolidin-2-oneHCID 674473689,6%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

To ethyl 4-(-2-oxooxazolidin-3-yl)benzoate (0.235 g) described in Preparation Example 12 were added 1 M aqueous sodium hydroxide solution (1.3 mL) and ethanol (5 mL), and the mixture was stirred at 50° C. 1N hydrochloric acid (1.3 mL) was added, 1-(2,4,6-trimethylphenyl)piperazine (0.215 g) and 4-(4,6-dimethoxy[1.3.5]triazin-2-yl)-4-methylmorpholinium chloride hydrate (0.277 g) were added, and the mixture was stirred at room temperature overnight. The mixture was extracted with ethyl acetate, washed with saturated brine, and the solvent was evaporated. The residue was purified by HPLC (ODS, 0.05% TFA aqueous solution-acetonitrile) to give the title compound (37.7 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08354401B2
Quelldatensatzuspto-grants-2013_01
ORD IDord-540f18ada2da4cee81800e4aebeff0b0
Quellennotizuspto-grants-2013_01