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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1983106Erstellt: 25. Oktober 2026

Thiomorpholine → 4-{3-Methoxy-4-[5-(5-methyl-3-phenyl-isoxazol-4-yl)-[1,3,4]oxadiazol-2-yl]-phenyl}-thiomorpholine

https://huagongshe.com/reaction/1983106

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThiomorpholineHCID 67164—
Edukt2-(4-Fluoro-2-methoxy-phenyl)-5-(5-methyl-3-phenyl-isoxazol-4-yl)-[1,3,4]oxadiazoleHCID 16722645—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt4-{3-Methoxy-4-[5-(5-methyl-3-phenyl-isoxazol-4-yl)-[1,3,4]oxadiazol-2-yl]-phenyl}-thiomorpholineHCID 1672264666,2%

Reaktionsbedingungen

Temperatur170 °C

Reaktionsschritte

To a solution of 2-(4-fluoro-2-methoxy-phenyl)-5-(5-methyl-3-phenyl-isoxazol-4-yl)-[1,3,4]oxadiazole (200 mg, 0.57 mmol) in DMSO (2 mL) was added thiomorpholine (0.29 mL, 2.85 mmol) and the reaction mixture was stirred for 5 h at 170° C. After cooling to ambient temperature it was extracted with water (20 mL) and ethyl acetate (20 mL). The aqueous layer was extracted with ethyl acetate (20 mL) and the combined organic layers were washed with brine (half-saturated, 20 mL) and aqueous sodium carbonate (saturated, 20 mL). Drying over sodium sulfate and purification by chromatography (SiO2, heptane:ethyl acetate:dichloromethane=70:10:20 to 40:40:20) afforded the title compound (164 mg, 66%) as an off-white solid. MS: m/e=435.3 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07541372B2
Quelldatensatzuspto-grants-2009_06
ORD IDord-53ac82823dd8475c9115fad6ecff1ec1
Quellennotizuspto-grants-2009_06