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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 349950Erstellt: 24. Oktober 2026

Dimethylformamide → Methyl 5-(5-methyl-2-phenyl-4-oxazolyl)methoxy-3-pyridinecarboxylate

https://huagongshe.com/de/reaction/349950

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktPotassium CarbonateHCID 11430—
EduktMethyl 5-hydroxypyridine-3-carboxylateHCID 354317—
Edukt4-(Chloromethyl)-5-methyl-2-phenyl-1,3-oxazoleHCID 9794289—
LösungsmittelWaterHCID 962—
ProduktMethyl 5-(5-methyl-2-phenyl-4-oxazolyl)methoxy-3-pyridinecarboxylateHCID 1786134159,6%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of methyl 5-hydroxy-3-pyridinecarboxylate (9.84 g), 4-chloromethyl-5-methyl-2-phenyloxazole (13.40 g), potassium carbonate (8.90 g) and N,N-dimethylformamide (100 ml) was stirred at 80° C. overnight. The reaction mixture was poured into water, which was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride solution, dried (MgSO4), and concentrated. The residue was subjected to silica gel column chromatography to obtain methyl 5-(5-methyl-2-phenyl-4-oxazolylmethoxy)-3-pyridinecarboxylate (12.42 g, yield 59%) as pale yellow crystals from the fraction eluted with ethyl acetate-hexane (1:2, volume ratio). This was recrystallized from ethyl acetate-hexane. Melting point: 119–120° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07179823B1
Quelldatensatzuspto-grants-2007_02
ORD IDord-4b6f402531fb40e68251360b27c030a2
Quellennotizuspto-grants-2007_02