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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 31469Erstellt: 25. Oktober 2026

Sodium ethoxide → 5-Fluoro-6-methyl-1,1'-biphenyl-3-carboxamide

https://huagongshe.com/reaction/31469

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium ethoxideHCID 2723922—
Edukt4'-[5-(chloromethyl)-1,3,4-oxadiazol-2-yl]-N-cyclopropyl-5-fluoro-6-methyl-1,1'-biphenyl-3-carboxamideHCID 69314917—
LösungsmittelEthanolHCID 702—
Produkt5-Fluoro-6-methyl-1,1'-biphenyl-3-carboxamideHCID 86604697—

Reaktionsschritte

Freshly prepared sodium ethoxide in ethanol (0.2M, 0.8 ml) was added to a solution of (4′-[5-(chloromethyl)-1,3,4-oxadiazol-2-yl]-N-cyclopropyl-5-fluoro-6-methyl-1,1′-biphenyl-3-carboxamide (Intermediate 34) (50 mg) in ethanol (1 ml) and the reaction stirred at room temperature for 18 hours. The reaction was reduced to dryness under vacuum and the residue partitioned between ethyl acetate and water. The organic phase dried (magnesium sulphate) and reduced to dryness under vacuum. The residue was purified by HPLC to give N-cyclopropyl-4′-[5-ethoxymethyl)-1,3,4-oxadiazol-2-yl]-5-fluoro-6-methyl-1,1′-biphenyl-3-carboxamide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07425555B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-01140e8d3fa24085a648bb18a36c93a3
Quellennotizuspto-grants-2008_09