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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 656868Erstellt: 25. Oktober 2026

Water → 7-Fluoro-1-(2-propen-1-yl)-1,5-naphthyridin-2(1H)-one

https://huagongshe.com/reaction/656868

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktAllyl iodideHCID 11166—
EduktSodium hydrideHCID 24758—
Edukt7-Fluoro-1,5-naphthyridin-2(1H)-oneHCID 46900801—
LösungsmittelDimethylformamideHCID 6228—
Produkt7-Fluoro-1-(2-propen-1-yl)-1,5-naphthyridin-2(1H)-oneHCID 5857946763%

Reaktionsschritte

7-Fluoro-1,5-naphthyridin-2(1H)-one (2.152 g, 13.122 mmol) was suspended in dry DMF (40 ml) under argon at 0° C., and the stirred suspension was treated with sodium hydride (1.155 g of a 60% w:w dispersion in oil, 2.2 eq.) added in portions. The suspension was allowed to warm to rt. After stirring for 30 mins at rt, the mixture was treated with allyl iodide (2.67 ml, 2.2 eq) and then stirred for a further 30 min before addition of water (100 ml). The mixture was then extracted with DCM (3×200 ml). The organic extracts were combined, dried over anhydrous magnesium sulphate, filtered and evaporated to give a residue which was purified by column chromatography on silica with a 0-10% methanol in DCM gradient to give the desired product as a light brown solid (1.683 g, 63%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08071592B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-99fd1e59768d4e9d81031f9de5e50b74
Quellennotizuspto-grants-2011_12