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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 513926Erstellt: 26. Oktober 2026

Benzyl Alcohol → 3-(Benzyloxy)-7-bromo-1,5-naphthyridine

https://huagongshe.com/reaction/513926

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl AlcoholHCID 244—
EduktSodium hydrideHCID 24758—
Edukt3,7-Dibromo-1,5-naphthyridineHCID 1236658—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-(Benzyloxy)-7-bromo-1,5-naphthyridineHCID 9041731036,7%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a solution of benzyl alcohol (2.25 g, 20.8 mmol) in DMF (25 mL) was added NaH (60% in mineral oil, 0.83 g, 20.8 mmol). The resulting mixture was heated to 60° C. for 10 minutes and was added to 3,7-dibromo-1,5-naphthyridine (Intermediate 3, 5.0 g, 17.4 mmol) in DMF (25.0 mL) at 100° C. The resulting mixture was stirred over night at 100° C., cooled, and concentrated under reduced pressure. Water (50 mL) was added and the aqueous layer was washed with DCM (3×50 mL). The organic layers were combined, dried over Na2SO4, filtered and concentrated under reduced pressure. Purification (FCC, SiO2, DCM/petroleum ether, 1:1) afforded the title compound as a white solid (2.0 g, 36.7%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09102674B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-344092db26ed41608b66559ff67c1940
Quellennotizuspto-grants-2015_08