Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 276855Erstellt: 25. Oktober 2026

3-Bromoaniline → 4-(3-Bromo-phenylamino)-6-fluoro-[1,7]naphthyridine-3-carbonitrile

https://huagongshe.com/reaction/276855

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-BromoanilineHCID 11562—
Edukt4-Chloro-6-fluoro-1,7-naphthyridine-3-carbonitrileHCID 18548960—
LösungsmittelEthanolHCID 702—
Produkt4-(3-Bromo-phenylamino)-6-fluoro-[1,7]naphthyridine-3-carbonitrileHCID 1854897987%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To 1.9 g of 4-chloro-6-fluoro-[1.7]naphthyridine-3-carbonitrile in 30 mL of absolute ethanol was added 1.6 mL of 3-bromoaniline. After refluxing the reaction under an inert atmosphere for 8 hours, the reaction mixture was cooled to 0° C. and the product was filtered and washed with cold ethanol. Drying in vacuo yielded 2.7 g (87%) of 4-(3-bromo-phenylamino)-6-fluoro-[1.7]naphthyridine-3-carbonitrile as an off-white solid: melting point 185-195° C.; mass spectrum (m/e): M+H 343.0, 345.1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06355636B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-da8df5cd0c6e46409fd2ba0f86b44905
Quellennotizuspto-grants-2002_03