Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 235815Erstellt: 26. Oktober 2026

Ethanol → N-(7-methoxy-1,8-naphthyridin-2-yl)-2,6-difluorobenzamide

https://huagongshe.com/reaction/235815

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
Edukt2,6-Difluorobenzoic acidHCID 9796—
Edukt7-methoxy-1,8-Naphthyridin-2-amineHCID 21793027—
LösungsmittelWaterHCID 962—
ProduktN-(7-methoxy-1,8-naphthyridin-2-yl)-2,6-difluorobenzamideHCID 2021754040,4%

Reaktionsbedingungen

Temperatur4 °C

Reaktionsschritte

The procedure is similar to that described in Example 1, but starting with 2,6-difluorobenzoic acid (5.1 g), N,N'-carbonyldiimidazole (5.2 g) and 2-amino-7-methoxy-1,8-naphthyridine (4.4 g). The product produced by precipitation in water (4.5 g; m.p. 215°-217° C.) is dissolved in boiling ethanol (70 cc). After 1 hour's cooling at 4° C., the crystallised solid is separated by filtration, washed with ethanol (10 cc) and dried at 45° C. under reduced pressure (0.067 kPa). N-(7-methoxy-1,8-naphthyridin-2-yl)-2,6-difluorobenzamide (3.2 g) is produced, m.p. 219°-220° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04642308
Quelldatensatzuspto-grants-1987_02
ORD IDord-48b605eb739444d7ad11458a312f483c
Quellennotizuspto-grants-1987_02