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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 656867Erstellt: 24. Oktober 2026

Sodium Bicarbonate → 7-Fluoro-2-methoxy-1,5-naphthyridine

https://huagongshe.com/de/reaction/656867

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium BicarbonateHCID 516892—
Edukt8-Bromo-7-fluoro-2-methoxy-1,5-naphthyridineHCID 45480320—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
Produkt7-Fluoro-2-methoxy-1,5-naphthyridineHCID 4690080287%

Reaktionsschritte

8-Bromo-7-fluoro-2-(methoxy)-1,5-naphthyridine (for a synthesis see WO2004058144, Example 53(g)) (5.040 g, 19.61 mmol) was stirred in MeOH (200 ml) with sodium hydrogen carbonate (3.29 g, 39.22 mmol) and 10% palladium on carbon (2.5 g), and the resulting suspension was hydrogenated at 1 atmosphere of hydrogen pressure under for 4 h. The mixture was filtered with suction through celite and the solids were washed with MeOH (500 ml). The combined filtrate plus washings were concentrated to about 50 ml under reduced pressure and then treated with water (200 ml) and DCM (300 ml). The aqueous phase was separated and extracted twice more with DCM (300 ml). The combined organic phases were separated, dried over anhydrous magnesium sulphate, filtered and evaporated to give the desired compound as an off-white solid (3.044 g, 87%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08071592B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-0da16db5eb034e5b957f54a901bcd029
Quellennotizuspto-grants-2011_12