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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2088985Erstellt: 25. Oktober 2026

Hydrochloric Acid → 5-Fluoro-1-[(6-fluoro-2-naphthyl)methyl]-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

https://huagongshe.com/reaction/2088985

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktLithium HydroxideHCID 3939—
EduktPotassium IodideHCID 4875—
EduktPotassium CarbonateHCID 11430—
Edukt2-(Bromomethyl)-6-fluoronaphthaleneHCID 594633—
EduktEthyl 5-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylateHCID 58398097—
LösungsmittelDimethylformamideHCID 6228—
Produkt5-Fluoro-1-[(6-fluoro-2-naphthyl)methyl]-4-oxo-1,4-dihydroquinoline-3-carboxylic acidHCID 46187671—

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

To a mixture of ethyl 5-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate (0.050 g, 0.21 mmol), potassium carbonate (0.088 g, 0.64 mmol) and potassium iodide (3 mg, 0.02 mmol) was added the above 2-(bromomethyl)-6-fluoronaphthalene in 1 mL of DMF. The reaction was stirred overnight at 40° C. and 1 mL of a saturated aqueous lithium hydroxide solution was then added to the reaction. After stirring for 30 min, the solution was acidified with 4 N HCl and the product was extracted three times with EtOAc. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The crude material was purified by reverse phase HPLC to provide the 5-fluoro-1-[(6-fluoro-2-naphthyl)methyl]-4-oxo-1,4-dihydroquinoline-3-carboxylic acid which gave a mass ion (ES+) of 366 for M+H+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08436016B2
Quelldatensatzuspto-grants-2013_05
ORD IDord-7bed42ae01484949851f3b1a1c04cc91
Quellennotizuspto-grants-2013_05