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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 217365Erstellt: 23. Oktober 2026

Sodium hydride → 4-hydroxy-1-phenyl-3-(4-trifluoromethoxyphenylacetyl)-1,8-naphthyridin-2(1H)-one

https://huagongshe.com/de/reaction/217365

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
EduktSodium BicarbonateHCID 516892—
Edukt4-Hydroxy-1-phenyl-1,8-naphthyridin-2(1H)-oneHCID 54686473—
Edukt4-(Trifluoromethoxy)phenylacetyl chlorideHCID 57430096—
EduktHCID 178418361HCID 178418361—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-hydroxy-1-phenyl-3-(4-trifluoromethoxyphenylacetyl)-1,8-naphthyridin-2(1H)-oneHCID 6894540723%

Reaktionsschritte

In accordance with a process described in JP-61-246183A, 4-hydroxy-1-phenyl-1,8-naphthyridin-2(1H)-one was synthesized. To a suspension of the synthesized compound (893 mg, 3.7 mmol) in DMF (16 mL) was added sodium hydride (purity of about 60%, 360 mg, 9.0 mmol, 2.4 eq.), and the mixture was stirred until no more hydrogen was generated. Then, 4-trifluoromethoxyphenylacetyl chloride (1.2 eq.) was added thereto, and the mixture was stirred at a room temperature for 3 hours. To the mixture was added water and further added a saturated sodium hydrogencarbonate solution, and the resulting mixture was subjected to extraction with dichloromethane. The extract was dried over anhydrous magnesium sulfate, and the solvent was distilled off from the extract. The resulting residue was purified by a flash column chromatography to give 4-hydroxy-1-phenyl-3-(4-trifluoromethoxyphenylacetyl)-1,8-naphthyridin-2(1H)-one (383 mg, yield 23%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08193356B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-232611ede40e4b2daeab917ef1811aab
Quellennotizuspto-grants-2012_06