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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2194518Generated: November 1, 2026

Water → 1-Benzyl-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylic acid

https://huagongshe.com/reaction/2194518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 1-benzyl-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylateHCID 67010119—
Solvent1,4-DioxaneHCID 31275—
Product1-Benzyl-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylic acidHCID 6700961497%

Reaction Conditions

Temperature50 °C

Reaction Steps

1.95 g (6.3 mmol) of ethyl 1-benzyl-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylate was dissolved in 1,4-dioxane (30 mL), and 1.31 g (9.5 mmol) of potassium carbonate and 60 mL of water were added to this solution at room temperature. The resulting mixture was stirred for 3 hours at 50° C. The solvent of the reaction mixture was distilled off under reduced pressure, and the residue was dissolved in water. Concentrated hydrochloric acid was added to make the solution acidic, and the mixture was extracted with chloroform. The organic phase was dried, filtered, and concentrated, and thus 1.71 g (yield: 97%) of the title compound was obtained as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08334236B2
Source datasetuspto-grants-2012_12
ORD IDord-3a78a15bb8e94ae5b574259b0ad4ee14
Source noteuspto-grants-2012_12