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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 1-benzyl-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylate | HCID 67010119 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-Benzyl-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylic acid | HCID 67009614 | 97% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08334236B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-3a78a15bb8e94ae5b574259b0ad4ee14 |
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| Source note | uspto-grants-2012_12 |
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