HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413122Generated: November 2, 2026
Potassium Carbonate → HCID 20430478, compound
https://huagongshe.com/reaction/2413122
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Fluoroethyl p-Toluenesulfonate | HCID 256019 | — |
| Reactant | 882865-15-8 | HCID 13268404 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 20430478 | HCID 20430478 | 77.6% |
Reaction Steps
Ethyl 7-(4-acetyl-1-piperazinyl)-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylate (7.2 g) and anhydrous potassium carbonate (4.1 g) are added to dimethylformamide (60 ml). The mixture is heated at 50° C. for 30 minutes with stirring. 2-Fluoroethyl p-toluenesulfonate (6.5 g) is added to the mixture, and the mixture is heated at 70°-80° C. with stirring. After the reaction is completed, the insoluble substance is removed by filtration. The filtrate is concentrated to dryness under reduced pressure, and the precipitate is collected by filtration. The precipitate is recrystallized from acetone to give 6.3 g of ethyl 7-(4-acetyl-1-piperazinyl)-6-fluoro-1-(2-fluoroethyl)-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylate (m.p. 183°-185° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04496566 |
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| Source dataset | uspto-grants-1985_01 |
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| ORD ID | ord-669fcbc9544a4b6cb297616487e6302d |
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| Source note | uspto-grants-1985_01 |
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