HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223154Generated: October 30, 2026
Potassium Carbonate → 1,8-Naphthyridine-3-carboxylic acid, 1,4-dihydro-6-chloro-1-ethenyl-4-oxo-7-(1-piperazinyl)-
https://huagongshe.com/reaction/223154
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 20519047 | HCID 20519047 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Azane;hydrate | HCID 12896473 | — |
| Product | 1,8-Naphthyridine-3-carboxylic acid, 1,4-dihydro-6-chloro-1-ethenyl-4-oxo-7-(1-piperazinyl)- | HCID 3058380 | 51.4% |
Reaction Steps
To a solution of potassium carbonate (1.52 g) in ethanol (40 ml) which was kept at 90°-95° C., was added ethyl 7-(4-acetyl-1-piperazinyl)-6-chloro-1-(2-chloroethyl)-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylate (4.0 g) and the mixture was heated to reflux for 1.5 hours. After the mixture was cooled, the resulting potassium 7-(4-acetyl-1-piperazinyl)-6-chloro-1,4-dihydro-4-oxo-1-vinyl-1,8-naphthyridine-3-carboxylate was collected, and dissolved in 30 ml of water and 20 ml of 1 N sodium hydroxide. The mixture was heated to reflux for 2 hours and acidified with acetic acid, and then adjusted to pH 8 with ammonia solution to give a precipitate. The precipitate was dissolved in diluted hydrochloric acid and adjusted again to pH 8 with ammonia water to give 1.56 g of 6-chloro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-1-vinyl-1,8-naphthyridine-3-carboxylic acid, m.p. 272°-274° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04352803 |
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| Source dataset | uspto-grants-1982_10 |
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| ORD ID | ord-772d87dec6c04a19bae6deeebe166cf2 |
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| Source note | uspto-grants-1982_10 |
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