HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084391Generated: November 2, 2026
Acetic Acid → 1,8-naphthyridine-3-carboxylic Acid
https://huagongshe.com/reaction/1084391
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 7,8,9-Trifluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid | HCID 19423678 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1,8-naphthyridine-3-carboxylic Acid | HCID 4738391 | — |
Reaction Steps
A suspension of 4 g of 7,8,9-trifluoro-1-methyl-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridine-3-carboxylic acid in 60 cm3 of dimethyl sulphoxide and 3 g of 1-methylpiperazine is heated at 80° C. for 1 hour and a half. After cooling to about 20° C., 150 cm3 of water are added. 18 cm3 of 10% acetic acid are added to the solution obtained. The precipitate formed is drained, washed with 3 times 50 cm3 of water and recrystallized from 50 cm3 of dimethylformamide. 4 g of 7,9-difluoro-1-methyl-8-(4-methyl-1-pip-erazinyl)-4-oxo-1,4-dihydrobenzo[b]1,8]naphthyridine-3-carboxylic acid are obtained in the form of a yellow solid melting at 316° C..
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05004745 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-1d9adb8e5949442181481b9b7b2da446 |
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| Source note | uspto-grants-1991_04 |
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