HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743660Generated: October 30, 2026
3-Ethoxycarbonyl-7,8,9-trifluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine → 7,8,9-Trifluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid
https://huagongshe.com/reaction/743660
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Ethoxycarbonyl-7,8,9-trifluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine | HCID 19423688 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 7,8,9-Trifluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid | HCID 19423678 | 93% |
Reaction Steps
A suspension of 0.88 g of 3-ethoxycarbonyl-7,8,9-trifluoro-1-methyl-4-oxo-1,4-dihydrobenzo-[b][1,8]naphthyridine in a mixture of 10 cm3 of 17.5% aqueous hydrochloric acid solution and 10 cm3 of acetic acid is heated with stirring to a temperature in the region of 100° C. for 3 hours. After cooling to approximately 20° C., the product is drained and washed with 3 times 10 cm3 of water. 0.75 g of 7,8,9-trifluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3carboxylic acid is obtained in the form of a pale yellow solid, which decomposes at 352° C. and which is used without further purification for the subsequent steps.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05556861 |
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| Source dataset | uspto-grants-1996_09 |
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| ORD ID | ord-6f56098e7f87448cb26483e4e2d65b9c |
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| Source note | uspto-grants-1996_09 |
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