Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 18523277 | HCID 18523277 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 18523349 | HCID 18523349 | 67.6% |
Reaction Steps
0.86 cm3 of 1 N aqueous potassium hydroxide was added, with stirring, to a suspension of 0.39 g of ethyl 7-fluoro-8-[4-hydroxy-4-(3-trifluoromethylphenyl)piperidin-1-yl]-4-methyl-1-oxo-1,4-dihydrobenzo[f][1,7]naphthyridine-2-carboxylate in 4.5 cm3 of ethanol and 3.5 cm3 of water. The mixture was heated at about 80° C. for 3 hours, and then after cooling, 20 cm3 of water were added and then the medium was acidified with 0.05 cm3 of acetic acid. The precipitate was filtered off, dewatered, washed with 2 cm3 of isopropanol and then washed twice with 2 cm3 of diisopropyl ether and dried. 0.25 g of 7-fluoro-8-[4-hydroxy-4-(3-trifluoromethylphenyl)piperidin-1-yl]-4-methyl-1-oxo-1,4-dihydrobenzo[f][1,7]naphthyridine-2-carboxylic acid was obtained in the form of a yellow solid, which melted above 260° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06566362B2 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-b4e30657ef3b4c7794d0e75396f67cae |
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| Source note | uspto-grants-2003_05 |
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