Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 13960202 | HCID 13960202 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13960207 | HCID 13960207 | 81% |
Reaction Steps
3.87 g (0.01 mole) of 9-fluoro-5-methyl-8-(1-piperazinyl)-6,7-dihydro-1,7-dioxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid ethyl ester was suspended in 12 ml of ethanol, 50 ml of a 2N aqueous solution of sodium hydroxide was added thereto, and this mixture was stirred at 20°-25° C. for 2 hours to hydrolyze the starting material. The resulting reaction solution was adjusted to pH 4-5 by the addition of acetic acid under cooling with ice. The precipitate which separated out was collected by filtration and recrystallized from ethanol to obtain 2.91 g (81.0% yield) of 9-fluoro-5-methyl-8-(1-piperazinyl)-6,7-dihydro-1,7-dioxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid in the form of yellow crystals. These crystals had a melting point of 261°-263° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04720495 |
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| Source dataset | uspto-grants-1988_01 |
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| ORD ID | ord-9999158176464418b649efd409c54e31 |
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| Source note | uspto-grants-1988_01 |
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