Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 53888048 | HCID 53888048 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13960227 | HCID 13960227 | 73.2% |
Reaction Steps
2.08 g (0.005 mole) of 9-fluoro-5-methyl-8-(3,4-dimethyl-1-piperazinyl)-6,7-dihydro-1,7-dioxo-1H,5H-benzo-[ij]quinolizine-2-carboxylic acid ethyl ester was suspended in 5 ml of ethanol, 30 ml of a 2N aqueous solution of sodium hydroxide was added thereto, and this mixture was stirred at 15°-20° C. for 3 hours to hydrolyze the starting material. The resulting reaction solution was adjusted to pH 1 by the addition of concentrated hydrochloric acid under cooling with ice. The crystals which separated out were collected by filtration and successively washed with small volumes of water and ethanol. These crystals were recrystallized from water to obtain 1.62 g (73.2% yield) of 9-fluoro-5-methyl-8-(3,4-dimethyl-1-piperazinyl)-6,7-dihydro-1,7-dioxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid hydrochloride monohydrate in the form of yellow crystals. These crystals had a melting point of 226°-228° 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-fb818a6a426f4f09af895bf79a8bc594 |
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| Source note | uspto-grants-1988_01 |
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