Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 21290575 | HCID 21290575 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 20133480 | HCID 20133480 | 39.3% |
Reaction Steps
To a solution of 6,8-Difluoro-1-(4-hydroxyphenyl)-7-(1-piperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (4.18 g) in DMF (29 ml) is added a solution of methyl iodide (7.7 g) in DMF (20 ml). The mixture is heated in a stainless steel autoclave on an oil bath at 110°-120° C. for 5 hours. DMF is distilled off under reduced pressure, and to the residue is added 10% aqueous sodium hydroxide to regulate pH 13. The insoluble substance is filtered off, and the remaining mixture is regulated to pH 8 with acetic acid. The precipitated crystals are separated by filtration, washed with water, dried, and then recrystallized from DMF to give 6,8-difluoro-1-(4-hydroxyphenyl)-7-(4-methyl-1-piperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (1.7 g) as pale yellowish white crystals, m.p. >300° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04755513 |
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| Source dataset | uspto-grants-1988_07 |
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| ORD ID | ord-ba9b987122254ca5a2cf2ea2a60442ef |
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| Source note | uspto-grants-1988_07 |
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