Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | (Chloromethyl)cyclopropane | HCID 80013 | — |
| Reactant | 8-Fluorociprofloxacin | HCID 122848 | — |
| Reactant | 1,3-Diethyl 2-(2,3,4,5-tetrafluorobenzoyl)propanedioate | HCID 13564973 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 13365560 | HCID 13365560 | — |
Reaction Steps
A mixture of 3 5 g (0.01 mol) of 1-cyclopropyl-6,8-difluoro-7-(piperazin-1-yl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid, 2.1 g of triethylamine, 1.8 g of cyclopropylmethyl chloride and 3.3 g of potassium iodide is heated to 80° C. for 6 hours. Thereafter, the mixture is evaporated down in vacuo, 30 ml of water are added, the mixture is adjusted to pH 5 and the precipitate is filtered off under suction, washed with water and methanol and recrystallised from glycol monomethyl ether. 1.8 g of 1-cyclopropyl-7-(4-cyclopropylmethylpiperazin-1-yl)-6,8-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid having a decomposition temperature of 246°-248° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04952695 |
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| Source dataset | uspto-grants-1990_08 |
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| ORD ID | ord-d1c79b1491354fb49495cd68ee634fa2 |
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| Source note | uspto-grants-1990_08 |
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