Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Levofloxacin | HCID 149096 | — |
| Solvent | Water | HCID 962 | — |
| Product | Levofloxacin monohydrate | HCID 178438 | 181.4% |
Reaction Steps
5 g of crude levofloxacine crystals were added to 25 ml of water and formulated into a slurry. The obtained slurry was stirred at 25° C. for 20 hours. The crystals were collected by filtering, washed with 5 ml of water and dried at room temperature under reduced pressure. When a constant weight was achieved, 4.76 g of (S)-9-fluoro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-2,3-dihydro-7H-pyrido[1,2,3-de][1,4]-benzoxazine-6-carboxylic acid monohydrate was obtained. The analysis on these crystals by the powdery method of X-ray diffraction proved that the product was the monohydrate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05545737 |
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| Source dataset | uspto-grants-1996_08 |
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| ORD ID | ord-61d73df7b7164803abc0defec7506bb4 |
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| Source note | uspto-grants-1996_08 |
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