Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Levofloxacin | HCID 149096 | — |
| Solvent | Toluene trichloromethane | HCID 22987606 | — |
| Product | Levofloxacin Hydrate | HCID 3033924 | — |
Reaction Steps
Levofloxacin crude is dissolved in mixture of toluene-chloroform at temperature of 20° C. to 40° C. by mixing for about 30 min to 2 hrs. Removed the insolubles by filtration, treated the clear solution with carbon and distilled off the toluene-chloroform at temperature below 60° C. Isopropanol is added to the mass, temperature is raised to 65° C. to 90° C., known quantity of water preferably to make-up the water content about 12% to about 20%, more selectively about 15% is added to the reaction mass at temperature of 60° C. to 90° C., mixed for about 5 min to 30 min, cooled to 15° C. to about 35° C., mixed for about 30 min to 4 hrs, isolated and dried at temperature of 45° C. to 85° C. preferably at 60° C. to 70° C. gives the levofloxacin hemihydrate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07678903B2 |
|---|
| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-e159a1dc868547618726dc0b2899ed0e |
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| Source note | uspto-grants-2010_03 |
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