Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | Levofloxacin q-acid | HCID 688333 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | Levofloxacin | HCID 149096 | 76.2% |
Reaction Steps
5 g (17.79 mmole) of (S)-(−)-9,10-difluoro-3-methyl-7-oxo-2,3-dihydro-7H-pyrido [1,2,3-de][1,4]benzoxazine-6-carboxylic acid was put in suspension in 6.8 mL (0.06 mole) of N-methyl piperazine. The reaction mixture was heated to reflux for 40 minutes until completion of the reaction. The mixture was then cooled to 80° C. IPA (10 mL) and n-heptane (10 mL) were added at this temperature. The solid was filtrated under vacuum and rinsed with n-heptane. The mother liquor also gave a precipitate after addition of n-heptane. Both precipitates were filtrated under vacuum and dried overnight to yield 4.9 g (76%) levofloxacin.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07629458B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-2704d4c9cba740c9913ea4ad96eac64c |
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| Source note | uspto-grants-2009_12 |
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