Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Heptane | HCID 8900 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | Levofloxacin q-acid | HCID 688333 | — |
| Solvent | 1-Methoxy-2-propanol | HCID 7900 | — |
| Product | Levofloxacin | HCID 149096 | 77.3% |
Reaction Steps
3 g (10.67 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 30 mL of PGME and 4.75 mL (43 mmole) of N-methyl piperazine. The reaction mixture was heated to reflux for 23 hours until completion of the reaction. During that time, the reaction mixture became soluble. The mixture was then cooled to 90° C. and n-Heptane (10 mL) was added at this temperature. The reaction mixture was then cooled to 0° C. and the precipitation occurred around 65° C. The reaction was left at 0° C. for 3 hours, filtrated under vacuum and dried overnight to obtain 2.98 g (77.3%) of 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-ac1b154497184dc0bfd8deb196e66413 |
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| Source note | uspto-grants-2009_12 |
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