| Identification | Back Directory | [Name]
(3S)-10-Fluoro-2,3-dihydro-3-Methyl-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic Acid | [CAS]
117620-84-5 | [Synonyms]
Levofloxacin-10 Levofloacin Impurity 8 Levofloacin Impurity J Levofloxacin Impurity J Levofloxacin Impurity 2 Levofloxacin Impurity 43 (S)-10-fluoro-3-methyl-7-oxo (S)-10-fluoro-3-methyl-7-oxo-2,3-dihydro-7H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylic acid (3S)-10-Fluoro-2,3-dihydro-3-Methyl-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic Acid 7H-Pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic acid, 10-fluoro-2,3-dihydro-3-methyl-7-oxo-, (3S)- Levofloxacin (3S)-10-Fluoro-2,3-dihydro-3-methyl-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic Acid Levofloxacin impurity 12/(3S)-10-Fluoro-2,3-dihydro-3-methyl-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic Acid | [Molecular Formula]
C13H10FNO4 | [MDL Number]
MFCD31579563 | [MOL File]
117620-84-5.mol | [Molecular Weight]
263.221 |
| Hazard Information | Back Directory | [Uses]
(3S)-10-Fluoro-2,3-dihydro-3-methyl-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic Acid is an intermediate in the synthesis of Levofloxacin (L360000), an antibiotic used against gram-negative organisms. | [Synthesis]
(3S)-10-Fluoro-2,3-dihydro-3-Methyl-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic Acid is synthesized by reacting ethyl (S)-10-fluoro-3-methyl-7-oxo- 2,3-dihydro-7H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylate with Potassium hydroxide in Tetrahydrofuran by reflux.1
![(3S)-10-Fluoro-2,3-dihydro-3-Methyl-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic Acid (3S)-10-Fluoro-2,3-dihydro-3-Methyl-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic Acid](/NewsImg/2026-01-07/6390337865069381401125048.png) | [References]
[1] JEFFREY L. GRAY. Synthesis and Biological Testing of Non-Fluorinated Analogues of Levofloxacin.[J]. ChemInform, 2003, 34 42. DOI:10.1002/chin.200342162.
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