Chinese Journal of Magnetic Resonance ›› 2012, Vol. 29 ›› Issue (1): 119-127.

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Pure and Mixed Enantiomer of Moxifloxacin Hydrochloride Studied by NMR Spectroscopy

 YANG Qiu-Qing1*, LIU Bo-Qian2, HAN Kang1   

  1. 1. Experimental Center, Hebei Normal University, Shijiazhuang 050016, China;
    2. Department of Chemistry, China Agricultural University, Beijing 100094, China
  • Received:2010-11-30 Revised:2011-05-04 Online:2012-03-05 Published:2012-03-05

Abstract:

The structures of pure and mixed enantiomer of moxifloxacin hydrochloride were elucidated by NMR. The chemical shift of the spectral peaks were assigned using 1H and 13C NMR, COSY, HSQC, HMBC and 2D NOESY techniques, as well as 19F-13C coupled splitting. It was found that 19F-13C coupling exists not only in the sixmembered ring, but also in the fivemembered heterocyclic ring, and that 4JFC in the five-membered heterocyclic ring is larger than 3JFC and 4JFC in the sixmembered ring. The spectral characteristics of the pure and mixed enantiomer of moxifloxacin hydrochloride were summarized. A method was proposed to differentiate the pure and mixed enantiomer of moxifloxacin hydrochloride.

Key words: NMR,  moxifloxacin hydrochloride, enantiomer, identification method

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