Synthesis of 2-Methyl-2,5-diazabicyclo[2.2.1]heptane, Side Chain to Danofloxacin

Various syntheses of the side chain of the quinolone antibiotic danofloxacin are described. The realization that the N-methyl substitution on the side chain 2-methyl-2,5-diazabicyclo[2.2.1]heptane can reside on either nitrogen, due to the symmetry of the molecule, played a major role in the design o...

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Veröffentlicht in:Organic process research & development 2009-03, Vol.13 (2), p.336-340
1. Verfasser: Braish, Tamim F
Format: Artikel
Sprache:eng
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Zusammenfassung:Various syntheses of the side chain of the quinolone antibiotic danofloxacin are described. The realization that the N-methyl substitution on the side chain 2-methyl-2,5-diazabicyclo[2.2.1]heptane can reside on either nitrogen, due to the symmetry of the molecule, played a major role in the design of the commercial synthetic route.
ISSN:1083-6160
1520-586X
DOI:10.1021/op8002618