发明名称
摘要 <p>Intermediates of formula (Ia) or (Ib) are provided: wherein R 11 and R 21 represents a hydrogen atom or an amino-protecting group, and R 16 represents an amino-protecting group, useful for the production of quinolone synthetic antibacterial agent of formula (I) wherein substituents R 6 and R 7 taken together with the carbon atoms to which they are bonded form a cyclic structure which may contain an oxygen atom as a ring constituent atom, the cyclic structure forming a 5-4, 5-5, or 5-6 fused bicyclic pyrrolidinyl substituent, the substituent being bonded to a quinolone mother skeleton Q containing a pyridobenzoxazine structure:</p>
申请公布号 JP2010515663(A) 申请公布日期 2010.05.13
申请号 JP20090527641 申请日期 2007.12.28
申请人 发明人
分类号 C07D401/04;A61K31/4709;A61K31/5383;A61P31/04;C07D401/14;C07D491/048;C07D491/052;C07D498/06;C07D519/00 主分类号 C07D401/04
代理机构 代理人
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