发明名称 Synthetic intermediate of oxazole compound and method for producing the same
摘要 An object of the present disclosure is to provide a method for producing an oxazole compound in a high yield. The object can be achieved by a compound represented by Formula (11): wherein R1 is a hydrogen atom or lower-alkyl group; R2 is a 1-piperidyl group substituted at the 4-position with a substituent selected from (A1a) a phenoxy group substituted on the phenyl moiety with one or more halogen-substituted lower-alkoxy groups, (A1b) a phenoxy-substituted lower-alkyl group substituted on the phenyl moiety with one or more halogen-substituted lower-alkyl groups, (A1c) a phenyl-substituted lower-alkoxy lower-alkyl group substituted on the phenyl moiety with halogen, (A1d) a phenyl-substituted lower-alkyl group substituted on the phenyl moiety with one or more halogen-substituted lower-alkoxy groups, (A1e) an amino group substituted with a phenyl group substituted with one or more halogen-substituted lower-alkoxy groups, and a lower-alkyl group, and (A1f) a phenyl-substituted lower-alkoxy group substituted on the phenyl moiety with one or more halogen-substituted lower-alkoxy groups; n is an integer from 1 to 6; and X3 is an organic sulfonyloxy group. In one embodiment the compound is (R)-1-[4-(2,3-epoxy-2-methylpropoxy)phenyl]-4-[4-(trifluoromethoxy)phenoxy]piperidine.
申请公布号 NZ601239(A) 申请公布日期 2014.10.31
申请号 NZ20110601239 申请日期 2011.01.28
申请人 OTSUKA PHARMACEUTICAL CO. LTD. 发明人 FUJITA NOBUHISA;YAMAMOTO AKIHIRO;SHINHAMA KOICHI;OGASAWARA SHIN;UTSUMI NAOTO;AKI SHINJI
分类号 C07D211/46;C07D405/12;C07D498/04 主分类号 C07D211/46
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