发明授权
US07645738B2 18-membered nitrobenzyl- and aminobenzyl-substituted cyclohexadepsipeptides for controlling endoparasites and a process for their preparation 失效
用于控制内寄生虫的18元硝基苄基 - 和氨基苄基取代的环己缩肽及其制备方法

  • 专利标题: 18-membered nitrobenzyl- and aminobenzyl-substituted cyclohexadepsipeptides for controlling endoparasites and a process for their preparation
  • 专利标题(中): 用于控制内寄生虫的18元硝基苄基 - 和氨基苄基取代的环己缩肽及其制备方法
  • 申请号: US10582555
    申请日: 2004-12-07
  • 公开(公告)号: US07645738B2
    公开(公告)日: 2010-01-12
  • 发明人: Peter JeschkeAchim Harder
  • 申请人: Peter JeschkeAchim Harder
  • 申请人地址: DE
  • 专利权人: Bayer Animal Health GmbH
  • 当前专利权人: Bayer Animal Health GmbH
  • 当前专利权人地址: DE
  • 代理商 Jessica Monachello
  • 优先权: DE10359798 20031219
  • 国际申请: PCT/EP2004/013896 WO 20041207
  • 国际公布: WO2005/063277 WO 20050714
  • 主分类号: A61K38/00
  • IPC分类号: A61K38/00
18-membered nitrobenzyl- and aminobenzyl-substituted cyclohexadepsipeptides for controlling endoparasites and a process for their preparation
摘要:
The invention relates to cyclic depsipeptides, especially 18-membered cyclohexadepsipeptides of general formula (I) and the salts thereof, wherein R1 represents nitrobenzyl or R′R″N-benzyl—wherein R′ and R″ independently represent hydrogen, optionally substituted C1-C4-alkyl, formyl, C1-C4-alkoxy-C1-C4-alkyl, C1-C4-alkoxycarbonyl, or hydroxy-C1-C2-alkyl-sulfonyl-C1-C2-alkyl, or, together with the nitrogen atom to which they are bound, R′ and R″ form an optionally substituted monocyclic or polycyclic, optionally bridged and/or spirocyclic, saturated or unsaturated heterocycle containing between one and three other heteroatoms from the group of nitrogen, oxygen and sulphur, or R′ and R″ together form C3-C5-alkylene monocarbonyl or an optionally substituted diacyl radical of a C4-C6-dicarboxylic acid—and R2, R3 and R4 independently represent C1-C4-alkyl. The invention also relates to the optical isomers and racemates of said cyclic depsipeptides, to a method for the production thereof, and to the use of the same for controlling endoparasites.
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