Imidazo[1,2-a]Pyridine Compounds As Receptor Tyrosine Kinase Inhibitors
    5.
    发明申请
    Imidazo[1,2-a]Pyridine Compounds As Receptor Tyrosine Kinase Inhibitors 审中-公开
    咪唑并[1,2-a]吡啶化合物作为受体酪氨酸激酶抑制剂

    公开(公告)号:US20110184013A1

    公开(公告)日:2011-07-28

    申请号:US13122095

    申请日:2009-09-30

    CPC分类号: C07D487/04 C07D471/04

    摘要: Compounds of Formula I and II: I II having the chemical names cis-6-fluoro-8-(3-fluoropiperidin-4-yloxy)-2-(7-(2-methoxyethoxy)imidazo[1,2-a]pyridin-3-yl)quinoline and 6-fluoro-8-(trans-3-fluoropiperidin-4-yloxy)-2-(7-(2-methoxyethoxy)imidazo[1,2-a]pyridin-3-yl)quinoline, respectively, and enantiomers and pharmaceutically acceptable salts thereof, are receptor tyrosine inhibitors useful in the treatment of diseases mediated by class 3 and class 5 receptor tyrosine kinases. The compounds of this invention have also been found to be inhibitors of Pim-1.

    摘要翻译: 具有化学名称的顺式-6-氟-8-(3-氟哌啶-4-基氧基)-2-(7-(2-甲氧基乙氧基)咪唑并[1,2-a]吡啶的式I和II化合物: 吡啶-3-基)喹啉和6-氟-8-(反式-3-氟哌啶-4-基氧基)-2-(7-(2-甲氧基乙氧基)咪唑并[1,2-a]吡啶-3-基)喹啉 和对映异构体及其药学上可接受的盐是可用于治疗由3类和5类受体酪氨酸激酶介导的疾病的受体酪氨酸抑制剂。 本发明化合物也被发现是Pim-1的抑制剂。