This invention relates to certain novel pyrazine derivatives (Formula I) as SHP2 inhibitors which is shown as formula I, their synthesis and their use for treating a SHP2 mediated disorder. More particularly, this invention is directed to fused heterocyclic group derivatives useful as inhibitors of SHP2, methods for producing such compounds and methods for treating a SHP2-mediated disorder.
这项发明涉及某些新颖的
吡嗪衍
生物(
化学式I)作为SHP2
抑制剂,其
化学式如下,以及它们的合成以及用于治疗SHP2介导的疾病的用途。更具体地,这项发明涉及融合杂环基衍
生物,可用作SHP2的
抑制剂,生产这类化合物的方法以及治疗SHP2介导的疾病的方法。