(1S,2R)-5'-methoxy-2-(3-((E)-2-(6-(4-methylpiperazin-1-yl)pyridin-3-yl)vinyl)-1H-indazol-6-yl)spiro[cyclopropane-1,3'-indolin]-2'-one | 1247002-26-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪烷类
• 英文名称: (1S,2R)-5'-methoxy-2-(3-((E)-2-(6-(4-methylpiperazin-1-yl)pyridin-3-yl)vinyl)-1H-indazol-6-yl)spiro[cyclopropane-1,3'-indolin]-2'-one
• 英文别名: (2'R,3S)-5-methoxy-2'-[3-[(E)-2-[6-(4-methylpiperazin-1-yl)pyridin-3-yl]ethenyl]-1H-indazol-6-yl]spiro[1H-indole-3,1'-cyclopropane]-2-one
• CAS: 1247002-26-1
• 化学式: C₃₀H₃₀N₆O₂
• 分子量: 506.607
• InChiKey: XMHCFCMVNKTYOH-XFGYKPTDSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  38
• 可旋转键数：
  5
• 环数：
  7.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  86.4
• 氢给体数：
  2
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  5-methoxy-3-[[3-[(E)-2-[6-(4-methylpiperazin-1-yl)pyridin-3-yl]ethenyl]-1H-indazol-6-yl]methylidene]-1H-indol-2-one 、 三乙胺 、 methylene chloride diethyl ether 以 chloroform methanol 为溶剂， 以gave the minor diastereomer title compound as a pale yellow solid (18 mg, 4%)的产率得到(1S,2R)-5'-methoxy-2-(3-((E)-2-(6-(4-methylpiperazin-1-yl)pyridin-3-yl)vinyl)-1H-indazol-6-yl)spiro[cyclopropane-1,3'-indolin]-2'-one
  参考文献：
  名称：

  Kinase inhibitors and method of treating cancer with same

  摘要：

  本发明涉及一种由以下结构式表示的化合物及其药学上可接受的盐：该结构式表示的化合物是激酶抑制剂，因此在此披露用于治疗癌症。该结构式中各变量的定义在此提供。

  公开号：

  US08481525B2

文献信息

• [EN] KINASE INHIBITORS AND METHOD OF TREATING CANCER WITH SAME<br/>[FR] INHIBITEURS DE KINASES ET PROCÉDÉ DE TRAITEMENT DU CANCER AVEC CEUX-CI
  申请人：UNIV HEALTH NETWORK

  公开号：WO2010115279A1

  公开（公告）日：2010-10-14

  The invention is directed to a compound represented by the following structural formula and pharmaceutically acceptable salts thereof: Compounds represented by this structural formula are kinase inhibitors and are therefore disclosed herein for the treatment of cancer. Definitions for the variables in the structural formula are provided herein.

  这项发明涉及一种由以下结构式表示的化合物及其药用可接受的盐：由该结构式表示的化合物是激酶抑制剂，因此在此披露用于治疗癌症。结构式中变量的定义在此提供。
• KINASE INHIBITORS AND METHOD OF TREATING CANCER
  申请人：Sampson Peter B.

  公开号：US20110263598A1

  公开（公告）日：2011-10-27

  The invention is directed to a compound represented by the following structural formula and pharmaceutically acceptable salts thereof: Compounds represented by this structural formula are kinase inhibitors and are therefore disclosed herein for the treatment of cancer. Definitions for the variables in the structural formula are provided herein.

  本发明涉及以下结构式和其药学上可接受的盐所代表的化合物：该结构式所代表的化合物是激酶抑制剂，因此本发明公开了用于治疗癌症的该类化合物。该结构式中变量的定义在此提供。
• KINASE INHIBITORS AND METHOD OF TREATING CANCER WITH SAME
  申请人：Sampson Peter B.

  公开号：US20120149686A1

  公开（公告）日：2012-06-14

  The invention is directed to a compound represented by the following structural formula and pharmaceutically acceptable salts thereof: Compounds represented by this structural formula are kinase inhibitors and are therefore disclosed herein for the treatment of cancer. Definitions for the variables in the structural formula are provided herein.

  本发明涉及以下结构式及其药物可接受的盐所表示的化合物：该结构式所表示的化合物是激酶抑制剂，因此在此披露用于治疗癌症。本结构式中变量的定义在此提供。
• Kinase inhibitors and method of treating cancer
  申请人：University Health Network

  公开号：US08263596B2

  公开（公告）日：2012-09-11

  The invention is directed to a compound represented by the following structural formula and pharmaceutically acceptable salts thereof: Compounds represented by this structural formula are kinase inhibitors and are therefore disclosed herein for the treatment of cancer. Definitions for the variables in the structural formula are provided herein.

  该发明涉及以下结构式及其药学上可接受的盐所表示的化合物：此结构式所表示的化合物是激酶抑制剂，因此在此透露用于治疗癌症。此处提供了结构式中变量的定义。
• SYNTHESIS OF CHIRAL 2-(1H-INDAZOL-6-YL)-SPIRO[CYCLOPROPANE-1,3'-INDOLIN]-2'-ONES
  申请人：University Health Network

  公开号：US20150133677A1

  公开（公告）日：2015-05-14

  The present invention is directed to novel synthetic methods for preparing a spiro cyclopropyl indolinone compound represented by Structural Formula (A): or its pharmaceutically acceptable salt thereof. Also included are synthetic intermediates described herein.

  本发明涉及一种新的合成方法，用于制备由结构式(A)所表示的螺环丙基吲哚酮化合物或其药学上可接受的盐。本发明还包括在此处描述的合成中间体。