(S)-4-(methylsulfonyl)-2-(((7-(4-(piperidin-4-yl)phenyl)pyridino[3,4-b]pyrazine-5-yl)oxy)methyl)morpholine | 1613256-72-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 英文名称: (S)-4-(methylsulfonyl)-2-(((7-(4-(piperidin-4-yl)phenyl)pyridino[3,4-b]pyrazine-5-yl)oxy)methyl)morpholine
• 英文别名: (S)-4-(methylsulfonyl)-2-(((7-(4-(piperidin-4-yl)phenyl)pyrido[3,4-b]pyrazin-5-yl)oxy)methyl)morpholine；5-[[(2S)-4-(methylsulfonyl)-2-morpholinyl]methoxy]-7-[4-(4-piperidinyl)phenyl]-pyrido[3,4-b]pyrazine；(2S)-4-methylsulfonyl-2-[[7-(4-piperidin-4-ylphenyl)pyrido[3,4-b]pyrazin-5-yl]oxymethyl]morpholine
• CAS: 1613256-72-6
• 化学式: C₂₄H₂₉N₅O₄S
• 分子量: 483.591
• InChiKey: IWWPDVITWKPCFP-FQEVSTJZSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.2
• 重原子数：
  34
• 可旋转键数：
  6
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.46
• 拓扑面积：
  115
• 氢给体数：
  1
• 氢受体数：
  9

反应信息

• 作为反应物：
  描述：

  (S)-4-(methylsulfonyl)-2-(((7-(4-(piperidin-4-yl)phenyl)pyridino[3,4-b]pyrazine-5-yl)oxy)methyl)morpholine 、 2-溴乙醇 在 TEA 作用下， 以 二氯甲烷 为溶剂， 反应 96.0h， 生成 (S)-2-(4-(4-(5-((4-(methylsulfonyl)morpholin-2-yl)methoxy)pyrido[3,4-b]pyrazin-7-yl)phenyl)piperidin-1-yl)ethanol
  参考文献：
  名称：

  [EN] SUBSTITUTED PYRIDOPYRAZINES AS SYK INHIBITORS
  [FR] PYRIDOPYRAZINES SUBSTITUÉES UTILISÉES EN TANT QU'INHIBITEURS DE SYK

  摘要：

  本发明涉及式(I)的吡啶吡嗪化合物，以及其药物组合物和使用方法，其中R1、R2、R3、L、m、p和W如规范中所定义。

  公开号：

  WO2014086032A1

文献信息

• Substituted Pyridopyrazines as Syk Inhibitors
  申请人：HUTCHISON MEDIPHARMA LIMITED

  公开号：US20160002221A1

  公开（公告）日：2016-01-07

  The present invention relates to pyridopyrazine compounds of formula (I), pharmaceutical compositions thereof and methods of use therefore, wherein R 1 , R 2 , R 3 , L, m, p and W are as defined in the specification.

  本发明涉及式(I)的吡啶吡嗪化合物、其制药组合物和使用方法，其中R1、R2、R3、L、m、p和W如规范中所定义。
• SUBSTITUTED PYRIDOPYRAZINES AS SYK INHIBITORS
  申请人：HUTCHISON MEDIPHARMA LIMITED

  公开号：US20150307491A1

  公开（公告）日：2015-10-29

  The present invention relates to pyridopyrazine compounds of formula (I), pharmaceutical compositions thereof and methods of use therefore, wherein R 1 , R 2 , R 3 , L, m, p and W are as defined in the specification.

  本发明涉及式(I)的吡啶吡嗪化合物，其制药组合物和使用方法，其中R1、R2、R3、L、m、p和W如规范中所定义。
• SYK INHIBITORS
  申请人：Gilead Sciences, Inc.

  公开号：US20180071303A1

  公开（公告）日：2018-03-15

  The application provides methods reducing the side effects of chemotherapy and radiotherapy, including, hematopoietic toxicity, anemia, myelosuppression, pancytopenia, thrombocytopenia, neutropenia, lymphopenia, leukopenia, stomatitis and alopecia. The application provides a method for increasing the number of, neutrophil counts and platelet counts in a patient in need thereof, comprising administering an effective of an inhibitor of spleen tyrosine kinase (SYKi). The present application provides methods for treating myelosuppresive disorders by the administration of a SYKi. In certain embodiments, the myelosuppression is induced by the administration of one or more myelosuppressive agents, for example, anti-cancer drugs. The present application provides methods for treating AML/ALL in a patient with 11q23/MLL abnormalities comprising the step of administering an effective amount of a SYKi to said patient.