1-pyridin-3-ylmethyl-1H-pyrazol-4-carboxylic acid | 1153373-34-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 1-pyridin-3-ylmethyl-1H-pyrazol-4-carboxylic acid
• 英文别名: 1-(Pyridin-3-ylmethyl)-1H-pyrazole-4-carboxylic acid；1-(pyridin-3-ylmethyl)pyrazole-4-carboxylic acid
• CAS: 1153373-34-2
• 化学式: C₁₀H₉N₃O₂
• 分子量: 203.2
• InChiKey: WCMWZVWZYCRAIW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.3
• 重原子数：
  15
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.1
• 拓扑面积：
  68
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  5-氯-4-氟-3-硝基-1H-吡咯并[2,3-B]吡啶 、 1-pyridin-3-ylmethyl-1H-pyrazol-4-carboxylic acid 在 三乙胺 、 N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate 作用下， 以 N,N-二甲基甲酰胺 、 正丁醇 为溶剂， 反应 26.0h， 生成 1-pyridin-4-ylmethyl-1H-pyrazol-4-carboxylic acid [4-((R)-3-aminopiperidin-1-yl)-5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl]amide
  参考文献：
  名称：

  [EN] 1H-PYRROLO[2,3-B] PYRIDINE DERIVATIVES AND THEIR USE AS KINASE INHIBITORS
  [FR] DÉRIVÉS DE 1H-PYRROLO[2,3-B]PYRIDINE ET LEUR UTILISATION COMME INHIBITEURS DE KINASES

  摘要：

  本发明涉及式(I)化合物的化合物及其治疗用途：(I) 其中Z、Y和R1的定义如权利要求中所述。

  公开号：

  WO2013114113A1

文献信息

• 1H-PYRROLO[2,3-B] PYRIDINE DERIVATIVES AND THEIR USE AS KINASE INHIBITORS
  申请人：Vernalis (R&D) Limited

  公开号：US20150011533A1

  公开（公告）日：2015-01-08

  The inventions relates to compounds of (I) and therapeutic uses thereof: (I) The terms Z, Y, and R 1 are as defined in the claims.

  这项发明涉及化合物(I)及其治疗用途：(I) 术语Z、Y和R1的定义如索赔中所述。
• Methods of Synthesizing Substituted Purine Compounds
  申请人：EPIZYME, INC.

  公开号：US20150011495A1

  公开（公告）日：2015-01-08

  The present invention provides an efficient process for the synthesis of (2R,3R,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-((((1r,3S)-3-(2-(5-(tert-butyl)-1H-benzo[d]imidazol-2-yl)ethyl)cyclobutyl)(isopropyl)amino)methyl)tetrahydrofuran-3,4-diol and hydrates thereof and methods for treating disorders in which DOT1-mediated protein methylation plays a part, such as cancer and neurological disorders, by administering these compounds and pharmaceutical compositions to subjects in need thereof. The present invention also provides novel crystalline forms of (2R,3R,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-((((1r,3S)-3-(2-(5-(tert-butyl)-1H-benzo[d]imidazol-2-yl)ethyl)cyclobutyl)(isopropyl)amino)methyl)tetrahydrofuran-3,4-diol and hydrates thereof (Form A, Form B, and Form C), characterized by a unique X-ray diffraction pattern and Differential Scanning Calorimetry profile, as well as a unique crystalline structure.

  本发明提供了一种有效的合成过程，用于合成(2R,3R,4S,5R)-2-(6-氨基-9H-嘌呤-9-基)-5-((((1r,3S)-3-(2-(5-(叔丁基)-1H-苯并[d]咪唑-2-基)乙基)环丁基)(异丙基)氨基)甲基)四氢呋喃-3,4-二醇及其水合物，并通过向需要治疗DOT1介导的蛋白质甲基化在内的疾病的受试者投与这些化合物和制药组合物来治疗这些疾病，例如癌症和神经系统疾病。本发明还提供了(2R,3R,4S,5R)-2-(6-氨基-9H-嘌呤-9-基)-5-((((1r,3S)-3-(2-(5-(叔丁基)-1H-苯并[d]咪唑-2-基)乙基)环丁基)(异丙基)氨基)甲基)四氢呋喃-3,4-二醇及其水合物的新型晶体形式(Form A、Form B和Form C)，其具有独特的X射线衍射图案和差示扫描量热分析曲线，以及独特的晶体结构。
• 1H-pyrrolo[2,3-B] pyridine derivatives and their use as kinase inhibitors
  申请人：VERNALIS (R&D) LIMITED

  公开号：US10000481B2

  公开（公告）日：2018-06-19

  The inventions relates to compounds of (I) and therapeutic uses thereof: (I) The terms Z, Y, and R1 are as defined in the claims.

  本发明涉及 (I) 的化合物及其治疗用途： (I) 术语 Z、Y 和 R1 如权利要求中所定义。
• 1H-pyrrolo [2,3-b] pyridine derivatives and their use as kinase inhibitors
  申请人：Vernalis (R&D) Limited

  公开号：US10889582B2

  公开（公告）日：2021-01-12

  The inventions relates to compounds of (I) and therapeutic uses thereof: (I) The terms Z, Y, and R1 are as defined in the claims.

  本发明涉及 (I) 的化合物及其治疗用途： (I) 术语 Z、Y 和 R1 如权利要求中所定义。
• Methods of synthesizing substituted purine compounds
  申请人：Epizyme, Inc.

  公开号：US10968247B2

  公开（公告）日：2021-04-06

  The present invention provides an efficient process for the synthesis of (2R,3R,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-((((1r,3S)-3-(2-(5-(tert-butyl)-1H-benzo[d]imidazol-2-yl)ethyl)cyclobutyl)(isopropyl)amino)methyl)tetrahydrofuran-3,4-diol and hydrates thereof and methods for treating disorders in which DOT1-mediated protein methylation plays a part, such as cancer and neurological disorders, by administering these compounds and pharmaceutical compositions to subjects in need thereof. The present invention also provides novel crystalline forms of (2R,3R,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-((((1r,3S)-3-(2-(5-(tert-butyl)-1H-benzo[d]imidazol-2-yl)ethyl)cyclobutyl)(isopropyl)amino)methyl)tetrahydrofuran-3,4-diol and hydrates thereof (Form A, Form B, and Form C), characterized by a unique X-ray diffraction pattern and Differential Scanning Calorimetry profile, as well as a unique crystalline structure.

  本发明提供了一种用于合成(2R,3R,4S,5R)-2-(6-氨基-9H-嘌呤-9-基)-5-((((1r,3S)-3-(2-(5-(叔丁基)-1H-苯并[d]咪唑-2-基)乙基)环丁基)(异丙基)氨基)甲基)四氢呋喃-3、4-二醇及其水合物，以及通过向有需要的受试者施用这些化合物和药物组合物来治疗由 DOT1 介导的蛋白质甲基化起作用的疾病（如癌症和神经系统疾病）的方法。本发明还提供了新型结晶形式的(2R,3R,4S,5R)-2-(6-氨基-9H-嘌呤-9-基)-5-((((1r,3S)-3-(2-(5-(叔丁基)-1H-苯并[d]咪唑-2-基)乙基)环丁基)(异丙基)氨基)甲基)四氢呋喃-3、4-二醇及其水合物（形式 A、形式 B 和形式 C），具有独特的 X 射线衍射图样和差示扫描量热曲线，以及独特的晶体结构。