2,3-dimethyl-N-(1,2,3,4-tetrahydronaphthalen-1-yl)-1H-pyrrolo[2,3-c]pyridine-7-amine

• 分子结构分类: 有机化合物 - 苯类化合物 - 四氢化萘
• 英文名称: 2,3-dimethyl-N-(1,2,3,4-tetrahydronaphthalen-1-yl)-1H-pyrrolo[2,3-c]pyridine-7-amine
• 英文别名: 2,3-dimethyl-N-(1,2,3,4-tetrahydronaphthalen-1-yl)-1H-pyrrolo[2,3-c]pyridin-7-amine
• 化学式: C₁₉H₂₁N₃
• 分子量: 291.396
• InChiKey: BQILPXJDRYSAFV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  22
• 可旋转键数：
  2
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.32
• 拓扑面积：
  40.7
• 氢给体数：
  2
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  2-氯-3-硝基吡啶 以 四氢呋喃 为溶剂， 反应 18.5h， 生成 2,3-dimethyl-N-(1,2,3,4-tetrahydronaphthalen-1-yl)-1H-pyrrolo[2,3-c]pyridine-7-amine
  参考文献：
  名称：

  Molecular Modeling, Design, Synthesis, and Biological Activity of 1<i>H</i>-Pyrrolo[2,3-<i>c</i>]pyridine-7-amine Derivatives as Potassium-Competitive Acid Blockers

  摘要：

  一系列1H-吡咯并[2,3-c]吡啶-7-胺衍生物被设计和合成，基于我们的对接模型作为钾竞争性酸拮抗剂（P-CABs）。这些衍生物的分子模型让我们在1位引入取代基，以获取两个亲脂性位点和极性残基。我们鉴定了表现出优异体外和体内抑制活性的强效P-CABs。这些结果表明1H-吡咯并[2,3-c]吡啶-7-胺衍生物是有前景的P-CABs的铅化合物。

  DOI：

  10.1248/cpb.c13-00878

文献信息

• Pyrrolo [2,3-C] Pyridine Compound, Process for Producing the Same, and Use
  申请人：Hasuoka Atsushi

  公开号：US20070293532A1

  公开（公告）日：2007-12-20

  Provision of a compound having a superior proton pump action, which shows an antiulcer activity and the like after conversion to an in vivo proton pump inhibitor, a production method thereof and use thereof. A pyrrolo[2,3-c]pyridine compound represented by the formula: wherein each symbol is as defined in the specification.

  提供一种具有卓越质子泵作用的化合物，经转化为体内质子泵抑制剂后，表现出抗溃疡活性等，其生产方法和用途。一种由以下式表示的吡咯并[2,3-c]吡啶化合物：其中每个符号如规范中所定义。
• PYRROLOÝ2,3-c¨PYRIDINE COMPOUND, PROCESS FOR PRODUCING THE SAME, AND USE
  申请人：Takeda Pharmaceutical Company Limited

  公开号：EP1787991A1

  公开（公告）日：2007-05-23

  Provision of a compound having a superior proton pump action, which shows an antiulcer activity and the like after conversion to an in vivo proton pump inhibitor, a production method thereof and use thereof. A pyrrolo[2,3-c]pyridine compound represented by the formula: wherein each symbol is as defined in the specification.

  提供一种具有优异质子泵作用的化合物，该化合物在转化为体内质子泵抑制剂后显示出抗溃疡活性等作用，及其生产方法和用途。 一种由式表示的吡咯并[2,3-c]吡啶化合物： 其中各符号如说明书中所定义。
• PYRROLO[2,3-c]PYRIDINE COMPOUND, PROCESS FOR PRODUCING THE SAME, AND USE
  申请人：Takeda Pharmaceutical Company Limited

  公开号：EP1787991B2

  公开（公告）日：2020-06-24
• PYRROLO [2,3-c] PYRIDINE COMPOUND, PROCESS FOR PRODUCING THE SAME, AND USE
  申请人：Takeda Pharmaceutical Company Limited

  公开号：US20180148446A1

  公开（公告）日：2018-05-31

  Provision of a compound having a superior proton pump action, which shows an antiulcer activity and the like after conversion to an in vivo proton pump inhibitor, a production method thereof and use thereof. A pyrrolo[2,3-c]pyridine compound represented by the formula: wherein each symbol is as defined in the specification.
• Molecular Modeling, Design, Synthesis, and Biological Activity of 1&lt;i&gt;H&lt;/i&gt;-Pyrrolo[2,3-&lt;i&gt;c&lt;/i&gt;]pyridine-7-amine Derivatives as Potassium-Competitive Acid Blockers
  作者：Yasuyoshi Arikawa、Atsushi Hasuoka、Keizo Hirase、Nobuhiro Inatomi、Fumihiko Sato、Yasunobu Hori、Terufumi Takagi、Naoki Tarui、Makiko Kawamoto、Masahiro Kajino

  DOI：10.1248/cpb.c13-00878

  日期：——

  A series of 1H-pyrrolo[2,3-c]pyridine-7-amine derivatives were designed and synthesized based on our docking model as potassium-competitive acid blockers (P-CABs). Molecular modeling of these derivatives led us to introduce a substituent at the 1-position to access two lipophilic sites and polar residues. We identified potent P-CABs that exhibit excellent inhibitory activity in vitro and in vivo. These results indicate that the 1H-pyrrolo[2,3-c]pyridine-7-amine derivatives are promising lead compounds as P-CABs.

  一系列1H-吡咯并[2,3-c]吡啶-7-胺衍生物被设计和合成，基于我们的对接模型作为钾竞争性酸拮抗剂（P-CABs）。这些衍生物的分子模型让我们在1位引入取代基，以获取两个亲脂性位点和极性残基。我们鉴定了表现出优异体外和体内抑制活性的强效P-CABs。这些结果表明1H-吡咯并[2,3-c]吡啶-7-胺衍生物是有前景的P-CABs的铅化合物。