3-amino-6-phenylthieno[2,3-b]pyridine-2-carboxylic acid | 340816-70-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: 3-amino-6-phenylthieno[2,3-b]pyridine-2-carboxylic acid
• CAS: 340816-70-8
• 化学式: C₁₄H₁₀N₂O₂S
• 分子量: 270.312
• InChiKey: TXLOBKPVDXIDCL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  19
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  104
• 氢给体数：
  2
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  3-amino-6-phenylthieno[2,3-b]pyridine-2-carboxylic acid 在 溶剂黄146 作用下， 反应 7.0h， 生成 2-methyl-3,7-diphenylpyrido[3',2':4,5]thieno[3,2-d]pyrimidin-4(3H)-one
  参考文献：
  名称：

  Synthesis and characterization of 6-(aryl)-2-thioxo-1,2-dihydropyridine-3-carbonitriles

  摘要：

  In the present study, 3-aminothieno[2,3-b] pyridines, pyrido[3',2' :4,5] thieno[3,2-d]pyrimidinones, and pyrido[3',2' : 4,5]thieno[3,2-d][1,3]oxazinones were prepared via the reaction of 6-(aryl)-2-thioxo-1,2-dihydropyridine-3-carbonitriles with active-halogen-containing compounds. The structures of all the newly synthesized heterocyclic compounds were established by considering elemental analysis and spectral data.[GRAPHICS].

  DOI：

  10.1080/17415993.2012.661734
• 作为产物：
  描述：

  1-phenyl-3-dimethylaminoprop-2-enone 在 三乙烯二胺 、 potassium hydroxide 、 lithium hydroxide 作用下， 以 四氢呋喃 、 甲醇 、 乙醇 、 水 、 N,N-二甲基甲酰胺 为溶剂， 生成 3-amino-6-phenylthieno[2,3-b]pyridine-2-carboxylic acid
  参考文献：
  名称：

  Discovery and structure–activity relationships study of novel thieno[2,3-b]pyridine analogues as hepatitis C virus inhibitors

  摘要：

  Current treatment for hepatitis C is barely satisfactory, there is an urgent need to develop novel agents for combating hepatitis C virus infection. This study discovered a new class of thieno[ 2,3-b] pyridine derivatives as HCV inhibitors. First, a hit compound characterized by a thienopyridine core was identified in a cell-based screening of our privileged small molecule library. And then, structure activity relationship study of the hit compound led to the discovery of several potent compounds without obvious cytotoxicity in vitro (12c, EC50 = 3.3 mu M, SI > 30.3, 12b, EC50 = 3.5 mu M, SI > 28.6, 10l, EC50 = 3.9 mu M, SI > 25.6, 12o, EC50 = 4.5 mu M, SI > 22.2, respectively). Although the mechanism of them had not been clearly elucidated, our preliminary optimization of this class of compounds had provided us a start point to develop new anti-HCV agents. (C) 2014 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2014.01.075

文献信息

• Identification of thienopyridine carboxamides as selective binders of HIV-1 <i>trans</i> Activation Response (TAR) and Rev Response Element (RRE) RNAs
  作者：Xue-Dong Li、Li Liu、Liang Cheng

  DOI：10.1039/c8ob02753f

  日期：——

  The synthesis, biochemical and structural studies of two novel thienopyridine carboxamide derivatives that selectively recognize HIV-1 TAR and RRE RNAs were described.

  合成、生化和结构研究了两类新型噻吩并吡啶甲酰胺衍生物，它们可以选择性地识别HIV-1 TAR和RRE RNAs。