3-Cyano-5-[(2-methylpropan-2-yl)oxycarbonyl]-1,4,6,7-tetrahydropyrrolo[3,2-c]pyridine-2-carboxylic acid | 1393847-09-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯并吡啶类
• 英文名称: 3-Cyano-5-[(2-methylpropan-2-yl)oxycarbonyl]-1,4,6,7-tetrahydropyrrolo[3,2-c]pyridine-2-carboxylic acid
• 英文别名: 3-cyano-5-[(2-methylpropan-2-yl)oxycarbonyl]-1,4,6,7-tetrahydropyrrolo[3,2-c]pyridine-2-carboxylic acid
• CAS: 1393847-09-0
• 化学式: C₁₄H₁₇N₃O₄
• 分子量: 291.307
• InChiKey: WTCKYCJRASKBHC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1
• 重原子数：
  21
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  106
• 氢给体数：
  2
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  sodium;1-cyano-3,3-diethoxyprop-1-en-2-olate 在 sodium chlorite 、 ammonium acetate 作用下， 以 乙醇 、 水 为溶剂， 反应 1.5h， 生成 3-Cyano-5-[(2-methylpropan-2-yl)oxycarbonyl]-1,4,6,7-tetrahydropyrrolo[3,2-c]pyridine-2-carboxylic acid
  参考文献：
  名称：

  Synthesis of 2,3-dicarbonylated pyrroles and furans via the three-component Hantzsch reaction

  摘要：

  Pyrroles containing a 2,3-dicarbonyl substitution pattern are synthesized in one step via a three-component Hantzsch procedure. The normally difficult-to-access substrates are readily obtained in short reaction times and in moderate to good yields, giving pharmaceutically attractive products containing multiple handles for further elaboration. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2012.04.022

文献信息

• Synthesis of 2,3-dicarbonylated pyrroles and furans via the three-component Hantzsch reaction
  作者：Thomas A. Moss、Thorsten Nowak

  DOI：10.1016/j.tetlet.2012.04.022

  日期：2012.6

  Pyrroles containing a 2,3-dicarbonyl substitution pattern are synthesized in one step via a three-component Hantzsch procedure. The normally difficult-to-access substrates are readily obtained in short reaction times and in moderate to good yields, giving pharmaceutically attractive products containing multiple handles for further elaboration. (C) 2012 Elsevier Ltd. All rights reserved.