4-(methylsulfonyl)-N-(pyridin-2-yl)benzamide | 940745-02-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 4-(methylsulfonyl)-N-(pyridin-2-yl)benzamide
• 英文别名: 4-methylsulfonyl-N-pyridin-2-ylbenzamide
• CAS: 940745-02-8
• 化学式: C₁₃H₁₂N₂O₃S
• 分子量: 276.316
• InChiKey: QLSSUKSFFOVWAV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.5
• 重原子数：
  19
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  84.5
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  在 四羟基二硼 作用下， 反应 0.17h， 以140 mg的产率得到4-(methylsulfonyl)-N-(pyridin-2-yl)benzamide
  参考文献：
  名称：

  Rapid and Selective in situ Reduction of Pyridine-N-oxides with Tetra­hydroxydiboron

  摘要：

  Pyridine-N-oxides are often used as reactive precursors in the syntheses of substituted pyridines. Isolation and subsequent reduction of the associated pyridine-N-oxide intermediates can be challenging. We have discovered that tetrahydroxydiboron functions as a mild, versatile, and remarkably selective reducing agent for pyridine-N-oxides and may be used in an in situ fashion, thus obviating the isolation of N-oxide-containing intermediates

  DOI：

  10.1055/s-0033-1340010

文献信息

• A One-Pot Copper Catalyzed Biomimetic Route to <i>N</i>-Heterocyclic Amides from Methyl Ketones via Oxidative C–C Bond Cleavage
  作者：Parthasarathi Subramanian、Satrajit Indu、Krishna P. Kaliappan

  DOI：10.1021/ol5031266

  日期：2014.12.5

  A direct one-pot Cu-catalyzed biomimetic oxidation of methyl ketones to pharmaceutically important N-heterocyclic amides is reported. The scope of the method is broad, scalable, and mild, and the reaction is tolerant with various acid, base sensitive functionalities with multiple heteroatoms and aryl halides. The extensive mechanistic studies suggest that this reaction follows the Luciferin-Luciferase-like

  据报道，直接一锅铜催化的甲基酮仿生氧化成药学上重要的N-杂环酰胺。该方法的范围广泛，可扩展且温和，并且该反应可耐受具有多种杂原子和芳基卤化物的各种酸，碱敏感性官能团。广泛的机理研究表明，该反应遵循荧光素-荧光素酶样途径。
• Rapid and Selective in situ Reduction of Pyridine-N-oxides with Tetra­hydroxydiboron
  作者：Allyn Londregan、David Piotrowski、Jun Xiao

  DOI：10.1055/s-0033-1340010

  日期：——

  Pyridine-N-oxides are often used as reactive precursors in the syntheses of substituted pyridines. Isolation and subsequent reduction of the associated pyridine-N-oxide intermediates can be challenging. We have discovered that tetrahydroxydiboron functions as a mild, versatile, and remarkably selective reducing agent for pyridine-N-oxides and may be used in an in situ fashion, thus obviating the isolation of N-oxide-containing intermediates