N-methyl-N-(3-nitrobenzyl)nitrous amide | 98736-52-8

• 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: N-methyl-N-(3-nitrobenzyl)nitrous amide
• 英文别名: Benzenemethanamine, N-methyl-3-nitro-N-nitroso-；N-methyl-N-[(3-nitrophenyl)methyl]nitrous amide
• CAS: 98736-52-8
• 化学式: C₈H₉N₃O₃
• 分子量: 195.178
• InChiKey: CZHXKPIRJQBHPY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.2
• 重原子数：
  14
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  78.5
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  3-硝基溴苄 在 盐酸 、 sodium nitrite 作用下， 以 乙醇 、 水 、 溶剂黄146 为溶剂， 反应 6.0h， 生成 N-methyl-N-(3-nitrobenzyl)nitrous amide
  参考文献：
  名称：

  Quantitative structure-activity relationship of the mutagenicity of substituted N-nitroso-N-benzylmethylamines: possible implications for carcinogenicity

  摘要：

  The relative mutagenicities of substituted N-nitroso-N-benzylmethylamines have been reexamined from a quantitative structure-activity relationship point of view. Most of the compounds were mutagenic toward Salmonella typhimurium TA 1535 with Aroclor-induced male hamster liver S9 activation. The dose-response data were subjected to a multiple linear regression equation calculated in a stepwise manner, which found that the differences in mutagenicities could be explained primarily by differences in the three-bond path molecular connectivity index, with smaller contributions from sigma and pi. Moreover, a polynomial regression analysis showed that the maximum mutagenicity could be explained by an optimal amount of electron withdrawal by the substituent which would cause a weakening, or activation, of the methylene C-H bond. The possible relevance of these observations to carcinogenesis is discussed.

  DOI：

  10.1021/jm00151a006

文献信息

• The Use of Potassium/Sodium Nitrite as a Nitrosating Agent in the Electrooxidative <i>N</i> ‐Nitrosation of Secondary Amines
  作者：Ying Wang、Shiqi You、Mengyao Ruan、Feiyi Wang、Chao Ma、Cuifen Lu、Guichun Yang、Zuxing Chen、Meng Gao

  DOI：10.1002/ejoc.202100363

  日期：2021.6.14

  An efficient and environmentally electrooxidative N-nitrosation of secondary amines using potassium/sodium nitrite as nitrosating agents has been developed. This strategy break through the innate combination of sodium nitrite and a strong acid. The reaction is compatible with the late-stage modification of pharmaceutical compounds and could be conducted in gram scale with high reaction efficiency.

  已经开发了一种使用亚硝酸钾/亚硝酸钠作为亚硝化剂的仲胺的有效和环境电氧化N-亚硝化。这种策略突破了亚硝酸钠和强酸的先天组合。该反应与药物化合物的后期修饰相容，可以以克级规模进行，反应效率高。
• Quantitative structure-activity relationship of the mutagenicity of substituted N-nitroso-N-benzylmethylamines: possible implications for carcinogenicity
  作者：George M. Singer、A. W. Andrews、Shu Mei Guo

  DOI：10.1021/jm00151a006

  日期：1986.1

  The relative mutagenicities of substituted N-nitroso-N-benzylmethylamines have been reexamined from a quantitative structure-activity relationship point of view. Most of the compounds were mutagenic toward Salmonella typhimurium TA 1535 with Aroclor-induced male hamster liver S9 activation. The dose-response data were subjected to a multiple linear regression equation calculated in a stepwise manner, which found that the differences in mutagenicities could be explained primarily by differences in the three-bond path molecular connectivity index, with smaller contributions from sigma and pi. Moreover, a polynomial regression analysis showed that the maximum mutagenicity could be explained by an optimal amount of electron withdrawal by the substituent which would cause a weakening, or activation, of the methylene C-H bond. The possible relevance of these observations to carcinogenesis is discussed.