1-phenyl-5-(4-nitrophenyl)-1H-tetrazole | 14213-27-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 1-phenyl-5-(4-nitrophenyl)-1H-tetrazole
• 英文别名: 5-(4-nitrophenyl)-1-phenyl-1H-tetrazole；5-(4-nitrophenyl)-1-phenyltetrazole；5-(4-nitro-phenyl)-1-phenyl-1H-tetrazole；5-(4-Nitro-phenyl)-1-phenyl-1H-tetrazol；1-Phenyl-5-(p-nitrophenyl)-tetrazol
• CAS: 14213-27-5
• 化学式: C₁₃H₉N₅O₂
• 分子量: 267.247
• InChiKey: IOLDWWUVEIYATK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  20
• 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：
  89.4
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  1-phenyl-5-(4-nitrophenyl)-1H-tetrazole 、 三氯苯 以34%的产率得到
  参考文献：
  名称：

  HOUGHTON, P. G.;PIPE, D. F.;REES, CH. W, J. CHEM. SOC. PERKIN TRANS., 1985, N 7, 1471-1479

  摘要：

  DOI：
• 作为产物：
  描述：

  对硝基苯甲腈 在 sodium azide 、 溶剂黄146 、 正丁醇 作用下， 生成 1-phenyl-5-(4-nitrophenyl)-1H-tetrazole
  参考文献：
  名称：

  Tetra- and Pentacyclic Benzimidazole Compounds as Analogs of Some Indole Alkaloids

  摘要：

  DOI：

  10.1021/jo01090a003

文献信息

• Efficient Synthesis of 1,5-Disubstituted Tetrazoles
  作者：Alan Katritzky、Chunming Cai、Nabin Meher

  DOI：10.1055/s-2007-966001

  日期：2007.4

  A general method for the synthesis of 1,5-disubstituted tetrazoles from imidoylbenzotriazoles that involves mild reaction conditions and short reaction times.

  一种由亚氨基苯并三唑合成 1,5-二取代四唑的通用方法，反应条件温和，反应时间短。
• Iron (III)‐porphyrin Complex FeTSPP as an efficient catalyst for synthesis of tetrazole derivatives <i>via</i> [2 + 3]cycloaddition reaction in aqueous medium
  作者：Mahmoud Abd El Aleem Ali Ali El‐Remaily、O.M. Elhady

  DOI：10.1002/aoc.4989

  日期：2019.8

  metal complex (5,10,15,20‐tetrakis‐(4‐sulfonatophenyl)‐porphyrin‐iron (III) chloride (FeTSPP) was new employed in an environmentally benign protocol as an efficient catalyst for a “click” chemistry approach for the synthesis of tetrazole and guanindinyltetrazole derivatives via [2 + 3] cycloaddition reaction of nitriles and azide derivatives in aqueous medium. The synthesized compounds were obtained in

  金属络合物（5,10,15,20-四（4-磺酰基苯基）-卟啉-氯化铁（FeTSPP）在环境友好的方案中被新用作一种有效的催化剂，用于“点击”化学方法。通过腈和叠氮化物衍生物在水性介质中的[2 + 3]环加成反应合成四唑和胍基四唑衍生物，得到的化合物收率高，反应时间短，催化剂可回收。
• Transition-metal-free multinitrogenation of amides by C–C bond cleavage: a new approach to tetrazoles
  作者：Lian-Hua Li、Zhi-Jie Niu、Ying-Xiu Li、Yong-Min Liang

  DOI：10.1039/c8cc06324a

  日期：——

  regioselective synthesis of 1,5-disubstituted tetrazoles has been developed. By means of electrophilic amide activation, and further C–C bond cleavage and rearrangement, a diverse set of functionalized 1,5-DST derivatives were selectively constructed under mild conditions. As showcased in the mechanisms, the chemoselectivity is easily switched by the selection of the starting materials in the reaction.

  开发了一种无金属的全新的一锅多酰胺酰胺，用于化学和区域选择性合成1,5-二取代的四唑。通过亲电酰胺的活化，以及进一步的C–C键裂解和重排，在温和条件下选择性地构建了多种功能化的1,5-DST衍生物。如机理所示，通过选择反应中的起始原料可以容易地切换化学选择性。
• Improved Schmidt Synthesis of 1,5-Disubstituted 1<i>H</i>-Tetrazoles from Ketones
  作者：Hitomi Suzuki、Young Seok Hwang、Chie Nakaya、Yoshihiro Matano

  DOI：10.1055/s-1993-26027

  日期：——

  On treatment with an excess of sodium azide in the presence of titanium(IV) chloride in boiling acetonitrile, both aliphatic and aromatic ketones are smoothly converted to 1,5-disubstituted 1H-tetrazoles in high yields.

  在沸腾的乙腈中，在氯化钛（IV）的存在下，用过量叠氮化钠进行处理，脂肪酮和芳香酮都能顺利转化为 1,5-二取代的 1H-四唑，产量很高。
• Synthesis of 1,5-Disubstituted Tetrazoles from Nitrones by Using Bis(p-nitrophenyl) Phosphorazidate in the Presence of 4-(Dimethylamino)pyridine
  作者：Masato Matsugi、Kotaro Ishihara、Takayuki Shioiri

  DOI：10.1055/a-1800-2011

  日期：2022.5

  A novel method has been developed for the synthesis of 1,5-disubstituted tetrazoles from nitrones by using bis(p-nitrophenyl) phosphorazidate in the presence of 4-(dimethylamino)pyridine. By this approach, various nitrones were converted into the corresponding tetrazoles. This method permits the preparation of 1,5-disubstituted tetrazoles without the need for toxic or explosive reagents.

  开发了一种在4-(二甲氨基)吡啶存在下使用叠氮化双(对硝基苯基)磷酸酯从硝酮合成1,5-二取代四唑的新方法。通过这种方法，各种硝酮转化为相应的四唑。该方法允许制备 1,5-二取代四唑，而不需要有毒或爆炸性试剂。