3-(5-苯基四唑-2-基)丙腈 | 124313-46-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 中文名称: 3-(5-苯基四唑-2-基)丙腈
• 英文名称: 3-(5-phenyltetrazol-2-yl)propionitrile
• 英文别名: 2-(2-cyanoethyl)-5-phenyltetrazole；3-(5-Phenyl-tetrazol-2-yl)-propionitrile；3-(5-phenyltetrazol-2-yl)propanenitrile
• CAS: 124313-46-8
• 化学式: C₁₀H₉N₅
• mdl: MFCD00844647
• 分子量: 199.215
• InChiKey: UOMGIELJQUNAPC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  15
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  67.4
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  3-(5-苯基四唑-2-基)丙腈 在 sodium azide 、 二乙胺盐酸盐 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 以49%的产率得到1-(5-phenyltetrazol-2-yl)-2-(tetrazol-5-yl)ethane
  参考文献：
  名称：

  Synthesis of Polynuclear Nonfused Azoles

  摘要：

  Polynuclear blocks consisting of nonfused heterocycles of the azole series, connected through methylene bridges, were synthesized by successive addition of azole units via cycloaddition of organic azides to the triple bond of N-(2-propynyl)azoles, as well as via reaction of azide ion at the cyano group of cyanomethylazoles. Initial N-(2-propynyl)azoles were prepared by reaction of 2-propynyl bromide with 1,2,3-triazoles, benzotriazole, and tetrazoles; cyanomethylazoles were obtained by alkylation of azoles with chloroacetonitrile. An analogous scheme was used to add heterocyclic units to 2-phenyl-1,2,3-triazole-4-carbonitrile. In this case, the first two heterocyclic units are linked through the ring carbon atom.

  DOI：

  10.1023/b:rujo.0000019746.10504.f3
• 作为产物：
  描述：

  5-苯基四氮唑 、 丙烯腈 在 三乙胺 作用下， 以 异丙醇 为溶剂， 反应 3.0h， 以48.5%的产率得到3-(5-苯基四唑-2-基)丙腈
  参考文献：
  名称：

  Dziklinska, H.; Dzierzgowski, S.; Jezewski, A., Bulletin des Societes Chimiques Belges, 1989, vol. 98, # 4, p. 277 - 284

  摘要：

  DOI：

文献信息

• Selective and Potent Monoamine Oxidase Type B Inhibitors: 2-Substituted 5-Aryltetrazoles Derivatives
  作者：Luc Lebreton、Olivier Curet、Salah Gueddari、Fathi Mazouz、Suzanne Bernard、Claude Burstein、Rene Milcent

  DOI：10.1021/jm00024a006

  日期：1995.11

  investigated in vitro for their abilities to inhibit selectively rat brain monoamine oxidase (MAO) B over MAO A. Most of them were MAO B inhibitors and those bearing a substituted 4-(arylmethoxy)phenyl group in the position 5 of the tetrazole ring had IC50 values between 8 microM for 18d and 2 nM for 16a (30 nM for lazabemide) with a selectivity toward MAO B of 37,000 for 16a. The reversibility of their

  合成了二十个新的2-（氰基烷基）四唑（15和16）和二十个新的2-（羟烷基）四唑（17和18），并在体外研究了其抑制MAO A选择性抑制大鼠脑单胺氧化酶（MAO）B的能力。它们中的大多数是MAO B抑制剂，在四唑环5位带有取代的4-（芳甲氧基）苯基的那些，其IC50值在18d时为8 microM，在16a时为2 nM（拉扎贝胺为30 nM），具有选择性。朝向37,000的MAO B（16a）。通过体外透析试验证明了其抑制活性的可逆性。5- [4-（苯基甲氧基）苯基] -2-（2-氰乙基）四唑（16a）及其衍生物16h和5- [4-（苯基甲氧基）苯基] -2-（2-羟乙基）四唑（18a）发现其衍生物18h是有效的，体外选择性和竞争性MAO B抑制剂。Tetrazole 16a可以被认为是迄今为止已知的最具活性和选择性的竞争性MAO B抑制剂之一。选择该化合物用于离体实验，并显示为强效和可逆的MAO
• ——
  作者：K. A. Esikov、V. Yu. Zubarev、E. V. Bezklubnaya、A. A. Malin、V. A. Ostrovskii

  DOI：10.1023/a:1020933900167

  日期：——
• DZIKLINSKA, H.;DZIERZGOWSKI, S.;JEZEWSKI, A.;PIENKIEWICZ, J., BULL. SOC. CHIM. BELG., 98,(1989) N, C. 277-283
  作者：DZIKLINSKA, H.、DZIERZGOWSKI, S.、JEZEWSKI, A.、PIENKIEWICZ, J.

  DOI：——

  日期：——
• Synthesis of Polynuclear Nonfused Azoles
  作者：O. N. Verkhozina、V. N. Kizhnyaev、L. I. Vereshchagin、A. V. Rokhin、A. I. Smirnov

  DOI：10.1023/b:rujo.0000019746.10504.f3

  日期：2003.12

  Polynuclear blocks consisting of nonfused heterocycles of the azole series, connected through methylene bridges, were synthesized by successive addition of azole units via cycloaddition of organic azides to the triple bond of N-(2-propynyl)azoles, as well as via reaction of azide ion at the cyano group of cyanomethylazoles. Initial N-(2-propynyl)azoles were prepared by reaction of 2-propynyl bromide with 1,2,3-triazoles, benzotriazole, and tetrazoles; cyanomethylazoles were obtained by alkylation of azoles with chloroacetonitrile. An analogous scheme was used to add heterocyclic units to 2-phenyl-1,2,3-triazole-4-carbonitrile. In this case, the first two heterocyclic units are linked through the ring carbon atom.
• Dziklinska, H.; Dzierzgowski, S.; Jezewski, A., Bulletin des Societes Chimiques Belges, 1989, vol. 98, # 4, p. 277 - 284
  作者：Dziklinska, H.、Dzierzgowski, S.、Jezewski, A.、Plenkiewicz, J.

  DOI：——

  日期：——

表征谱图