3,4,5,6-Tetrahydro-2H-[1,4']bipyridinyl-2'-carbonitrile | 127680-88-0

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: 3,4,5,6-Tetrahydro-2H-[1,4']bipyridinyl-2'-carbonitrile
• 英文别名: 4-(Piperidin-1-yl)pyridine-2-carbonitrile；4-piperidin-1-ylpyridine-2-carbonitrile
• CAS: 127680-88-0
• 化学式: C₁₁H₁₃N₃
• 分子量: 187.244
• InChiKey: KUNVHZKYKVYNCK-UHFFFAOYSA-N

物化性质

• 熔点：
  78-79 °C
• 沸点：
  363.6±27.0 °C(Predicted)
• 密度：
  1.15±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  14
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.45
• 拓扑面积：
  39.9
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  3,4,5,6-Tetrahydro-2H-[1,4']bipyridinyl-2'-carbonitrile 在 吡啶 、 硫化氢 、 三乙胺 作用下， 以71%的产率得到3,4,5,6-Tetrahydro-2H-[1,4']bipyridinyl-2'-carbothioic acid amide
  参考文献：
  名称：

  New pyridine derivatives as potential antimicrobial agents

  摘要：

  A set of pyridine derivatives bearing a substituted alkylthio chain or a piperidyl ring in position 2 or 4 were synthesized, and their antimycobacterial and antifugal activities were evaluated. Chemical structures were confirmed by IR and NMR data, and by elemental analysis. Minimum inhibitory concentrations (MIC) were used for the evaluation of microbiological activity in vitro. The compounds were moderately active against both Mycobacterium tuberculosis and nontuberculous mycobacteria. The most active compound was 2-cyanomethylthiopyridine-4-carbonitrile (7) with MTC against Mycobacterium kansasii in the range of 8-4 mu mol/l. The antifungal activities of the compounds were relatively low. (C) 1999 Elsevier Science S.A. All rights reserved.

  DOI：

  10.1016/s0014-827x(99)00078-6
• 作为产物：
  描述：

  哌啶 、 4-氯-2-氰基吡啶 在 1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下， 以 1,4-二氧六环 为溶剂， 生成 3,4,5,6-Tetrahydro-2H-[1,4']bipyridinyl-2'-carbonitrile
  参考文献：
  名称：

  氨基嗪甲腈哌啶基缩氨基硫脲的合成及生物活性

  摘要：

  为了研究结构修饰如何影响结核抑制效力，我们合成了七种新的哌啶基缩氨基硫酮衍生物8-14，其中三个用吡嗪环取代了吡啶环。衍生物 8-9 和 13-14 对标准菌株表现出显着的活性（最低抑菌浓度 (MIC) 2-4 μg/mL），对耐药结核分枝杆菌菌株表现出更高的活性（MIC 0.5-4 μg/mL）。此外，化合物 8-9 的作用完全具有选择性（对其他微生物的 MIC ≥ 1000 μg/mL）且无毒（对 HaCaT 细胞的 IC50 5.8 至 >50 μg/mL）。吡嗪衍生物 11-12 的抗分枝杆菌活性可以忽略不计（MIC 256 至 >500 μg/mL），表明在这种情况下取​​代芳环通常不是一个有前途的研究方向。使用X射线晶体学测定化合物11的两性离子结构。吸收、分布、代谢和排泄 (ADME) 计算表明，除 11 种之外的所有化合物都可以考虑作为未来药物进行测试。对构效关系进行了分析

  DOI：

  10.3390/ph16091267

文献信息

• A study of the photochemically induced reaction of pyridine-2,4-dicarbonitrile with primary and secondary amines. A direct synthesis of aminocyano-pyridines
  作者：Rosanna Bernardi、Tullio Caronna、Sergio Morrocchi、Maurizio Ursini、Bruno M. Vittimberga

  DOI：10.1039/p19900000097

  日期：——

  A novel synthesis of alkylaminopyridinecarbonitriles by a photoinitiated substitution reaction between pyridine-2,4-dicarbonitrile and certain amines is described. The mechanism is discussed.

  描述了通过吡啶-2，4-二甲腈和某些胺之间的光引发的取代反应的烷基氨基吡啶甲腈的新颖合成。讨论了该机制。
• BERNARDI, ROSANNA;CARONNA, TULLIO;MORROCCHI, SERGIO;URSINI, MAURIZIO;VITT+, J. CHEM. SOC. PERKIN TRANS. PT 1,(1990) N, C. 97-100
  作者：BERNARDI, ROSANNA、CARONNA, TULLIO、MORROCCHI, SERGIO、URSINI, MAURIZIO、VITT+

  DOI：——

  日期：——
• New pyridine derivatives as potential antimicrobial agents
  作者：Věra Klimešová、Martin Svoboda、Karel Waisser、Milan Pour、Jarmila Kaustová

  DOI：10.1016/s0014-827x(99)00078-6

  日期：1999.10

  A set of pyridine derivatives bearing a substituted alkylthio chain or a piperidyl ring in position 2 or 4 were synthesized, and their antimycobacterial and antifugal activities were evaluated. Chemical structures were confirmed by IR and NMR data, and by elemental analysis. Minimum inhibitory concentrations (MIC) were used for the evaluation of microbiological activity in vitro. The compounds were moderately active against both Mycobacterium tuberculosis and nontuberculous mycobacteria. The most active compound was 2-cyanomethylthiopyridine-4-carbonitrile (7) with MTC against Mycobacterium kansasii in the range of 8-4 mu mol/l. The antifungal activities of the compounds were relatively low. (C) 1999 Elsevier Science S.A. All rights reserved.
• Synthesis and Biological Activity of Piperidinothiosemicarbazones Derived from Aminoazinecarbonitriles
  作者：Dagmara Ziembicka、Katarzyna Gobis、Małgorzata Szczesio、Ewa Augustynowicz-Kopeć、Agnieszka Głogowska、Izabela Korona-Głowniak、Krzysztof Bojanowski

  DOI：10.3390/ph16091267

  日期：——

  significant activity against the standard strain (minimum inhibitory concentration (MIC) 2–4 μg/mL) and even greater activity against the resistant M. tuberculosis strain (MIC 0.5–4 μg/mL). Additionally, the effects of compounds 8–9 were entirely selective (MIC toward other microorganisms ≥ 1000 μg/mL) and non-toxic (IC50 to HaCaT cells 5.8 to >50 μg/mL). The antimycobacterial activity of pyrazine

  为了研究结构修饰如何影响结核抑制效力，我们合成了七种新的哌啶基缩氨基硫酮衍生物8-14，其中三个用吡嗪环取代了吡啶环。衍生物 8-9 和 13-14 对标准菌株表现出显着的活性（最低抑菌浓度 (MIC) 2-4 μg/mL），对耐药结核分枝杆菌菌株表现出更高的活性（MIC 0.5-4 μg/mL）。此外，化合物 8-9 的作用完全具有选择性（对其他微生物的 MIC ≥ 1000 μg/mL）且无毒（对 HaCaT 细胞的 IC50 5.8 至 >50 μg/mL）。吡嗪衍生物 11-12 的抗分枝杆菌活性可以忽略不计（MIC 256 至 >500 μg/mL），表明在这种情况下取​​代芳环通常不是一个有前途的研究方向。使用X射线晶体学测定化合物11的两性离子结构。吸收、分布、代谢和排泄 (ADME) 计算表明，除 11 种之外的所有化合物都可以考虑作为未来药物进行测试。对构效关系进行了分析