1-benzyl-4-dodecyl-1,2,3-triazole | 1244564-33-7

• 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: 1-benzyl-4-dodecyl-1,2,3-triazole
• 英文别名: 1-benzyl-4-dodecyl-1H-1,2,3-triazole；1-Benzyl-4-dodecyl-triazole；1-benzyl-4-dodecyltriazole
• CAS: 1244564-33-7
• 化学式: C₂₁H₃₃N₃
• 分子量: 327.513
• InChiKey: XCWDZGDPYJIDOF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.3
• 重原子数：
  24
• 可旋转键数：
  13
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.62
• 拓扑面积：
  30.7
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  1-benzyl-4-dodecyl-1,2,3-triazole 在 copper dichloride 、 三甲基乙酸 作用下， 以 neat (no solvent) 为溶剂， 反应 46.0h， 以53%的产率得到1-benzyl-5-chloro-4-dodecyl-1H-1,2,3-triazole
  参考文献：
  名称：

  无溶剂新戊酸/氯化铜共同促进 1,2,3-三唑的氯化

  摘要：

  通过在新戊酸中使用氯化铜 (II)，直接从 5H 取代的 1,2,3-三唑在 1,2,3-三唑的 5-位上开发了一种新的氯化反应。因此，一系列三唑以低到高的收率被氯化。

  DOI：

  10.1055/s-0032-1317446
• 作为产物：
  描述：

  溴甲苯 在 sodium azide 、 copper(II) sulfate 、 sodium ascorbate 、 sodium iodide 作用下， 以 水 、 N,N-二甲基甲酰胺 、 叔丁醇 为溶剂， 反应 24.0h， 生成 1-benzyl-4-dodecyl-1,2,3-triazole
  参考文献：
  名称：

  Chemical synthesis and biological evaluation of triazole derivatives as inhibitors of InhA and antituberculosis agents

  摘要：

  A series of triazoles have been prepared and evaluated as inhibitors of InhA as well as inhibitors of Mycobacterium tuberculosis H37Rv. Several of these new compounds possess a good activity against InhA, particularly compounds 17 and 18 for which molecular docking has been performed. Concerning their activities against M. tuberculosis H37Rv strain, two of them, 3 and 12, were found to be good inhibitors with MIC values of 0.50 and 0.25 mu g/ml, respectively. Particularly, compound 12 presenting the best MIC value of all compounds tested (0.6 mu M) is totally inactive against InhA. (C) 2012 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2012.03.029

文献信息

• Antimicrobial 1,3,4-trisubstituted-1,2,3-triazolium salts
  作者：James T. Fletcher、Jill M. Sobczyk、Sarah C. Gwazdacz、Aaron J. Blanck

  DOI：10.1016/j.bmcl.2018.09.011

  日期：2018.11

  A series of 1,3,4-trisubstituted-1,2,3-triazolium bromide salts were prepared by efficient two-step sequences of azide-alkyne cycloaddition and benzylic substitution. The antimicrobial activity of each triazolium salt and correlating triazole precursor was evaluated using a minimum inhibitory concentration (MIC) assay. MIC activities as low as 1 µM against Gram-positive bacteria, 8 µM against Gram-negative

  通过叠氮化物-炔烃环加成和苄基取代的有效两步序列，制备了一系列1,3,4-三取代-1,2,3-三唑鎓溴化物盐。使用最小抑菌浓度（MIC）分析评估每种三唑鎓盐和相关的三唑前体的抗菌活性。盐类似物对革兰氏阳性菌的MIC活性低至1 µM，对革兰氏阴性菌的MIC活性低至4 µM，而对中性三唑则无活性。分别鉴定了代表选择性和广谱抗菌活性的类似物。在此基序中观察到的MIC结构与活性的关系表明，阳离子电荷的存在和整体疏水性的平衡具有强烈的影响力，而苄基vs.
• Copper(I)-Catalyzed Azide-Alkyne Cycloadditions in Ionic Liquids under Amine-Free Conditions
  作者：Alberto Marra、Alessandro Dondoni、Alessandra Vecchi、Angela Chambery、Cinzia Chiappe

  DOI：10.1055/s-0029-1218760

  日期：2010.6

  Copper(I) iodide catalyzed cycloadditions of various combinations of structurally diverse organic azides and terminal alkynes were carried out in a commercially available, polyoxygenated ionic liquid (AMMOENG 100™) without addition of free amine. Unlike the previously tested ionic liquids, this solvent led exclusively to the 1,4-disubstituted triazole regioisomer. alkynes - azides - carbohydrates -

  在不添加游离胺的情况下，在市售的多氧化离子液体（AMMOENG 100™）中进行结构多样的有机叠氮化物和末端炔烃的各种组合的碘化亚铜（I）催化的环加成反应。与先前测试过的离子液体不同，该溶剂仅产生1,4-二取代的三唑区域异构体。 炔烃-叠氮化物-碳水化合物-铜-环加成
• Chemical synthesis and biological evaluation of triazole derivatives as inhibitors of InhA and antituberculosis agents
  作者：Christophe Menendez、Aurélien Chollet、Frédéric Rodriguez、Cyril Inard、Maria Rosalia Pasca、Christian Lherbet、Michel Baltas

  DOI：10.1016/j.ejmech.2012.03.029

  日期：2012.6

  A series of triazoles have been prepared and evaluated as inhibitors of InhA as well as inhibitors of Mycobacterium tuberculosis H37Rv. Several of these new compounds possess a good activity against InhA, particularly compounds 17 and 18 for which molecular docking has been performed. Concerning their activities against M. tuberculosis H37Rv strain, two of them, 3 and 12, were found to be good inhibitors with MIC values of 0.50 and 0.25 mu g/ml, respectively. Particularly, compound 12 presenting the best MIC value of all compounds tested (0.6 mu M) is totally inactive against InhA. (C) 2012 Elsevier Masson SAS. All rights reserved.
• Solvent-Free Pivalic Acid/Copper Chloride Jointly Promoted Chlorination of 1,2,3-Triazoles
  作者：Christian Lherbet、Michel Baltas、Christophe Menendez、Nathalie Saffon

  DOI：10.1055/s-0032-1317446

  日期：——

  A novel chlorination reaction on the 5-position of 1,2,3-triazoles, directly from 5H-substituted 1,2,3-triazoles was developed by using copper(II) chloride in pivalic acid. A series of triazoles were thus chlorinated in low to good yields.

  通过在新戊酸中使用氯化铜 (II)，直接从 5H 取代的 1,2,3-三唑在 1,2,3-三唑的 5-位上开发了一种新的氯化反应。因此，一系列三唑以低到高的收率被氯化。