2-(1,2,4-triazol-1-yl)-3-(3,4,5-trimethoxyphenyl)sulfanyl-1H-indole | 1416576-25-4

• 分子结构分类: 有机化合物 - 有机硫化合物 - 硫醚类
• 英文名称: 2-(1,2,4-triazol-1-yl)-3-(3,4,5-trimethoxyphenyl)sulfanyl-1H-indole
• CAS: 1416576-25-4
• 化学式: C₁₉H₁₈N₄O₃S
• 分子量: 382.443
• InChiKey: UHSZRFLAZMNXCF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.1
• 重原子数：
  27
• 可旋转键数：
  6
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.16
• 拓扑面积：
  99.5
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  3,4,5-trimethoxybenzenethiol 在 碘 、 sodium hydride 作用下， 以 乙醇 、 N,N-二甲基甲酰胺 为溶剂， 生成 2-(1,2,4-triazol-1-yl)-3-(3,4,5-trimethoxyphenyl)sulfanyl-1H-indole
  参考文献：
  名称：

  吲哚的需氧氧化C–H偶氮化和黄素-碘偶联的有机催化一锅法合成氮唑基硫吲哚

  摘要：

  已开发了由黄素-碘偶联的有机催化驱动的吲哚与唑类的需氧氧化交叉偶联，用于2-（azol-1-yl）吲哚的绿色合成。偶联的有机催化系统通过利用分子氧作为唯一的牺牲试剂，以原子经济的方式从吲哚，唑类和硫醇一锅法合成2-偶氮基-3-硫代吲哚。

  DOI：

  10.1021/acs.orglett.1c00241

文献信息

• Toward Highly Potent Cancer Agents by Modulating the C-2 Group of the Arylthioindole Class of Tubulin Polymerization Inhibitors
  作者：Giuseppe La Regina、Ruoli Bai、Whilelmina Maria Rensen、Erica Di Cesare、Antonio Coluccia、Francesco Piscitelli、Valeria Famiglini、Alessia Reggio、Marianna Nalli、Sveva Pelliccia、Eleonora Da Pozzo、Barbara Costa、Ilaria Granata、Amalia Porta、Bruno Maresca、Alessandra Soriani、Maria Luisa Iannitto、Angela Santoni、Junjie Li、Marlein Miranda Cona、Feng Chen、Yicheng Ni、Andrea Brancale、Giulio Dondio、Stefania Vultaggio、Mario Varasi、Ciro Mercurio、Claudia Martini、Ernest Hamel、Patrizia Lavia、Ettore Novellino、Romano Silvestri

  DOI：10.1021/jm3013097

  日期：2013.1.10

  New arylthioindole derivatives having different cyclic substituents at position 2 of the indole were synthesized as anticancer agents. Several compounds inhibited tubulin polymerization at submicromolar concentration and inhibited cell growth at low nanomolar concentrations. Compounds 18 and 57 were superior to the previously synthesized S. Compound 18 was exceptionally potent as an inhibitor of cell growth: it showed IC50 = 1.0 nM in MCF-7 cells, and it was uniformly active in the whole panel of cancer cells and superior to colchicine and combretastatin A-4. Compounds 18, 20, 55, and 57 were notably more potent than vinorelbine, vinblastine, and paclitaxel in the NCl/ADR-RES and Messa/Dx5 cell lines, which overexpress P-glycoprotein. Compounds 18 and 57 showed initial vascular disrupting effects in a tumor model of liver rhabdomyosarcomas at 15 mg/kg intravenous dosage. Derivative 18 showed water solubility and higher metabolic stability than 5 in human liver microsomes.
• Aerobic Oxidative C–H Azolation of Indoles and One-Pot Synthesis of Azolyl Thioindoles by Flavin–Iodine-Coupled Organocatalysis
  作者：Kazumasa Tanimoto、Hayaki Okai、Marina Oka、Ryoma Ohkado、Hiroki Iida

  DOI：10.1021/acs.orglett.1c00241

  日期：2021.3.19

  The aerobic oxidative cross-coupling of indoles with azoles driven by flavin-iodine-coupled organocatalysis has been developed for the green synthesis of 2-(azol-1-yl)indoles. The coupled organocatalytic system enabled the one-pot three-component synthesis of 2-azolyl-3-thioindoles from indoles, azoles, and thiols in an atom-economical manner by utilizing molecular oxygen as the only sacrificial reagent

  已开发了由黄素-碘偶联的有机催化驱动的吲哚与唑类的需氧氧化交叉偶联，用于2-（azol-1-yl）吲哚的绿色合成。偶联的有机催化系统通过利用分子氧作为唯一的牺牲试剂，以原子经济的方式从吲哚，唑类和硫醇一锅法合成2-偶氮基-3-硫代吲哚。