3-乙硫基-5-(3-(乙硫基)-1,2,4-三嗪-5-基)-1,2,4-三嗪 | 1010071-37-0

• 分子结构分类: 有机化合物 - 有机硫化合物 - 硫醚类
• 中文名称: 3-乙硫基-5-(3-(乙硫基)-1,2,4-三嗪-5-基)-1,2,4-三嗪
• 英文名称: 3,3'-bis(ethylsulfanyl)-5,5'-bi-1,2,4-triazine
• 英文别名: 3-ethylthio-5-(3-(ethylthio)-1,2,4-triazin-5-yl)-1,2,4-triazine；3-Ethylsulfanyl-5-(3-ethylsulfanyl-1,2,4-triazin-5-yl)-1,2,4-triazine
• CAS: 1010071-37-0
• 化学式: C₁₀H₁₂N₆S₂
• 分子量: 280.377
• InChiKey: APQZYWUDYDMQHK-UHFFFAOYSA-N

物化性质

• 熔点：
  129-130 °C
• 沸点：
  559.8±60.0 °C(Predicted)
• 密度：
  1.39±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.6
• 重原子数：
  18
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  128
• 氢给体数：
  0
• 氢受体数：
  8

反应信息

• 作为反应物：
  描述：

  3-乙硫基-5-(3-(乙硫基)-1,2,4-三嗪-5-基)-1,2,4-三嗪 在 2,5-降冰片二烯 作用下， 以 4-异丙基甲苯 为溶剂， 反应 30.0h， 生成 6,6'-bis(ethylsulfanyl)-2,2'-bipyridine
  参考文献：
  名称：

  Synthesis of Enantiomerically Enriched Mono and Bis 2,2′-Bipyridine Alkyl Sulfoxides and Their First Application as Chiral Auxiliaries

  摘要：

  The direct asymmetric oxidation of 6,6'-bis(alkylsulfanyl)-2,2'-bipyridines 2a-e to non-racemic mono sulfoxides 3a-e and bis-sulfoxides 4a,c-e using either Davis oxaziridine or a modified Sharples reagent is reported. The use of isolated mono- and bis-sulfoxides as chiral auxiliaries was tested in either the asymmetric addition of the diethylzinc or allyl(trichloro)silane to benzaldehyde.

  DOI：

  10.1080/10426500902856347
• 作为产物：
  描述：

  3-(ethylsulfanyl)-1,2,4-triazine 在 potassium cyanide 作用下， 以 水 为溶剂， 反应 2.0h， 以81%的产率得到3-乙硫基-5-(3-(乙硫基)-1,2,4-三嗪-5-基)-1,2,4-三嗪
  参考文献：
  名称：

  光学活性的2,2'-联吡啶烷基亚砜的第一种方法

  摘要：

  6,6'-双（烷基硫烷基）-2,2'-联吡啶的合成及其使用（+）-（8,8-二氯樟脑磺酰基磺酰基）恶唑烷或不对称氧化为非外消旋的2,2'-联吡啶烷基亚砜报道了一种改良的Sharpless试剂。

  DOI：

  10.1016/j.tetlet.2007.11.104

文献信息

• The first approach to optically active 2,2′-bipyridine alkyl sulfoxides
  作者：Justyna Ławecka、Bogdan Bujnicki、Józef Drabowicz、Andrzej Rykowski

  DOI：10.1016/j.tetlet.2007.11.104

  日期：2008.1

  The synthesis of 6,6′-bis(alkylsulfanyl)-2,2′-bipyridines and their asymmetric oxidation to non-racemic 2,2′-bipyridine alkyl sulfoxides using either (+)-(8,8-dichlorocamphorylsulfonyl)oxaziridine or a modified Sharpless reagent is reported.

  6,6'-双（烷基硫烷基）-2,2'-联吡啶的合成及其使用（+）-（8,8-二氯樟脑磺酰基磺酰基）恶唑烷或不对称氧化为非外消旋的2,2'-联吡啶烷基亚砜报道了一种改良的Sharpless试剂。
• 3-Alkylthio-1,2,4-triazine dimers with potent antimalarial activity
  作者：Kung Ban、Sandra Duffy、Yelena Khakham、Vicky M. Avery、Andrew Hughes、Oliver Montagnat、Kasiram Katneni、Eileen Ryan、Jonathan B. Baell

  DOI：10.1016/j.bmcl.2010.08.065

  日期：2010.10

  We report on the discovery of 3-alkylthio-1,2,4-triazine dimers that are potently toxic to Plasmodium falciparum, with single digit nanomolar activity, and up to several thousand-fold lower toxicity to mammalian cells. They are equipotent against chloroquine-resistant strains of P. falciparum. (c) 2010 Elsevier Ltd. All rights reserved.
• 3,3′-Disubstituted 5,5′-Bi(1,2,4-triazine) Derivatives with Potent in Vitro and in Vivo Antimalarial Activity
  作者：Lian Xue、Da-Hua Shi、Jitendra R. Harjani、Fei Huang、Julia G. Beveridge、Tamir Dingjan、Kung Ban、Sarah Diab、Sandra Duffy、Leonardo Lucantoni、Sabine Fletcher、Francis C. K. Chiu、Scott Blundell、Katherine Ellis、Stuart A. Ralph、Grennady Wirjanata、Silvia Teguh、Rintis Noviyanti、Marina Chavchich、Darren Creek、Ric N. Price、Jutta Marfurt、Susan A. Charman、Matthew E. Cuellar、Jessica M. Strasser、Jayme L. Dahlin、Michael A. Walters、Michael D. Edstein、Vicky M. Avery、Jonathan B. Baell

  DOI：10.1021/acs.jmedchem.8b01799

  日期：2019.3.14

  A series of 3,3'-disubstituted 5,5'-bi(1,2,4-triazine) derivatives was synthesized and screened against the erythrocytic stage of Plasmodium falciparum 3D7 line. The most potent dimer, 6k, with an IC50 (50% inhibitory concentration) of 0.008 μM, had high in vitro potency against P. falciparum lines resistant to chloroquine (W2, IC50 = 0.0047 ± 0.0011 μM) and artemisinin (MRA1240, IC50 = 0.0086 ± 0

  合成了一系列 3,3'-二取代的 5,5'-双 (1,2,4-三嗪) 衍生物，并针对恶性疟原虫 3D7 系的红细胞期进行了筛选。最有效的二聚体 6k，IC50（50% 抑制浓度）为 0.008 μM，在体外对抗氯喹（W2，IC50 = 0.0047 ± 0.0011 μM）和青蒿素（MRA1240，IC50 = 0.0086 ± 0.0010 微米）。6k 的出色离体效力显示出对来自无并发症疟疾门诊患者血液的恶性疟原虫 (IC50 = 0.022-0.034 μM) 和间日疟原虫 (IC50 = 0.0093-0.031 μM) 的临床现场分离株。尽管 6k 在小鼠中被相对快速地清除，但它在 Peters 4 天试验中抑制了寄生虫血症，口服给药后的平均 ED50 值（50% 有效剂量）为 1.47 mg kg-1 day-1。
• Synthesis of Enantiomerically Enriched Mono and Bis 2,2′-Bipyridine Alkyl Sulfoxides and Their First Application as Chiral Auxiliaries
  作者：Justyna Ławecka、Bogdan Bujnicki、Józef Drabowicz、Jerzy Łuczak、Andrzej Rykowski

  DOI：10.1080/10426500902856347

  日期：2009.5.14

  The direct asymmetric oxidation of 6,6'-bis(alkylsulfanyl)-2,2'-bipyridines 2a-e to non-racemic mono sulfoxides 3a-e and bis-sulfoxides 4a,c-e using either Davis oxaziridine or a modified Sharples reagent is reported. The use of isolated mono- and bis-sulfoxides as chiral auxiliaries was tested in either the asymmetric addition of the diethylzinc or allyl(trichloro)silane to benzaldehyde.