3-(2-Chlorophenyl)-5-ethylthio-1,2,4-triazole | 80590-36-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 3-(2-Chlorophenyl)-5-ethylthio-1,2,4-triazole
• 英文别名: 5-(2-Chlorophenyl)-3-(ethylsulfanyl)-1H-1,2,4-triazole；5-(2-chlorophenyl)-3-ethylsulfanyl-1H-1,2,4-triazole
• CAS: 80590-36-9
• 化学式: C₁₀H₁₀ClN₃S
• 分子量: 239.728
• InChiKey: VKXLNSGXIICFEP-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.5
• 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：
  66.9
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  3-(2-Chlorophenyl)-5-ethylthio-1,2,4-triazole 在 potassium permanganate 、 溶剂黄146 作用下， 反应 2.0h， 以45%的产率得到3-(2-Chlorophenyl)-5-(ethanesulfonyl)-1H-1,2,4-triazole
  参考文献：
  名称：

  Preparation of 5-aryl-3-alkylthio-l,2,4-triazoles and corresponding sulfones with antiinflammatory–analgesic activity

  摘要：

  In this study, a series of 5-aryl-3-alkylthio-1,2,4-triazoles and corresponding sulfones were prepared with the objective of developing better analgesic-antiinflammatory compounds with minimum ulcerogenic risk. The structures of the compounds were elucidated by spectral and elemental analysis. The compounds were assayed per os in mice for their antiinflammatory and analgesic activity as well as the ulcerogenic risk and acute toxicity. Several of these compounds showed significant activity. Alkylsulfone derivatives were found to be much more potent analgesic-antimflammatory agents than the corresponding alkylthio analogs. Compounds 9 and 11 were the most active of the series in both analgesic and antiinflammatory activity tests. In contrast to reference compound acetyl salicylic acid, these compounds did not induce gastric lesions in the stomach of experimental animals at the doses that exhibited analgesic/antiinflammatory activity. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2006.11.029

文献信息

• Pesticidal heterocyclic compounds, processes for preparing them, compositions containing them, and their use
  申请人：FBC LIMITED

  公开号：EP0036711A2

  公开（公告）日：1981-09-30

  The compounds of the formula: wherein R represents phenyl substituted in at least the 2- position by fluorine, chlorine, bromine or iodine, R2 represents a group R3, -OR3, -SR3 or -NR3R4 where R3 represents hydrogen, alkyl of 1 to 6 carbon atoms, cycloalkyl of 3 to 7 carbon atoms, alkenyl of 2 to 6 carbon atoms, cycloalkenyl of 3 to 7 carbon atoms, alkynyl of 2 to 6 carbon atoms, phenyl, phenylalkyl of 7 to 10 carbon atoms or naphthyl, each of which may be unsubstituted or substituted by one or more halogen atoms, alkyl or alkoxy or alkylthio groups of 1 to 6 carbon atoms, nitro groups, cyano groups or mercapto groups, R4 represents a group as defined for R3 but not necessarily identical thereto, and A and B, together with the carbon atoms to which they are attached, form a 3,6-disubstituted pyridazine, a 3,6-disubstituted dihydropyridazine, a 2,5-disubstituted pyrimidine, a 1,2,4-oxadiazole, a 1,2,4-oxadiazoline or a 1,2,4-triazole ring, and the quaternary salts thereof, are novel compounds which are pesticidal, notably with respect to acarids, insects and aphids and their eggs and larvae. Compositions containing the compounds are also described as well as processes for their preparation and methods of using them.

  式中的化合物： 其中 R 代表至少在 2-位被氟、氯、溴或碘取代的苯基，R2 代表基团 R3、-OR3、-SR3 或 -NR3R4 其中 R3 代表氢、1 至 6 个碳原子的烷基、3 至 7 个碳原子的环烷基、2 至 6 个碳原子的烯基、3 至 7 个碳原子的环烯基、2 至 6 个碳原子的炔基、苯基、7 至 10 个碳原子的苯基烷基或萘基、其中 R3 代表氢、1 至 6 个碳原子的烷基、3 至 7 个碳原子的环烷基、2 至 6 个碳原子的烯基、3 至 7 个碳原子的环烯基、2 至 6 个碳原子的炔基、2 至 6 个碳原子的炔基、苯基、7 至 10 个碳原子的苯基烷基或萘基，其中每个烷基可以是未取代的，也可以被一个或多个卤素原子、1 至 6 个碳原子的烷基或烷氧基或烷硫基取代、硝基、氰基或巯基，R4 代表 R3 所定义的基团，但不一定与之相同，A 和 B 与它们所连接的碳原子一起形成 3,6-二取代的哒嗪、3,6-二取代的二氢哒嗪、2,5-二取代的哒嗪、2,5-二取代的二氢哒嗪、2,5-二取代的二氢哒嗪、2,5-二取代的二氢哒嗪、2,5-二取代的二氢哒嗪、2,5-二取代嘧啶、1,2,4-噁二唑、1,2,4-噁二唑啉或 1,2,4-三唑环，以及它们的季盐，这些新型化合物具有杀虫作用，特别是对螨、昆虫和蚜虫及其卵和幼虫。此外，还介绍了含有这些化合物的组合物及其制备工艺和使用方法。
• US4414221A
  申请人：——

  公开号：US4414221A

  公开（公告）日：1983-11-08
• Preparation of 5-aryl-3-alkylthio-l,2,4-triazoles and corresponding sulfones with antiinflammatory–analgesic activity
  作者：Birsen Tozkoparan、Esra Küpeli、Erdem Yeşilada、Mevlüt Ertan

  DOI：10.1016/j.bmc.2006.11.029

  日期：2007.2

  In this study, a series of 5-aryl-3-alkylthio-1,2,4-triazoles and corresponding sulfones were prepared with the objective of developing better analgesic-antiinflammatory compounds with minimum ulcerogenic risk. The structures of the compounds were elucidated by spectral and elemental analysis. The compounds were assayed per os in mice for their antiinflammatory and analgesic activity as well as the ulcerogenic risk and acute toxicity. Several of these compounds showed significant activity. Alkylsulfone derivatives were found to be much more potent analgesic-antimflammatory agents than the corresponding alkylthio analogs. Compounds 9 and 11 were the most active of the series in both analgesic and antiinflammatory activity tests. In contrast to reference compound acetyl salicylic acid, these compounds did not induce gastric lesions in the stomach of experimental animals at the doses that exhibited analgesic/antiinflammatory activity. (c) 2006 Elsevier Ltd. All rights reserved.