4-(4-bromophenyl)-1-(4-chlorobenzoyl)thiosemicarbazide | 356576-31-3

• 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: 4-(4-bromophenyl)-1-(4-chlorobenzoyl)thiosemicarbazide
• 英文别名: N-(4-bromophenyl)-2-[(4-chlorophenyl)carbonyl]hydrazinecarbothioamide；1-(4-bromophenyl)-3-[(4-chlorobenzoyl)amino]thiourea
• CAS: 356576-31-3
• 化学式: C₁₄H₁₁BrClN₃OS
• 分子量: 384.684
• InChiKey: JFGZEQBKWPITBF-UHFFFAOYSA-N

物化性质

• 密度：
  1.632±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  21
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  85.2
• 氢给体数：
  3
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  4-(4-bromophenyl)-1-(4-chlorobenzoyl)thiosemicarbazide 在 sodium hydroxide 作用下， 以 乙醇 为溶剂， 反应 2.5h， 生成 4-(4-bromophenyl)-5-(4-chlorophenyl)-2-(pyrrolidin-1-ylmethyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione
  参考文献：
  名称：

  微生物活性曼尼希碱衍生自 1,2,4-三唑。C-5取代基对抗菌活性的影响。

  摘要：

  我们的研究证明，C-5 取代基的化学性质显着决定了衍生自 4,5-二取代 1,2,4-三唑-3-硫酮的曼尼希碱的抗菌活性。通过在苯环中引入氯原子，该活性显着​​增加。获得的化合物对机会性细菌（枯草芽孢杆菌和蜡状芽孢 杆菌）特别有效。某些曼尼希碱的抗菌活性与氨苄西林、头孢呋辛等常用抗生素的抗菌活性相似或更高。

  DOI：

  10.1007/s00044-012-0248-y
• 作为产物：
  描述：

  4-氯苯甲酸苯酯 在 一水合肼 作用下， 以 甲醇 、 乙醇 为溶剂， 反应 3.5h， 生成 4-(4-bromophenyl)-1-(4-chlorobenzoyl)thiosemicarbazide
  参考文献：
  名称：

  1,3,4-Thiadiazole Derivatives. Synthesis, Structure Elucidation, and Structure−Antituberculosis Activity Relationship Investigation

  摘要：

  A series of 2,5-disubstituted-1,3,4-thiadiazoles were synthesized, the compounds structures were elucidated and screened for the antituberculosis activity against Mycobacterium tuberculosis H37Rv using the BACTEC 460 radiometric system. Among the tested compounds, 2-phenylamino-5-(4-fluorophenyl)-1,3,4-thiadiazole 22 showed the highest inhibitory activity. The relationships between the structures of compounds and their antituberculosis activity were investigated by the Electronic-Topological Method (ETM) and feed forward neural networks (FFNNs) trained with the back-propagation algorithm. As a result of the approach, a system of pharmacophores and anti-pharmacophores has been found that effectively separates compounds of the examination set into groups of active and inactive compounds. The system can be applied to the screening and design of new active compounds possessing skeletons similar to those used in the present study.

  DOI：

  10.1021/jm0495632

文献信息

• A Novel Strategy for the Construction of Azole Heterocycles via an Oxidative Desulfurization Approach Using Iodobenzene and Oxone®
  作者：Vikas Telvekar、Kavitkumar Patel、Nikhil Jadhav、Prashant Jagadhane

  DOI：10.1055/s-0031-1290439

  日期：2012.8

  The oxidative desulfurization approach has been utilized for the construction of oxadiazole and thiadiazole heterocycles using iodobenzene and Oxone ® . The use of iodobenzene and the inexpensive readily available oxidant Oxone ® makes the reaction system simple and versatile for desulfurization.

  氧化脱硫方法已用于使用碘苯和 Oxone ® 构建恶二唑和噻二唑杂环。碘苯和廉价易得的氧化剂 Oxone ® 的使用使反应系统简单且适用于脱硫。
• Studies on the Anticonvulsant Activity and Influence on GABA-ergic Neurotransmission of 1,2,4-Triazole-3-thione- Based Compounds
  作者：Tomasz Plech、Barbara Kaproń、Jarogniew Łuszczki、Monika Wujec、Agata Paneth、Agata Siwek、Marcin Kołaczkowski、Maria Żołnierek、Gabriel Nowak

  DOI：10.3390/molecules190811279

  日期：——

  The anticonvulsant activity of several 1,2,4-triazole-3-thione derivatives on mouse maximal electroshock-induced seizures was tested in this study. Characteristic features of all active compounds were rapid onset of action and long lasting effect. Structure-activity observations showed that the probability of obtaining compounds exerting anticonvulsant activity was much higher when at least one of the phenyl rings attached to 1,2,4-triazole nucleus had a substituent at the para position. The obtained results, moreover, permit us to conclude that despite the structural similarity of loreclezole (second-generation anticonvulsant drug) and the titled compounds, their anticonvulsant activity is achieved via completely different molecular mechanisms.

  本研究测试了几种 1,2,4-三唑-3-硫酮衍生物对小鼠最大电休克诱发癫痫发作的抗惊厥活性。所有活性化合物的特点都是起效迅速、作用持久。结构-活性观察结果表明，当 1,2,4-三唑核上连接的苯基环中至少有一个在对位上具有取代基时，化合物具有抗惊厥活性的几率要高得多。此外，研究结果还让我们得出结论：尽管洛雷克唑（第二代抗惊厥药物）和标题化合物的结构相似，但它们的抗惊厥活性是通过完全不同的分子机制实现的。
• The antinociceptive effect of 4-substituted derivatives of 5-(4-chlorophenyl)-2-(morpholin-4-ylmethyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione in mice
  作者：Listos Joanna、Sylwia Talarek、Jolanta Orzelska、Sylwia Fidecka、Monika Wujec、Tomasz Plech

  DOI：10.1007/s00210-013-0938-0

  日期：2014.4

  The aim of the present experiments was to examine the antinociceptive activity of 4-substituted derivatives of 5-(4-chlorophenyl)-2-(morpholin-4-ylmethyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione in mice. The compounds were synthesized using the so-called Mannich reaction and their structures were confirmed using IR and 1H-NMR spectra. The antinociceptive activity was investigated in two behavioral tests: the hot plate test and the writhing test. For preliminary estimation of other behavioral effects, the locomotor activity of mice, the motor coordination in the rota-rod test, and the myorelaxation in the chimney test were also studied. The changes in body temperature of animals were also recorded. We demonstrated that all examined compounds produced antinociceptive effect, both in the hot plate test and in the writhing test, without impact on the motor coordination and myorelaxation of animals. The pharmacological effect of all drugs has been developed within 60 min after administration of drugs; and in two cases (T-103 and T-104), it has been a short-lasting effect (up to 90 min). Two compounds (T-100 and T-102) also inhibited the locomotor activity of animals. T-104 induced the changes in body temperature of mice. Generally, we demonstrated that combination of two different heterocyclic systems (morpholine and 1,2,4-triazole) might be beneficial for reduction of nociception.