2-[(5-Methyl-1,3,4-thiadiazol-2-yl)thio]-1-(2-naphthyl)ethanone | 677760-45-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 2-[(5-Methyl-1,3,4-thiadiazol-2-yl)thio]-1-(2-naphthyl)ethanone
• 英文别名: 2-[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanyl]-1-naphthalen-2-ylethanone
• CAS: 677760-45-1
• 化学式: C₁₅H₁₂N₂OS₂
• 分子量: 300.405
• InChiKey: NDKKOEVLQIIHGT-UHFFFAOYSA-N

物化性质

• 沸点：
  515.2±52.0 °C(Predicted)
• 密度：
  1.36±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  20
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.13
• 拓扑面积：
  96.4
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  2-[(5-Methyl-1,3,4-thiadiazol-2-yl)thio]-1-(2-naphthyl)ethanone 在 selenium(IV) oxide 、 sodium acetate 作用下， 以 四氢呋喃 、 乙醇 为溶剂， 反应 3.0h， 生成 2-methyl-5-[4-(2-naphthyl)-1,2,3-selenadiazol-5-yl]sulfanyl-1,3,4-thiadiazole
  参考文献：
  名称：

  5-杂芳基硫烷基-4-芳基1,2,3-硒代/噻二唑的合成与表征

  摘要：

  2-甲基-5-[（4-芳基-1,2,3-硒基二氮杂-5-基）硫烷基] -1,3,4-噻二唑，5- [4-芳基-1,2-的合成及光谱表征，3-selenadiazol-5-yl] sulfanyl-1-phenyl-1 H -1,2,3,4-tetraazoles，4-aryl-5-[（5-methyl-1,3,4-thiadiazol-2- ）]，1,2,3-噻二唑和5- [4-芳基-1,2,3-噻二唑-5-基]硫烷基-1-苯基-1 H -1,2,3,4-四唑已经报道。 2-甲基-5-[（4-芳基-1,2,3-硒基二氮杂-5-基）硫烷基] -1,3,4-噻二唑，5- [4-芳基-1,2-的合成及光谱表征，3-selenadiazol-5-yl] sulfanyl-1-phenyl-1 H -1,2,3,4-tetraazoles，4-aryl-5-[（5-methyl-1,3,4-thiadiazol-2-

  DOI：

  10.1007/s12039-011-0160-x

文献信息

• Synthesis of 3-heteroarylthioquinoline derivatives and their in vitro antituberculosis and cytotoxicity studies
  作者：Selvam Chitra、Nidhin Paul、Shanmugam Muthusubramanian、Paramasivam Manisankar、Perumal Yogeeswari、Dharmarajan Sriram

  DOI：10.1016/j.ejmech.2011.07.046

  日期：2011.10

  A series of 3-heteroarylthioquinoline derivatives has been synthesized by the Friedlander annulation of 2-[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanyl]-1-aryl-1-ethanone/2-(1,3-benzothiazol-2-ylsulfanyl)-1-aryl-1-ethanone/1-aryl-2-[(2-phenyl-2H-1,2,3,4-tetraazol-5-yl)sulfanyl]-1-ethanone with 2-aminobenzophenone in good yields using YbCl3 as the catalyst. These compounds have been screened for their in vitro activity against Mycobacterium tuberculosis H37Rv (MTB) and among the 21 compounds screened, 2-[2-(4-bromophenyl)-4-phenyl-3-quinolyl]sulfanyl-5-methyl-1,3,4-thiadiazole (5d) and 2-[2-(4-chlorophenyl)-4-phenyl-3-quinolyl]sulfanyl-5-methyl-1,3,4-thiadiazole (5c) were found to be the most active compounds with MIC of 3.2 and 3.5 mu M respectively against MTB. The cytotoxic effects against mouse fibroblasts (NIH 3T3) in vitro were evaluated for 5c and 5d, which displayed no toxic effects (IC50 > 1000 mu M) against the mouse fibroblast cell line NIH 3T3. (C) 2011 Elsevier Masson SAS. All rights reserved.
• Synthesis and characterization of 5-heteroarylsulfanyl-4-aryl- 1,2,3-selena/thiadiazoles
  作者：RAMAIYAN MANIKANNAN、MASILAMANI SHANMUGARAJA、SEETHARAMAN MANOJVEER、SHANMUGAM MUTHUSUBRAMANIAN

  DOI：10.1007/s12039-011-0160-x

  日期：2012.3

  Synthesis and spectral characterization of 2-methyl-5-[(4-aryl-1,2,3-selenadiazol-5-yl)sulfanyl]-1,3,4-thiadiazoles, 5-[4-aryl-1,2,3-selenadiazol-5-yl]sulfanyl-1-phenyl-1H-1,2,3,4-tetraazoles, 4-aryl-5-[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanyl]-1,2,3-thiadiazole and 5-[4-aryl-1,2,3-thiadiazol-5-yl]sulfanyl-1-phenyl-1H-1,2,3,4-tetraazole have been reported. Synthesis and spectral characterization of

  2-甲基-5-[（4-芳基-1,2,3-硒基二氮杂-5-基）硫烷基] -1,3,4-噻二唑，5- [4-芳基-1,2-的合成及光谱表征，3-selenadiazol-5-yl] sulfanyl-1-phenyl-1 H -1,2,3,4-tetraazoles，4-aryl-5-[（5-methyl-1,3,4-thiadiazol-2- ）]，1,2,3-噻二唑和5- [4-芳基-1,2,3-噻二唑-5-基]硫烷基-1-苯基-1 H -1,2,3,4-四唑已经报道。 2-甲基-5-[（4-芳基-1,2,3-硒基二氮杂-5-基）硫烷基] -1,3,4-噻二唑，5- [4-芳基-1,2-的合成及光谱表征，3-selenadiazol-5-yl] sulfanyl-1-phenyl-1 H -1,2,3,4-tetraazoles，4-aryl-5-[（5-methyl-1,3,4-thiadiazol-2-