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5-[2,6-Dimethyl-4-(4-nitrophenyl)-5-(5-sulfanylidene-1,2-dihydro-1,2,4-triazol-3-yl)pyridin-3-yl]-1,2-dihydro-1,2,4-triazole-3-thione | 1075237-16-9

中文名称
——
中文别名
——
英文名称
5-[2,6-Dimethyl-4-(4-nitrophenyl)-5-(5-sulfanylidene-1,2-dihydro-1,2,4-triazol-3-yl)pyridin-3-yl]-1,2-dihydro-1,2,4-triazole-3-thione
英文别名
——
5-[2,6-Dimethyl-4-(4-nitrophenyl)-5-(5-sulfanylidene-1,2-dihydro-1,2,4-triazol-3-yl)pyridin-3-yl]-1,2-dihydro-1,2,4-triazole-3-thione化学式
CAS
1075237-16-9
化学式
C17H14N8O2S2
mdl
——
分子量
426.483
InChiKey
GWHASLBXWLCOMC-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    2.2
  • 重原子数:
    29
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    196
  • 氢给体数:
    4
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    2,2'-(2,6-dimethyl-4-(4-nitrophenyl)pyridine-3,5-dicarbonyl)bis(hydrazine-1-carbothioamide) 在 sodium hydroxide 作用下, 以58%的产率得到5-[2,6-Dimethyl-4-(4-nitrophenyl)-5-(5-sulfanylidene-1,2-dihydro-1,2,4-triazol-3-yl)pyridin-3-yl]-1,2-dihydro-1,2,4-triazole-3-thione
    参考文献:
    名称:
    Microwave Assisted Synthesis of Some Pyridine Derivatives Containing Mercaptotriazole and Thiazolidinone as a New Class of Antimicrobial Agents
    摘要:
    A fast and facile procedure for the synthesis of pyridomereaptotriazole 4a-e and pyridothiazolidinone 5a-e is being reported starting from diliydropyridine 1a-e. Subsequent oxidation with nitrating mixture (HNO3/H2SO4) produced the anticipated 2,6-dimethylpyridine derivatives 2a-e, which were subsequently condensed with thiosemicarbazide in ethanol to produce the key intermediate 2,2'-[4(4-substituted phenyl)- 2,6-dimethylpyridine-3,5-diyl]dicarbonyldihydrazine carbothioamides 3a-e. In the final step pyridomercaptotriazole derivatives 4a-e were synthesized by treating 3a-e in alkaline media. In parallel pyridothiazolidinone derivatives 5a-e were obtained by the reaction of 3a-e with ClCH2COOH/CH3COONa. All the reactions were carried out on microwave irradiation in good yield with short time. The structures of all the compounds have been confirmed on the basis of their analytical, IR, H-1 NMR, and Mass spectral data (Tables I and II). The potent antimicrobial effects of the synthesized compounds were also investigated.
    DOI:
    10.1080/10426500701557138
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文献信息

  • Microwave Assisted Synthesis of Some Pyridine Derivatives Containing Mercaptotriazole and Thiazolidinone as a New Class of Antimicrobial Agents
    作者:Sarika Mehta、Neelam Swarnkar、Ritu Vyas、Jitendra Vardia、Pinki B. Punjabi、Suresh C. Ameta
    DOI:10.1080/10426500701557138
    日期:2007.12.24
    A fast and facile procedure for the synthesis of pyridomereaptotriazole 4a-e and pyridothiazolidinone 5a-e is being reported starting from diliydropyridine 1a-e. Subsequent oxidation with nitrating mixture (HNO3/H2SO4) produced the anticipated 2,6-dimethylpyridine derivatives 2a-e, which were subsequently condensed with thiosemicarbazide in ethanol to produce the key intermediate 2,2'-[4(4-substituted phenyl)- 2,6-dimethylpyridine-3,5-diyl]dicarbonyldihydrazine carbothioamides 3a-e. In the final step pyridomercaptotriazole derivatives 4a-e were synthesized by treating 3a-e in alkaline media. In parallel pyridothiazolidinone derivatives 5a-e were obtained by the reaction of 3a-e with ClCH2COOH/CH3COONa. All the reactions were carried out on microwave irradiation in good yield with short time. The structures of all the compounds have been confirmed on the basis of their analytical, IR, H-1 NMR, and Mass spectral data (Tables I and II). The potent antimicrobial effects of the synthesized compounds were also investigated.
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