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4-(4-Methoxy-phenyl)-5-(5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridin-2-ylmethyl)-2,4-dihydro-[1,2,4]triazole-3-thione

中文名称
——
中文别名
——
英文名称
4-(4-Methoxy-phenyl)-5-(5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridin-2-ylmethyl)-2,4-dihydro-[1,2,4]triazole-3-thione
英文别名
4-(4-methoxyphenyl)-3-(5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridin-2-ylmethyl)-1H-1,2,4-triazole-5-thione
4-(4-Methoxy-phenyl)-5-(5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridin-2-ylmethyl)-2,4-dihydro-[1,2,4]triazole-3-thione化学式
CAS
——
化学式
C16H18N6OS
mdl
——
分子量
342.425
InChiKey
HYFXNXFHQBXBCB-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):
    1.9
  • 重原子数:
    24
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    99.7
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    4-甲氧基苯基 异硫氰酸酯 、 5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridine-2-acetic acid hydrazide 在 sodium hydroxide 作用下, 反应 7.0h, 以62%的产率得到4-(4-Methoxy-phenyl)-5-(5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridin-2-ylmethyl)-2,4-dihydro-[1,2,4]triazole-3-thione
    参考文献:
    名称:
    Synthesis, antitumor and antiviral properties of some 1,2,4-triazole derivatives
    摘要:
    A series of 1,5-dialkyl-1,2,4-triazole derivatives of acetic acid alkylidene hydrazides 8-12, the acid 13, 1,5-dialkyl-3-(5-mercapto-4-N-aryl-1H-[1,2,4]-triazol-3-ylmethylene)-1H-[1,2,4] triazoles 14-16, their 1,3,4-oxadiazole analogues 17-21, as well as the 1,2,4-triazolo-indoles 25 and 27 were prepared. The Z/E conformations of some acetic acid alkylidene derivatives were studied by NMR spectroscopy. Most of the target compounds were evaluated in a series of human cancer cell in cultures and none have shown activity except 25 which exhibited remarkable activity against nine cancer types. No in vitro antiviral activity against HIV-1, HIV-2, HSV-1, HSV-2, SV, CV-B4, RSV, P3V, RV, SinV, PTV has been found for all the synthesized compounds.
    DOI:
    10.1016/j.farmac.2004.05.006
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