5-(p-chlorophenyl)-5-phenyl-2-(2-propynyl)-2,4-dihydro-3H-1,2,4-triazol-3-one | 1351071-20-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 5-(p-chlorophenyl)-5-phenyl-2-(2-propynyl)-2,4-dihydro-3H-1,2,4-triazol-3-one
• CAS: 1351071-20-9
• 化学式: C₁₇H₁₂ClN₃O
• 分子量: 309.755
• InChiKey: BBVXZXDBAVEGIR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.99
• 重原子数：
  22.0
• 可旋转键数：
  3.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.06
• 拓扑面积：
  39.82
• 氢给体数：
  0.0
• 氢受体数：
  4.0

反应信息

• 作为反应物：
  描述：

  聚合甲醛 、 5-(p-chlorophenyl)-5-phenyl-2-(2-propynyl)-2,4-dihydro-3H-1,2,4-triazol-3-one 、 2,6-二甲基哌啶 在 copper(l) chloride 作用下， 以 1,4-二氧六环 为溶剂， 反应 3.0h， 以27.86%的产率得到4-phenyl-5-(p-chlorophenyl)-2,[4-(2,6-dimethylpiperidino)-2-butynyl]-2,4-dihydro-3H-1,2,4-triazol-3-one
  参考文献：
  名称：

  Synthesis and antimicrobial evaluation of 4,5-diaryl-2-[4-(t-amino)-2-butynyl]-2,4-dihydro-3H-1,2,4-triazol-3-ones

  摘要：

  A series of 4,5-diaryl-2-[4-(t-amino)-2-butynyl]-2,4-dihydro-3H-1,2,4-triazol-3-ones were synthesized and characterized by infrared spectrum (IR), H-1-NMR spectra and elemental analyses. Investigation of their antimicrobial activity was performed. Antimicrobial activity profile of the title compounds were evaluated against Gram- positive bacteria, Gram-negative bacteria and fungi. The synthesized compounds displayed different degrees of antimicrobial activities as shown in Table 3. Compound 12 was the most active one. This may be attributed to 4,5-diphenylsubstituent on the triazoline-3-one ring and the nature of the amino groups at terminal acetylenic moiety.

  DOI：

  10.1007/s00044-011-9840-9
• 作为产物：
  描述：

  1-(4-chloro-benzoyl)-4-phenyl-semicarbazide 在 potassium hydroxide 作用下， 以 乙醇 、 水 为溶剂， 反应 1.08h， 生成 5-(p-chlorophenyl)-5-phenyl-2-(2-propynyl)-2,4-dihydro-3H-1,2,4-triazol-3-one
  参考文献：
  名称：

  Synthesis and antimicrobial evaluation of 4,5-diaryl-2-[4-(t-amino)-2-butynyl]-2,4-dihydro-3H-1,2,4-triazol-3-ones

  摘要：

  A series of 4,5-diaryl-2-[4-(t-amino)-2-butynyl]-2,4-dihydro-3H-1,2,4-triazol-3-ones were synthesized and characterized by infrared spectrum (IR), H-1-NMR spectra and elemental analyses. Investigation of their antimicrobial activity was performed. Antimicrobial activity profile of the title compounds were evaluated against Gram- positive bacteria, Gram-negative bacteria and fungi. The synthesized compounds displayed different degrees of antimicrobial activities as shown in Table 3. Compound 12 was the most active one. This may be attributed to 4,5-diphenylsubstituent on the triazoline-3-one ring and the nature of the amino groups at terminal acetylenic moiety.

  DOI：

  10.1007/s00044-011-9840-9