5-(Azidomethyl)-3-(4-fluorophenyl)-1,2-oxazole

• 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: 5-(Azidomethyl)-3-(4-fluorophenyl)-1,2-oxazole
• 英文别名: 5-(azidomethyl)-3-(4-fluorophenyl)-1,2-oxazole
• 化学式: C₁₀H₇FN₄O
• 分子量: 218.19
• InChiKey: LVZMIHCUDFZEKE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.1
• 拓扑面积：
  40.4
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  7-(prop-2-yn-1-yl)-7H-pyrrolo[2,3-d]pyrimidine 、 5-(Azidomethyl)-3-(4-fluorophenyl)-1,2-oxazole 在 copper(ll) sulfate pentahydrate 、 sodium ascorbate 作用下， 以 水 、 叔丁醇 为溶剂， 以90%的产率得到5-((4-((7H-pyrrolo[2,3-d]pyrimidin-7-yl)methyl)-1H-1,2,3-triazol-1-yl)methyl)-3-(4-fluorophenyl)isoxazole
  参考文献：
  名称：

  Synthesis and biological evaluation of 1H-pyrrolo[2,3-d]pyrimidine-1,2,3-triazole derivatives as novel anti-tubercular agents

  摘要：

  A series of novel 1H-pyrrolo[2,3-d]pyrimidine-1,2,3-triazole derivatives have been synthesized in good to excellent yields. Through the copper-catalyzed azide-alkyne cycloaddition via reaction of 7-(prop-2-ynyl)-7H-pyrrolo[2,3-d]pyrimidine and aryl, heteroaryl and alkyl azides in the presence of CuSO4 center dot 5H(2)O and sodium ascorbate. These compounds were evaluated for their in vitro antimycobacterial activity against Mycobacterium tuberculosis H37Rv strain. Most of these pyrrolopyrimidine-triazole hybrids exhibited good anti tubercular activity. The antimycobacterial assay results showed that the minimum inhibitory concentration of compounds 4q and 4r were 0.78 mu g/mL. The molecular docking results also had shown highest Moldock score for same compounds. These novel compounds exhibited good inhibition activities and further structure-activity studies of the derivatives had shown promising features to use in antitubercular therapy.

  DOI：

  10.1016/j.bmcl.2018.11.036