4-((1-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)-1H-1,2,3-triazol-4-yl)methoxy)-2-(trifluoromethyl)quinazoline | 1213232-29-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二氮杂萘
• 英文名称: 4-((1-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)-1H-1,2,3-triazol-4-yl)methoxy)-2-(trifluoromethyl)quinazoline
• 英文别名: 4-[[1-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-Heptadecafluorodecyl)triazol-4-yl]methoxy]-2-(trifluoromethyl)quinazoline
• CAS: 1213232-29-1
• 化学式: C₂₂H₁₁F₂₀N₅O
• 分子量: 741.33
• InChiKey: GPEQRYOQAKUZEP-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  8.2
• 重原子数：
  48
• 可旋转键数：
  12
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.55
• 拓扑面积：
  65.7
• 氢给体数：
  0
• 氢受体数：
  25

反应信息

• 作为产物：
  描述：

  癸烷,10-叠氮-1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-十七氟- 、 4-Prop-2-ynoxy-2-(trifluoromethyl)quinazoline 在 copper(l) iodide 作用下， 以 四氢呋喃 为溶剂， 以85.91%的产率得到4-((1-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)-1H-1,2,3-triazol-4-yl)methoxy)-2-(trifluoromethyl)quinazoline
  参考文献：
  名称：

  Click chemistry: Studies on the synthesis of novel fluorous tagged triazol-4-yl substituted quinazoline derivatives and their biological evaluation – Theoretical and experimental validation

  摘要：

  The formation of N- and O-propargylated quinazoline derivatives 2, 3 from quinazol-4-ones 1 was theoretically predicted by optimizations at B3LYP/6-31G* level, analysed kinetically and thermodynamically. Theoretical predictions are validated by experiment to observe the trends and found deviation. Thus, compound I was propargylated in basic media to obtain compound 2 and 3 in definite proportions. Each compound was further subjected to [3 + 2] cycloaddition using perfluoroalkyl azides through Click reaction under Sharpless conditions, and obtained a series of novel perfluoroalkyl-1H,1,2,3-triazol-4-yl substituted quinazolines 4, 5, and 6. All the compounds were screened for antimicrobial activity and identified potential compounds. (C) 2009 Published by Elsevier Masson SAS.

  DOI：

  10.1016/j.ejmech.2009.09.027