2-phenyl-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)methyl}oxy)-5,6-dimethylthieno[2,3-d]pyrimidine | 1225505-07-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 噻吩并嘧啶酮衍生物
• 英文名称: 2-phenyl-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)methyl}oxy)-5,6-dimethylthieno[2,3-d]pyrimidine
• 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]-5,6-dimethyl-2-phenylthieno[2,3-d]pyrimidine
• CAS: 1225505-07-6
• 化学式: C₂₇H₁₈F₁₇N₅OS
• 分子量: 783.512
• InChiKey: QWUUAAFSBVAYQY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  9.7
• 重原子数：
  51
• 可旋转键数：
  13
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.48
• 拓扑面积：
  94
• 氢给体数：
  0
• 氢受体数：
  23

反应信息

• 作为产物：
  描述：

  5,6-dimethyl-2-phenyl-4-(prop-2-yn-1-yloxy)thieno[2,3-d]pyrimidine 、 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- 在 copper(l) iodide 作用下， 以 四氢呋喃 为溶剂， 反应 12.33h， 以42.45%的产率得到2-phenyl-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)methyl}oxy)-5,6-dimethylthieno[2,3-d]pyrimidine
  参考文献：
  名称：

  Synthesis and theoretical studies on energetics of novel N- and O- perfluoroalkyl triazole tagged thienopyrimidines – Their potential as adenosine receptor ligands

  摘要：

  A series of novel N- and O- perfluoroalkyl triazole tagged thienopyrimidines 6a-c and 7a-d was synthesized in two steps from thienopyrimidin-4-ones 2 through O- and N-propargylated regioisomers 3a-i and 4a-i respectively. Compound 2 was reacted with propargyl bromide to form O- and N-propargylated regioisomers 3 and 4 in definite proportions. Each regioisomer was separated and independently subjected to [3 + 2] cycloaddition using perfluoroalkyl azides through Click reaction under Sharpless conditions and obtained exclusively anti product in each case. The formation of two regioisomers in the first step and single anti addition product in the next step could be explained based on computational studies carried out at B3LYP/6-31G(d) level of theory. Results of Fukui function indices at the reactive centers are in accordance with the observations. On evaluation of the synthesized molecules for their binding affinities towards adenosine receptors, 4d and 4f were found to be selective to A(1) over A(2A) receptors. (C) 2010 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2009.12.075

文献信息

• Synthesis and theoretical studies on energetics of novel N- and O- perfluoroalkyl triazole tagged thienopyrimidines – Their potential as adenosine receptor ligands
  作者：B. Sirisha、B. Narsaiah、T. Yakaiah、G. Gayatri、G. Narahari Sastry、M. Raghu Prasad、A. Raghuram Rao

  DOI：10.1016/j.ejmech.2009.12.075

  日期：2010.5

  A series of novel N- and O- perfluoroalkyl triazole tagged thienopyrimidines 6a-c and 7a-d was synthesized in two steps from thienopyrimidin-4-ones 2 through O- and N-propargylated regioisomers 3a-i and 4a-i respectively. Compound 2 was reacted with propargyl bromide to form O- and N-propargylated regioisomers 3 and 4 in definite proportions. Each regioisomer was separated and independently subjected to [3 + 2] cycloaddition using perfluoroalkyl azides through Click reaction under Sharpless conditions and obtained exclusively anti product in each case. The formation of two regioisomers in the first step and single anti addition product in the next step could be explained based on computational studies carried out at B3LYP/6-31G(d) level of theory. Results of Fukui function indices at the reactive centers are in accordance with the observations. On evaluation of the synthesized molecules for their binding affinities towards adenosine receptors, 4d and 4f were found to be selective to A(1) over A(2A) receptors. (C) 2010 Elsevier Masson SAS. All rights reserved.