N-((1-(2-fluoroethyl)-1H-1,2,3-triazol-4-yl)methyl)-5-nitrothiazol-2-amine | 1356919-07-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: N-((1-(2-fluoroethyl)-1H-1,2,3-triazol-4-yl)methyl)-5-nitrothiazol-2-amine
• 英文别名: N-[[1-(2-fluoroethyl)triazol-4-yl]methyl]-5-nitro-1,3-thiazol-2-amine
• CAS: 1356919-07-7
• 化学式: C₈H₉FN₆O₂S
• 分子量: 272.263
• InChiKey: OYUKUYVQOYIAOX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1
• 重原子数：
  18
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  130
• 氢给体数：
  1
• 氢受体数：
  8

反应信息

• 作为产物：
  描述：

  1-azido-2-fluoroethane 、 5-nitro-N-(prop-2-ynyl)thiazol-2-amine 在 copper(II) sulfate 、 sodium ascorbate 作用下， 以 四氢呋喃 、 水 为溶剂， 生成 N-((1-(2-fluoroethyl)-1H-1,2,3-triazol-4-yl)methyl)-5-nitrothiazol-2-amine
  参考文献：
  名称：

  A fluorous and click approach for screening potential PET probes: Evaluation of potential hypoxia biomarkers

  摘要：

  Radiopharmaceuticals for nuclear imaging are essentially targeting molecules, labeled with short-lived radionuclides (e. g., F-18 for PET). A significant drawback of radiopharmaceuticals development is the difficulty to access radiolabeled molecule libraries for initial in vitro evaluation, as radiolabeling has to be optimized for each individual molecule. The present paper discloses a method for preparing libraries of F-18-labeled radiopharmaceuticals using both the fluorous-based F-18-radiochemistry and the Huisgen 1,3-dipolar (click) conjugation reaction. As a proof of concept, this approach allowed us to obtain a series of readily accessible F-18-radiolabeled nitroaromatic molecules, for exploring their structure-activity relationship and further in vitro evaluation of their hypoxic selectivity. Crown Copyright (C) 2011 Published by Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2011.10.084

文献信息

• A fluorous and click approach for screening potential PET probes: Evaluation of potential hypoxia biomarkers
  作者：Romain Bejot、Laurence Carroll、Kishore Bhakoo、Jérôme Declerck、Veronique Gouverneur

  DOI：10.1016/j.bmc.2011.10.084

  日期：2012.1

  Radiopharmaceuticals for nuclear imaging are essentially targeting molecules, labeled with short-lived radionuclides (e. g., F-18 for PET). A significant drawback of radiopharmaceuticals development is the difficulty to access radiolabeled molecule libraries for initial in vitro evaluation, as radiolabeling has to be optimized for each individual molecule. The present paper discloses a method for preparing libraries of F-18-labeled radiopharmaceuticals using both the fluorous-based F-18-radiochemistry and the Huisgen 1,3-dipolar (click) conjugation reaction. As a proof of concept, this approach allowed us to obtain a series of readily accessible F-18-radiolabeled nitroaromatic molecules, for exploring their structure-activity relationship and further in vitro evaluation of their hypoxic selectivity. Crown Copyright (C) 2011 Published by Elsevier Ltd. All rights reserved.