3-ethyl-6,7-dihydro-5H-pyrrolo[1,2-c]imidazole | 1394843-43-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 3-ethyl-6,7-dihydro-5H-pyrrolo[1,2-c]imidazole
• CAS: 1394843-43-6
• 化学式: C₈H₁₂N₂
• 分子量: 136.197
• InChiKey: IYSQGLDWEYXTMD-UHFFFAOYSA-N

物化性质

• 沸点：
  283.8±9.0 °C(Predicted)
• 密度：
  1.14±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.2
• 重原子数：
  10
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.62
• 拓扑面积：
  17.8
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  丙腈 、 5-azidopent-1-yne 在 gold(III) chloride 、 甲烷磺酸 作用下， 反应 10.0h， 以78%的产率得到3-ethyl-6,7-dihydro-5H-pyrrolo[1,2-c]imidazole
  参考文献：
  名称：

  Synthesis of Bicyclic Imidazoles via [2 + 3] Cycloaddition between Nitriles and Regioselectively Generated α-Imino Gold Carbene Intermediates

  摘要：

  The cyclic alpha-imino gold carbene intermediate B is most likely generated in situ via regioselective nitrene transfer from an azido group to a tethered terminal alkyne in the presence of a gold catalyst and at ambient temperature. This highly electrophilic intermediate can react with a weakly nucleophilic nitrile, which is used as the reaction solvent, to deliver a bicyclic imidazole rapidly in an overall bimolecular [2 + 2 + 1] cycloaddition and in mostly serviceable yield. The competing intramolecular Huisgen reaction, although likely also catalyzed by gold, is minimized by using AuCl3 as the catalyst.

  DOI：

  10.1021/ol302102h

文献信息

• Sufonamides and Uses Thereof
  申请人：Saunders Jeffrey O.

  公开号：US20080261970A1

  公开（公告）日：2008-10-23

  Compounds of formula (I), including methods of making and methods of using are described in formula (I).
• Synthesis of Bicyclic Imidazoles via [2 + 3] Cycloaddition between Nitriles and Regioselectively Generated α-Imino Gold Carbene Intermediates
  作者：Yuanjing Xiao、Liming Zhang

  DOI：10.1021/ol302102h

  日期：2012.9.7

  The cyclic alpha-imino gold carbene intermediate B is most likely generated in situ via regioselective nitrene transfer from an azido group to a tethered terminal alkyne in the presence of a gold catalyst and at ambient temperature. This highly electrophilic intermediate can react with a weakly nucleophilic nitrile, which is used as the reaction solvent, to deliver a bicyclic imidazole rapidly in an overall bimolecular [2 + 2 + 1] cycloaddition and in mostly serviceable yield. The competing intramolecular Huisgen reaction, although likely also catalyzed by gold, is minimized by using AuCl3 as the catalyst.