ethyl 2-(2-(1H-pyrazol-1-yl)phenyl)acetate | 1436430-74-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: ethyl 2-(2-(1H-pyrazol-1-yl)phenyl)acetate
• 英文别名: Ethyl 2-(2-pyrazol-1-ylphenyl)acetate
• CAS: 1436430-74-8
• 化学式: C₁₃H₁₄N₂O₂
• 分子量: 230.266
• InChiKey: KWHADXMKGGAINY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  17
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.23
• 拓扑面积：
  44.1
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  5-重氮米氏酸(=5-重氮-2,2-二甲基-1,3-二氧杂环己烷-4,6-二酮) 、 1-苯基吡唑 在 silver hexafluoroantimonate 、 dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer 作用下， 以 乙醇 为溶剂， 反应 7.0h， 以71%的产率得到ethyl 2-(2-(1H-pyrazol-1-yl)phenyl)acetate
  参考文献：
  名称：

  Rhodium(III)-Catalyzed Azacycle-Directed Intermolecular Insertion of Arene C–H Bonds into α-Diazocarbonyl Compounds

  摘要：

  Cp*Rh(III)-catalyzed intermolecular C C couplings between activated alpha-diazocarbonyl compounds and arenes bearing a range of azacyclic directing groups have been achieved. This catalytic alkylation reaction operates under mild conditions with good functional group tolerance.

  DOI：

  10.1021/jo400572h

文献信息

• USE OF 4-AMINO-PIPERIDINES FOR TREATING SLEEP DISORDERS
  申请人：van Kammen Daniel

  公开号：US20080051429A1

  公开（公告）日：2008-02-28

  Inverse agonists and antagonists of serotonin receptors are disclosed for use in treating sleep disorders such as insomnia, and specifically sleep maintenance insomnia. The compound increase slow wave sleep, decrease the number of awakenings after sleep onset, and decrease the time awake after sleep onset.

  揭示了逆向激动剂和拮抗剂的血清素受体，用于治疗睡眠障碍，如失眠，特别是睡眠维持失眠。该化合物增加慢波睡眠，减少入睡后醒来的次数，减少入睡后清醒的时间。
• Rhodium(III)-Catalyzed Azacycle-Directed Intermolecular Insertion of Arene C–H Bonds into α-Diazocarbonyl Compounds
  作者：Xinzhang Yu、Songjie Yu、Jian Xiao、Boshun Wan、Xingwei Li

  DOI：10.1021/jo400572h

  日期：2013.6.7

  Cp*Rh(III)-catalyzed intermolecular C C couplings between activated alpha-diazocarbonyl compounds and arenes bearing a range of azacyclic directing groups have been achieved. This catalytic alkylation reaction operates under mild conditions with good functional group tolerance.