2-{4-[4-(1H-indol-3-yl)piperidin-1-yl]-butyl}-4-(4-methoxyphenyl)pyrido[1,2-c]pyrimidine-1,3-dione | 1149339-66-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: 2-{4-[4-(1H-indol-3-yl)piperidin-1-yl]-butyl}-4-(4-methoxyphenyl)pyrido[1,2-c]pyrimidine-1,3-dione
• 英文别名: 2-{4-[4-(1H-Indol-3-yl)-piperidin-1-yl]-butyl}-4-(4-methoxyphenyl)-pyrido[1,2-c]pyrimidine-1,3-dione；2-[4-[4-(1H-indol-3-yl)piperidin-1-yl]butyl]-4-(4-methoxyphenyl)pyrido[1,2-c]pyrimidine-1,3-dione
• CAS: 1149339-66-1
• 化学式: C₃₂H₃₄N₄O₃
• 分子量: 522.647
• InChiKey: WDBRYUHRFVVVLM-UHFFFAOYSA-N

物化性质

• 熔点：
  235-236 °C
• 沸点：
  744.0±70.0 °C(predicted)
• 密度：
  1.31±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5
• 重原子数：
  39
• 可旋转键数：
  8
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  68.9
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  2-(4-bromobutyl)-4-(4-methoxyphenyl)-1H-pyrido[1,2-c]pyrimidine-1,3(2H)-dione 、 3-(4’-哌啶基)-1H-吲哚 在 potassium carbonate 、 potassium iodide 作用下， 以 乙腈 为溶剂， 以90%的产率得到2-{4-[4-(1H-indol-3-yl)piperidin-1-yl]-butyl}-4-(4-methoxyphenyl)pyrido[1,2-c]pyrimidine-1,3-dione
  参考文献：
  名称：

  Novel 4-aryl-pyrido[1,2-c]pyrimidines with dual SSRI and 5-HT1A activity, Part 1

  摘要：

  A series of new derivatives of 4-aryl-pyrido[1,2-c]pyrimidine containing the 3-(4-piperidyl)-1H-indole residue or its 5-methoxy derivative were synthesized. They were characterized (i) in vitro by binding to 5-HT1A receptors and 5-HT transporter proteins in rat brain cortex membranes and (ii) in vivo in the mouse by induced hypothermia and forced swimming models for antagonist/agonist activity against the 5-HT1A autoreceptors and postsynaptic 5-HT1A receptors, respectively. Structure activity relationship evaluation indicated that the presence of the 3-(4-piperidyl)-1H-indole residue and ortho- or para-substituents with -F or -CH3 groups in the aryl ring as well as an unsubstituted aryl in the 4-aryl-pyrido[1,2-c]pyrimidine moiety promoted low K-i values for both receptors. In contrast, the presence of a 5-methoxy-3-(4-piperidyl)-1H-indole methoxy-3-(4-piperidyl)-1H-indole residue as well as -CI or -OCH3 substituents at the para position markedly reduced the receptor affinity. (c) 2008 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2008.09.021

文献信息

• Novel 4-aryl-pyrido[1,2-c]pyrimidines with dual SSRI and 5-HT1A activity, Part 1
  作者：Franciszek Herold、Andrzej Chodkowski、Łukasz Izbicki、Marek Król、Jerzy Kleps、Jadwiga Turło、Gabriel Nowak、Katarzyna Stachowicz、Małgorzata Dybała、Agata Siwek

  DOI：10.1016/j.ejmech.2008.09.021

  日期：2009.4

  A series of new derivatives of 4-aryl-pyrido[1,2-c]pyrimidine containing the 3-(4-piperidyl)-1H-indole residue or its 5-methoxy derivative were synthesized. They were characterized (i) in vitro by binding to 5-HT1A receptors and 5-HT transporter proteins in rat brain cortex membranes and (ii) in vivo in the mouse by induced hypothermia and forced swimming models for antagonist/agonist activity against the 5-HT1A autoreceptors and postsynaptic 5-HT1A receptors, respectively. Structure activity relationship evaluation indicated that the presence of the 3-(4-piperidyl)-1H-indole residue and ortho- or para-substituents with -F or -CH3 groups in the aryl ring as well as an unsubstituted aryl in the 4-aryl-pyrido[1,2-c]pyrimidine moiety promoted low K-i values for both receptors. In contrast, the presence of a 5-methoxy-3-(4-piperidyl)-1H-indole methoxy-3-(4-piperidyl)-1H-indole residue as well as -CI or -OCH3 substituents at the para position markedly reduced the receptor affinity. (c) 2008 Elsevier Masson SAS. All rights reserved.