6-chloro-2-N-[1-(4-fluorophenyl)ethyl]-1,3,5-triazine-2,4-diamine | 756851-67-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 三嗪类
• 英文名称: 6-chloro-2-N-[1-(4-fluorophenyl)ethyl]-1,3,5-triazine-2,4-diamine
• CAS: 756851-67-9
• 化学式: C₁₁H₁₁ClFN₅
• 分子量: 267.693
• InChiKey: ITHKMQSKGBSZOB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  18
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  76.7
• 氢给体数：
  2
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  2-(4-氟苯氧基)乙胺 、 6-chloro-2-N-[1-(4-fluorophenyl)ethyl]-1,3,5-triazine-2,4-diamine 在 N,N-二异丙基乙胺 作用下， 以 四氢呋喃 为溶剂， 生成 N2-[2-(4-Fluorophenoxy)ethyl]-N4-[1-(4-fluorophenyl)ethyl]-1,3,5-triazine-2,4,6-triamine
  参考文献：
  名称：

  Aminotriazine 5-HT7 antagonists

  摘要：

  The present studies have identified a series of aminotriazines as novel 5-HT7 receptor antagonists. Compounds 10 and 17 have high affinity for the 5-HT7 receptor and do not bind to either the 5-HT2C or 5-HT6 receptors. These compounds produce no agonist effects by themselves, and shift the dose-response curve of 5-CT to the right in the manner of an antagonist. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2004.06.008
• 作为产物：
  描述：

  1-(4-氟苯基)乙胺 在 ammonium hydroxide 、 N,N-二异丙基乙胺 作用下， 以 四氢呋喃 为溶剂， 生成 6-chloro-2-N-[1-(4-fluorophenyl)ethyl]-1,3,5-triazine-2,4-diamine
  参考文献：
  名称：

  Aminotriazine 5-HT7 antagonists

  摘要：

  The present studies have identified a series of aminotriazines as novel 5-HT7 receptor antagonists. Compounds 10 and 17 have high affinity for the 5-HT7 receptor and do not bind to either the 5-HT2C or 5-HT6 receptors. These compounds produce no agonist effects by themselves, and shift the dose-response curve of 5-CT to the right in the manner of an antagonist. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2004.06.008

文献信息

• Aminotriazine 5-HT7 antagonists
  作者：Ronald J Mattson、Derek J Denhart、John D Catt、Michael F Dee、Jeffrey A Deskus、Jonathan L Ditta、James Epperson、H Dalton King、Aiming Gao、Michael A Poss、Ashok Purandare、David Tortolani、Yufen Zhao、Hua Yang、Suresh Yeola、Jane Palmer、John Torrente、Arlene Stark、Graham Johnson

  DOI：10.1016/j.bmcl.2004.06.008

  日期：2004.8

  The present studies have identified a series of aminotriazines as novel 5-HT7 receptor antagonists. Compounds 10 and 17 have high affinity for the 5-HT7 receptor and do not bind to either the 5-HT2C or 5-HT6 receptors. These compounds produce no agonist effects by themselves, and shift the dose-response curve of 5-CT to the right in the manner of an antagonist. (C) 2004 Elsevier Ltd. All rights reserved.