(4,6-Bis-trichloromethyl-[1,3,5]triazin-2-yl)-(1-ethyl-piperidin-3-yl)-amine | 110045-47-1

• 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: (4,6-Bis-trichloromethyl-[1,3,5]triazin-2-yl)-(1-ethyl-piperidin-3-yl)-amine
• 英文别名: N-(1-ethylpiperidin-3-yl)-4,6-bis(trichloromethyl)-1,3,5-triazin-2-amine
• CAS: 110045-47-1
• 化学式: C₁₂H₁₅Cl₆N₅
• 分子量: 442.003
• InChiKey: PWUCKHFRYSYFNL-UHFFFAOYSA-N

物化性质

• 沸点：
  462.1±55.0 °C(Predicted)
• 密度：
  1.565±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.6
• 重原子数：
  23
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.75
• 拓扑面积：
  53.9
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  3-氨基-N-乙基哌啶 、 四异硫氰酸化硅 以 乙酸乙酯 为溶剂， 以69%的产率得到(4,6-Bis-trichloromethyl-[1,3,5]triazin-2-yl)-(1-ethyl-piperidin-3-yl)-amine
  参考文献：
  名称：

  Antimalarial activity of 2-(substituted amino)-4,6-bis(trichloromethyl)-1,3,5-triazines and N-(chlorophenyl)-N'-[4-(substituted amino)-6-(trichloromethyl)-1,3,5-triazin-2-yl]guanidines

  摘要：

  A series of 2-[[(dialkylamino)alkyl]amino]-4,6-bis(trichloromethyl)-1,3,5-triazines (III) and N-(4-chlorophenyl)-N'-[4-[[(dialkylamino)alkyl]amino]-6- (trichloromethyl)-1,3,5-triazin-2-yl]guanidines (IV) were prepared from 2,4,6-tris(trichloromethyl)-1,3,5-triazine and 2-chloro-4,6-bis(trichloromethyl)-1,3,5-triazine. Compounds of type III showed modest antimalarial activity while XIa with the camoquin side chain was more potent. Analogues of type IV broadly exhibited modest antimalarial activity.

  DOI：

  10.1021/jm00394a002

文献信息

• Antimalarial activity of 2-(substituted amino)-4,6-bis(trichloromethyl)-1,3,5-triazines and N-(chlorophenyl)-N'-[4-(substituted amino)-6-(trichloromethyl)-1,3,5-triazin-2-yl]guanidines
  作者：Leslie M. Werbel、Edward F. Elslager、Carolyn Hess、Marland P. Hutt

  DOI：10.1021/jm00394a002

  日期：1987.11

  A series of 2-[[(dialkylamino)alkyl]amino]-4,6-bis(trichloromethyl)-1,3,5-triazines (III) and N-(4-chlorophenyl)-N'-[4-[[(dialkylamino)alkyl]amino]-6- (trichloromethyl)-1,3,5-triazin-2-yl]guanidines (IV) were prepared from 2,4,6-tris(trichloromethyl)-1,3,5-triazine and 2-chloro-4,6-bis(trichloromethyl)-1,3,5-triazine. Compounds of type III showed modest antimalarial activity while XIa with the camoquin side chain was more potent. Analogues of type IV broadly exhibited modest antimalarial activity.