(4,6-dichloro-[1,3,5]triazin-2-yl)-[4-(3,4-dimethoxyphenyl)-6-methylsulfanyl-pyrimidin-2-yl]-amine | 1160591-34-3

• 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: (4,6-dichloro-[1,3,5]triazin-2-yl)-[4-(3,4-dimethoxyphenyl)-6-methylsulfanyl-pyrimidin-2-yl]-amine
• 英文别名: 4,6-dichloro-N-[4-(3,4-dimethoxyphenyl)-6-methylsulfanylpyrimidin-2-yl]-1,3,5-triazin-2-amine
• CAS: 1160591-34-3
• 化学式: C₁₆H₁₄Cl₂N₆O₂S
• 分子量: 425.298
• InChiKey: FMSIEDLEWNSSBD-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.8
• 重原子数：
  27
• 可旋转键数：
  6
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.19
• 拓扑面积：
  120
• 氢给体数：
  1
• 氢受体数：
  9

反应信息

• 作为反应物：
  描述：

  (4,6-dichloro-[1,3,5]triazin-2-yl)-[4-(3,4-dimethoxyphenyl)-6-methylsulfanyl-pyrimidin-2-yl]-amine 、 N,N-二乙基乙二胺 在 potassium carbonate 作用下， 以 四氢呋喃 为溶剂， 反应 8.0h， 以68%的产率得到N2,N4-bis(2-(diethylamino)ethyl)-N6-(4-(3,4-dimethoxyphenyl)-6-(methylthio)pyrimidin-2-yl)-1,3,5-triazine-2,4,6-triamine
  参考文献：
  名称：

  Synthesis and antileishmanial activity of novel 2,4,6-trisubstituted pyrimidines and 1,3,5-triazines

  摘要：

  A series of 2,4,6-trisubstituted pyrimidines and 1,3,5-triazines have been synthesized and screened for their in vitro and in vivo antileishmanial activity against Leishmania donovani. Among all, 14 compounds have shown promising inhibition of 80-100% at 10 mu g/ml against promastigotes and IC50 in the range of 0.89-9.68 mu g/ml against amastigotes. Three compounds 13, 32 and 33 with good selectivity index (S.I.) were screened for their in vivo activity in golden hamsters (Mesocricetus auratus) infected with MHOM/IN/80/Dd(8) strain of L. donovani and have shown moderate in vivo inhibition of 48-56% at a dose of 50 mg/kg x 5, i.p. route for 5 days. (C) 2009 Published by Elsevier Masson SAS.

  DOI：

  10.1016/j.ejmech.2009.01.016
• 作为产物：
  描述：

  三聚氯氰 、 4-(3,4-dimethoxyphenyl)-6-methylsulfanyl-pyrimidin-2-ylamine 在 potassium carbonate 作用下， 以 四氢呋喃 为溶剂， 反应 9.0h， 以70%的产率得到(4,6-dichloro-[1,3,5]triazin-2-yl)-[4-(3,4-dimethoxyphenyl)-6-methylsulfanyl-pyrimidin-2-yl]-amine
  参考文献：
  名称：

  Synthesis and antileishmanial activity of novel 2,4,6-trisubstituted pyrimidines and 1,3,5-triazines

  摘要：

  A series of 2,4,6-trisubstituted pyrimidines and 1,3,5-triazines have been synthesized and screened for their in vitro and in vivo antileishmanial activity against Leishmania donovani. Among all, 14 compounds have shown promising inhibition of 80-100% at 10 mu g/ml against promastigotes and IC50 in the range of 0.89-9.68 mu g/ml against amastigotes. Three compounds 13, 32 and 33 with good selectivity index (S.I.) were screened for their in vivo activity in golden hamsters (Mesocricetus auratus) infected with MHOM/IN/80/Dd(8) strain of L. donovani and have shown moderate in vivo inhibition of 48-56% at a dose of 50 mg/kg x 5, i.p. route for 5 days. (C) 2009 Published by Elsevier Masson SAS.

  DOI：

  10.1016/j.ejmech.2009.01.016

文献信息

• Synthesis and antileishmanial activity of novel 2,4,6-trisubstituted pyrimidines and 1,3,5-triazines
  作者：Naresh Sunduru、Nishi、Shraddha Palne、Prem M.S. Chauhan、Suman Gupta

  DOI：10.1016/j.ejmech.2009.01.016

  日期：2009.6

  A series of 2,4,6-trisubstituted pyrimidines and 1,3,5-triazines have been synthesized and screened for their in vitro and in vivo antileishmanial activity against Leishmania donovani. Among all, 14 compounds have shown promising inhibition of 80-100% at 10 mu g/ml against promastigotes and IC50 in the range of 0.89-9.68 mu g/ml against amastigotes. Three compounds 13, 32 and 33 with good selectivity index (S.I.) were screened for their in vivo activity in golden hamsters (Mesocricetus auratus) infected with MHOM/IN/80/Dd(8) strain of L. donovani and have shown moderate in vivo inhibition of 48-56% at a dose of 50 mg/kg x 5, i.p. route for 5 days. (C) 2009 Published by Elsevier Masson SAS.