2-dimethylamino-4-oxo-6,7-dihydro-4H-imidazo[1,2-a]-1,3,5-triazine-8-dithiocarbonic acid potassium salt | 1161796-57-1

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: 2-dimethylamino-4-oxo-6,7-dihydro-4H-imidazo[1,2-a]-1,3,5-triazine-8-dithiocarbonic acid potassium salt
• 英文别名: Potassium;2-(dimethylamino)-4-oxo-6,7-dihydroimidazo[1,2-a][1,3,5]triazine-8-carbodithioate
• CAS: 1161796-57-1
• 化学式: C₈H₁₀N₅OS₂*K
• 分子量: 295.431
• InChiKey: KEISDFXKMLQVHI-UHFFFAOYSA-M

计算性质

• 辛醇/水分配系数(LogP)：
  -3.64
• 重原子数：
  17
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  84.6
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  二硫化碳 、 5,6-dihydro-2-dimethylaminoimidazo<1,2-a>-sym-triazin-8-one 在 氢氧化钾 作用下， 以 乙醇 为溶剂， 反应 0.5h， 以88%的产率得到2-dimethylamino-4-oxo-6,7-dihydro-4H-imidazo[1,2-a]-1,3,5-triazine-8-dithiocarbonic acid potassium salt
  参考文献：
  名称：

  Derivatives of imidazo-sym-triazine

  摘要：

  2-Dimethylamino-4,6,7,8-tetrahydroimidazo[1,2-a]-sym-triazin-4-one synthesized by us previously is converted by the action of aryl isocyanates and arenesulfonyl chlorides into the corresponding derivatives of urea and N-arenesulfonyl-substituted imidazo-sym-triazinones. It was shown that 6-(2-chloroethoxy)-2-dimethylamino-4-(methoxycarbonylmethylamino)-sym-triazine is converted by thermolysis into 2-dimethylamino-8-methoxycarbonylmethyl-4,6,7,8-tetrahydroimidazo[1,2-a]-1,3,5-triazin-4-one, which is also obtained by the action of methyl bromoacetate on the imidazo-sym-triazinone.

  DOI：

  10.1007/s10593-008-0143-0

文献信息

• Derivatives of imidazo-sym-triazine
  作者：V. V. Dovlatyan、K. A. Eliazyan、V. A. Pivazyan、A. P. Yengoyan

  DOI：10.1007/s10593-008-0143-0

  日期：2008.8

  2-Dimethylamino-4,6,7,8-tetrahydroimidazo[1,2-a]-sym-triazin-4-one synthesized by us previously is converted by the action of aryl isocyanates and arenesulfonyl chlorides into the corresponding derivatives of urea and N-arenesulfonyl-substituted imidazo-sym-triazinones. It was shown that 6-(2-chloroethoxy)-2-dimethylamino-4-(methoxycarbonylmethylamino)-sym-triazine is converted by thermolysis into 2-dimethylamino-8-methoxycarbonylmethyl-4,6,7,8-tetrahydroimidazo[1,2-a]-1,3,5-triazin-4-one, which is also obtained by the action of methyl bromoacetate on the imidazo-sym-triazinone.