5-chloro-1-({4-[4-chlorobenzyl]piperazin-1-yl}-methyl)indoline-2,3-dione

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: 5-chloro-1-({4-[4-chlorobenzyl]piperazin-1-yl}-methyl)indoline-2,3-dione
• 英文别名: 5-chloro-1-[[4-[(4-chlorophenyl)methyl]piperazin-1-yl]methyl]indole-2,3-dione
• 化学式: C₂₀H₁₉Cl₂N₃O₂
• 分子量: 404.296
• InChiKey: VIETUGSVLYJPOV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  27
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  43.9
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  聚合甲醛 、 1-(4-氯苄基)哌嗪 、 5-氯靛红 以 乙醇 、 水 为溶剂， 反应 3.0h， 以77%的产率得到5-chloro-1-({4-[4-chlorobenzyl]piperazin-1-yl}-methyl)indoline-2,3-dione
  参考文献：
  名称：

  A Study on Hydrolytic Stability of Isatin N-Mannich Bases

  摘要：

  Stability parameters of biologically active compounds with N-Mannich base motif in their structure, which is susceptible to hydrolysis, have been studied. A procedure for the synthesis of small molecule compounds reactivating the function of the p53 tumor suppressor protein was developed, and the dependence of the Mannich base degradation rate on the structure of the compounds was established. For the hydrolysis reaction we determined the rate constants and calculated rho, Delta G#, Delta H, and Delta S. Modifications of active compounds that retain the activity at the maximum possible stability were proposed.

  DOI：

  10.1134/s1070363218010085

文献信息

• A Study on Hydrolytic Stability of Isatin N-Mannich Bases
  作者：D. D. Orlova、D. S. Novikova、A. V. Garabadzhiu、V. G. Tribulovich

  DOI：10.1134/s1070363218010085

  日期：2018.1

  Stability parameters of biologically active compounds with N-Mannich base motif in their structure, which is susceptible to hydrolysis, have been studied. A procedure for the synthesis of small molecule compounds reactivating the function of the p53 tumor suppressor protein was developed, and the dependence of the Mannich base degradation rate on the structure of the compounds was established. For the hydrolysis reaction we determined the rate constants and calculated rho, Delta G#, Delta H, and Delta S. Modifications of active compounds that retain the activity at the maximum possible stability were proposed.