3-chloro-14-methyl-8,13,13b,14-tetrahydro-7H-indolo[2',3':3,4]pyrido[2,1-b]quinazolin-5-one

• 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: 3-chloro-14-methyl-8,13,13b,14-tetrahydro-7H-indolo[2',3':3,4]pyrido[2,1-b]quinazolin-5-one
• 英文别名: 3-chloro-14-methyl-8,13,13b,14-tetrahydroindolo[2',3':3,4]pyrido[2,1-b]quinazolin-5(7H)-one；3-Chloroevodiamine；17-chloro-21-methyl-3,13,21-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,15(20),16,18-heptaen-14-one
• 化学式: C₁₉H₁₆ClN₃O
• 分子量: 337.809
• InChiKey: YPANHQUQZMGGSB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  24
• 可旋转键数：
  0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  39.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  5-氯靛红酸酐 在 三乙烯二胺 、 potassium carbonate 、 三氟乙酸酐 作用下， 以 N,N-二甲基乙酰胺 、 N,N-二甲基甲酰胺 为溶剂， 反应 5.0h， 生成 3-chloro-14-methyl-8,13,13b,14-tetrahydro-7H-indolo[2',3':3,4]pyrido[2,1-b]quinazolin-5-one
  参考文献：
  名称：

  连续双环化反应一锅法合成乙二胺及其类似物

  摘要：

  使用三组分反应可实现一锅法合成乙二胺及其类似物。通过连续的双环化，容易将具有良好官能团耐受性的各种容易获得的底物掺入具有生物活性的喹唑啉代咔啉主链中。三乙氧基甲烷作为助溶剂的使用对于这种快速而直接的转化至关重要。

  DOI：

  10.1021/acs.orglett.8b02667

文献信息

• One-Pot Total Synthesis of Evodiamine and Its Analogues through a Continuous Biscyclization Reaction
  作者：Zi-Xuan Wang、Jia-Chen Xiang、Miao Wang、Jin-Tian Ma、Yan-Dong Wu、An-Xin Wu

  DOI：10.1021/acs.orglett.8b02667

  日期：2018.10.19

  The one-pot total synthesis of evodiamine and its analogues is achieved using a three-component reaction. Through continuous biscyclization, various readily available substrates with good functional group tolerance were easily incorporated into biologically active quinazolinocarboline backbones. The use of triethoxymethane as a cosolvent was crucial for this quick and straightforward transformation

  使用三组分反应可实现一锅法合成乙二胺及其类似物。通过连续的双环化，容易将具有良好官能团耐受性的各种容易获得的底物掺入具有生物活性的喹唑啉代咔啉主链中。三乙氧基甲烷作为助溶剂的使用对于这种快速而直接的转化至关重要。
• Synthesis of evodiamine and its derivatives through a visible-light-driven intramolecular C N cross-coupling reaction
  作者：Linfeng Zhang、Dong Chen、Chao Zhou、Yutong Yin、Guixia Wang、Qiping Zhu、Shiqing Li、Xiangfei Kong

  DOI：10.1016/j.tetlet.2022.154305

  日期：2023.1

  A visible-light-initiated CNcross-coupling reaction is described, featuring metal-free and photocatalyst-free, at ambient temperature, with air as the oxidant and pinacolborane as the reducing agent. The substrates with electron-withdrawing groups give higher yields than those with electron-donating groups, but the substituent position has a negligible influence on yields. Moreover, DFT calculations

  描述了一种可见光引发的 C N交叉偶联反应，其特点是无金属和无光催化剂，在环境温度下，以空气为氧化剂，频哪醇硼烷为还原剂。具有吸电子基团的底物比具有给电子基团的底物具有更高的产率，但取代基位置对产率的影响可以忽略不计。此外，进行了DFT计算，结果与自由基反应机理相吻合。该反应为吴茱萸碱及其衍生物的合成提供了一种简单且环保的方法。
• New Tricks for an Old Natural Product: Discovery of Highly Potent Evodiamine Derivatives as Novel Antitumor Agents by Systemic Structure–Activity Relationship Analysis and Biological Evaluations
  作者：Guoqiang Dong、Shengzheng Wang、Zhenyuan Miao、Jianzhong Yao、Yongqiang Zhang、Zizhao Guo、Wannian Zhang、Chunquan Sheng

  DOI：10.1021/jm300605m

  日期：2012.9.13

  Evodiamine is a quinazolinocarboline alkaloid isolated from the fruits of traditional Chinese herb Evodiae fructus. Previously, we identified N13-substituted evodiamine derivatives as potent topoisomerase I inhibitors by structure-based virtual screening and lead optimization. Herein, a library of novel evodiamine derivatives bearing various substitutions or modified scaffold were synthesized. Among them, a number of evodiamine derivatives showed substantial increase of the antitumor activity, with GI(50) values lower than 3 nM. Moreover, these highly potent compounds can effectively induce the apoptosis of A549 cells. Interestingly, further computational target prediction calculations in combination with biological assays confirmed that the evodiamine derivatives acted by dual inhibition of topoisomerases I and II. Moreover, several hydroxyl derivatives, such as 10-hydroxyl evodiamine (10j) and 3-amino-10-hydroxyl evodiamine (18g), also showed good in vivo antitumor efficacy and low toxicity at the dose of 1 mg/kg or 2 mg/kg. They represent promising candidates for the development of novel antitumor agents.
• Discovery of evodiamine derivatives as potent insecticide candidates
  作者：Jingbo Liu、Yabing Shi、Shuting Chen、Fengyun Li、Wen Wen、Yuanhong Wang

  DOI：10.1016/j.bmc.2022.116727

  日期：2022.5

  search for novel more effective insecticides, natural products could be used as ideal template compounds due to their good environmental compatibility, various bioactivities, unique scaffolds and mode of action. We have found that natural product evodiamine, the main active component from the fruits of Evodia rutaecarpa (Juss.) Benth, displayed obvious insecticidal activities against lepidoptera pests

  在寻找新型更有效的杀虫剂时，天然产物具有良好的环境相容性、多种生物活性、独特的支架和作用方式，可作为理想的模板化合物。我们发现吴茱萸果实的主要活性成分天然产物吴茱萸碱对鳞翅目具有明显的杀虫活性。害虫。为了继续我们的研究，我们合理设计和合成了一系列吴茱萸碱衍生物3a-3aa。杀幼虫活性结果表明，大部分目标化合物对Mythimna separata、Plutella xylostella和Helicoverpa armigera的效果优于吴茱萸碱、苦参碱和鱼藤酮，其中3z表现出优异的杀幼虫活性（2.5 mg/L对M. separata的杀幼虫活性为65%， 75% 1.0 mg/L 对P. xylostella和 85% 10 mg/L 对H. armigera，分别），远优于吴茱萸碱（0%）、苦参碱（0%）和鱼藤酮（0%）。初步构效关系表明吴茱萸碱E环上的氟原子对杀幼虫活性有正向影响。钙显像