6-Methoxy-1-methyl-9H-carbazole-2,3-dicarboxylic acid dimethyl ester | 213604-81-0

• 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: 6-Methoxy-1-methyl-9H-carbazole-2,3-dicarboxylic acid dimethyl ester
• 英文别名: dimethyl 6-methoxy-1-methyl-9H-carbazole-2,3-dicarboxylate
• CAS: 213604-81-0
• 化学式: C₁₈H₁₇NO₅
• 分子量: 327.337
• InChiKey: HRNDYMAYQRNZJG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  24
• 可旋转键数：
  5
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  77.6
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  6-Methoxy-1-methyl-9H-carbazole-2,3-dicarboxylic acid dimethyl ester 在 一水合肼 、 N,N-二乙基苯胺 、 三氯氧磷 作用下， 以 1,4-二氧六环 为溶剂， 反应 4.5h， 生成 N'-(1-Chloro-9-methoxy-5-methyl-6H-pyridazino[4,5-b]carbazol-4-yl)-N,N-diethyl-propane-1,3-diamine
  参考文献：
  名称：

  Synthesis of Pyridazino[4,5-b]carbazoles as Potential Antitumor Agents

  摘要：

  The synthesis of a series of new pyridazino[4,5-b]carbazoles (8, 9, 12-14), representing 3-aza analogs of pyridol [4,3-b]carbazole antitumor agents, is described. The key intermediates, d-fused dichloropyridazines of type 5, were subjected to nucleophilic displacement reactions and/or to reductive dehalogenation.

  DOI：

  10.3987/com-98-8217
• 作为产物：
  描述：

  丁炔二酸二甲酯 、 6-Methoxy-1-methyl-9H-pyrano[3,4-b]indol-3-one 以 various solvent(s) 为溶剂， 反应 1.5h， 以57%的产率得到6-Methoxy-1-methyl-9H-carbazole-2,3-dicarboxylic acid dimethyl ester
  参考文献：
  名称：

  Synthesis of Pyridazino[4,5-b]carbazoles as Potential Antitumor Agents

  摘要：

  The synthesis of a series of new pyridazino[4,5-b]carbazoles (8, 9, 12-14), representing 3-aza analogs of pyridol [4,3-b]carbazole antitumor agents, is described. The key intermediates, d-fused dichloropyridazines of type 5, were subjected to nucleophilic displacement reactions and/or to reductive dehalogenation.

  DOI：

  10.3987/com-98-8217

文献信息

• Synthesis of Pyridazino[4,5-b]carbazoles as Potential Antitumor Agents
  作者：Norbert Haider、Rami Jbara、Forouzandeh Khadami、Richard Wanko

  DOI：10.3987/com-98-8217

  日期：——

  The synthesis of a series of new pyridazino[4,5-b]carbazoles (8, 9, 12-14), representing 3-aza analogs of pyridol [4,3-b]carbazole antitumor agents, is described. The key intermediates, d-fused dichloropyridazines of type 5, were subjected to nucleophilic displacement reactions and/or to reductive dehalogenation.