[3-(4-Methoxy-4-oxobutyl)-7-methyl-6,8-dioxo-5-phenylisochromen-7-yl] cyclopentanecarboxylate | 1013888-89-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 氮杂非酮类
• 英文名称: [3-(4-Methoxy-4-oxobutyl)-7-methyl-6,8-dioxo-5-phenylisochromen-7-yl] cyclopentanecarboxylate
• CAS: 1013888-89-5
• 化学式: C₂₇H₂₈O₇
• 分子量: 464.515
• InChiKey: UVYYLKATRLKHLS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  34
• 可旋转键数：
  9
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.41
• 拓扑面积：
  96
• 氢给体数：
  0
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  4-氨基-1-丁醇 、 [3-(4-Methoxy-4-oxobutyl)-7-methyl-6,8-dioxo-5-phenylisochromen-7-yl] cyclopentanecarboxylate 在 Amberlite IRC₇₆ resin 作用下， 以 水 、 乙腈 为溶剂， 反应 8.5h， 生成 [2-(4-Hydroxybutyl)-3-(4-methoxy-4-oxobutyl)-7-methyl-6,8-dioxo-5-phenylisoquinolin-7-yl] cyclopentanecarboxylate
  参考文献：
  名称：

  Synthesis of Azaphilone-Based Chemical Libraries

  摘要：

  The synthesis of azaphilone scaffolds that have been further diversified by cross coupling acylation and amine addition is reported. Methodology development also led to novel modifications including CS acetoxylation and condensations producing isoquinolin-6(7H) structures. Overall, the library synthesis afforded three azaphilone sublibraries, including vinylogous pyridones which project diversity elements in four sectors of the azaphilone core.

  DOI：

  10.1021/co300002x
• 作为产物：
  描述：

  5-bromo-3-(4-methoxy-4-oxobutyl)-7-methyl-6,8-dioxo-7,8-dihydro-6H-isochromen-7-yl cyclopentanecarboxylate 、 三丁基苯基锡 在 palladium diacetate 、 三(邻甲基苯基)磷 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 12.0h， 以76%的产率得到[3-(4-Methoxy-4-oxobutyl)-7-methyl-6,8-dioxo-5-phenylisochromen-7-yl] cyclopentanecarboxylate
  参考文献：
  名称：

  Synthesis of Azaphilone-Based Chemical Libraries

  摘要：

  The synthesis of azaphilone scaffolds that have been further diversified by cross coupling acylation and amine addition is reported. Methodology development also led to novel modifications including CS acetoxylation and condensations producing isoquinolin-6(7H) structures. Overall, the library synthesis afforded three azaphilone sublibraries, including vinylogous pyridones which project diversity elements in four sectors of the azaphilone core.

  DOI：

  10.1021/co300002x

文献信息

• Synthesis of Azaphilone-Based Chemical Libraries
  作者：Mathieu Achard、Aaron B. Beeler、John A. Porco

  DOI：10.1021/co300002x

  日期：2012.3.12

  The synthesis of azaphilone scaffolds that have been further diversified by cross coupling acylation and amine addition is reported. Methodology development also led to novel modifications including CS acetoxylation and condensations producing isoquinolin-6(7H) structures. Overall, the library synthesis afforded three azaphilone sublibraries, including vinylogous pyridones which project diversity elements in four sectors of the azaphilone core.