1-Morpholino-1-(4-pyridyl)aethylen | 55482-77-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 恶嗪烷类
• 英文名称: 1-Morpholino-1-(4-pyridyl)aethylen
• 英文别名: 4-(1-pyridin-4-yl-vinyl)-morpholine；4-[1-(Pyridin-4-yl)ethenyl]morpholine；4-(1-pyridin-4-ylethenyl)morpholine
• CAS: 55482-77-4
• 化学式: C₁₁H₁₄N₂O
• 分子量: 190.245
• InChiKey: ZLMJPYPBXMIKQY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.2
• 重原子数：
  14
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  25.4
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  1-Morpholino-1-(4-pyridyl)aethylen 、 对苯醌 以 乙醇 为溶剂， 反应 0.75h， 以3.9%的产率得到2-(pyridin-4-yl)benzofuran-5-ol
  参考文献：
  名称：

  A new synthetic access to furo[3,2-f]chromene analogues of an antimycobacterial

  摘要：

  From the structure of 3,3-dimethyl-3H-benzofuro[3,2-f][1]-benzopyran, a selective in vitro inhibitor of mycobacterial growth, we have undertaken a structure-activity relationship investigation. We wish to report here our results on the use of [2+3] cycloadditions between 2-formylbenzoquinone and various enol derivatives to give various 4-formyl-5-hydroxy benzofurans. In the next step, an ytterbium triflate-catalysed reaction with 2-methylpropene allowed the preparation of various original furo[3,2-f]chromenes derivatives. Their biological evaluation on the growth of Mycobacterium smegmatis as well as Mycobacterium tuberculosis pointed out that some analogues were four times more active than the initial hit. (C) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2008.06.057
• 作为产物：
  描述：

  吗啉 、 4-乙酰吡啶 生成 1-Morpholino-1-(4-pyridyl)aethylen
  参考文献：
  名称：

  胺。第三十八部分 1-芳基-1-二烷基氨基丙烯的构型

  摘要：

  从1 H nmr数据中已经指定了几种1-芳基-1-二烷基氨基丙烯的构型。与相应的Z-异构体相比，E-异构体的烯烃质子在更高的电场下共振。

  DOI：

  10.1039/p19740002671

文献信息

• US4026900A
  申请人：——

  公开号：US4026900A

  公开（公告）日：1977-05-31
• US4075217A
  申请人：——

  公开号：US4075217A

  公开（公告）日：1978-02-21
• US4111946A
  申请人：——

  公开号：US4111946A

  公开（公告）日：1978-09-05
• US4127583A
  申请人：——

  公开号：US4127583A

  公开（公告）日：1978-11-28
• A new synthetic access to furo[3,2-f]chromene analogues of an antimycobacterial
  作者：Luke Alvey、Soizic Prado、Valérie Huteau、Brigitte Saint-Joanis、Sylvie Michel、Michel Koch、Stewart T. Cole、François Tillequin、Yves L. Janin

  DOI：10.1016/j.bmc.2008.06.057

  日期：2008.9

  From the structure of 3,3-dimethyl-3H-benzofuro[3,2-f][1]-benzopyran, a selective in vitro inhibitor of mycobacterial growth, we have undertaken a structure-activity relationship investigation. We wish to report here our results on the use of [2+3] cycloadditions between 2-formylbenzoquinone and various enol derivatives to give various 4-formyl-5-hydroxy benzofurans. In the next step, an ytterbium triflate-catalysed reaction with 2-methylpropene allowed the preparation of various original furo[3,2-f]chromenes derivatives. Their biological evaluation on the growth of Mycobacterium smegmatis as well as Mycobacterium tuberculosis pointed out that some analogues were four times more active than the initial hit. (C) 2008 Elsevier Ltd. All rights reserved.