5-(2-isopropylphenyl)-2-methoxypyridine | 1186126-60-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: 5-(2-isopropylphenyl)-2-methoxypyridine
• 英文别名: 2-Methoxy-5-(2-propan-2-ylphenyl)pyridine
• CAS: 1186126-60-2
• 化学式: C₁₅H₁₇NO
• 分子量: 227.306
• InChiKey: ZOTVLZXJGYBFHL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  17
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  22.1
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  4-­-phenylphenol xtosylate 、 2-甲氧基-5-吡啶硼酸 在 potassium phosphate 、 2-(二环己基膦)3,6-二甲氧基-2′,4′,6′-三异丙基-1,1′-联苯 、 palladium diacetate 作用下， 以 2-甲基-2-丁醇 为溶剂， 以89%的产率得到5-(2-isopropylphenyl)-2-methoxypyridine
  参考文献：
  名称：

  A Versatile Catalyst System for Suzuki−Miyaura Cross-Coupling Reactions of C(sp²)-Tosylates and Mesylates

  摘要：

  A catalyst system for the Suzuki-Miyaura cross-coupling reactions of aryl and vinyl tosylates and mesylates has been developed. This catalyst displays excellent functional group tolerance and allows the coupling of heteroarylboronic acids with aryl tosylates and mesylates to be performed in high yields. Moreover, reactions employing alkylboronic acids, as well as heteroaryl, vinyl, and allylic pinacol boronate esters, were conducted with high efficiencies.

  DOI：

  10.1021/ol9015892

文献信息

• Potassium Channel Inhibitors
  申请人：Trotter B. Wesley

  公开号：US20090233897A1

  公开（公告）日：2009-09-17

  The present invention relates to compounds having the structure useful as potassium channel inhibitors to treat cardiac arrhythmias, and the like.

  本发明涉及具有结构的化合物，可用作钾通道抑制剂以治疗心律失常等。
• Arylsulfonylnaphthalene Derivatives As 5Ht2a Antagonists
  申请人：Chambers Stuart Mark

  公开号：US20070281952A1

  公开（公告）日：2007-12-06

  Compounds of formula (I) are potent and selective 5-HT 2A antagonists, useful in treatment of a variety of adverse conditions of the CNS.

  公式为（I）的化合物是有效且选择性的5-HT2A拮抗剂，可用于治疗中枢神经系统的各种不良状况。
• US7592456B2
  申请人：——

  公开号：US7592456B2

  公开（公告）日：2009-09-22
• US8148535B2
  申请人：——

  公开号：US8148535B2

  公开（公告）日：2012-04-03
• A Versatile Catalyst System for Suzuki−Miyaura Cross-Coupling Reactions of C(sp²)-Tosylates and Mesylates
  作者：Brijesh Bhayana、Brett P. Fors、Stephen L. Buchwald

  DOI：10.1021/ol9015892

  日期：2009.9.3

  A catalyst system for the Suzuki-Miyaura cross-coupling reactions of aryl and vinyl tosylates and mesylates has been developed. This catalyst displays excellent functional group tolerance and allows the coupling of heteroarylboronic acids with aryl tosylates and mesylates to be performed in high yields. Moreover, reactions employing alkylboronic acids, as well as heteroaryl, vinyl, and allylic pinacol boronate esters, were conducted with high efficiencies.