3-methyl-N-[(2-methylphenyl)-phenylmethyl]pyridin-2-amine | 1388624-26-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 3-methyl-N-[(2-methylphenyl)-phenylmethyl]pyridin-2-amine
• CAS: 1388624-26-7
• 化学式: C₂₀H₂₀N₂
• 分子量: 288.392
• InChiKey: DINDEKMJLZRVFO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.1
• 重原子数：
  22
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.15
• 拓扑面积：
  24.9
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  2-氯-3-甲基吡啶 在 十二羰基三钌 、 palladium diacetate 、 potassium carbonate 、 R-(+)-1,1'-联萘-2,2'-双二苯膦 作用下， 以 频哪酮 、 甲苯 为溶剂， 反应 16.0h， 生成 3-methyl-N-[(2-methylphenyl)-phenylmethyl]pyridin-2-amine
  参考文献：
  名称：

  Ruthenium(0)-Catalyzed sp³ C–H Bond Arylation of Benzylic Amines Using Arylboronates

  摘要：

  A Ru-catalyzed direct arylation of benzylic sp(3) carbons of acyclic amines with arylboronates is reported. This highly regioselective and efficient transformation can be performed with various combinations of N-(2-pyridyl) substituted benzylamines and arylboronates. Substitution of the pyridine directing group in the 3-position proved to be crucial in order to achieve high arylation yields. Furthermore, the pyridine directing group can be removed in high yields via a two-step protocol.

  DOI：

  10.1021/ol300627p

文献信息

• Ruthenium(II)-Catalyzed sp³ C–H Bond Arylation of Benzylic Amines Using Aryl Halides
  作者：Navid Dastbaravardeh、Michael Schnürch、Marko D. Mihovilovic

  DOI：10.1021/ol301680v

  日期：2012.7.20

  protocol for the direct arylation of benzylic amines was developed. Employing 3-substituted pyridines as directing groups, arylation was achieved using aryl bromides or aryl iodides as the aryl source. Potassium pivalate proved to be an important additive in this transformation. The arylation took place selectively in the benzylic sp3 position, and no significant competitive sp2 arylation was observed

  建立了钌（II）催化的苄基胺直接芳基化的方案。使用3-取代的吡啶作为指导基团，使用芳基溴化物或芳基碘化物作为芳基源实现芳基化。新戊酸钾被证明是该转化过程中的重要添加剂。芳基化选择性地发生在苄基sp 3位置，没有观察到明显的竞争性sp 2芳基化。观察到少量的丙烯酸化亚胺为副产物。另外，建立了裂解吡啶基的反应条件，使得能够获得双芳基甲胺。
• Ruthenium(0)-Catalyzed sp³ C–H Bond Arylation of Benzylic Amines Using Arylboronates
  作者：Navid Dastbaravardeh、Michael Schnürch、Marko D. Mihovilovic

  DOI：10.1021/ol300627p

  日期：2012.4.6

  A Ru-catalyzed direct arylation of benzylic sp(3) carbons of acyclic amines with arylboronates is reported. This highly regioselective and efficient transformation can be performed with various combinations of N-(2-pyridyl) substituted benzylamines and arylboronates. Substitution of the pyridine directing group in the 3-position proved to be crucial in order to achieve high arylation yields. Furthermore, the pyridine directing group can be removed in high yields via a two-step protocol.