4-(5-Bromo-2-methoxyphenyl)-2-methylpyrimidine | 1360444-92-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: 4-(5-Bromo-2-methoxyphenyl)-2-methylpyrimidine
• CAS: 1360444-92-3
• 化学式: C₁₂H₁₁BrN₂O
• 分子量: 279.136
• InChiKey: OJJDQSUZBIPWKD-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  16
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.17
• 拓扑面积：
  35
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  4-(5-Bromo-2-methoxyphenyl)-2-methylpyrimidine 在 四(三苯基膦)钯 、 三氟二甲基硫醚络合物 作用下， 以 乙二醇二甲醚 、 二氯甲烷 、 1,2-二氯乙烷 为溶剂， 反应 16.67h， 生成 5'-allyl-2'-methoxy-3-(2-methylpyrimidin-4-yl)-[1,1'-biphenyl]-4-ol
  参考文献：
  名称：

  Synthesis and neurite growth evaluation of new analogues of honokiol, a neolignan with potent neurotrophic activity

  摘要：

  A versatile synthetic route is reported towards the preparation of new analogues for potent neurotrophic agent biaryl-type lignan honokiol. A focused 24-membered library of derivatives containing five different groups at 5'-position of honokiol has been prepared in fair to good overall yields. Compared to the natural product, or to analogues with a short alkyl chain in this position, these new derivatives have lost most of the neurotrophic activity. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2011.12.015
• 作为产物：
  描述：

  5-溴-2-甲氧基苯甲醛 在 Jones reagent 、 sodium carbonate 作用下， 以 四氢呋喃 、 丙酮 、 乙腈 为溶剂， 反应 8.5h， 生成 4-(5-Bromo-2-methoxyphenyl)-2-methylpyrimidine
  参考文献：
  名称：

  Synthesis and neurite growth evaluation of new analogues of honokiol, a neolignan with potent neurotrophic activity

  摘要：

  A versatile synthetic route is reported towards the preparation of new analogues for potent neurotrophic agent biaryl-type lignan honokiol. A focused 24-membered library of derivatives containing five different groups at 5'-position of honokiol has been prepared in fair to good overall yields. Compared to the natural product, or to analogues with a short alkyl chain in this position, these new derivatives have lost most of the neurotrophic activity. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2011.12.015