2-(biphenyl-4-yl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol | 1527518-42-8

• 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: 2-(biphenyl-4-yl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol
• 英文别名: 2-(Biphenyl-4-yl)-3-cyclopropyl-1-(1h-1,2,4-triazol-1-yl)butan-2-ol；3-cyclopropyl-2-(4-phenylphenyl)-1-(1,2,4-triazol-1-yl)butan-2-ol
• CAS: 1527518-42-8
• 化学式: C₂₁H₂₃N₃O
• 分子量: 333.433
• InChiKey: HLSYFEIZKHNHCT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  25
• 可旋转键数：
  6
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  50.9
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  环唑醇 在 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodide 、 氨 、 sodium 、 三苯基膦 、 cesium fluoride 作用下， 以 甲苯 为溶剂， 反应 49.5h， 生成 2-(biphenyl-4-yl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol
  参考文献：
  名称：

  Arylation of aryl chlorides, a convenient method for the synthesis of new potential triazolic fungicides

  摘要：

  We evaluated two alternative routes for the arylation of known chlorinated fungicides. The first pathway involved a SRN1 substitution, followed by Stille reaction, while the second consisted in a one step reaction by the Suzuki coupling. Both methodologies were useful to obtain new products that could be potential fungicides. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2013.11.067

文献信息

• Arylation of aryl chlorides, a convenient method for the synthesis of new potential triazolic fungicides
  作者：Natividad Herrera Cano、Ana N. Santiago

  DOI：10.1016/j.tet.2013.11.067

  日期：2014.1

  We evaluated two alternative routes for the arylation of known chlorinated fungicides. The first pathway involved a SRN1 substitution, followed by Stille reaction, while the second consisted in a one step reaction by the Suzuki coupling. Both methodologies were useful to obtain new products that could be potential fungicides. (C) 2013 Elsevier Ltd. All rights reserved.