2-((5-bromothiazol-2-yl)oxy)-5-isobutoxyaniline | 936247-49-3

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 2-((5-bromothiazol-2-yl)oxy)-5-isobutoxyaniline
• CAS: 936247-49-3
• 化学式: C₁₃H₁₅BrN₂O₂S
• 分子量: 343.244
• InChiKey: DRPPIQNDSGDCMT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.31
• 重原子数：
  19.0
• 可旋转键数：
  5.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  57.37
• 氢给体数：
  1.0
• 氢受体数：
  5.0

反应信息

• 作为反应物：
  描述：

  2-((5-bromothiazol-2-yl)oxy)-5-isobutoxyaniline 在 bis-triphenylphosphine-palladium(II) chloride copper(l) iodide 、 三乙胺 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 生成 N-{3-[2-(2-acetylamino-4-isobutoxy-phenoxy)-thiazol-5-yl]-1-methyl-prop-2-ynyl}-acetamide
  参考文献：
  名称：

  Phenoxy thiazole derivatives as potent and selective acetyl-CoA carboxylase 2 inhibitors: Modulation of isozyme selectivity by incorporation of phenyl ring substituents

  摘要：

  A phenyl ring substitution strategy was employed to optimize the ACC2 potency and selectivity profiles of a recently discovered phenoxy thiazolyl series of acetyl-CoA carboxylase inhibitors. Ring substituents were shown to dramatically affect isozyme selectivity. Modifications that generally impart high levels of ACC2 selectivity (> 3000-fold) while maintaining excellent ACC2 potency (IC(50)s similar to 9-20 nM) were identified. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2007.01.022
• 作为产物：
  描述：

  4-甲氧基-2-硝基酚 在 钾硼氢 、 三溴化硼 、 potassium carbonate 、 potassium iodide 、 copper(l) chloride 作用下， 以 甲醇 、 二氯甲烷 、 N,N-二甲基甲酰胺 为溶剂， 生成 2-((5-bromothiazol-2-yl)oxy)-5-isobutoxyaniline
  参考文献：
  名称：

  Phenoxy thiazole derivatives as potent and selective acetyl-CoA carboxylase 2 inhibitors: Modulation of isozyme selectivity by incorporation of phenyl ring substituents

  摘要：

  A phenyl ring substitution strategy was employed to optimize the ACC2 potency and selectivity profiles of a recently discovered phenoxy thiazolyl series of acetyl-CoA carboxylase inhibitors. Ring substituents were shown to dramatically affect isozyme selectivity. Modifications that generally impart high levels of ACC2 selectivity (> 3000-fold) while maintaining excellent ACC2 potency (IC(50)s similar to 9-20 nM) were identified. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2007.01.022