[4-(4-Cyclopentyl-piperazin-1-yl)-phenyl]-[6-methoxy-2-(4-methoxy-phenyl)-benzo[b]thiophen-3-yl]-methanone | 849662-59-5

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: [4-(4-Cyclopentyl-piperazin-1-yl)-phenyl]-[6-methoxy-2-(4-methoxy-phenyl)-benzo[b]thiophen-3-yl]-methanone
• CAS: 849662-59-5
• 化学式: C₃₂H₃₄N₂O₃S
• 分子量: 526.7
• InChiKey: FTKJSCFOHMEVPS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.88
• 重原子数：
  38.0
• 可旋转键数：
  7.0
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.34
• 拓扑面积：
  42.01
• 氢给体数：
  0.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  [4-(4-Cyclopentyl-piperazin-1-yl)-phenyl]-[6-methoxy-2-(4-methoxy-phenyl)-benzo[b]thiophen-3-yl]-methanone 在 三氯化铝 、 乙硫醇 作用下， 生成 [4-(4-Cyclopentyl-piperazin-1-yl)-phenyl]-[6-hydroxy-2-(4-hydroxy-phenyl)-benzo[b]thiophen-3-yl]-methanone
  参考文献：
  名称：

  Benzothiophenes containing a piperazine side chain as selective ligands for the estrogen receptor α and their bioactivities in vivo

  摘要：

  The synthesis of benzothiophenes containing a piperazine side chain and their binding affinities for estrogen receptors are described. These compounds bearing piperazine side chains were identified to be high-affinity ligands with high selectivity for ER alpha subtype. They were also potent agonists in bone tissue. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2004.12.074
• 作为产物：
  描述：

  6-甲氧基-2-(4-甲氧基苯基)-3-(4-氟苯甲酰基)苯并[b]噻吩 在 palladium on activated charcoal 甲酸铵 、 potassium carbonate 作用下， 以 四氢呋喃 、 N-甲基吡咯烷酮 、 甲醇 为溶剂， 反应 21.5h， 生成 [4-(4-Cyclopentyl-piperazin-1-yl)-phenyl]-[6-methoxy-2-(4-methoxy-phenyl)-benzo[b]thiophen-3-yl]-methanone
  参考文献：
  名称：

  Benzothiophenes containing a piperazine side chain as selective ligands for the estrogen receptor α and their bioactivities in vivo

  摘要：

  The synthesis of benzothiophenes containing a piperazine side chain and their binding affinities for estrogen receptors are described. These compounds bearing piperazine side chains were identified to be high-affinity ligands with high selectivity for ER alpha subtype. They were also potent agonists in bone tissue. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2004.12.074