1-(4-甲氧基苯磺酰基)高哌嗪 | 937618-33-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 1-(4-甲氧基苯磺酰基)高哌嗪
• 英文名称: 1-(4-Methoxybenzenesulfonyl)-1,4-diazepane
• 英文别名: 1-(4-methoxyphenyl)sulfonyl-1,4-diazepane
• CAS: 937618-33-2
• 化学式: C₁₂H₁₈N₂O₃S
• mdl: MFCD07364372
• 分子量: 270.353
• InChiKey: AVROALWVWITGTM-UHFFFAOYSA-N

物化性质

• 沸点：
  424.7±55.0 °C(Predicted)
• 密度：
  1.214±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.7
• 重原子数：
  18
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  67
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  1-(4-甲氧基苯磺酰基)高哌嗪 在 水 、 caesium carbonate 、 lithium hydroxide 作用下， 以 四氢呋喃 、 甲醇 、 乙腈 为溶剂， 生成 4-[4-(4-Methoxyphenyl)sulfonyl-1,4-diazepan-1-yl]butanoic acid
  参考文献：
  名称：

  Solution-Phase Parallel Synthesis and SAR of Homopiperazinyl Analogs as Positive Allosteric Modulators of mGlu₄

  摘要：

  Using a functional high-throughput screening (HTS) and subsequent solution-phase parallel synthesis approach, we have discovered a novel series of positive allosteric modulators for mGlu(4), a G-protein coupled receptor. This series is comprised of a homopiperazine central core. The solution-phase parallel synthesis and SAP, of analogs derived from this series will be presented. This series of positive allosteric modulators of mGlu(4) provide critical research tools to further probe the mGlu(4)-mediated effects in Parkinson's disease.

  DOI：

  10.1021/co1000508
• 作为产物：
  描述：

  tert-butyl 4-((4-methoxyphenyl)sulfonyl)-1,4-diazepane-1-carboxylate 在 盐酸 、 水 作用下， 以 1,4-二氧六环 为溶剂， 以100%的产率得到1-(4-甲氧基苯磺酰基)高哌嗪
  参考文献：
  名称：

  Solution-Phase Parallel Synthesis and SAR of Homopiperazinyl Analogs as Positive Allosteric Modulators of mGlu₄

  摘要：

  Using a functional high-throughput screening (HTS) and subsequent solution-phase parallel synthesis approach, we have discovered a novel series of positive allosteric modulators for mGlu(4), a G-protein coupled receptor. This series is comprised of a homopiperazine central core. The solution-phase parallel synthesis and SAP, of analogs derived from this series will be presented. This series of positive allosteric modulators of mGlu(4) provide critical research tools to further probe the mGlu(4)-mediated effects in Parkinson's disease.

  DOI：

  10.1021/co1000508