5-[2-(2-(6-(methoxymethoxy)-2,5,7,8-tetramethylchroman-2-yl)methoxy)-5-pyridylmethyl]-2,4-thiazolidinedione | 695171-59-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并吡喃
• 英文名称: 5-[2-(2-(6-(methoxymethoxy)-2,5,7,8-tetramethylchroman-2-yl)methoxy)-5-pyridylmethyl]-2,4-thiazolidinedione
• CAS: 695171-59-6
• 化学式: C₂₅H₃₀N₂O₆S
• 分子量: 486.589
• InChiKey: DINDABLIZSIUFS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.05
• 重原子数：
  34.0
• 可旋转键数：
  8.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.48
• 拓扑面积：
  95.98
• 氢给体数：
  1.0
• 氢受体数：
  8.0

反应信息

• 作为反应物：
  描述：

  5-[2-(2-(6-(methoxymethoxy)-2,5,7,8-tetramethylchroman-2-yl)methoxy)-5-pyridylmethyl]-2,4-thiazolidinedione 在 硫酸 、 溶剂黄146 、 间氯过氧苯甲酸 作用下， 以 甲醇 、 氯仿 、 水 为溶剂， 反应 20.0h， 生成
  参考文献：
  名称：

  Studies on some glitazones having pyridine as the linker unit

  摘要：

  Molecular modeling on various well-known glitazones carrying a pyridine ring instead of benzene ring as the middle linker unit showed conformational rigidity as compared to their parent molecules. Blocking the lone pair of electrons on the pyridine N, made them flexible once again. A few representatives of these analogues were synthesized and their efficacy as PPARgamma agonists evaluated. (C) 2003 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2003.11.027
• 作为产物：
  描述：

  5-[2-(2-(6-(methoxymethoxy)-2,5,7,8-tetramethylchroman-2-yl)methoxy)-5-pyridylmethylene]-2,4-thiazolidinedione 在 palladium on activated charcoal 氢气 作用下， 以 1,4-二氧六环 为溶剂， 反应 24.0h， 生成 5-[2-(2-(6-(methoxymethoxy)-2,5,7,8-tetramethylchroman-2-yl)methoxy)-5-pyridylmethyl]-2,4-thiazolidinedione
  参考文献：
  名称：

  Studies on some glitazones having pyridine as the linker unit

  摘要：

  Molecular modeling on various well-known glitazones carrying a pyridine ring instead of benzene ring as the middle linker unit showed conformational rigidity as compared to their parent molecules. Blocking the lone pair of electrons on the pyridine N, made them flexible once again. A few representatives of these analogues were synthesized and their efficacy as PPARgamma agonists evaluated. (C) 2003 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2003.11.027