ethyl (2E,4E)-5-[2-[3,5-di(propan-2-yl)-2-propoxyphenyl]cyclopenten-1-yl]-3-methylpenta-2,4-dienoate | 330935-10-9

• 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: ethyl (2E,4E)-5-[2-[3,5-di(propan-2-yl)-2-propoxyphenyl]cyclopenten-1-yl]-3-methylpenta-2,4-dienoate
• CAS: 330935-10-9
• 化学式: C₂₈H₄₀O₃
• 分子量: 424.624
• InChiKey: MYYAPMWKCWOMHY-VXUIJSMJSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.7
• 重原子数：
  31
• 可旋转键数：
  11
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.54
• 拓扑面积：
  35.5
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  ethyl (2E,4E)-5-[2-[3,5-di(propan-2-yl)-2-propoxyphenyl]cyclopenten-1-yl]-3-methylpenta-2,4-dienoate 在 lithium hydroxide 作用下， 以 乙醇 为溶剂， 反应 3.0h， 以88%的产率得到5-[2-(3,5-Diisopropyl-2-propoxy-phenyl)-cyclopent-1-enyl]-3-methyl-penta-2,4-dienoic acid
  参考文献：
  名称：

  Design, Synthesis, and Structure−Activity Relationship Studies of Novel 6,7-Locked-[7-(2-alkoxy-3,5-dialkylbenzene)-3-methylocta]-2,4,6-trienoic Acids

  摘要：

  Retinoid X receptor:peroxisome proliferative-activated receptor (RXR:PPAR) heterodimers play a critical role in the regulation of glucose (RXR/PPARy) and lipid metabolism (RXR/PPARalpha). Previously, we described a concise structure-activity relationship study of selective RXR modulators possessing a (2E,4E,6Z)-3-methyl-7-(3,5-dialkyl-6-Eilkoxyphenyl)-octa-2,4,6-trienoic acid scaffold. These studies were focused on the 2-position alkoxy side chain. We describe here the design and synthesis of a novel series of RXR selective modulators possessing the same aromatic core structure with the addition of a ring locked 6--7-Z-olefin on the trienoic acid moiety. The synthesis and structure- activity relationship studies of these 6,7-locked cyclopentenyl, phenyl, thienyl, furan, and pyridine-trienoic acid derivatives is presented herein.

  DOI：

  10.1021/jm020401k
• 作为产物：
  描述：

  2,4-二异丙基苯酚 在 盐酸 、 N,N-二甲基丙烯基脲 、 N-碘代丁二酰亚胺 、 四(三苯基膦)钯 、 正丁基锂 、 四丙基高钌酸铵 、 氢化铝钠 、 sodium hydride 、 sodium carbonate 、 对甲苯磺酸 、 N-甲基吗啉氧化物 、 cesium fluoride 作用下， 以 四氢呋喃 、 乙醚 、 乙醇 、 正己烷 、 二氯甲烷 、 N,N-二甲基甲酰胺 、 甲苯 为溶剂， 反应 112.66h， 生成 ethyl (2E,4E)-5-[2-[3,5-di(propan-2-yl)-2-propoxyphenyl]cyclopenten-1-yl]-3-methylpenta-2,4-dienoate
  参考文献：
  名称：

  Design, Synthesis, and Structure−Activity Relationship Studies of Novel 6,7-Locked-[7-(2-alkoxy-3,5-dialkylbenzene)-3-methylocta]-2,4,6-trienoic Acids

  摘要：

  Retinoid X receptor:peroxisome proliferative-activated receptor (RXR:PPAR) heterodimers play a critical role in the regulation of glucose (RXR/PPARy) and lipid metabolism (RXR/PPARalpha). Previously, we described a concise structure-activity relationship study of selective RXR modulators possessing a (2E,4E,6Z)-3-methyl-7-(3,5-dialkyl-6-Eilkoxyphenyl)-octa-2,4,6-trienoic acid scaffold. These studies were focused on the 2-position alkoxy side chain. We describe here the design and synthesis of a novel series of RXR selective modulators possessing the same aromatic core structure with the addition of a ring locked 6--7-Z-olefin on the trienoic acid moiety. The synthesis and structure- activity relationship studies of these 6,7-locked cyclopentenyl, phenyl, thienyl, furan, and pyridine-trienoic acid derivatives is presented herein.

  DOI：

  10.1021/jm020401k