2-(aminocarbonyl)-5,11-trans-diethyl-8-methoxy-5,6,11,12-tetrahydrochrysene | 138090-14-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 菲及其衍生物
• 英文名称: 2-(aminocarbonyl)-5,11-trans-diethyl-8-methoxy-5,6,11,12-tetrahydrochrysene
• 英文别名: (5R,11S)-5,11-diethyl-8-methoxy-5,6,11,12-tetrahydrochrysene-2-carboxamide
• CAS: 138090-14-9
• 化学式: C₂₄H₂₇NO₂
• 分子量: 361.484
• InChiKey: XXXVSGMHKYJVDU-LSDHHAIUSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.87
• 重原子数：
  27.0
• 可旋转键数：
  4.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  52.32
• 氢给体数：
  1.0
• 氢受体数：
  2.0

反应信息

• 作为反应物：
  描述：

  2-(aminocarbonyl)-5,11-trans-diethyl-8-methoxy-5,6,11,12-tetrahydrochrysene 在 四氯化钛 、 三乙胺 作用下， 以 四氢呋喃 、 四氯化碳 为溶剂， 以99%的产率得到2-cyano-8-methoxy-5,11-trans-diethyl-5,6,11,12-tetrahydrochrysene
  参考文献：
  名称：

  5,6,11,12-Tetrahydrochrysenes: synthesis of rigid stilbene systems designed to be fluorescent ligands for the estrogen receptor

  摘要：

  We have prepared a series of tetrahydrochrysenes as fluorescent ligands for the estrogen receptor. The stilbene chromophore in this tetracyclic system is held rigid and is adorned with an electron-donating hydroxyl group at C-8 that corresponds to the phenolic hydroxyl of estrogens and an electron acceptor at C-2 to give a donor-acceptor fluorophore. Additional substituents at C-5 and C-11 provide additional bulk that improves receptor binding affinity without distorting the planar conjugated system. The tetrahydrochrysene core was prepared by an acyloin condensation of alpha-alkyl m-methoxyhydrocinnamate esters, followed by a double dehydrative cyclization. The cis and trans isomers of the alkyl substituted systems could be separated and their stereochemistry ascertained by X-ray crystallographic analysis; the trans isomer has the higher receptor binding affinity, and the derivative with ethyl substituents at C-5 and C-11 has the best affinity. The donor-acceptor systems were prepared by functional group manipulations on one of the aromatic methoxy groups: conversion to the trifluoromethanesulfonate was followed by a palladium-mediated carbonylation to give the acetyl derivative and methoxycarbonylation to give the ester. The ester was further elaborated to the amide and nitrile. The nitro compound was prepared by nitration of protio system, itself prepared by hydrogenolysis of the trifluoromethanesulfonate. As will be described later, these tetrahydrochrysenes provide a favorable combination of estrogen receptor binding affinity and long wavelength, high quantum yield fluorescence to make them useful as fluorescent ligands for the estrogen receptor.

  DOI：

  10.1021/jo00030a039
• 作为产物：
  描述：

  5,11-trans-diethyl-2-<(trifluoromethanesulfonyl)oxy>-8-methoxy-5,6,11,12-tetrahydrochrysene 在 palladium diacetate ammonium chloride-trimethylaluminium 、 1,3-双(二苯基膦)丙烷 、 三乙胺 作用下， 以 二甲基亚砜 、 苯 为溶剂， 反应 16.5h， 生成 2-(aminocarbonyl)-5,11-trans-diethyl-8-methoxy-5,6,11,12-tetrahydrochrysene
  参考文献：
  名称：

  5,6,11,12-Tetrahydrochrysenes: synthesis of rigid stilbene systems designed to be fluorescent ligands for the estrogen receptor

  摘要：

  We have prepared a series of tetrahydrochrysenes as fluorescent ligands for the estrogen receptor. The stilbene chromophore in this tetracyclic system is held rigid and is adorned with an electron-donating hydroxyl group at C-8 that corresponds to the phenolic hydroxyl of estrogens and an electron acceptor at C-2 to give a donor-acceptor fluorophore. Additional substituents at C-5 and C-11 provide additional bulk that improves receptor binding affinity without distorting the planar conjugated system. The tetrahydrochrysene core was prepared by an acyloin condensation of alpha-alkyl m-methoxyhydrocinnamate esters, followed by a double dehydrative cyclization. The cis and trans isomers of the alkyl substituted systems could be separated and their stereochemistry ascertained by X-ray crystallographic analysis; the trans isomer has the higher receptor binding affinity, and the derivative with ethyl substituents at C-5 and C-11 has the best affinity. The donor-acceptor systems were prepared by functional group manipulations on one of the aromatic methoxy groups: conversion to the trifluoromethanesulfonate was followed by a palladium-mediated carbonylation to give the acetyl derivative and methoxycarbonylation to give the ester. The ester was further elaborated to the amide and nitrile. The nitro compound was prepared by nitration of protio system, itself prepared by hydrogenolysis of the trifluoromethanesulfonate. As will be described later, these tetrahydrochrysenes provide a favorable combination of estrogen receptor binding affinity and long wavelength, high quantum yield fluorescence to make them useful as fluorescent ligands for the estrogen receptor.

  DOI：

  10.1021/jo00030a039