2-[2-(4-benzyloxyphenyl)ethoxy]ethanol | 86902-15-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 酚类
• 英文名称: 2-[2-(4-benzyloxyphenyl)ethoxy]ethanol
• 英文别名: 2-[2-(4-Phenylmethoxyphenyl)ethoxy]ethanol
• CAS: 86902-15-0
• 化学式: C₁₇H₂₀O₃
• 分子量: 272.344
• InChiKey: JPFHREAMFXRYAI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  20
• 可旋转键数：
  8
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  38.7
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-[2-(4-benzyloxyphenyl)ethoxy]ethanol 在 palladium on activated charcoal 吡啶 、 氢气 、 sodium hydride 作用下， 以 乙醇 、 乙酸乙酯 为溶剂， 反应 1.25h， 生成 4-<2-(2-phenoxyethoxy)ethyl>phenol
  参考文献：
  名称：

  .beta.1-Selective adrenoceptor antagonists. 2. 4-Ether-linked phenoxypropanolamines

  摘要：

  A series of 4-substituted phenoxypropanolamines was prepared and examined for beta-adrenoceptor activity. Some of the compounds, especially the [4-[2-[[2-(4-fluorophenyl)ethyl] oxy]ethoxy]phenoxy]propanolamines (14, 15, and 24), showed potent beta 1-blockade with virtually no beta 2-blockade at doses over a 1000 times greater. The compounds also possessed partial agonist activity. Structure-activity relationships are discussed, and conclusions are drawn about the binding sites on beta-adrenoceptors.

  DOI：

  10.1021/jm00365a005
• 作为产物：
  描述：

  2-(4-苯甲氧基苯基)乙醇 在 lithium aluminium tetrahydride 、 sodium hydride 作用下， 以 四氢呋喃 为溶剂， 反应 3.67h， 生成 2-[2-(4-benzyloxyphenyl)ethoxy]ethanol
  参考文献：
  名称：

  .beta.1-Selective adrenoceptor antagonists. 2. 4-Ether-linked phenoxypropanolamines

  摘要：

  A series of 4-substituted phenoxypropanolamines was prepared and examined for beta-adrenoceptor activity. Some of the compounds, especially the [4-[2-[[2-(4-fluorophenyl)ethyl] oxy]ethoxy]phenoxy]propanolamines (14, 15, and 24), showed potent beta 1-blockade with virtually no beta 2-blockade at doses over a 1000 times greater. The compounds also possessed partial agonist activity. Structure-activity relationships are discussed, and conclusions are drawn about the binding sites on beta-adrenoceptors.

  DOI：

  10.1021/jm00365a005

文献信息

• WO2008/96093
  申请人：——

  公开号：——

  公开（公告）日：——
• MACHIN, P. J.;HURST, D. N.;BRADSHAW, R. M.;BLABER, L. C.;BURDEN, D. T.;FR+, J. MED. CHEM., 1983, 26, N 11, 1570-1576
  作者：MACHIN, P. J.、HURST, D. N.、BRADSHAW, R. M.、BLABER, L. C.、BURDEN, D. T.、FR+

  DOI：——

  日期：——
• [EN] OXAZOLE AND THIAZOLE DERIVATIVES AND THEIR USES<br/>[FR] DÉRIVÉS D'OXAZOLE ET DE THIAZOLE ET LEURS UTILISATIONS
  申请人：ARGENTA DISCOVERY LTD

  公开号：WO2008096093A1

  公开（公告）日：2008-08-14

  [EN] A quaternary ammonium compound of formula (I) having M3 receptor antagonist activity; a composition comprising such a compound; the use of such a compound in therapy (such as asthma or COPD); and a method of treating a patient with such a compound.
  [FR] L'invention concerne un composé d'ammonium quaternaire de formule (I) ayant une activité antagoniste du récepteur M3; une composition comprenant ce composé; l'utilisation de ce composé en thérapie (telle que le traitement de l'asthme ou de COPD (maladie pulmonaire obstructive chroniquesdu cheval)); et une méthode visant à traiter un patient avec ce composé.
• .beta.1-Selective adrenoceptor antagonists. 2. 4-Ether-linked phenoxypropanolamines
  作者：Peter J. Machin、David N. Hurst、Rachel M. Bradshaw、Leslie C. Blaber、David T. Burden、Allison D. Fryer、Rosemary A. Melarange、Celia Shivdasani

  DOI：10.1021/jm00365a005

  日期：1983.11

  A series of 4-substituted phenoxypropanolamines was prepared and examined for beta-adrenoceptor activity. Some of the compounds, especially the [4-[2-[[2-(4-fluorophenyl)ethyl] oxy]ethoxy]phenoxy]propanolamines (14, 15, and 24), showed potent beta 1-blockade with virtually no beta 2-blockade at doses over a 1000 times greater. The compounds also possessed partial agonist activity. Structure-activity relationships are discussed, and conclusions are drawn about the binding sites on beta-adrenoceptors.