(+)-N-<(2R)-7-hydroxy-1,2,3,4-tetrahydronaphth-2-yl>-(S)-mandelamide | 121216-36-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 四氢化萘
• 英文名称: (+)-N-<(2R)-7-hydroxy-1,2,3,4-tetrahydronaphth-2-yl>-(S)-mandelamide
• 英文别名: N-[(2R)-7-hydroxy-1,2,3,4-tetrahydronaphth-2-yl]-(S)-mandelamide；(+)-N-((2R)-7-hydroxy-1,2,3,4-tetrahydronaphth-2-yl)-(S)-mandelamide；(2S)-2-hydroxy-N-[(2R)-7-hydroxy-1,2,3,4-tetrahydronaphthalen-2-yl]-2-phenylacetamide
• CAS: 121216-36-2
• 化学式: C₁₈H₁₉NO₃
• 分子量: 297.354
• InChiKey: DCKGATCXENEYCB-WBVHZDCISA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  22
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.28
• 拓扑面积：
  69.6
• 氢给体数：
  3
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (+)-N-<(2R)-7-hydroxy-1,2,3,4-tetrahydronaphth-2-yl>-(S)-mandelamide 在 dimethyl sulfide borane 作用下， 以 四氢呋喃 为溶剂， 反应 4.0h， 生成 (7R)-7-[[(2S)-2-hydroxy-2-phenylethyl]amino]-5,6,7,8-tetrahydronaphthalen-2-ol
  参考文献：
  名称：

  Synthesis and β-adrenergic activity of atypical β-adrenergic phenylethanolaminotetralin stereoisomers

  摘要：

  A series of substituted phenylethanolaminotetralins were synthesized as pure stereoisomers and their ability to stimulate atypical beta-adrenoceptors selectively was evaluated. The compounds in vitro relative potencies were assessed using the atypical beta response of inhibition of rat proximal colon motility and the typical beta 1 (increase in guinea-pig right atrial frequency) and beta 2 (guinea-pig tracheal relaxation and rat uterus motility inhibition) responses. Compound 42 (SR 58611A) was found to be the most potent and selective.

  DOI：

  10.1016/0223-5234(94)90095-7
• 作为产物：
  描述：

  2-氨基-7-甲氧基四氢萘 在 ammonium hydroxide 、 TEA 、 氢溴酸 、 (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate 作用下， 以 二氯甲烷 为溶剂， 反应 8.0h， 生成 (+)-N-<(2R)-7-hydroxy-1,2,3,4-tetrahydronaphth-2-yl>-(S)-mandelamide
  参考文献：
  名称：

  Synthesis and β-adrenergic activity of atypical β-adrenergic phenylethanolaminotetralin stereoisomers

  摘要：

  A series of substituted phenylethanolaminotetralins were synthesized as pure stereoisomers and their ability to stimulate atypical beta-adrenoceptors selectively was evaluated. The compounds in vitro relative potencies were assessed using the atypical beta response of inhibition of rat proximal colon motility and the typical beta 1 (increase in guinea-pig right atrial frequency) and beta 2 (guinea-pig tracheal relaxation and rat uterus motility inhibition) responses. Compound 42 (SR 58611A) was found to be the most potent and selective.

  DOI：

  10.1016/0223-5234(94)90095-7

文献信息

• Procédé pour la préparation de phényléthanolaminotétralines
  申请人：ELF SANOFI

  公开号：EP0303545B1

  公开（公告）日：1992-06-17
• US5198586A
  申请人：——

  公开号：US5198586A

  公开（公告）日：1993-03-30
• US5235103A
  申请人：——

  公开号：US5235103A

  公开（公告）日：1993-08-10
• Synthesis and β-adrenergic activity of atypical β-adrenergic phenylethanolaminotetralin stereoisomers
  作者：R Cecchi、T Croci、R Boigegrain、S Boveri、M Baroni、G Boccardi、JP Guimbard、U Guzzi

  DOI：10.1016/0223-5234(94)90095-7

  日期：1994.1

  A series of substituted phenylethanolaminotetralins were synthesized as pure stereoisomers and their ability to stimulate atypical beta-adrenoceptors selectively was evaluated. The compounds in vitro relative potencies were assessed using the atypical beta response of inhibition of rat proximal colon motility and the typical beta 1 (increase in guinea-pig right atrial frequency) and beta 2 (guinea-pig tracheal relaxation and rat uterus motility inhibition) responses. Compound 42 (SR 58611A) was found to be the most potent and selective.