6-phenyl-5,6,7,8-tetrahydroquinolin-8-one

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 英文名称: 6-phenyl-5,6,7,8-tetrahydroquinolin-8-one
• 英文别名: 6-phenyl-6,7-dihydroquinolin-8(5H)-one；Ijrzsljquollsz-uhfffaoysa-；6-phenyl-6,7-dihydro-5H-quinolin-8-one
• 化学式: C₁₅H₁₃NO
• 分子量: 223.274
• InChiKey: IJRZSLJQUOLLSZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  17
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  30
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  6-phenyl-5,6,7,8-tetrahydroquinolin-8-one 在 三氟甲磺酸 作用下， 反应 0.75h， 以93%的产率得到11-hydroxy-6,11-dihydro-6,11-methano-5H-benzo[5,6]cyclohepta[1,2-b]pyridine
  参考文献：
  名称：

  摘要：

  According to the H-1 and C-13 NMR data, 5-azonia-4-hydroxynaphthalen-1-onium cation, generated by protonation of 8-hydroxyquinoline in the system CF3SO3H-SbF5, reacts with cyclohexane to give diprotonated 5,6,7,8-tetrahydroquinolin-8-one. Further reaction of the latter with cyclohexane yields 5,6,7,8-tetrahydroquinolinium ion. The reaction of 8-hydroxyquinoline with benzene in the presence of aluminum bromide or chloride gives 6-phenyl-5,6,7,8-tetrahydroquinolin-8-one and product of its intramolecular cyclization, 11-hydroxy-6,11-dihydro-6,11-methano-5H-benzo[5,6]cyclohepta[1,2-b]pyridine. The effect of the protonated nitrogen atom on the electrophilicity of dications is discussed.

  DOI：

  10.1023/a:1016306814374
• 作为产物：
  描述：

  8-羟基喹啉 、 苯 在 aluminum tri-bromide 、 氢溴酸 作用下， 反应 48.0h， 生成 6-phenyl-5,6,7,8-tetrahydroquinolin-8-one
  参考文献：
  名称：

  [EN] PYRIDINE CGRP RECEPTOR ANTAGONISTS
  [FR] ANTAGONISTES DE RÉCEPTEUR DE CGRP À BASE DE PYRIDINE

  摘要：

  本发明涉及吡啶衍生物，其为CGRP受体拮抗剂，在治疗或预防涉及CGRP的疾病，如偏头痛等方面有用。该发明还涉及包含这些化合物的药物组合物，以及在预防或治疗涉及CGRP的这类疾病中使用这些化合物和组合物。

  公开号：

  WO2013169563A1

文献信息

• [EN] PYRIDINE CGRP RECEPTOR ANTAGONISTS<br/>[FR] ANTAGONISTES DE RÉCEPTEUR DE CGRP À BASE DE PYRIDINE
  申请人：MERCK SHARP & DOHME

  公开号：WO2013169563A1

  公开（公告）日：2013-11-14

  The present invention is directed to pyridine derivatives which are antagonists of CGRP receptors and useful in the treatment or prevention of diseases in which CGRP is involved, such as migraine. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which CGRP is involved.

  本发明涉及吡啶衍生物，其为CGRP受体拮抗剂，在治疗或预防涉及CGRP的疾病，如偏头痛等方面有用。该发明还涉及包含这些化合物的药物组合物，以及在预防或治疗涉及CGRP的这类疾病中使用这些化合物和组合物。
• PYRIDINE CGRP RECEPTOR ANTAGONISTS
  申请人：Merck Sharp & Dohme Corp.

  公开号：US20150099771A1

  公开（公告）日：2015-04-09

  The present invention is directed to pyridine derivatives which are antagonists of CGRP receptors and useful in the treatment or prevention of diseases in which CGRP is involved, such as migraine. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which CGRP is involved.

  本发明涉及吡啶衍生物，其为CGRP受体拮抗剂，可用于治疗或预防涉及CGRP的疾病，例如偏头痛。本发明还涉及包含这些化合物的制药组合物以及使用这些化合物和组合物预防或治疗涉及CGRP的这些疾病的方法。
• Pyridine CGRP receptor antagonists
  申请人：Merck Sharp & Dohme Corp.

  公开号：US09227973B2

  公开（公告）日：2016-01-05

  The present invention is directed to pyridine derivatives which are antagonists of CGRP receptors and useful in the treatment or prevention of diseases in which CGRP is involved, such as migraine. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which CGRP is involved.

  本发明涉及吡啶衍生物，其为CGRP受体拮抗剂，可用于治疗或预防涉及CGRP的疾病，例如偏头痛。该发明还涉及包含这些化合物的制药组合物以及在预防或治疗涉及CGRP的这些疾病中使用这些化合物和组合物的用途。
• US9227973B2
  申请人：——

  公开号：US9227973B2

  公开（公告）日：2016-01-05
• ——
  作者：K. Yu. Koltunov、I. B. Repinskaya

  DOI：10.1023/a:1016306814374

  日期：——

  According to the H-1 and C-13 NMR data, 5-azonia-4-hydroxynaphthalen-1-onium cation, generated by protonation of 8-hydroxyquinoline in the system CF3SO3H-SbF5, reacts with cyclohexane to give diprotonated 5,6,7,8-tetrahydroquinolin-8-one. Further reaction of the latter with cyclohexane yields 5,6,7,8-tetrahydroquinolinium ion. The reaction of 8-hydroxyquinoline with benzene in the presence of aluminum bromide or chloride gives 6-phenyl-5,6,7,8-tetrahydroquinolin-8-one and product of its intramolecular cyclization, 11-hydroxy-6,11-dihydro-6,11-methano-5H-benzo[5,6]cyclohepta[1,2-b]pyridine. The effect of the protonated nitrogen atom on the electrophilicity of dications is discussed.

表征谱图