4-Benzyloxy-6(1H)-pyrimidinon | 13566-56-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: 4-Benzyloxy-6(1H)-pyrimidinon
• 英文别名: 6-benzyloxy-3H-pyrimidin-4-one；4-phenylmethoxy-1H-pyrimidin-6-one
• CAS: 13566-56-8
• 化学式: C₁₁H₁₀N₂O₂
• 分子量: 202.213
• InChiKey: WIOVWZOLMLEBHY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1
• 重原子数：
  15
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.09
• 拓扑面积：
  50.7
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  [4-(2-chloroethyl)phenyl]methanol 、 4-Benzyloxy-6(1H)-pyrimidinon 在 potassium carbonate 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 3.0h， 以36%的产率得到6-benzyloxy-3-[2-(4-hydroxymethyl-phenyl)-ethyl]-3H-pyrimidin-4-one
  参考文献：
  名称：

  WO2008/22979

  摘要：

  公开号：

文献信息

• Substituted pyrimidinones
  申请人：——

  公开号：US20040242608A1

  公开（公告）日：2004-12-02

  Disclosed are compounds Formula I 1 and pharmaceutically acceptable salts thereof, wherein R 1 , R 2 , R 4 , and R 5 are defined herein. These compounds are useful for treating diseases and conditions caused or exacerbated by unregulated p38 MAP Kinase and/or TNF activity. Pharmaceutical compositions containing the compounds, methods of preparing the compounds and methods of treatment using the compounds are also disclosed.

  本发明涉及化合物I1及其药学上可接受的盐，其中R1、R2、R4和R5的定义如下。这些化合物可用于治疗由未调节的p38 MAP激酶和/或TNF活性引起或恶化的疾病和病况。本发明还涉及含有这些化合物的药物组合物、制备这些化合物的方法以及使用这些化合物进行治疗的方法。
• NEW PYRIDONE DERIVATES WITH MCH ANTAGONISTIC ACTIVITY AND MEDICAMENTS COMPRISING THESE COMPOUNDS
  申请人：Stenkamp Dirk

  公开号：US20080255083A1

  公开（公告）日：2008-10-16

  The present invention relates to compounds of general formula I wherein the groups and radicals B, k, L, U, V, W, X, Y, Z, R 1 , R 2 , have the meanings given in claim 1 . Moreover the invention relates to pharmaceutical compositions containing at least one compound according to the invention. By virtue of their MCH-receptor antagonistic activity the pharmaceutical compositions according to the invention are suitable for the treatment of metabolic disorders and/or eating disorders, particularly obesity, bulimia, anorexia, hyperphagia and diabetes.

  本发明涉及一般式I的化合物，其中B、k、L、U、V、W、X、Y、Z、R1、R2的基团和基团具有权利要求1中所给出的含义。此外，本发明涉及含有至少一种根据本发明的化合物的制药组合物。由于它们的MCH受体拮抗活性，本发明的制药组合物适用于治疗代谢障碍和/或进食障碍，特别是肥胖症、暴食症、厌食症、过度进食和糖尿病。
• SUBSTITUTED PYRIMIDINONES
  申请人：Durley C. Richard

  公开号：US20070167621A1

  公开（公告）日：2007-07-19

  Disclosed are compounds Formula I and pharmaceutically acceptable salts thereof, wherein R 1 , R 2 , R 4 , and R 5 are defined herein. These compounds are useful for treating diseases and conditions caused or exacerbated by unregulated p38 MAP Kinase and/or TNF activity. Pharmaceutical compositions containing the compounds, methods of preparing the compounds and methods of treatment using the compounds are also disclosed.

  本发明涉及化合物I的公式及其药学上可接受的盐，其中R1、R2、R4和R5在此定义。这些化合物可用于治疗由未经调节的p38 MAP激酶和/或TNF活性引起或恶化的疾病和病况。本发明还涉及含有这些化合物的药物组合物、制备这些化合物的方法以及使用这些化合物的治疗方法。
• Pyridone derivates with MCH antagonistic activity and medicaments comprising these compounds
  申请人：Boehringer Ingelheim International GmbH

  公开号：US08067590B2

  公开（公告）日：2011-11-29

  The present invention relates to compounds of general formula I wherein the groups and radicals B, k, L, U, V, W, X, Y, Z, R1, R2, have the meanings given in claim 1. Moreover the invention relates to pharmaceutical compositions containing at least one compound according to the invention. By virtue of their MCH-receptor antagonistic activity the pharmaceutical compositions according to the invention are suitable for the treatment of metabolic disorders and/or eating disorders, particularly obesity, bulimia, anorexia, hyperphagia and diabetes.

  本发明涉及通式I的化合物，其中B、k、L、U、V、W、X、Y、Z、R1、R2的基团和基团具有权利要求1所给出的含义。此外，本发明涉及含有至少一种根据本发明的化合物的制药组合物。由于它们的MCH受体拮抗活性，根据本发明的制药组合物适用于治疗代谢紊乱和/或进食障碍，特别是肥胖症、暴食症、厌食症、过度进食和糖尿病。
• New pyridone derivatives with MCH antagonistic activity and medicaments comprising these compounds
  申请人：Boehringer Ingelheim International GmbH

  公开号：EP2383259A1

  公开（公告）日：2011-11-02

  The present invention relates to compounds of general formula I wherein the groups and radicals B, k, L, U,V, W, X, Y, Z, R1, R2, have the meanings given in claim 1. Moreover the invention relates to pharmaceutical compositions containing at least one compound according to the invention. By virtue of their MCH-receptor antagonistic activity the pharmaceutical compositions according to the invention are suitable for the treatment of metabolic disorders and/or eating disorders, particularly obesity, bulimia, anorexia, hyperphagia and diabetes.

  本发明涉及通式 I 的化合物 其中基团 B、k、L、U、V、W、X、Y、Z、R1、R2 具有权利要求 1 所述的含义。此外，本发明还涉及含有至少一种根据本发明的化合物的药物组合物。由于其 MCH 受体拮抗活性，根据本发明的药物组合物适用于治疗代谢紊乱和/或饮食失调，特别是肥胖症、贪食症、厌食症、食欲过盛和糖尿病。