4-(5-bromo-pyridin-2-ylmethoxy)-1H-pyridin-2-one | 1008518-18-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: 4-(5-bromo-pyridin-2-ylmethoxy)-1H-pyridin-2-one
• 英文别名: 4-[(5-bromopyridin-2-yl)methoxy]-1H-pyridin-2-one
• CAS: 1008518-18-0
• 化学式: C₁₁H₉BrN₂O₂
• 分子量: 281.109
• InChiKey: ZNMVCKYESBJGQD-UHFFFAOYSA-N

物化性质

• 沸点：
  521.1±50.0 °C(Predicted)
• 密度：
  1.62±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1
• 重原子数：
  16
• 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：
  51.2
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  4-(5-bromo-pyridin-2-ylmethoxy)-1H-pyridin-2-one 在 三溴化磷 、 caesium carbonate 作用下， 以 二氯甲烷 为溶剂， 生成 1-[2-(4-bromomethyl-phenyl)-2-oxo-ethyl]-4-(5-bromo-pyridin-2-ylmethoxy)-1H-pyridin-2-one
  参考文献：
  名称：

  Design, synthesis and evaluation of MCH receptor 1 antagonists—Part III: Discovery of pre-clinical development candidate BI 186908

  摘要：

  Although overweight and obesity are highly prevalent conditions, options to treat them are still very limited. As part of our search for safe and effective MCH-R1 antagonists for the treatment of obesity, two series of pyridones and pyridazinones were evaluated. Optimization was aimed at improving DMPK properties by increasing metabolic stability and improving the safety profile by reducing inhibition of the hERG channel and reducing the potential to induce phospholipidosis. Steric shielding of a labile keto moiety with an ortho-methyl group and fine-tuning of the polarity in several parts of the molecule resulted in BI 186908 (11g), a potent and selective MCH-R1 antagonist with favorable DMPK and CMC properties. Chronic administration of BI 186908 resulted in significant body weight reduction comparable to sibutramine in a 4 week diet-induced obesity model in rats. Based on its favorable safety profile, BI 186908 was advanced to pre-clinical development. (C) 2015 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2015.05.065
• 作为产物：
  描述：

  2,4-二羟基吡啶 、 5-溴-2-(溴甲基)吡啶 在 potassium carbonate 作用下， 以 乙腈 为溶剂， 生成 4-(5-bromo-pyridin-2-ylmethoxy)-1H-pyridin-2-one
  参考文献：
  名称：

  Design, synthesis and evaluation of MCH receptor 1 antagonists—Part III: Discovery of pre-clinical development candidate BI 186908

  摘要：

  Although overweight and obesity are highly prevalent conditions, options to treat them are still very limited. As part of our search for safe and effective MCH-R1 antagonists for the treatment of obesity, two series of pyridones and pyridazinones were evaluated. Optimization was aimed at improving DMPK properties by increasing metabolic stability and improving the safety profile by reducing inhibition of the hERG channel and reducing the potential to induce phospholipidosis. Steric shielding of a labile keto moiety with an ortho-methyl group and fine-tuning of the polarity in several parts of the molecule resulted in BI 186908 (11g), a potent and selective MCH-R1 antagonist with favorable DMPK and CMC properties. Chronic administration of BI 186908 resulted in significant body weight reduction comparable to sibutramine in a 4 week diet-induced obesity model in rats. Based on its favorable safety profile, BI 186908 was advanced to pre-clinical development. (C) 2015 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2015.05.065

文献信息

• NEW COMPOUNDS, PHARMACEUTICAL COMPOSITIONS AND USES THEREOF
  申请人：OOST Thorsten

  公开号：US20130237515A1

  公开（公告）日：2013-09-12

  The present invention relates to compounds of general formula I, wherein the groups R 1 , R 2 , L 1 , L 2 , U and B are as defined in the application, which have valuable pharmacological properties, and in particular modulate the activity of the MCH receptor.

  本发明涉及一般式I的化合物，其中基团R1、R2、L1、L2、U和B如申请中所定义，具有有价值的药理特性，特别是调节MCH受体的活性。
• [EN] PYRIDINONE AND PYRIDAZINONE DERIVATIVES AS MCH - RECEPTOR MODULATORS<br/>[FR] DÉRIVÉS DE PYRIDINONE ET PYRIDAZINONE EN TANT QUE MODULATEURS DU RÉCEPTEUR DE MCH
  申请人：BOEHRINGER INGELHEIM INT

  公开号：WO2013131935A1

  公开（公告）日：2013-09-12

  The present invention relates to compounds of general formula I, wherein the groups R1, R2, L1, L2, U and B are as defined in the application, which have valuable pharmacological properties, and in particular modulate the activity of the MCH receptor.

  本发明涉及一般式I的化合物，其中R1、R2、L1、L2、U和B组分如申请中所定义，具有有价值的药理特性，特别是调节MCH受体活性。
• [EN] PYRIDONE AND PYRIDAZINONE DERIVATIVES AS MCH ANTAGONISTS<br/>[FR] DÉRIVÉS DE PYRIDONE ET DE PYRIDAZINONE COMME ANTAGONISTES DE LA MCH
  申请人：BOEHRINGER INGELHEIM INT

  公开号：WO2009103478A1

  公开（公告）日：2009-08-27

  The present invention relates to pyridone and pyridazinone derivatives as listed in claim 1 including their salts. 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.

  本发明涉及权利要求1中所列的吡啶酮和吡啶并二嗪酮衍生物及其盐。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。凭借其黑色素细胞刺激素受体拮抗活性，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、贪食症、厌食症、过食和糖尿病。
• 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。
• 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。