6-Bromo-2-(4-fluorophenyl)-8-methylimidazo[1,2-a]pyridine-3-carbaldehyde | 481049-66-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 6-Bromo-2-(4-fluorophenyl)-8-methylimidazo[1,2-a]pyridine-3-carbaldehyde
• CAS: 481049-66-5
• 化学式: C₁₅H₁₀BrFN₂O
• 分子量: 333.16
• InChiKey: VURIWCFMYAZFMC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.4
• 重原子数：
  20
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  34.4
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  6-Bromo-2-(4-fluorophenyl)-8-methylimidazo[1,2-a]pyridine-3-carbaldehyde 在 palladium diacetate manganese(IV) oxide 、 potassium carbonate 、 caesium carbonate 、 R-(+)-1,1'-联萘-2,2'-双二苯膦 作用下， 以 四氢呋喃 、 乙醇 、 二氯甲烷 为溶剂， 生成 3-[2-(cyclopentylamino)pyrimidin-4-yl]-N-cyclopropyl-2-(4-fluorophenyl)-8-methylimidazo[1,2-a]pyridin-6-amine
  参考文献：
  名称：

  Imidazo[1,2-a]pyridines with potent activity against herpesviruses

  摘要：

  Synthesis of a series of 2-aryl-3-pyrimidyl-imidazo[1,2-a]pyridines with potent activity against herpes simplex viruses is described. Synthetic approaches allowing for variation of the 2-aryl, 3-heteroaryl as well as other imidazopyridine substituents are outlined and resulting effects on antiviral activity are highlighted. Several compounds with in vitro antiviral activity similar or better than acyclovir are described. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2007.02.079
• 作为产物：
  描述：

  2-氨基-3-甲基-5-溴吡啶 在 碳酸氢钠 、 三氯氧磷 作用下， 以 乙醇 为溶剂， 生成 6-Bromo-2-(4-fluorophenyl)-8-methylimidazo[1,2-a]pyridine-3-carbaldehyde
  参考文献：
  名称：

  Imidazo[1,2-a]pyridines with potent activity against herpesviruses

  摘要：

  Synthesis of a series of 2-aryl-3-pyrimidyl-imidazo[1,2-a]pyridines with potent activity against herpes simplex viruses is described. Synthetic approaches allowing for variation of the 2-aryl, 3-heteroaryl as well as other imidazopyridine substituents are outlined and resulting effects on antiviral activity are highlighted. Several compounds with in vitro antiviral activity similar or better than acyclovir are described. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2007.02.079

文献信息

• Imidazo[1,2-a]pyridine derivatives for treatment of herpes viral infections
  申请人：Gudmundsson Kristjan

  公开号：US20060167252A1

  公开（公告）日：2006-07-27

  The present invention provides compounds of formula (I) wherein all variables are as defined herein, pharmaceutical compositions containing the same, processes for preparing the same and their use as pharmaceutical agents.

  本发明提供了式(I)的化合物，其中所有变量在此定义，包含它们的药物组成物，制备它们的方法以及它们作为药物代理的用途。
• Imidazo'1,2-a!pyridine derivatives for the prophylaxis and treatment of herpes viral infections
  申请人：Gudmundsson S Kristjan

  公开号：US20050228004A1

  公开（公告）日：2005-10-13

  The present invention provides compounds of formula (I): wherein all variables are as defined herein, pharmaceutical compositions containing the same, processes for preparing the same and their use as pharmaceutical agents.

  本发明提供了式(I)的化合物：其中所有变量如本文所定义，包含这些化合物的制药组合物，制备这些化合物的过程以及它们作为制药剂的用途。
• Imidazo[1,2-a]Pyridine Derivatives for Treatment Of Herpes Viral Infections
  申请人：Gudmundsson S. Kristjan

  公开号：US20070135451A1

  公开（公告）日：2007-06-14

  The present invention provides compounds of formula (I): wherein all variables are as defined herein pharmaceutical compositions containing the same, processes for preparing the same and their use as pharmaceutical agents.

  本发明提供了公式(I)的化合物：其中所有变量均如本文所定义的制药组合物，制备它们的过程以及它们作为制药剂的用途。
• Imidazo[1,2-α]pyridine derivatives for the prophylaxis and treatment of herpes viral infections
  申请人：SmithKline Beecham Corporation

  公开号：US07186714B2

  公开（公告）日：2007-03-06

  The present invention provides compounds of formula (I) wherein all variables are as defined herein, pharmaceutical compositions containing the same, processes for preparing the same and their use as pharmaceutical agents

  本发明提供公式(I)的化合物，其中所有变量均如本文所定义，包含这些化合物的药物组合物，制备这些化合物的方法以及它们作为药物剂的用途。
• IMIDAZO¬1,2-A|PYRIDINE DERIVATIVES FOR THE PROPHYLAXIS AND TREATMENT OF HERPES VIRAL INFECTIONS
  申请人：SMITHKLINE BEECHAM CORPORATION

  公开号：EP1401836B1

  公开（公告）日：2006-08-23