Benzimidazole deriv. 9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并咪唑类
• 英文名称: Benzimidazole deriv. 9
• 英文别名: 4-(1-phenylbenzimidazol-5-yl)-1-(2-piperidin-1-ylethyl)pyridin-2-one
• 化学式: C₂₅H₂₆N₄O
• 分子量: 398.508
• InChiKey: NPCYXGHGFVADQP-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  30
• 可旋转键数：
  5
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.28
• 拓扑面积：
  41.4
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  4-bromo-N1-phenylbenzene-1,2-diamine 在 盐酸 、 (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride 、 potassium acetate 、 sodium hydride 、 联硼酸频那醇酯 作用下， 以 甲醇 、 N,N-二甲基甲酰胺 为溶剂， 生成 Benzimidazole deriv. 9
  参考文献：
  名称：

  Design and synthesis of 1,5-diarylbenzimidazoles as inhibitors of the VEGF-receptor KDR

  摘要：

  1, 5-Diarylbenzimidazoles have been identified as potent inhibitors of KDR kinase activity. The series was developed with a goal of finding compounds with optimal drug-like properties. This communication describes structural modifications in the series that enhance solubility, lower protein binding, and provide compounds with excellent potency and pharmacokinetic profiles. (C) 2003 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(03)00485-2

文献信息

• US6162804A
  申请人：——

  公开号：US6162804A

  公开（公告）日：2000-12-19
• US6465484B1
  申请人：——

  公开号：US6465484B1

  公开（公告）日：2002-10-15
• Design and synthesis of 1,5-diarylbenzimidazoles as inhibitors of the VEGF-receptor KDR
  作者：Mark T. Bilodeau、April M. Cunningham、Timothy J. Koester、Patrice A. Ciecko、Kathleen E. Coll、William R. Huckle、Randall W. Hungate、Richard L. Kendall、Rosemary C. McFall、Xianzhi Mao、Ruth Z. Rutledge、Kenneth A. Thomas

  DOI：10.1016/s0960-894x(03)00485-2

  日期：2003.8

  1, 5-Diarylbenzimidazoles have been identified as potent inhibitors of KDR kinase activity. The series was developed with a goal of finding compounds with optimal drug-like properties. This communication describes structural modifications in the series that enhance solubility, lower protein binding, and provide compounds with excellent potency and pharmacokinetic profiles. (C) 2003 Elsevier Ltd. All rights reserved.