phenylmethyl 4-[(2-fluoro-4-nitrophenyl)oxy]-1-piperidinecarboxylate

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: phenylmethyl 4-[(2-fluoro-4-nitrophenyl)oxy]-1-piperidinecarboxylate
• 英文别名: benzyl 4-(2-fluoro-4-nitrophenoxy)piperidine-1-carboxylate
• 化学式: C₁₉H₁₉FN₂O₅
• 分子量: 374.369
• InChiKey: FTDBCLYHFYAVHJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.8
• 重原子数：
  27
• 可旋转键数：
  5
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.32
• 拓扑面积：
  84.6
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  phenylmethyl 4-[(2-fluoro-4-nitrophenyl)oxy]-1-piperidinecarboxylate 在 氢溴酸 、 溶剂黄146 作用下， 反应 0.5h， 以50%的产率得到4-[(2-fluoro-4-nitrophenyl)oxy]piperidine hydrobromide
  参考文献：
  名称：

  [EN] THIAZOLE SULFONAMIDE AND OXAZOLE SULFONAMIDE KINASE INHIBITORS
  [FR] INHIBITEURS DE THIAZOLE SULFONAMIDE ET OXAZOLE SULFONAMIDE KINASES

  摘要：

  本发明提供了噻唑磺酰胺和恶唑磺酰胺化合物、含有该化合物的组合物，以及它们的制备方法和作为药物的使用方法。

  公开号：

  WO2010104899A1
• 作为产物：
  描述：

  4-羟基-1-哌啶甲酸苄酯 、 3,4-二氟硝基苯 在 sodium hydride 作用下， 以 四氢呋喃 为溶剂， 生成 phenylmethyl 4-[(2-fluoro-4-nitrophenyl)oxy]-1-piperidinecarboxylate
  参考文献：
  名称：

  Structure–activity relationship in the oxazolidinone–quinolone hybrid series: influence of the central spacer on the antibacterial activity and the mode of action

  摘要：

  Oxazolidinone-quinolone hybrids, which combine the pharmacophores of a quinolone and an oxazolidinone, were synthesised and shown to be active against a variety of susceptible and resistant Gram-positive and Gram-negative bacteria. The nature of the spacer greatly influences the antibacterial activity by directing the mode of action, that is quinotone- and/or oxazolidinone-like activity. The best compounds in this series have a balanced dual mode of action and overcome all types of resistance, including resistance to quinolones and linezolid, in clinically relevant Gram-positive pathogens. (C) 2003 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2003.07.028

文献信息

• [EN] THIAZOLE AND OXAZOLE KINASE INHIBITORS<br/>[FR] INHIBITEURS DE KINASE À BASE DE THIAZOLE ET D'OXAZOLE
  申请人：SMITHKLINE BEECHAM CORP

  公开号：WO2009032667A1

  公开（公告）日：2009-03-12

  The present invention provides thiazole and oxazole compounds, compositions containing the same, as well as processes for the preparation and methods for their use as pharmaceutical agents.

  本发明提供噻唑和氧唑化合物，含有这些化合物的组合物，以及用作药用剂的制备方法和使用方法。
• Thiazole And Oxazole Kinase Inhibitors
  申请人：Adjabeng George

  公开号：US20110190280A1

  公开（公告）日：2011-08-04

  The present invention provides thiazole and oxazole compounds, compositions containing the same, as well as processes for the preparation and methods for their use as pharmaceutical agents.

  本发明提供噻唑和氧唑化合物，含有这些化合物的组合物，以及制备这些化合物的方法和将其用作药物的方法。
• Thiazole Sulfonamide And Oxazole Sulfonamide Kinase Inhibitors
  申请人：Adjabeng George

  公开号：US20110319392A1

  公开（公告）日：2011-12-29

  The present invention provides thiazole sulfonamide and oxazole sulfonamide compounds, compositions containing the same, as well as processes for the preparation and methods for their use as pharmaceutical agents.

  本发明提供了噻唑磺酰胺和噁唑磺酰胺化合物，含有它们的组合物，以及制备它们的过程和作为药物剂的方法。
• THIAZOLE AND OXAZOLE KINASE INHIBITORS
  申请人：Glaxosmithkline LLC

  公开号：EP2197876A1

  公开（公告）日：2010-06-23
• THIAZOLE SULFONAMIDE AND OXAZOLE SULFONAMIDE KINASE INHIBITORS
  申请人：GlaxoSmithKline LLC

  公开号：EP2406234A1

  公开（公告）日：2012-01-18