4-(4-benzhydryl-piperazin-1-yl)-3-fluoro-phenylamine | 952950-43-5

• 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: 4-(4-benzhydryl-piperazin-1-yl)-3-fluoro-phenylamine
• 英文别名: 4-(4-benzhydrylpiperazin-1-yl)-3-fluoroaniline
• CAS: 952950-43-5
• 化学式: C₂₃H₂₄FN₃
• 分子量: 361.462
• InChiKey: ZENDNQVNJDIBFH-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.5
• 重原子数：
  27
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  32.5
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  4-(4-benzhydryl-piperazin-1-yl)-3-fluoro-phenylamine 在 正丁基锂 、 碳酸氢钠 作用下， 以 四氢呋喃 、 正己烷 为溶剂， 生成 (R)-3-[4-(4-Benzhydryl-piperazin-1-yl)-3-fluoro-phenyl]-5-hydroxymethyl-oxazolidin-2-one
  参考文献：
  名称：

  Synthesis and antibacterial activity of linezolid analogues

  摘要：

  Several new compounds of oxazolidinone class were designed and synthesized referring to the structure-activity relationship studies and the synthesis of Linezolid, and their antibacterial activity was studied. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(02)00043-4
• 作为产物：
  描述：

  二苯甲基哌嗪 在 palladium on activated charcoal ammonium formate 、 N,N-二异丙基乙胺 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 生成 4-(4-benzhydryl-piperazin-1-yl)-3-fluoro-phenylamine
  参考文献：
  名称：

  Synthesis and antibacterial activity of linezolid analogues

  摘要：

  Several new compounds of oxazolidinone class were designed and synthesized referring to the structure-activity relationship studies and the synthesis of Linezolid, and their antibacterial activity was studied. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(02)00043-4

文献信息

• ORGANIC COMPOUNDS
  申请人：Nozulak Joachim

  公开号：US20090099199A1

  公开（公告）日：2009-04-16

  The invention relates to compound of the formula I wherein the substituents are as defined in the specification; in free base form or in acid addition salt form; to its preparation, to its use as medicament and to medicaments comprising it.

  这项发明涉及公式I的化合物 其中取代基如规范中定义；以自由碱形式或酸盐形式存在；其制备，用作药物以及包含它的药物。
• PIPERAZINYL DERIVATIVES USEFUL AS MODULATORS OF THE NEUROPEPTIDE Y2 RECEPTOR
  申请人：Chai Wenying

  公开号：US20120129870A1

  公开（公告）日：2012-05-24

  The present invention is directed to piperidinyl and piperazinyl derivatives of formula (II) useful as inhibitors of the NPY Y2 receptor, pharmaceutical compositions comprising said compounds, processes for the preparation of said compounds and the use of said compounds for the treatment and/or prevention of disorders, diseases and conditions mediated by the NPY Y2 receptor.

  本发明涉及公式（II）的哌啶基和哌嗪基衍生物，其可用作NPY Y2受体的抑制剂，包括该化合物的制药组合物，制备该化合物的过程以及利用该化合物治疗和/或预防由NPY Y2受体介导的疾病、疾病和病情的用途。
• SUBSTITUTED PIPERAZINES AND PIPERIDINES AS MODULATORS OF THE NEUROPEPTIDE Y2 RECEPTOR
  申请人：Novartis AG

  公开号：EP2205561A2

  公开（公告）日：2010-07-14
• [EN] ORGANIC COMPOUNDS<br/>[FR] COMPOSÉS ORGANIQUES
  申请人：NOVARTIS AG

  公开号：WO2009050197A2

  公开（公告）日：2009-04-23

  The invention relates to compound of the formula (I): wherein the substituents are as defined in the specification; in free base form or in acid addition salt form; to its preparation, to its use as medicament and to medicaments comprising it.
• Synthesis and antibacterial activity of linezolid analogues
  作者：Du Yu、Guo Huiyuan

  DOI：10.1016/s0960-894x(02)00043-4

  日期：2002.3

  Several new compounds of oxazolidinone class were designed and synthesized referring to the structure-activity relationship studies and the synthesis of Linezolid, and their antibacterial activity was studied. (C) 2002 Elsevier Science Ltd. All rights reserved.