(S)-N-[3-[3-fluoro-4-[piperazin-1-yl]phenyl]-2-oxooxazolidin-5-ylmethyl]thioacetamide | 612056-04-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪烷类
• 英文名称: (S)-N-[3-[3-fluoro-4-[piperazin-1-yl]phenyl]-2-oxooxazolidin-5-ylmethyl]thioacetamide
• 英文别名: (S)-N-[[3-fluoro-4-(N-1-piperazinyl)-phenyl]-2-oxo-5-oxazolidinyl]methyl-thioacetamide；N-[[(5S)-3-(3-fluoro-4-piperazin-1-ylphenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl]ethanethioamide
• CAS: 612056-04-9
• 化学式: C₁₆H₂₁FN₄O₂S
• 分子量: 352.433
• InChiKey: OUKXIYKSIWIMKC-ZDUSSCGKSA-N

物化性质

• 沸点：
  527.0±60.0 °C(Predicted)
• 密度：
  1.296±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1
• 重原子数：
  24
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  88.9
• 氢给体数：
  2
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  3-(4-氯苯甲酰)丙酸 、 (S)-N-[3-[3-fluoro-4-[piperazin-1-yl]phenyl]-2-oxooxazolidin-5-ylmethyl]thioacetamide 在 4-二甲氨基吡啶 吡啶 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 作用下， 反应 20.0h， 生成 N-{[(5S)-3-(4-{4-[4-(4-chlorophenyl)-4-oxobutanoyl]piperazinyl}-3-fluorophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}ethanethioamide
  参考文献：
  名称：

  [EN] N-(4-(PIPERAZIN-1-YL)-PHENYL-2-OXAZOLIDINONE-5-CARBOXAMIDE DERIVATES AND RELATED COMPOUNDS AS ANTIBACTERIAL AGENTS
  [FR] DERIVES DE N-(4-(PIPERAZINE-1-YL)-PHENYL-2-OXAZOLIDINONE-5-CARBOXAMIDES ET COMPOSES ASSOCIES SERVANT D'AGENTS ANTIBACTERIENS

  摘要：

  本发明提供了具有以下式I的抗菌剂，或其药学上可接受的盐，其中：A是结构i、ii、iii或iv，W是N(H)C(X)-R、Het或-Y HET，在其中Hot或Y HET可以选择地被=S或'0取代，但当A是结构iv时，W不是-Y--1-MT或Het。

  公开号：

  WO2004045616A1
• 作为产物：
  描述：

  (S)-N-((3-(3-氟-4-(哌嗪-1-基)苯基)-2-氧代噁唑啉-5-基)甲基)乙酰胺 在 劳森试剂 作用下， 以 甲苯 为溶剂， 反应 5.0h， 生成 (S)-N-[3-[3-fluoro-4-[piperazin-1-yl]phenyl]-2-oxooxazolidin-5-ylmethyl]thioacetamide
  参考文献：
  名称：

  [EN] ANTIINFECTVE COMPOUNDS, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
  [FR] NOUVEAUX COMPOSES ANTI-INFECTIEUX, PROCESSUS DE PREPARATION DE CES COMPOSES ET COMPOSITIONS PHARMACEUTIQUES LES CONTENANT

  摘要：

  公开号：

  WO2003082864A3

文献信息

• [EN] NOVEL ANTIBACTERIAL AGENTS<br/>[FR] NOUVEAUX AGENTS ANTIBACTERIENS
  申请人：ORCHID CHEMICALS & PHARM LTD

  公开号：WO2004018439A1

  公开（公告）日：2004-03-04

  The present invention provides novel compounds of the general formula (I), their derivatives, their analogs, their tautomeric forms, their stereoisomers, their polymorphs, their hydrates, their solvates, their pharmaceutically acceptable salts and pharmaceutically acceptable compositions containing them. The present invention more particularly provides novel oxazolidinone derivatives of the general formula (I).

  本发明提供了一般式(I)的新化合物，它们的衍生物、类似物、互变异构体、立体异构体、多晶形态、水合物、溶剂合物、药学上可接受的盐以及含有它们的药学上可接受的组合物。本发明特别提供了一般式(I)的新噁唑啉酮衍生物。
• Novel antibacterial agents
  申请人：Agarwal Kumar Shiv

  公开号：US20050070526A1

  公开（公告）日：2005-03-31

  The present invention provides novel compounds of the general formula (I), their derivatives, their analogs, their tautomeric forms, their stereoisomers, their polymorphs, their hydrates, their solvates, their pharmaceutically acceptable salts and pharmaceutically acceptable compositions containing them. The present invention more particularly provides novel oxazolidinone derivatives of the general formula (I).

  本发明提供了一般式（I）的新化合物，它们的衍生物、类似物、互变异构体、立体异构体、多晶形态、水合物、溶剂化物、药学上可接受的盐及含有它们的药学上可接受的组合物。本发明更特别地提供了一般式（I）的新的噁唑烷酮衍生物。
• Novel and potent oxazolidinone antibacterials featuring 3-indolylglyoxamide substituents
  作者：Mohamed Takhi、Gurpreet Singh、C. Murugan、Nirvesh Thaplyyal、Soma Maitra、K.M. Bhaskarreddy、P.V.S. Amarnath、Arundhuti Mallik、T. Harisudan、Ravi Kumar Trivedi、K. Sreenivas、N. Selvakumar、Javed Iqbal

  DOI：10.1016/j.bmcl.2008.03.043

  日期：2008.9

  Novel oxazolidinone antibacterials bearing a variety of 3-indolylglyoxamide substituents have been explored in an effort to improve the spectrum and potency of this class of agents. A subclass of this series was also made with the diversity at C-5 terminus. These derivatives have been screened against a panel of clinically relevant Gram-positive pathogens and fastidious Gram-negative organisms. Several analogs in this series were identified with in vitro activity superior to linezolid ( MIC = 0.25-2 mu g/ mL). Compounds 10a, 10c, 10e and 10f displayed activity against linezolid resistant Gram-positive organisms (MIC = 2-4 mu g/ mL). Selected oxazolidinones were evaluated for in vivo efficacy against a mouse systemic infection model. (C) 2008 Elsevier Ltd. All rights reserved.
• WO2008/10070
  申请人：——

  公开号：——

  公开（公告）日：——
• Novel Mannich ketones of oxazolidinones as antibacterial agents
  作者：Brijesh Kumar Srivastava、Prashant B. Kapadnis、Purvi Pandya、Vidya Bhushan Lohray

  DOI：10.1016/j.ejmech.2004.07.007

  日期：2004.11

  A few Mannich ketones of piperazinyl oxazolidinone derivatives have been synthesized and their antibacterial activity in various Gram-positive organisms such as Bacillus subtilis, Staphylococcus aureus, Staphylococcus epidermidis and Enterococcus faecalis were evaluated by MIC determination. Compound 12 showed comparable activity (MIC) to linezolid and superior to eperezolid. (C) 2004 Elsevier SAS. All rights reserved.