(S)-n-[[3-(3,5-二氟苯基)-2-氧代-5-噁唑]甲基]乙酰胺 | 167010-30-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: (S)-n-[[3-(3,5-二氟苯基)-2-氧代-5-噁唑]甲基]乙酰胺
• 中文别名: (S)-N-[[3-(3,5-二氟苯基)-2-氧代-5-噁唑]甲基]乙酰胺
• 英文名称: (S)-N-((3-(3,5-Difluorophenyl)-2-oxooxazolidin-5-yl)methyl)acetamide
• 英文别名: N-[[(5S)-3-(3,5-difluorophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl]acetamide
• CAS: 167010-30-2
• 化学式: C₁₂H₁₂F₂N₂O₃
• 分子量: 270.23
• InChiKey: KDZFVXPBLHNVNS-NSHDSACASA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1
• 重原子数：
  19
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  58.6
• 氢给体数：
  1
• 氢受体数：
  5

安全信息

• 海关编码：
  2934999090
• 危险性防范说明：
  P261,P305+P351+P338
• 危险性描述：
  H302,H315,H319,H335

文献信息

• Antibiotic oxazolidinone derivatives
  申请人：Syngenta Limited

  公开号：US20030216374A1

  公开（公告）日：2003-11-20

  The invention concerns a compound of formula (I): 1 wherein, for example: T is of formula (IB) or (IC): 2 R 1 is of the formula —NHC(═O)R b wherein R b is (1-4C)alkyl; R 2 and R 3 are hydrogen or fluoro; A—B— is C═CH— or CH—CH 2 —; wherein when T is of formula (IB); R 6 is, for example, (1-4C)alkyl; R 5 is hydrogen, R 10 CO—, R 10 SO 2 — or R 10 CS— wherein R 10 is, for example, optionally substituted phenyl, or (1-10C)alkyl; or when T is of formula (IB) or (IC); R 5 and R 6 are linked to give a 5- or 6-membered ring which is fused to the ring shown in (IB) or (IC) so as to give an optionally substituted bicyclic ring; and pharmaceutically-acceptable salts thereof, processes for their preparation; pharmaceutical compositions containing them and their use as antibacterial agents.

  本发明涉及式(I)的化合物：1其中，例如：T为式(IB)或式(IC)：2R1为式—NHC(═O)Rb的形式，其中Rb为(1-4C)烷基；R2和R3为氢或氟；A—B—为C═CH—或CH—CH2—；当T为式(IB)时，R6为例如(1-4C)烷基；R5为氢、R10CO—、R10SO2—或R10CS—，其中R10为例如可选取代的苯基或(1-10C)烷基；或当T为式(IB)或式(IC)时，R5和R6连接形成一个5-或6-成员环，与(IB)或(IC)中所示的环融合，从而形成一个可选取代的双环；以及其药学上可接受的盐，制备它们的方法；含有它们的制药组合物和它们作为抗菌剂的用途。
• OXAZOLIDINONE DERIVATIVES AS ANTIMICROBIALS
  申请人：Das Biswajit

  公开号：US20100286211A1

  公开（公告）日：2010-11-11

  The present invention relates to certain substituted phenyl oxazolidinones and to processes for the synthesis of the same. This invention also relates to pharmaceutical compositions containing the compounds of the present invention as antimicrobials. The compounds are useful antimicrobial agents, effective against a number of human and veterinary pathogens, including gram-positive aerobic bacteria, for example, multiple-resistant staphylococci, streptococci and enterococci as well as anaerobic organisms, for example, Bacterioides spp. and Clostridia spp. species, and acid fast organisms, for example, Mycobacterium tuberculosis, Mycobacterium avium and Mycobacterium spp.

  本发明涉及某些取代苯基噁唑烷酮以及其合成方法。本发明还涉及包含本发明化合物作为抗微生物药物的制药组合物。这些化合物是有用的抗微生物剂，对多种人类和兽医病原体具有有效作用，包括革兰氏阳性的好氧菌，例如多重耐药葡萄球菌、链球菌和肠球菌，以及厌氧菌，例如拟杆菌属和梭菌属物种，以及酸性快速菌，例如结核分枝杆菌、埃及分枝杆菌和分枝杆菌属。
• TROPONE-SUBSTITUTED PHENYLOXAZOLIDINONE ANTIBACTERIAL AGENTS
  申请人：PHARMACIA & UPJOHN COMPANY

  公开号：EP0673370B1

  公开（公告）日：1998-01-07
• ANTIBIOTIC OXAZOLIDINONE DERIVATIVES
  申请人：ZENECA LIMITED

  公开号：EP1005468A1

  公开（公告）日：2000-06-07
• US5523403A
  申请人：——

  公开号：US5523403A

  公开（公告）日：1996-06-04