期刊文献+

利奈唑胺合成路线图解 被引量:17

Graphical Synthetic Routes of Linezolid
下载PDF
导出
摘要 利奈唑胺(linezolid,1),化学名为N-[[(5S)-3-[3-氟-4-(4-吗啉基)苯基]-2-氧代-5-噁唑烷基]甲基]乙酰胺,是美国Pfizer公司研发的第一个噫唑烷酮类抗菌药,可用于治疗耐万古霉素肠球菌(VRE)引起的菌血症,耐甲氧西林金黄色葡萄糖菌(MRSA)引起的肺炎和综合性皮肤感染以及耐青霉素肺炎链球菌(PRSP)引起的菌血症,2000年4月首次在美国上市,商品名Zyvox。
出处 《中国医药工业杂志》 CAS CSCD 北大核心 2010年第1期62-63,69,共3页 Chinese Journal of Pharmaceuticals
  • 相关文献

参考文献11

  • 1Swaney SM, Aoki H, Ganoza C, et al. The oxazolidinone linezolid inhibits initiation of protein synthesis in bacteria [J]. Antimicrob Agents Chemother, 1998, 42 (12) : 3251-3255.
  • 2Aoki H, Ke LZ, Poppe SM, et al. Oxazolidinone antibiotics target the P site on Escherichia coli ribosomes [J]. Antimicrob Agents Chemother, 2002, 46 (4): 1080-1085.
  • 3Brickner S J, Hutchinson DK, Barbachyn MR, et al. Synthesis and antibacterial activity of U-100592 and U-100766, two oxazolidinone antibacterial agents for the potential treatment of multidrug-resistant gram-positive bacterial infections [J]. JMed Chem, 1996, 39 (3) : 673-679.
  • 4徐广宇,吴希罕,谢毓元.N-[4(R)-(1,3-二噁烷基)甲基]苯胺、制备方法和用途:中国,100369909[P].2008-02-20.(CA2006,145:188857).
  • 5Lohray BB, Baskaran S, Rao BS, et al. A short synthesis of oxazolidinone derivatives linezolid and eperezolid : A new class of antibacteriais [J]. Tetrahedron Lett, 1999, 40(26) : 4855-4856.
  • 6Lohray BB, Chatterjee M, Jayamma Y. A practical approach.to the synthesis of dianhydro sugars [J]. Synth Commun, 1997, 27(10): 1711-1724.
  • 7黄强,李华,牛柏林,等.(R)-N-(3-氟-4-吗啉苯基)-噁唑酮-5-甲基醇制备工艺:中国,1772750[P].2006-05-17.(CA2006,145:62909).
  • 8Moran-Ramallal R, Liz R, Gotor V. Regioselective and stereospecific synthesis of enantiopure 1,3-oxazolidin- 2-ones by intramolecular ring opening of 2- (Bocarninomethyl) aziridines, preparation of the antibiotic linezolid [J]. Org Lett, 2008, 10 (10) : 1935-1938.
  • 9Immordino RJ, Perrault WR, Reeder MR. Process for preparing linezolid: WO, 2007116284 [P]. 2007-10-18. (CA 2007, 147: 469356).
  • 10余德胜,王志谦,熊莺,赵燕芳,宫平.利奈唑酮合成新工艺[J].中国药物化学杂志,2005,15(2):89-90. 被引量:8

二级参考文献2

  • 1Brickners SJ, Hutchinson DK, Barbachyn MR, et al.Synthesis and antibacterial activity of U-100766 and U-100592[J] .J Med Chem, 1996, 39(3):673 - 679.
  • 2孟庆国,刘浚.利奈唑酮的合成工艺改进[J].中国药物化学杂志,2003,13(1):28-30. 被引量:13

共引文献7

同被引文献102

  • 1T.Satyanarayana Raju,O.Vishweshwari Kutty,V.Ganesh,P.Yadagiri Swamy.A validated stability-indicating LC method for the separation of enantiomer and potential impurities of Linezolid using polar organic mode[J].Journal of Pharmaceutical Analysis,2012,2(4):272-278. 被引量:4
  • 2王鲁燕,陈代杰.噁唑烷酮类抗菌药物的研究[J].药学进展,2002,26(1):16-22. 被引量:9
  • 3余德胜,王志谦,熊莺,赵燕芳,宫平.利奈唑酮合成新工艺[J].中国药物化学杂志,2005,15(2):89-90. 被引量:8
  • 4赵肖玉,马燕如,徐正.利奈唑胺合成工艺的改进[J].华西药学杂志,2007,22(2):179-181. 被引量:9
  • 5黄强,李华,牛柏林,等.(R)-N-(3-氟-4-吗啉基)嗯唑酮-5-甲基醇制备工艺:中国,1772750[P].2005-11-15.
  • 6徐广宇,吴希罕,谢毓元.N-[4(R)-(1,3-二嗯烷基)甲基]-苯胺制备方法和用途:中国,1673224[P].2004-03-23.
  • 7Madhusudhan G, Reddy GO, Rajesh T, et al. Stereoselective synthesis of novel (R)- and (S)-5-azidomethyl-2- oxazolidinones from (S) -epichlorohydrin: a key precursorfor the oxazolidinone class of antibacterial agents [J] Tetrahedron Lett, 2008, 49 (19) : 3060-3062.
  • 8Barbachym MR, Brickner S J, Hutchinson DK. Substituted oxazine and thiazine oxazolidinone antimicrobials: WO, 1995007271 [P]. 1995-03-16.
  • 9Aoki H, Ke L Z, Poppe S M, et al. Oxazolidinone antibiotics targe the P site on Escherichia coli ribosomes [J]. Antimicrob Agents Chemother,2002,46(4):1080-1085.
  • 10Junzo O, Yoshiro F, Hiroshi Y. Preparation of oxazolidin- 2-ones:JP,2003206282 [P].2003-07-22.

引证文献17

二级引证文献25

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部