期刊文献+

巴洛沙星的合成路线 被引量:2

Graphical synthetic routes of balofloxacin
下载PDF
导出
摘要 目的:合成巴洛沙星。方法:对其合成路线进行了分类和比较。结果与结论:路线1②和2②适于工业化生产。 A comparison of various synthetic methods of balofloxacin,a new quinolone type ofantibacterial agent,was made,suggesting that both routes 1② and 2② are favorable to the manufactur-ing.
出处 《中国新药杂志》 CAS CSCD 北大核心 2004年第12期1130-1133,共4页 Chinese Journal of New Drugs
关键词 巴洛沙星 氟喹诺酮 合成路线图解 balofloxacin fluoroquinolone graphical synthetic routes
  • 相关文献

参考文献20

  • 1廖斌,丛欣,廖清江.2002年世界上市的新药[J].药学进展,2003,27(3):190-192. 被引量:17
  • 2Ito T,Matsumoto M,Nishino T,et al.Improved bactericidal activity of Q-35 against quinolone-resistant staphylococci[J].Antimicrob Agents Chemother,1995,39(7):1522-1525.
  • 3NakaneT NakajimaC MitsuhashiS.In vitro antibacterial activity of balafloxacin[J].日本化学疗法学会杂志,1995,43(5):1-9.
  • 4Marutani K,Matsumoto M,Otable Y,et al.Reduced phototoxicity of a fluoroquinolone antibacterial agent with long-wavelength UV light[J].Antimicrob Agents Chemother,1993,37(10):2217-2223.
  • 5Hirohito S,Kyshige O.Preparaton of quinolonecarboxylic acid derivatives and their intermediates[P].JP:117238,1993-05-14.
  • 6Damagala JM,Heifeitz C L,Hutt M P,et al.1-Substituted 7-[3-[(ethylamino)methyl]-1-pyrrolidinyl]-6,8-difluoro-1,4-dihydro-4-oxo-3- quinolonecarboxylic acids,new quantitative structure-activity relationships at N1 for the quinolone antibacterials[J].J Med Chem,1988,31(5):991-1001.
  • 7Clay RJ,Collom TA,Karrick GL,et al.A safe,economical method for the preparation of β-oxo esters[J].Synthesis,1993,3:290-292.
  • 8Yohe LG,Baldev S,Michae IR,et al.Preparation of pyridinylquinolones as antibacterials[P].EP:417669,1991-03-20.
  • 9Thomas MF,Joseph SP,John DM,et al.1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3- quinolonecarboxylic acids;1-cyclopropyl-1,4-dihydro- 6-fluoro -4-oxo-1,8-naphthyride-3-carboxylic acids and their derivatives[P].EP:153828,1985-09-04.
  • 10Hirohito S,Yasuo F,Yutaka M.Process for producing quinolonecarboxylic acid derivatives[P].WO:22308,1993-11-11.

二级参考文献2

  • 1[1]Pharma Mar ket letter, 2003,30 (6): 24 - 25.
  • 2[2]Scrip, 2003,No2823:26.

共引文献16

同被引文献13

  • 1刘明亮,刘秉全,孙兰英,郭慧元.巴洛沙星的合成[J].中国医药工业杂志,2004,35(7):385-388. 被引量:18
  • 2Ochi Kiyoshigo, Sift Hirohito. Preparation of 6-fluoro-7- (heterocyclic amino )-3-quinolonecarboxyllc acid derivatives as intermediates for antibacterial agents: WO, 9302055 [ P]. 1991-07-16.
  • 3Nagano Hiroyuki, Suzuki Nobuyuki. Quinolone carboxylic derivative hydrate: WO,9315070 [ P]. 1992-01-31.
  • 4Masuzana Ktmiyoshi, Suzue Seigo,Hirai Keiji,et al. Preparation of 8-alkoxy-quinolonecarboxylic acids as antibactefials with selective toxicity : EP, 230295 [ P ]. 1987-07 -29.
  • 5Hirohito S, Kyshige O. Preparation of quinolonecarboxylic acid derivatives and their intermediates: JP, 117238 [ P ]. 1993-05-14.
  • 6Shimizu Hirohito, Fujimura Yasuo, Miura Yutaka. Process for producing quinolonecarboxylic acid defivatives:WO, 9322308 [ P]. 1993-11-11.
  • 7Iwata Masayukl, Kimura Tomio, Fujiwara Yoshiml, et al. Preparation of alkoxyfluoroquinolonecarboxylic acid derivatives as medical bactericides: EP,241206 [ P]. 1987-10- 14.
  • 8李倩,赵世明,罗振福,孙有光.加替沙星合成工艺改进研究[J].精细化工中间体,2009,39(5):37-40. 被引量:3
  • 9周文,李荣东.加替沙星的合成研究[J].中南药学,2010,8(10):751-753. 被引量:2
  • 10王堃,邹龙,刘根炎,谈弋.莫西沙星及其杂质的合成研究进展[J].化学通报,2018,81(5):414-424. 被引量:9

引证文献2

二级引证文献2

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