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3-甲胺基哌啶二醋酸盐的合成工艺改进 被引量:2

An improved method for synthesis of 3-methylaminopiperidine diacetate
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摘要 目的:合成3-甲胺基哌啶二醋酸盐。方法:以3-氨基吡啶为起始原料,经3步反应制得3-甲胺基哌啶二醋酸盐。结果:目标化合物经1H-NMR和MS确证,总收率为41.4%。结论:本方法优化了反应条件和投料比,缩短了反应时间,提高了收率,适合工业化生产。 Objective : To synthesize 3-methylaminopiperidine diacetate. Methods : 3-Methylaminopiperidine diacetate was synthesized via 3-step reactions with 3-aminopyridine as the starting material. Results: The total yield of 3-methylaminopiperidine diacetate was 41.4%. Conclusion: The improved method optimizes the synthetic process and is worthy to a further pilot manufacture.
出处 《中国新药杂志》 CAS CSCD 北大核心 2008年第20期1774-1775,共2页 Chinese Journal of New Drugs
关键词 3-甲胺基哌啶二醋酸盐 中间体 巴洛沙星 合成 3-methylaminopiperidine diacetate intermediate balofloxaein synthesis
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  • 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
  • 2王道林,姜莉莉,李春芳.新一代氟喹诺酮类抗菌素——巴洛沙星的合成[J].中国药物化学杂志,2005,15(6):340-343. 被引量:5
  • 3[2]Nakane T, Nakajima C, Mitsuhashi S. In vitro antibacterial activity of balofloxacin [J]. Nippon Kagaku Ryoho Gakkai Zasshi, 1995, 43 (S-5): 1-9.
  • 4[3]Marutani K, Matsumoto M, Otable Y, et al. Reduced phototoxicity of a fluoroquinolone antibacterial agent with a methoxy group at the 8 position in mice irradiated with longwavelength UV light [J]. Antimicrob Agents Chemother, 1993,37 (10): 2217-2223.
  • 5[4]Shimizu H, Fujimura Y, Miura Y. Process for producing quinolonecarboxylic acid derivative [P]. WO: 9322308, 1993-11-11. (CA 1994, 120: 163997r)
  • 6[5]Masuzawa K, Suzue S, Hirai K, et al. Preparaton of 8-alkoxyquinolonecarboxylic acids as antibacterials with selective toxicity [P]. EP: 230295, 1987-07-29. (CA 1988, 108:75230g)
  • 7[6]Ataka K, Oku M, Kono M, et al. Preparaton of 7-amino-4-quinolonecarboxylic acids [P]. JP: 06157464, 1994-06-03. (CA 1994, 121: 230674u)
  • 8[7]Iwata M, Kimura T, Fujiwara Y, et al. Preparation of alkoxyfluoroquinolonecarboxylic acid derivatives as medical bactericides[P]. EP: 241206, 1987-10-14. (CA 1989, 110:135095v)
  • 9[8]Takagi N, Fubasami H, Matsukubo H. (6,7-Substituted-8-alkoxy- 1-cyclopropyl- 1,4-dihydro-4-oxo-3-quinolinecarboxylic acid O3,O4) bis (acyloxy-O) borates and the salts thereof, and methods for their manufacture [P]. EP: 464823,1992-01-08. (CA 1992, 116: 152003e)
  • 10[9]Spaith E, Lintner J. Uber die bildung yon lactamen aus lactonen [J]. Bericht, 1936, 69: 2727-2731.

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