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头孢噻呋钠的合成工艺研究 被引量:6

Study on the Synthetic Process of Ceftiofur Sodium
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摘要 设计了新的头孢噻呋钠的合成路线:7-氨基头孢烷酸(7-ACA)先与呋喃-2-甲硫羟酸缩合,再与AE-活性酯反应,后与异辛酸钠反应得到头孢噻呋钠。以7-ACA计算,反应总收率为39.9%。改进的新工艺反应步骤缩短。 This article designed a new synthetic route of ceftiofur sodium. The condensation product of 7-ACA and furan-2-thiol-formic acid reacted with AE thiolester, and then treated with sodium-2-ethyl hexanoate ,At last ,ceftiofur sodium was prepared. If caculated by 7-ACA, the total yield rate of ceftiofur sodium was 39.9%. The new method shortened the process.
出处 《中国兽药杂志》 2007年第2期19-20,共2页 Chinese Journal of Veterinary Drug
关键词 头孢噻呋钠 7-氨基头孢烷酸(7-ACA) 合成 ceftiofur sodium 7-ACA synthesis
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参考文献5

  • 1Mahendra I,Campbell J A.Crystalline Cephalosporin Hydro-halide Salts:US4902683[P].1990-02-02.
  • 2Sacks E,Dill H.Conversion of Cephalosporin Hydrohalide Salt to Alkal Metal:US4937330[P].1990-06-26.
  • 3Kumar U,Sivakumaran M,Handa V.Process for the Preparation of Furaca:US6476220[P].2002-11-05.
  • 4Deshpande P,Deshpande P,Kulkarni M.Method for the Preparation of Ceftiofur Sodium:US6555680[P].2003-04-29.
  • 5Deshpande P,Luthra P,Sathe P.Method for the Preparation of Ceftiofur Sodium and Its Intermediates:US6800756[P].2004-11-05.

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