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A modified procedure for synthesis of the side chain of ceftazidime-activated thioester

机译:头孢他啶活化的硫酯侧链合成的改进程序

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摘要

A modified procedure for synthesis of the side chain of ceftazidime-activated thioester has been established. This key intermediate of ceftazidime was obtained by a more eco-friendly process than conventional methods, and the yield was much higher (up to 92.4 %). It was found that different organic bases (triethylamine or pyridine) used in this reaction had different effects. The reaction conditions were also optimized to make the route more competitive and suitable for large-scale industrial production.
机译:建立了头孢他啶活化的硫酯侧链合成的改进程序。该头孢他啶的关键中间体是通过比传统方法更环保的方法制得的,收率更高(高达92.4%)。发现在该反应中使用的不同有机碱(三乙胺或吡啶)具有不同的作用。还优化了反应条件,以使路线更具竞争力并适合大规模工业生产。

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