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Research On Synthesis Of Cefoxitin

Posted on:2011-06-14Degree:MasterType:Thesis
Country:ChinaCandidate:Y F WangFull Text:PDF
GTID:2284330338977853Subject:Organic Chemistry
Abstract/Summary:PDF Full Text Request
Cefoxitin, the second-generation cephalosporins is permanece and have a broad spectrum of antibacterial activity. Because of its strutural characteristics. It has a high resistance to theβ-lactanase, which producted by bacteria. Thus, the cefoxitin has a great market potential.Starting from cephalosporanic acid as raw material, the cefoxitin was obtained via 4 steps amidation, methoxylation, deacetylation, and carbamo -ylation. We have improved the original process., the total yield of 71.5%. In the amidation reaction, we selected cephalosporanic acid as a reaction macterial which is simpler and lower; in reaction methoxy we selected tert-butyl hypochlorite to repalce the NBS as the halogenated reagent reduce the cost applicable for mass production; in the deacetylation reaction, we use enzymes as reagents to acetylation, and all intermediate conditions were optimized to obtain a low cost, simple green industrial synthesis route.
Keywords/Search Tags:cefoxitin, drug synthesis, improved synthesis
PDF Full Text Request
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