首页> 外文会议>International Conference on Chemical Engineering and Advanced Materials >A Convenient Method for the Chlorination of P-Methoxybenzyl 2-(3-Phenylacetamido-4-Benzenesulfonylthio-2-Azetidinone-1 -yI)-3-Methyl-3-Butenate
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A Convenient Method for the Chlorination of P-Methoxybenzyl 2-(3-Phenylacetamido-4-Benzenesulfonylthio-2-Azetidinone-1 -yI)-3-Methyl-3-Butenate

机译:对氯化甲氧基苄基的氯化2-(3-苯基乙酰胺-4-苯并磺酰酮-2-氮丁胺酮-1-甲基-3-丁酯的方便方法

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A convenient method for the chlorination of p-methoxybenzyl 2-(3- phenylacetamido-4-benzenesulfonylthio-2-azetidinone-l-yl)-3-methyl-3-butenate from penicillin G with sulfuryl chloride ( SO_2Cl_2), which is subsequently converted to p-methoxybenzyl 2-(3- phenylacetamido-4-benzenesulfonylthio-2-azetidinone-l-yl)-3-chloromethyl-3-butenate, versatile intermediates for the synthesis of cephalosporin antibiotics was developed. The method has the advantage of cheap reagents, mild reaction conditions and convenient operation. The quantity and the feeding rate of the chlorination reagent can be controlled easily. The method is particularly suitable for the chlorination in an industral process.
机译:从青霉素G用硫酰氯(SO_2Cl_2)的P-甲氧基苄基二甲氧苄基氯化二甲氧基苄基的氯化二甲氧基苄基2-(3-苯基乙酰氨基-4-苯甲磺酰硫胺-3-丁酯)-3-甲基-3-丁酯,随后转化为对甲氧基苄基2-(3-苯基乙酰胺-4-苯磺酰硫磺酰硫代-2-阿哌啶酮-1-基)-3-氯甲基-3-丁酯,开发了合成头孢菌素抗生素的通用中间体。该方法具有廉价试剂,温和的反应条件和操作方便的优势。可以容易地控制氯化试剂的量和进料速率。该方法特别适用于行业过程中的氯化。

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