http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7335767-B2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-36
filingDate 2003-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2008-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_817b92b9474035459facecbeec7c3f71
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5b569a1216cdcc20b57b5a8f0ab0fa75
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_68277fcc480d17395f319b451b314e84
publicationDate 2008-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-7335767-B2
titleOfInvention Method for preparation of ceftiofur and salts thereof
abstract A process for preparation of ceftiofur sodium of formula (Ib) n npossessing high stability and having purity of more than 97% and substantially free of impurities, is disclosed. The process comprises:n ni) reacting cefotaxime or its salts or its esters of formula (VI)n n nwherein R 3 is hydrogen, an alkali or alkaline earth metal, or an easily hydrolysable ester, with thiofuroic acid, employed in a molar proportion of 1.5 to 3.0 moles per mole of compound (VI), in the presence of acetonitrile as solvent and in the presence of large excess of methanesulfonic acid, employed in molar proportions of 12 to 18 moles per mole of compound (VI), and at a temperature of between −5° C. to 30° C. to give after necessary neutralization of the alkali or alkaline earth metal or removal of the ester group of the 4-carboxylic acid function, wherever applicable, ceftiofur of formula (Ia), possessing high stability and having purity of more than 97% and substantially free of impurities;n n nii) converting the ceftiofur of formula (Ia) thus obtained to its salt with an organic amine by treating a solution of ceftiofur in a mixture of water and a water-miscible organic solvent with an organic amine, at a temperature ranging from −10° C. to 10° C.;n niii) reacting of the amine salt thus obtained with a sodium metal carrier in a mixture of water and water-miscible organic solvent and in presence of sodium hydrogen sulfite to give ceftiofur sodium of formula (Ib).
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