http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DD-295162-A5

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D499-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D241-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D499-68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-43
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-495
filingDate 1990-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d037b831d79d592c9c92362596cbe430
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e1474eb864fd70ff2a582f0883796ebf
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publicationDate 1991-10-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DD-295162-A5
titleOfInvention PROCESS FOR PREPARING D-ALPHA- (4-ETHYL-2,3-DIOXO-PIPERAZINE-1-CARBONYLAMINO) -BENZYLPENICILLINE
abstract The invention relates to a technically feasible process for the preparation of * in high yield, of very good quality and crystallinity, which is characterized in that ampicillin, ampicillin salts or hydrolytically easily cleavable esters with * as a technical solution in a chlorinated organic solvent such as methylene chloride in the presence of Acid is acidified and during or after Ansaeuerung in a two-phase system water / organic solvent, wherein the organic solvent is a mixture of chlorinated hydrocarbon and esters, such as ethyl acetate, with pure seed crystals of * is added. The reaction product precipitates in this way in high yield and constant very good purity from the reaction mixture, is very easy to isolate and handle technically. {Piperacillin; acylation; ampicillin}
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104910178-B
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priorityDate 1990-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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