http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DD-248594-A5

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_97a285d8ecd0184a7e5d89a1e4e07997
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-545
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-545
filingDate 1986-07-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8428ca284342536af05284a010e50841
publicationDate 1987-08-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DD-248594-A5
titleOfInvention PROCESS FOR PREPARING A CRYSTALLINE DIMETHYLFORMAMIDEOLVATE OF THE 7 - ((D) -2-AMINO-2- (4-HYDROXYPHENYL) -ACETAMIDO) -3 - ((Z) -1-PROPENYL) -CEPH-3-EM-4-CARBON ACID
abstract The invention relates to a process for preparing a crystalline Dimethylformamidsolvats of 7- ((D) -2-amino-2- (4-hydroxyphenyl) acetamido) -3 - ((Z) -1-propenyl) -ceph-3 em-4-carboxylic acid. This solvate is an intermediate compound which is crystalline in form and therefore highly pure. In addition, this intermediate compound is more stable in storage than the free acid. From the dimethylformamide solvate obtainable according to the invention, said acid can be released without difficulty, which is an effective broad-spectrum antibiotic.
priorityDate 1985-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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