http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2009072-A6

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-495
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-10
filingDate 1988-10-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9330b31e19d8c9948084ff5640207c69
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9bdf373ebaae8f09baa00d6dcaf39110
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_71c57789097e655cfafdba67d4ad4333
publicationDate 1989-08-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2009072-A6
titleOfInvention PROCEDURE FOR OBTAINING CYPROFLOXACIN.
abstract PROCEDURE FOR OBTAINING CYMPROFLOXACIN FROM FORMULA INCLUDING: CONDENSATION OF 2,4-CHLORO-5-FLUOROACETOPHENONE WITH DIMETHYL CARBONATE GIVING 2,4-DICLORO-5-FLUOROBENZOYLACETATE, WHICH REACTION ENOL, TO WHICH CYCLOPROPYLAMINE IS ADDED, ORIGINATING THE ENAMINONE, WHICH BECAUSE OF CYCLATION GIVES PLACE TO A CYCLIC ETHER, WHOSE HYDROLYSIS PROVIDES THE ACID QUINOLIN-3-CARBOXYLIS, POSITIONING, WITH N-ETOXICARBONYLPIPER, AND TO CIPROFLOXACINA. THIS COMPOUND IS A WIDE SPECTRUM BACTERICIDE AGENT, VERY EFFECTIVE BOTH AGAINST GRAM-POSITIVE AND GRAM-NEGATIVE BACTERIA.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114105792-A
priorityDate 1988-10-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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