http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S61218585-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D215-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-47
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-04
filingDate 1985-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5c2c209420e4fad000e1eac5c1861bda
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ee727517e86a41e8550b8a01b821e983
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publicationDate 1986-09-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S61218585-A
titleOfInvention Novel quinoline carboxylic acid derivative and fungicide containing the same as active ingredient
abstract NEW MATERIAL:1-Cyclopropyl-6,8-difluoro-1,4-dihydro-7-(3-hydroxypyrro-lidin- 1-yl)-4-oxoquinoline-3-carboxylic acid o formula I and its salt. USE:It is used as a remedy for a variety of infectious diseases, because it has strong antibacterial activity. It shows strong proliferation inhibition against both gram-positive and gram-negative bacteria. PREPARATION:The reaction between 6,7,8-trifluoroquinoline carboxylic acid derivative of formula II and 3-hydroxypyrrolidine of formula III is carried out in a solvent such as methanol in the presence of an acid acceptor such as triethylamine at room temperature to 150 deg.C to give a compound of formula I.
priorityDate 1985-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 30.