http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-88103507-A

Outgoing Links

Predicate Object
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-89
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D237-32
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D491-056
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D521-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P3-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D498-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-89
filingDate 1988-06-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1988-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-88103507-A
titleOfInvention Preparation method of oxo-2,3-diazinyl acetic acid with benzothiazole or other heterocyclic branched chains
abstract The invention discloses a method for preparing oxo-2,3-naphthyridine acetic acid with benzothiazole or other heterocyclic branched chains, the method comprising: making oxo-2,3-naphthyridine acetic acid Esters react with aniline derivatives. The invention also discloses a method for preparing such oxo-2,3-naphthyridine esters.
priorityDate 1987-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID467688690

Total number of triples: 25.