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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_966a6c1f382ec9bcb5e3839dfd73e5b8
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-48
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D498-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-48
filingDate 1982-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1984-12-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cec7e7494f7fddf42128c5cc49f62ca6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5f2671d4ec783251857a5708a037ba54
publicationDate 1984-12-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1179344-A
titleOfInvention Process for the preparation of 6-¬3,6-dihydro-1(2h)- pyridyl| pyrimidine-3-oxides
abstract Abstract The intermediates of the formula I wherein R1 signifies lower alkyl or lower alkoxy-lower alkyl, R2 signifies hydrogen or -COOR3 and R3 signifies lower alkyl or lower alkoxy-lower alkyl, which are important for the manufacture of therapeutically valuable 1,2,5,6-tetrahydropyridyl-substituted 2-oxo-2H--[1,2,4]oxadiazolopyrimidinecarbamates, are obtained by reacting the corresponding arylsulphonyloxy- or alkyl-sulphonyloxy-substituted derivatives with 1,2,5,6-tetra-hydropyridine.
priorityDate 1981-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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