http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-8601913-A1

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2e5edd48190cba3fa70dd3975efd9831
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D235-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D235-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D235-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-415
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4184
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-12
filingDate 1984-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1985-11-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-8601913-A1
titleOfInvention PROCEDURE FOR PREPARING BENZIMIDAZOLES
abstract PROCEDURE TO PREPARE NEW BENZHIMIDAZOLES. IT CONSISTS OF CYCLING A COMPOUND OF FORMULA (II) TO OBTAIN BENZIMIDAZOLES FROM FORMULA (I) WHERE R MEANS A GROUP HYDROXY, ALCOXI, FENYLALCOXI, CYANOALCOXI, ALKYLSULFENILO, ALKYLSULFINOS; R2 MEANS A HYDROGEN ATOM, A HYDROXY, ALCOXY, PHENYLALCOXY, AMINE, ALKYLAMINE OR DIALKYLAMINE GROUP; R3 MEANS A HYDROGEN ATOM, A CYAN, NITRO, AMINO, CARBOXI, ALCOXICARBONYL AND OTHERS GROUP. THE REACTION IS CARRIED OUT IN A SOLVENT, AN ANCILLATING AGENT, A CONDENSING AGENT OR A BASE AND AT A TEMPERATURE BETWEEN 0 AND 250 C. THEY HAVE PHARMACEUTICAL USEFULNESS BECAUSE OF THEIR EFFECT ON BLOOD PRESSURE AND ON THE CONTRACTILITY OF THE MYOCARDIUM.
priorityDate 1983-12-23-04:00^^<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/SID458397310
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458392451
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458396411

Total number of triples: 20.