http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SU-1324261-A1
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_969b8616d26f6a341ca57c97f37d094a |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-341 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-498 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-495 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-28 |
filingDate | 1985-10-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 1991-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a3248a6efa3820de004c3512cc464f5b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ec76e6dfdf6d0fa24bd56b53c9d10cb9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8d057ad0d6077bc756d37abc6b801ef0 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_45026726bdf06e9f14f111800eb69591 |
publicationDate | 1991-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | SU-1324261-A1 |
titleOfInvention | Method of producing 3-(5-aryl-2,3-dihydrofurane-3-on-2-yl)-1,2,3,4-tetrahydro-2-quinoxalons |
abstract | The invention relates to heterocyclic compounds, and in particular, ZCh5-phenyl (or 5-top 1) -2,3-dihydrofuran-3-one-2-yl 1, 2, 3, -tetra 8 .-- ".-.-. -2-Hickox. Polo (PC), which have prottopog, are lyurl {friendly and can be used opasch, medicine. The goal is to co-act with: selecting an inecTH of the specified class, providing a better actypnost. This is achieved by the synthesis of PCs; 2-methoxycarbonylmethyl-1CHP. N-5-phenyl (or 5-p-tolyl) -2,3-dihydrofur n-3-one with phenylenediamine n benzene in the presence of boiling. Output (where 5-Fekil) 58%, so pl.228-229 C-, output PF (where 5-p-tolyl), t, pl. 234-233 C, Tests show that PF has a better prothypoinflammatory effect than amidopyrine and has less toxicity. 1 tab. with; S Yu Yu |
priorityDate | 1985-10-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 32.