http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2007514-A6
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f2d3599fb8f8f479dba95ca9bb504884 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-41 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-14 |
| filingDate | 1988-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fd353bc9b009350567061c9d0ce4b4a2 |
| publicationDate | 1989-06-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | ES-2007514-A6 |
| titleOfInvention | PROCEDURE FOR PREPARING 2,4-DIHYDRO-3H-1,2,4-TRIAZOL-3-ONAS. |
| abstract | A PROCEDURE FOR PREPARING 2,4-DIHYDRO-3H-1,2,4-TRIAZOLE-3-ONAS. THE FORMULA (I) COMPOUNDS IN WHICH R IS ALKYL C1-6 ARE OBTAINED BY CYCLE OF A FORMULA (II) INTERMEDIATE IN WHICH L1 IS HYDROGEN AND LY IS A REACTIVE OUTGOING GROUP AND LY TOGETHER FORM AN EXTRA LINK , WITH A HYDRAZINE DERIVATIVE FROM FORMULA (III) IN WHICH R3 IS A REACTIVE OUTGOING GROUP AND R IS DEFINED ABOVE, OPTIONALLY FOLLOWED BY FORMATION OF PHARMACEUTICALLY ACCEPTABLE SALTS OR BY OBTAINING THE FREE BASE FROM SALES. (I) THEY ARE USEFUL FOR THEIR FUNGICIDE AND ANTIBACTERIAL ACTIVITY. |
| priorityDate | 1988-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 16.