http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-350955-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_966a6c1f382ec9bcb5e3839dfd73e5b8 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-62 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-515 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-515 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-62 |
| filingDate | 1968-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1969-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | ES-350955-A1 |
| titleOfInvention | A PROCEDURE FOR PREPARING DERIVATIVES OF BARBITURIC ACID. |
| abstract | Novel compounds of the general formula wherein R1 and R2 individually represent an hydroxy, C 1-7 alkoxy or C 7-12 aralkoxy group, R3 represents a hydrogen atom, a C 1-7 alkyl, C 2-7 alkenyl or C 2-7 alkynyl group and n stands for 0, 1 or 2, and salts thereof with bases, are prepared by condensing a malonate of the general formula wherein R1, R2, R3 and n have the significance given above and R4 represents an alkyl group, with urea, and if desired, converting the resulting barbituric acid into a salt with a base. Pharmaceutical compositions of the above compounds elicit tranquillization without depression and are administered orally or parenterally. |
| priorityDate | 1967-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 20.