http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0105131-B1
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-46 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D403-06 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-403 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4035 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-46 |
| filingDate | 1983-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 1987-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1987-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | EP-0105131-B1 |
| titleOfInvention | 2-(omega-alkylaminoalkyl)- and 2-(omega-dialkylaminoalkyl)-3-(4-x-benzylidene)-phthalimidines |
| abstract | The 2-(ω-aikylaminoalkyl)- and 2-(m-dialkylaminoalkyl)-3-(4-X-benzylidene)phtalimidines are useful as local anesthetics.For the preparation, the adduct is formed between the suitable 3-(4-X-benzylidene)phtalide and a substituted aminoalkylamine, the adduct being then reacted with acetic anhydride; the X substituent at the position 4 of the benzylidene group then can be suitably converted according to the requirements. |
| priorityDate | 1982-08-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 49.