| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_85f07c75f85d843baf29f4a3379c3f2f |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P7-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D303-36
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-04 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C215-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D303-36
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C213-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P7-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C213-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-13 |
| filingDate |
1983-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8bb6f7ff13bf77046021c977fcba77ba
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_44bfc4884234ca3d21bfb4f4ab8eb06a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_09d1bea0005324763c9372c645a218e3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_123980eb9477cef9f71cf3a38b5bce63
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3bea3f4dffbeb74ca80a018c6ef3db52
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8057386bb71d17f3d2627135a011b0b6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0ebefa9f57679d64f815efaac436753c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2b2e55f2270b61db52dcb21d6e8e9c09 |
| publicationDate |
1985-06-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
FR-2557103-A1 |
| titleOfInvention |
NOVEL CYCLOALKYLAMINO-1 TERTIOBUTYLAMINO-3 PROPANOLS-2, THEIR PREPARATION METHOD AND THEIR THERAPEUTIC APPLICATION |
| abstract |
THE PRESENT INVENTION CONCERNS NEW CYCLOALKYLAMINO-1 TERTIOBUTYLAMINO-3 PROPANOLS-2 OF GENERAL FORMULA: (CF DRAWING IN BOPI) IN WHICH N REPRESENTS AN ENTIRE WHOLE MAY TAKE ANY OF THE VALUES BETWEEN 6 AND 11; THESE PRODUCTS MAY BE IN THE FORM OF FREE BASE OR PHARMACEUTICALLY ACCEPTABLE SALTS. THESE PRODUCTS ARE GENERALLY PREPARED IN TWO STEPS: THE AMINE IS REACTED: (CF DRAWING IN BOPI) (OR N REPRESENTS A WHOLE THAT CAN TAKE ANY OF THE VALUES BETWEEN 6 AND 11) AND EPICHLORHYDRINE: ( CF DRAWING IN BOPI) IN A SOLVENT, THEN THE EPOXIDE CHLORYDRATE SO OBTAINED WITH TERTIOBUTYLAMINE, IN A SOLVENT SUCH AS ETHANOL AT THE SOLVENT'S BOILING TEMPERATURE. THE PRODUCTS ACCORDING TO THE PRESENT INVENTION ARE USEFUL THERAPEUTICALLY IN PARTICULAR AS ANTIMICROBIALS. |
| priorityDate |
1983-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |