http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-3969522-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c7ad58d3c0b071069a8ee0cb8c8ba2e8 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-44 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-44 |
| filingDate | 1975-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 1976-07-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b2e83294cd892c17c084151dfa055399 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a9516b64b403b9d3e848b4c5ddf4cf13 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dbacd84ae8ab5a1235e3d08624bed937 |
| publicationDate | 1976-07-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | US-3969522-A |
| titleOfInvention | Diaryl-pyridyl-imidazole methanes for treating mycotic infections |
| abstract | Diaryl-pyridyl-imidazolyl methanes of the formula AND PHARMACEUTICALLY ACCEPTABLE NON-TOXIC SALTS THEREOF, WHEREIN R1 and R2 are the same or different alkyl of 1 to 4 carbon atoms, are produced either by A. REACTING A (DIALKYLPHENYL-PHENYL-PYRIDYL)-METHANOL OF THE FORMULA WHEREIN R1 and R2 are as above defined, with thionyl-bis-imidazole in the presence of an inert organic diluent at a temperature of from -20 DEG C to about 150 DEG C; or B. REACTING A (DIALKYLPHENYL-PHENYL-PYRIDYL)-METHYL HALIDE OF THE FORMULA WHEREIN R1 and R2 are as above defined and Hal is chlorine or bromine, with imidazole in the presence of an acid binding agent at a temperature of from 20 DEG C to about 180 DEG C. The diaryl-pyridyl-imidazole methanes of the present invention are useful for their antimycotic activity. |
| priorityDate | 1972-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 484.