http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DD-296080-A5
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c986d997e1f61f2bc6f4b7f09e16da63 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-415 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-12 |
filingDate | 1989-09-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_41ceea3ba082d2f352b704b538916532 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_47880b6d532c54c58041e3c25ca9fb1b |
publicationDate | 1991-11-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | DD-296080-A5 |
titleOfInvention | PROCESS FOR PREPARING NEW 3- (1-IMIDAZOLIN-2-YL-METHOXY) PYRAZOLES AND THEIR SALTS |
abstract | The invention relates to a process for the preparation of new * and their salts with physiologically acceptable acids in higher alcohols from the monotoluensulfonsauren salt of 1,2-diamino-ethane and also new 3- (cyanomethyloxy) pyrazoles. The latter is obtained virtually quantitatively and O-regiospecifically from the 3-hydroxy-pyrazoles or D4-pyrazolin-3-ones used as a mixture of two tautomers under the technically simple reaction conditions of the invention. Only under the mild conditions according to the invention can the title compounds be released and converted into any salts which are interesting as antiarrhythmic and antihypertensive agents, avoiding, according to the invention, a hitherto unknown, anchimerically accelerated cleavage of the imidazoline ring of the title compounds ; 3- (cyano-methyloxy) pyrazole; antiarrhythmic agent; antihypertensive agent; anchime cleavage of the imidazoline ring} |
priorityDate | 1989-09-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 95.