http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DD-296080-A5

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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

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