http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4532239-A

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filingDate 1983-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1985-07-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_52dbb658d62628315873a5d0d46608be
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_96e8e63d8f903a5a57404daa17b377be
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publicationDate 1985-07-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4532239-A
titleOfInvention N-phenoxypropanol-N'-pyridazinyl ethylendiamines as β-receptor blockers
abstract Basically-substituted pyridazines of the formula: <IMAGE> (I) wherein R1, R2 and R3, independently of one another, denote hydrogen, halogen, hydroxyl, nitro, trifluoromethyl, alkyl, alkoxyalkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, phenyl, alkoxy, hydroxyalkoxy, alkoxy-alkoxy, alkenyloxy, alkynyloxy, cycloalkoxy, phenalkoxy, alkanoyl, alkanoylamino and -NH-CO-R9, R9 representing morpholino, piperidino or 1-pyrrolididinyl, or an optionally substituted ureido radical, R4 denotes hydrogen or lower alkyl and W denotes hydrogen, chlorine or bromine; and the acid-addition salts thereof are useful alone or in pharmaceutical preparations for treating cardiac complaints, circulatory complaints and high blood pressure. Several methods for preparing the basically-substituted pyridazines are also provided.
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Total number of triples: 489.