http://rdf.ncbi.nlm.nih.gov/pubchem/patent/FR-2043503-A1
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_39ae96c0ecc22ff90ff986371a3cea0f |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D263-24 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-135 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-135 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D263-24 |
filingDate | 1970-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 1971-02-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | FR-2043503-A1 |
titleOfInvention | NEW AMINOPROPANOLS DERIVATIVES, THEIR OBTAINING AND THEIR APPLICATIONS |
abstract | Aminopropanols (I) of formula, R'OCH2CH(OH)CH2 NHR2 where R'=tetrahydronaphthyl or alkyl opt. substd by alkenyl, aryl, alkoxy, aryloxy, or aralkoxy and R2=diphenylalkyl opt. substd. by hal. and salts of (I) are beta-adrenergic blocking agents and coronary vasodilators. (I) may be prepd. by e.g. (a) reaction of an amine R2NH2 with the appropriate epoxide, halide etc., (b) reductive condensation of I (R2=H) with a ketone or aldehyde, (c) reaction of I(R2b=H) with a reactive cpd. R2X, where X is an acid residue. (d) condensation of oxazolidine-2-one (IIe R'OCH2CH - CH2 with R2X, followed by acid or base hydrolysis. |
priorityDate | 1969-05-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 17.