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filingDate 1988-11-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c682cd234d6b7bf9e9545a2022f95fa8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_377ce352b2651bc03132ac5d01f8c1a7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_554735ee2ee54b3d5a07abbae492a32d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_10ef1eff0e7421a8ddd1866ebbbeb181
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bc9992c70451cdb8c7c56fb4b06d75ae
publicationDate 1990-07-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0375791-A1
titleOfInvention Phenyl ethanol amines, their use as pharmaceutical compounds and as performance stimulants in animals, as well as processes for their preparation
abstract The invention relates to new phenylethanolamines of the general formula in the A is a straight-chain or branched alkylene group, B is a bond, an alkylene group, a carbonyl or hydroxymethylene group, R₁ represents a hydrogen atom, a halogen atom or a trifluoromethyl group, R₂ is a hydrogen atom or an amino group, R₃ is a cyano group, a hydrogen, chlorine or bromine atom and R₄ represents a hydrogen or halogen atom, an alkyl, hydroxy, alkoxy, carboxy, alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl or dialkylaminocarbonyl group or an alkoxy group which is terminated by a carboxy, alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl, Dialkylaminocarbonyl, hydroxy, alkoxy, amino, alkylamino, dialkylamino, pyrrolidino, piperidino or hexamethyleneimino group is substituted, mean their optical isomers and their diastereomers and their acid addition salts. n n n The new compounds of the formula I, their optical isomers and their diastereomers and their acid addition salts, in particular their physiologically tolerable acid addition salts with inorganic or organic acids, have valuable pharmacological properties, namely an action on the metabolism, preferably an antihypertensive and body fat reducing effect these are used as performance enhancers in animals.n n n The new compounds of the general formula I above can be prepared by processes which are known per se.
priorityDate 1987-06-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 539.