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filingDate 1993-02-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1995-03-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5dcf6e84a9917a2ec32a44fc7cc0affb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_13cef998400c3df5a35c6c2b6883e6a2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dbb8634b030f439996de3ee18f81a02e
publicationDate 1995-03-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5401879-A
titleOfInvention Phenylethanolamino- and phenylethanolaminomethyltetralines, process for the preparation thereof, intermediates in said process and pharmaceutical compositions containing them
abstract Phenylethanolamino- and phenylethanolaminomethyltetralines of formula (I) ##STR1## wherein X represents a hydrogen atom, a halogen atom, a (C 1 -C 4 )alkyl group or a trifluoromethyl group, n A represents a bond between the --COOR group and the tetraline ring, a (C 1 -C 4 )alkylene or a (C 2 -C 4 )alkenylene group, n R is hydrogen or a (C 1 -C 4 )alkyl group, and n n is 0 or 1 n and their salts, are typically prepared by reaction of an epoxide of formula (IIa) ##STR2## with a tetraline derivative of formula (III) ##STR3## wherein A and n are as defined above and R' is a (C 1 -C 4 )alkyl group, optionally followed by basic hydrolysis to obtain the compounds (I) wherein R is hydrogen. The new compounds show very interesting properties as antidepressant and intestinal spasmolytic agents. n The new intermediates of formula (III) are also claimed.
priorityDate 1991-02-18-04:00^^<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: 401.