http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0512901-B1

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filingDate 1992-04-30^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1999-06-23^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_18f581a499cfc3b78310496ce95992ae
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9e61480aca97c2a4daea522072aa31f8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8cb83d587abbc3f36e192d6f78aee926
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ae8c7f9821c5322ad75158117200a88c
publicationDate 1999-06-23^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0512901-B1
titleOfInvention Aminated polycyclic compounds and their enantiomers, process for their preparation and pharmaceutical compositions containing them
abstract The invention relates to compounds of formula (I): <IMAGE> in which - Y represents - either a Cy-N or Cy-CH2-N group in which Cy represents an optionally substituted phenyl; - or a group <IMAGE> in which .Ar represents an optionally substituted phenyl; .x is zero or one; .X represents a hydrogen, a hydroxyl, an alkoxy; an acyloxy; a carboxy; a carbalkoxy; a cyano; a -N(X1)2 group in which the groups X1 independently represent hydrogen, an alkyl, a hydroxyalkyl, an acyl, or alternatively -(X1)2 constitutes, with the nitrogen atom to which it is attached, a heterocycle; an -S-X2 group in which X2 represents hydrogen or an alkyl group; or alternatively X forms, with the carbon atom to which it is attached and with the adjacent carbon atom in the heterocycle, a double bond; - m is 2 or 3; - Ar' represents an optionally substituted phenyl or a phenyl substituted one or more times with a thienyl; a benzothienyl; a naphthyl or an indolyl; - n is 0, 1, 2 or 3; - p is 1 or 2 and when p = 2, then n = 1 and Q represents two hydrogen atoms; - Q represents oxygen or two hydrogen atoms; - T represents a group chosen from <IMAGE> - q is 0, 1, 2 or 3; - Z represents an optionally substituted phenyl; an optionally substituted naphthyl; a pyridyl; a thienyl; an indolyl; a quinolyl; a benzothienyl; an imidazolyl; or alternatively, when T is -C=O, -(CH2)q-Z may also represent a benzyl group substituted on the -CH- and optionally substituted on the aromatic ring; an optionally substituted mono-, di- or tricyclic aromatic or heteroaromatic group; or one of their possible salts with inorganic or organic acids, or when <IMAGE> one of their quaternary ammonium salts with the nitrogen (b) of piperidine or N-oxide derivatives with the same nitrogen atom. The invention also relates to the process for preparing them and to their enantiomers. Application: antagonists of neurokinin receptors.
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priorityDate 1991-05-03^^<http://www.w3.org/2001/XMLSchema#date>
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID233939502
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128417970
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID233950993
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID233938913
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129710170
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226645778
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128935768
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID233939411
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11126223
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226457894
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID233928564
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID228790484

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