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filingDate 1989-12-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8acc5d0a6cf2ce783a69e49d6fa20e26
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_10292d786dc5c931600d64c5eb16da98
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9e61480aca97c2a4daea522072aa31f8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_58805ae07275869223b359d75c51ac45
publicationDate 1990-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0373998-A1
titleOfInvention Propenone oxime ethers, method for their preparation and pharmaceutical compositions containing them
abstract The present invention relates to new ethers of propenone oximes, a process for their preparation and the pharmaceutical compositions containing them.n n n - Ar et Ar représentent indépendamment un groupe phényle non substitué, mono ou polysubstitué; un radical anthryle-9 ou naphtyle, un groupe pyridyle, thiényle, ou furyle, - R 1 et R 2 désignent indépendamment un atome d'hydrogène, un alkyle en C 1 -C 4 ou avec l'atome d'azote auquel ils sont liés un groupe pyrrolidinyl-1, pipéridino, morpholino ou pipérazinyl-1, -n = 2 ou 3, - M = H, CI, Br ou un groupe alkyle en C 1 -C 6 . The propenone oxime ethers according to the invention correspond to the formula: in which - Ar and Ar independently represent an unsubstituted, mono or polysubstituted phenyl group; an anthryl-9 or naphthyl radical, a pyridyl, thienyl or furyl group, - R 1 and R 2 independently denote a hydrogen atom, a C 1 -C 4 alkyl or with the nitrogen atom to which they are linked a pyrrolidinyl-1, piperidino, morpholino or piperazinyl-1 group, -n = 2 or 3, - M = H, CI, Br or a C 1 -C 6 alkyl group. n n n The invention also relates to the salts of the compounds of formula (1).n n n These compounds have antiplatelet properties and are 5HT 2 receptor antagonists.
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priorityDate 1988-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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