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filingDate 1977-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_543d3a46147f8f1a869b2225cc8d3604
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b040ca8d26954911a63bb6aa4725654e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dd6307542a11e9450eec66ca6a760427
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5d416b876ba11e71b23561961117acb5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4beb0b921bc081a3a8c84b0505203d16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e7fb4525a1e2dc775dc4d30746eee6da
publicationDate 1981-10-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-177453-B
titleOfInvention Process for preparing new basic substituted o-propyloximes and pharmaceutical preparations containing thereof
abstract Compounds of general formula <IMAGE> (I) wherein R1 represents a radical selected from the group consisting of (a) hydrogen, carboxyl; (b) alkyl, alkenyl each having up to 6 carbon atoms and their phenyl substituted derivatives; (c) at most binuclear unsubstituted aryl, at most binuclear aryl substituted by from 1 to 3 substituents selected from the group consisting of alkyl and alkoxy each having up to 6 carbon atoms, benzloxy, haloalkyl having up to 2 carbon atoms, halogen, cyano and nitro; amino, carboxyl and hydroxy; amino, carboxyl and hydroxy each being substituted by alkyl having at most 2 carbon atoms, methylenedioxy groups and O-<3-[4-(2-methoxyphenyl)-1-piperazinyl]-2-hydroxypropyl>-hydroximinom ethyl groups; (d) at most bicyclic unsubstituted heteroaromatic group having 1 to 4 heteroatoms selected from the group consisting of nitrogen, one sulphur and one oxygen in the ring system and such a heteroaromatic group being substituted by at most 3 substituents selected from the group consisting of alkyl, alkoxy each having up to 2 carbon atoms, phenylalkyl having up to 3 carbon atoms in the alkyl moiety, halogen, methylamino and dimethylamino; R2 represents a member selected from the group consisting of hydrogen, alkyl having up to 3 carbon atoms, cycloalkyl having up to 6 carbon atoms and phenyl; and R1 and R2, together with the carbon atom to which they are attached, form a radical selected from the group consisting of fluorene-9-ylidene and a cycloaliphatic group having up to 10 carbon atoms and such a cycloaliphatic group containing a hydrocarbon bridging group; R3 represents a member selected from the group consisting of hydrogen hydroxy and acyloxy; R4 represents a member selected from the group consisting of hydrogen alkyl having up to 3 carbon atoms and phenyl; R5 represents a member selected from the group consisting of halogen, alkoxy having up to 2 carbon atoms and hydroxy; and X represents a member selected from the group consisting of nitrogen and methine and physiologically acceptable acid addition salts thereof; a pharmaceutical composition containing said compounds.
priorityDate 1976-12-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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