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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P7-02
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00
filingDate 1990-11-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_eb0c757fe2e56dee0f67895a8bf62b58
publicationDate 1994-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-209305-B
titleOfInvention Process for producing 1h-imidazo(4,5-b)quinolinyl oxyalkanecarboxylic acid amides having increased water solubility, as well as pharmaceutical compositions comprising same
abstract A novel series of 2,3-dihydro-2-oxo-1 H -imidazo­[4,5-b]quinolinyloxyalkanoic acid amides having enhanced water solubility is disclosed of the formulan wherein n is 3 to 5; R₁ is alkyl of 1 to 4 carbon atoms; R₂ is hydrogen; R₃ is 1-piperidinylethyl, 1-benzylpiperidin-4-­yl, 4-(1-piperidinyl)piperidine, (1-alkyl-2-pyrrolidinyl)­alkyl where alkyl is 1 to 4 carbon atoms, 3-quinuclidinyl; R₂ and R₃ together with the nitrogen atom to which they are attached form 4-R₄-piperazin-1-yl wherein R₄ is alkyl of 1 to 7 carbon atoms, alkoxyethyl of 3 to 7 carbon atoms, pyridinyl, pyrimidinyl, tetrahydropyranylmethyl, thienyl­methyl, cycloalkyl-(CH₂) m where m is zero or one and cycloalkyl is 5 to 7 carbon atoms except m is zero when cycloalkyl is 7 carbon atoms, benzyl, 4-fluorobenzyl, 3-trifluoromethylbenzyl, 4-alkoxybenzyl where alkoxy is 1 to 4 carbon atoms. n The compounds are cyclic AMP phosphodiesterase inhibitors and are particularly useful as inhibitors of blood platelet aggregation and/or as cardiotonic agents.
priorityDate 1989-11-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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