http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0344414-B1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P7-02
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00
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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/A61P7-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-00
filingDate 1989-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1994-10-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_124ffb377ea0d083552e8b8c005159cb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ec4c16c78d7c59db057056d5b6b24d89
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3a99e7179104cda9539d5de66c694fc4
publicationDate 1994-10-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0344414-B1
titleOfInvention 5-Substitued imidazo[4,5-c]pyridines
abstract This invention relates to novel substituted imidazopyridine dervatives having the following formula <CHEM> or a pharmaceuticaly acceptable acid addition salt: wherein R1 and R2 are each independently selected from hydrogen; straight or branched chain alkyl of 1 to 15 carbon atoms; cycloalkyl having 3 to 8 carbon atoms; substituted cycloalkyl which can be substituted one or more by alkyl of 1 to 6 carbon atoms; bicycloalkyl having 3 to 8 carbon atoms in each ring; heterocyclicalkyl having 4 to 8 carbon atoms which can be optionally substituted by alkyl of 1 to 6 carbon atoms; heteroaromatic having 5 or 6 carbon atoms which can be optionally substituted by alkyl of 1 to 6 carbon atoms; phenyl; substituted phenyl which can be substituted one or more by a group independently selected from alkyl of 1 to 6 carbon atoms or halogen; straight or branched alkenyl having 3 to 15 carbon atoms with the proviso that the double bond of the alkenyl group cannot be adjacent to the nitrogen; cycloalkenyl having 5 to 8 carbon atoms with the proviso that the double bond cannot be adjacent to the nitrogen; R1 and R2 cannot both be hydrogen Y is phenyl or phenyl substituted once or more than at one or more of the 2, 3, 5 or 6 position of the phenyl ring by substituents independently selected from the group consisting of alkoxy wherein the alkyl is 1 to 6 carbon atoms; halogen wherein the halogen is selected from bromo, fluoro, or chloro; straight or brnached chain alkyl having 1 to 6 carbon atoms; substituted straight or branched chain alkyl which can be substituted one or more by halogen; thioalkyl wherein the alkyl is 1 to 6 carbon atoms; alkoxyalkyl wherein the alkyl groups are each 1 to 6 carbon atoms; hydroxyalkyl wherein the alkyl is 1 to 6 carbon atoms; alkylthioalkyl wherein the alkyl group are each 1 to 6 carbon atoms; cyano; mercaptoalkyl wherein the alkyl is 1 to 6 carbon atoms; hydroxy; amino; alkylamino wherein the alkyl group are each 1 to 6 carbon atoms; and dialkylamino wherein the alkyl group are each 1 to 6 carbon atoms. n is an integer of 1 to 5. R3 is a group substituted at one or more of the 4, 6, or 7 positions of the pyridine ring said group being independently selected from hydrogen; alkyl of 1 to 6 carbon atoms; halogen wherein the halogen is selected from bromo, fluoro or chloro; alkoxy wherein the alkyl is 1 to 6 carbon atoms. R4 is hydrogen or alkyl of 1 to 6 carbon atoms. useful in the treatment of diseases or disorders mediated by platelet-activating factor. This invention relates to pharmaceutical compositions of such substituted imidazopyridines.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8779141-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8329727-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7737162-B2
priorityDate 1988-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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