http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-3946008-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D491-052
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-535
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-535
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-54
filingDate 1974-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1976-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aab27483ec26e867497cbf9273709bb6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_37db79e72770fc992a5153e1dc03ae7a
publicationDate 1976-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-3946008-A
titleOfInvention Substituted benzopyrano[3,4-c]pyridines
abstract Substituted benzopyrano[3,4-c]pyridines having the following structural formula are disclosed: ##SPC1## n In the above formula, R 1 and R 2 are hydrogen, a hydroxyl group or a lower alkoxyl group of from 1 to 6 carbon atoms; and X is an oxygen atom, a sulfur atom, a methylene group or a nitrogen atom substituted by hydrogen, a lower alkyl group of from 1 to 6 carbon atoms or a lower alkanoyl group of from 1 to 6 carbon atoms. The compounds of this invention are prepared by reacting an R 1 , R 2 -substituted phenol with a 3-carbethoxy-4-piperidone in the presence of an acid catalyst to give an intermediate R 1 , R 2 -substituted benzopyrano[3,4-c]pyridine. N-aminoalkylbenzopyrano[3,4-c]pyridines are obtained by treating the benzopyrano[3,4-c]pyridine with an appropriately substituted alkyl halide. The compounds of this invention are useful as bronchodilators for the treatment of bronchial asthma.
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priorityDate 1973-03-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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