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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_79751aeaa9923745648e5ae7d9c35782
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D211-98
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-79
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-84
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D217-26
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-79
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-84
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D217-26
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D221-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-98
filingDate 1988-09-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1990-05-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bfae16f596bf9169a5da5686fa1334af
publicationDate 1990-05-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4923993-A
titleOfInvention Process for the preparation of 2-pyridinecarboxylic acid derivatives and 1-amino-1,4-dihydropyridine-2-carboxylic acid derivatives
abstract The process of the invention relates to the reaction of hydrazones of formula II ##STR1## with α-chloro- or α-bromoarylonitrile or α-chloro- or α-bromoacrylates of formula III ##STR2## to 1-amino-2-cyano-1,4-dihydropyridines or 1-amino-1,4-dihydropyridine-2-carboxylic acid esters of formula IV ##STR3## which are converted into pyridine derivatives of formula I ##STR4## by treatment with an acid, with removal of R 4 R 5 NH. Y is --CN or --COOR 3 and R 1 to R 5 may be alkyl.
priorityDate 1985-10-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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