http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1510977-A

Outgoing Links

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-50
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-44
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-435
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-50
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-445
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D-
filingDate 1975-08-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1978-05-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1510977-A
titleOfInvention Tetrahydropyridine and piperidine derivatives and processes for the production thereof
abstract The novel piperidine derivatives of the general formula I <IMAGE> in which R1 denotes a saturated aliphatic hydrocarbon radical having 1-12 or a saturated cycloaliphatic hydrocarbon radical having 3-12 carbon atoms, which radicals can be substituted by hydroxyl groups and/or interrupted by oxygen, or a phenyl-(lower alkyl) or cinnamyl radical which is optionally substituted in a specific manner, R2 denotes hydrogen or a lower alkyl group, R3 and R4 independently of one another denote hydrogen, lower alkyl or lower alkoxy groups, halogen atoms up to atomic number 35, benzyloxy or hydroxyl groups, and R3 also denotes a trifluoromethyl group, a lower 1-hydroxyalkyl group, a 1-hydroxycycloalkyl or cycloalkyl group each having 5-8 carbon atoms, or R3 and R4 together denote the trimethylene, tetramethylene or 1,3-butadienylene radical, R5 denotes hydrogen or an alkyl group having at most 4 carbon atoms and A and B denote divalent saturated aliphatic hydrocarbon radicals and B can also denote the direct bond, where A and B together always form 3 ring members and together with R5 have a total of at most 9 carbon atoms, and their acid addition salts have antidepressant activity. They are prepared by hydrogenation of the corresponding tetrahydropyridine derivatives.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AU-668026-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5716971-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5891895-A
priorityDate 1974-08-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 32.