http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-437081-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D211-58
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4465
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D295-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-58
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-445
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4468
filingDate 1975-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1977-01-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-437081-A1
titleOfInvention PROCEDURE FOR THE PREPARATION OF NEW 1- (N- (PARA-FLUO-ROBENZOILPROPIL) -4-PIPERIDIL) -UREAS.
abstract Novel 1-[N-(p-fluorobenzoylpropyl)-4-piperidyl]ureas of the formula I below, in which R is a hydrogen atom, an acetyl group, an alkyl group with 1 to 3 carbon atoms or the phenyl group, are prepared by reacting a correspondingly substituted N-(4-piperidyl)-2-imidazolidinone with a p-fluorobutyrophenone which has in the omega position a group which can be eliminated under the reaction conditions. The products of the process can be converted into their physiologically tolerated acid addition salts. It is additionally possible for resulting compounds of the formula I in which R is hydrogen to be acetylated by reaction with acetyl chloride or acetic anhydride. The novel compounds show the typical range of effects of the neuroleptics and can therefore be employed as CNS-depressant agents, sedatives and tranquillizers.
priorityDate 1974-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 30.