http://rdf.ncbi.nlm.nih.gov/pubchem/patent/HU-191459-B

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C325-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C323-44
filingDate 1982-05-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5989e4f1738b7c1f78608c38a353d9d1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ab8125b2922b266ab9a2d2d7e71b72d5
publicationDate 1987-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-191459-B
titleOfInvention Process for preparing n-/aryl-thio-alkyl/-n'-/amino-alkyl/-carbamide derivatives and pharmaceutical compositions containing thereof
abstract The present invention relates to a process for the preparation of the N- (arylthioalkyl) -N '- (aminoalkyl) urea of the formula (I) and its thiourea derivatives and their sulfinyl and sulfonyl analogues, acid addition salts and laxates thereof. , Ar1-B1-N-C-N-alk2-N (I) R4 is phenyl substituted with Ar 1 or 2-naphthyl, order or 1-3, wherein the substituents are identical or may be different and have 1 to 4 carbon atoms, alkoxy of 1 to 4 carbon atoms or halogen, and Ar may include a group-linked intermediate methylene group, R 1 and R 2 hydrogen, C 1-5 alkyl or phenyl-C 1-4 means alkyl, X represents oxygen or sulfur, II represents thio, sulfinyl or sulfimyl, R3 and R4 have the same or different meanings and C1-4 alkyl or phenyl-C1-4 alkyl group; or R 3 and R 4 are piperidinyl or C 1-4 alkyl-piperazinyl at the adjacent nitrogen atom and alk 1 and C 2 are C 1-7 -alkylene or C 1-4 -alkylene-C 1-4 -alkyl and may have the same or different meanings . The compounds exhibit antiarrhythmic activity. -1-
priorityDate 1981-05-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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