http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DD-289529-A5

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_571b8abacacea64d3f7089d0983b8b3b
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-50
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-5025
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
filingDate 1988-08-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3963ed93687ca77c9b7eeb6ba3943ad7
publicationDate 1991-05-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DD-289529-A5
titleOfInvention METHOD FOR PRODUCING HETEROCYCLIC COMPOUNDS
abstract The invention relates to a process for the preparation of heterocyclic compounds. These have the general formula wherein R1 represents an optionally substituted carbocyclic or heterocyclic aryl group or an optionally substituted alkyl, alkenyl, cycloalkyl or cycloalkenyl group; R 2 represents an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl or cycloalkenyl group or an optionally substituted carbocyclic or heterocyclic aryl or aralkyl group; R3 represents a hydrogen atom or an alkyl group; and either X represents an oxygen or sulfur atom, a group CH 2 or a group NR 4, wherein R 4 represents a hydrogen atom or a C 1-4 alkyl group, and Y represents a group CH 2 or CH 2 CH 2, or X-Y together represent the group CHCH. The compounds, their salts and physiologically functional derivatives are useful in the treatment of tumors. Formula (I) {method; manufacture; Links; heterocyclic; salts; tumors}
priorityDate 1987-08-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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