http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0114864-B1
Outgoing Links
Predicate | Object |
---|---|
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D295-15 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D295-15 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-34 |
filingDate | 1983-06-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 1988-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 1988-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | EP-0114864-B1 |
titleOfInvention | 2-pyrimidyl alkanesulfonates and methods for their preparation and use |
abstract | Novel 2-pyrimidyl alkanesulfonates are prepared by reacting a 2-hydroxypyrimidine acid salt with an alkanesulfonyl chloride in the presence of an acid acceptor. The novel 2-pyrimidyl alkanesulfonates are advantageously employed to prepare 1-(cyanoalkyl)-4-(2-pyrimidyl)piperazines by reacting them with a novel 1-(cyanoalkyl)piperazine in the presence of an acid acceptor which in turn are useful to prepare 8- ADomega- AD4-(2-pyrimidyl)-1-piperazinyl BDalkyl BD-8-azaspiro AD4.5 BDdecane-7,9-diones, such as buspirone. |
priorityDate | 1982-08-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 88.