http://rdf.ncbi.nlm.nih.gov/pubchem/patent/BR-0213557-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e911305f2cb02b43368a069a93d30519
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P17-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H19-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H19-173
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H19-167
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-173
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-167
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-16
filingDate 2002-10-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9dd161bfd80c427def5dd95c29661b69
publicationDate 2004-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber BR-0213557-A
titleOfInvention Method for the synthesis of a 2-aralkyloxyadenosine or a 2-alkoxydenosine and process for the preparation of a compound
abstract "METHOD FOR THE SYNTHESIS OF A 2-ARALKYLOXYADENOSIN OR A 2-ALCOXYADENOSINE AND PROCESS FOR PREPARING A COMPOUND". The invention provides novel methods for the synthesis of 2-aralkyloxyadenosines and 2-alkoxydenosines. The invention is particularly useful for the synthesis of 2- [2- (4-chlorophenyl) ethoxy] adenosine. Preferred methods of the invention include activating a guanosine compound followed by hydrolysis; alkylating the hydrolyzed compound with subsequent amination to provide a 2-aralkyloxyadenosine compound or a 2-alkoxyadenosine compound.
priorityDate 2001-10-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426152050
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426132189
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9910098
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID135768161

Total number of triples: 20.