http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20050083883-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_9f0efdc4af4970c7f1a1a1d1282a4df6
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K8-4966
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D253-075
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C281-18
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C281-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D253-075
filingDate 2003-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_210d6fc293897c266e933408e4a7acdb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f953268eaf0f59397bfc115fdc497373
publicationDate 2005-08-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20050083883-A
titleOfInvention Process for preparing a pharmaceutically active compound and for preparing its intermediate
abstract The present invention provides intermediate 2 (2,3-dichlorophenyl) -2 of the formula (II) comprising reacting 2,3-dichlorobenzoyl cyanide with an aminoguanidine bicarbonate in the presence of methanesulfonic acid in a non-aqueous medium. A method for preparing-(aminoguanidine) acetonitrile, wherein the reaction provides excellent yield and short reaction time. Such intermediates are useful for the preparation of 3,5-diamino-6- (2,3-dichlorophenyl) -1,2,4-triazine of formula (I). The invention also relates to a process for the preparation of compounds of formula (I) in high purity.n n n Formula In n n n n n n n Formula II
priorityDate 2002-10-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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