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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-073
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-067
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B43-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B43-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-167
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D473-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-54
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-173
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-04
filingDate 1993-05-21^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b1c8094804392162a9120ba133c7fc52
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e22cf90c1bdd0791fdaf367fe10beb7d
publicationDate 1994-11-29^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H06329560-A
titleOfInvention Method for introducing imide group into heterocyclic compound
abstract (57) [Summary] [Structure] A compound having a heterocycle to which a tetrazolyl group or a nitrotriazolyl group is bound is reacted with a succinimide derivative or a phthalimide derivative in the presence of a base to give a succinimide group to the above heterocyclic compound. Alternatively, a phthalimidoimide group is introduced. [Effect] Since the exocyclic amino group can be introduced at a high yield, it is preferably used as a method for introducing 15 N into a nucleoside exocyclic amino group. According to this 15 N introduction method, since the label compound used ([ 15 N] succinimide, [ 15 N] phthalimide, etc.) is solid at room temperature, the label compound is excellent in storability and reaction operability, The number of equivalents of the labeling compound used can be minimized.
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6822090-B2
priorityDate 1993-05-21^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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