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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1010e3862914acdd087e73d76911ec6d
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-52
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
filingDate 2000-07-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9bf21360ad52dbf223324605a632af41
publicationDate 2002-02-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2002037788-A
titleOfInvention N-fused pentaphylline and efficient method for its synthesis
abstract PROBLEM TO BE SOLVED: To provide a novel N-fused pentaphyrin and an efficient method for synthesizing the same. SOLUTION: The oxidized and reduced N- of the general formula (A) is provided. Condensed ring pentaphyrin embedded image General formula (A) (Where Ar is fluoro, chloro, bromo, iodo, A phenyl group which is independently selected from lower alkyl having 1 to 4 carbon atoms or lower alkoxy and has at least hydrogens at the 2- and 6-positions substituted by substituents, and each Ar may be different. ). A method for isolating Compound A by column chromatography using a mixed solvent of dichloromethane and n-hexane in a mixing ratio of 0: 1 to 1: 4 as an eluent.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2006182734-A
priorityDate 2000-07-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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