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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-47
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D498-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P3-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P3-08
filingDate 1992-10-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7e71d281d39cc5283bf73ce6e2bce717
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cb4b0df97fbad96454c06004cfbd0a15
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_95602db5e9f3af9838ab40ff9643ec9b
publicationDate 1994-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H06128266-A
titleOfInvention Process for producing oxazopyrroloquinoline compound
abstract (57) [Summary] (Modified) [Structure] Oxazopyrroloquinoline represented by the following formula III is produced by reacting pyrroloquinoline quinone represented by the following formula I with aldehyde represented by the following formula II. R-CHO II [In the formula, R represents an alkyl group, a phenyl group, a substituted phenyl group, a benzyl group, and a substituted benzyl group.] [Effect] Oxazopyrroloquinoline can be produced at a lower cost than the conventional reactions using various amino acids. it can.
priorityDate 1992-10-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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