http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20130074801-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a6209e5a437bf57ab1a4d6d690e27f42
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-06
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-96
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-505
filingDate 2011-12-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_99594dd38da149188248914a8a336200
publicationDate 2013-07-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20130074801-A
titleOfInvention One-Pod Synthesis of Quinazolin-2,4-Dione Derivatives
abstract The present invention comprises a first reaction step of reacting isatoic anhydride and a primary amine (NH 2 R); And a second reaction step of reacting the reaction product, triphosgene, and a base by mixing the reaction product of the first reaction step; and a method for synthesizing a one-pot of quinazoline-2,4-dione derivative comprising a . According to the synthesis method of the present invention, various quinazoline-2,4-dione derivatives can be synthesized in one-pot, and the separation and purification of intermediate materials are omitted, and thus the synthesis reaction proceeds easily. In addition, the overall reaction can be made at room temperature has the advantage that can be synthesized under mild conditions.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2015169999-A1
priorityDate 2011-12-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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