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Unprecedented reactivity of 3-amino-1H,3H-quinoline-2,4-diones with urea: An efficient synthesis of 2,6-dihydro-imidazo[1,5-c]quinazoline-3,5-diones

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dc.title Unprecedented reactivity of 3-amino-1H,3H-quinoline-2,4-diones with urea: An efficient synthesis of 2,6-dihydro-imidazo[1,5-c]quinazoline-3,5-diones en
dc.contributor.author Klásek, Antonín
dc.contributor.author Kořistek, Kamil
dc.contributor.author Lyčka, Antonín
dc.contributor.author Holčapek, Michal
dc.relation.ispartof Tetrahedron
dc.identifier.issn 0040-4020 Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued 2003
utb.relation.volume 59
utb.relation.issue 8
dc.citation.spage 1283
dc.citation.epage 1288
dc.type article
dc.language.iso en
dc.publisher Elsevier, Pergamon Press en
dc.identifier.doi 10.1016/S0040-4020(03)00028-0
dc.relation.uri https://www.sciencedirect.com/science/article/pii/S0040402003000280
dc.subject molekulární přesmyk cs
dc.subject deriváty močoviny cs
dc.subject alfa-aminoketony cs
dc.subject reakční mechanismus cs
dc.subject NMR cs
dc.subject MS cs
dc.subject molecular rearrangement en
dc.subject urea derivatives en
dc.subject alfa-aminoketones en
dc.subject reaction mechanism en
dc.subject NMR en
dc.subject MS en
dc.description.abstract Substituted 3-amino-1H,3H-quinoline-2,4-diones react with urea in acetic acid to give novel 2,6-dihydro-imidazol[1,5-c]-quinazoline-3,5-diones in high yields. The same compounds were obtained, albeit with small yields, from 3-chloro-1H,3H-quinoline-2,4-diones and urea. In the proposed reaction mechanism, a molecular rearrangement of the primarily formed mono-substituted urea takes splace. The prepared 2,6-dihydro-imidazo[1,5-c]quinazoline-3,5-diones were characterized by their 1H, 13C, 15N NMR and IR spectra and atmospheric pressure chemical ionisation mass spectra. en
utb.faculty Faculty of Technology
dc.identifier.uri http://hdl.handle.net/10563/1000239
utb.identifier.rivid RIV/70883521:28110/03:63501409
utb.identifier.obdid 11552839
utb.identifier.scopus 2-s2.0-0037450420
utb.identifier.wok 000181019900017
utb.source j-riv
utb.contributor.internalauthor Klásek, Antonín
utb.contributor.internalauthor Kořistek, Kamil
utb.fulltext.affiliation Antonín Klásek *a, Kamil Kořistek a, Antonín Lyčka b and Michal Holčapek c a Department of Chemistry and Environmental Technology, Faculty of Technology, Tomas Bata University, 762 72 Zlín, Czech Republic b Research Institute for Organic Syntheses, 532 18 Pardubice, Czech Republic c Department of Analytical Chemistry, Faculty of Chemical Technology, University of Pardubice, 53210 Pardubice, Czech Republic
utb.fulltext.dates Received 22 October 2002; revised 4 December 2002; accepted 19 December 2002
utb.fulltext.sponsorship This study was supported by the Ministry of Education Youth and Sports of the Czech Republic (Grant No. MSM 265200015). One of us (M. H.) acknowledges the support of grant project No. 203/02/0023 sponsored by the Grant Agency of the Czech Republic. The authors thank Mrs H. Gerzova (Faculty of Technology, Tomas Bata University in Zlín) for technical help.
utb.fulltext.projects MSM 265200015
utb.fulltext.projects GACR 203/02/0023
utb.fulltext.faculty Faculty of Technology
utb.fulltext.ou Department of Chemistry and Environmental Technology
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