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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 |