Kontaktujte nás | Jazyk: čeština English
Název: | 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 | ||||||||||
Autor: | Klásek, Antonín; Kořistek, Kamil; Lyčka, Antonín; Holčapek, Michal | ||||||||||
Typ dokumentu: | Recenzovaný odborný článek (English) | ||||||||||
Zdrojový dok.: | Tetrahedron. 2003, vol. 59, issue 8, p. 1283-1288 | ||||||||||
ISSN: | 0040-4020 (Sherpa/RoMEO, JCR) | ||||||||||
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DOI: | https://doi.org/10.1016/S0040-4020(03)00028-0 | ||||||||||
Abstrakt: | 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. | ||||||||||
Plný text: | https://www.sciencedirect.com/science/article/pii/S0040402003000280 | ||||||||||
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