Reaction of 3-amino-1H,3H-quinoline-2,4-diones with nitrourea. Synthetic route to novel 3-ureidoquinoline-2,4-diones and imidazo[4,5-c]quinoline-2,4-diones.

Klásek, Antonín; Hoza, Ignác; Lyčka, Antonín; Holčapek, Michal

Title:

Author:

Klásek, Antonín; Hoza, Ignác; Lyčka, Antonín; Holčapek, Michal

Document type:

Peer-reviewed article (English)

Source document:

Tetrahedron. 2004, vol. 60, issue 44, p. 9953-9961

ISSN:

0040-4020 (Sherpa/RoMEO, JCR)

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DOI:

https://doi.org/10.1016/j.tet.2004.07.106

Abstract:

1-Unsubstituted 3-amino-1H,3H-quinoline-2,4-diones react with nitrourea in dioxane affords novel 3-ureidoquinoline-2,4-diones or imidazo[4,5-c]quinoline-2,4-diones. All products were converted to 2,6-dihydro-imidazo[1,5-c]quinazoline-3,5-diones by refluxing in acetic acid.

Full text:

https://www.sciencedirect.com/science/article/pii/S0040402004013432

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Citace článku v časopise:
KLÁSEK, Antonín, Ignác HOZA, Antonín LYČKA a Michal HOLČAPEK. Reaction of 3-amino-1H,3H-quinoline-2,4-diones with nitrourea. Synthetic route to novel 3-ureidoquinoline-2,4-diones and imidazo[4,5-c]quinoline-2,4-diones. Tetrahedron [online]. 2004, vol. 60, iss. 44, s. 9953-9961. [cit. 2024-04-26]. ISSN 0040-4020. Dostupné z: https://www.sciencedirect.com/science/article/pii/S0040402004013432.

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