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Synthesis and antioxidant activity of new analogs of Quin-C1

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Chemistry of Heterocyclic Compounds Aims and scope

New derivatives of 4-oxo-1,2,3,4-tetrahydroquinazoline, analogs of Quin-C1, have been synthesized by the condensation of aroyl- and heteroaroylhydrazides of anthranilic acid with cinnamic, crotonic, and 4-hydroxy-3-methoxybenzoic aldehydes. The antioxidant activity of the obtained compounds has been determined.

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Authors and Affiliations

  1. Riga Technical University, 1 Kaļķu St., Riga, 1658, Latvia

    I. Mieriņa, Z. Tetere, D. Zicāne, I. Rāviņa, M. Turks & M. Jure

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  1. I. Mieriņa
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  2. Z. Tetere
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  3. D. Zicāne
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  4. I. Rāviņa
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  5. M. Turks
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  6. M. Jure
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Correspondence to M. Jure.

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1948-1955, December, 2012.

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Mieriņa, I., Tetere, Z., Zicāne, D. et al. Synthesis and antioxidant activity of new analogs of Quin-C1. Chem Heterocycl Comp 48, 1824–1831 (2013). https://doi.org/10.1007/s10593-013-1215-3

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  • DOI: https://doi.org/10.1007/s10593-013-1215-3

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