Synthesis of novel 4(3H)-quinazolinones with 1,2,3-triazoles moiety conjugated by Schiff base

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Abstract

We describe the synthesis of a novel quinazolin-4(3H)-ones i.e., (E)-3-[4-{4-(hydroxymethyl)-1H-1,2,3-triazol-1-yl}benzylideneamino]-7-fluoro-2-methylquinazolin-4(3H)-one (7). Treatment of 4-(4-(hydroxymethyl)-1H-1,2,3-triazol-1-yl)benzaldehyde, which is synthesized via a click reaction of 4-azidobenzaldehyde and alkyne, with 3-amino-7-fluoro-2-methylquinazolin-4(3H)-one afforded the corresponding product in toluene catalyzed by TiCl4. in vitro Cytotoxic activity of compound 7 against human hepatoma hepg2 cells is evaluated.

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Su, C., & Liu, X. (2014). Synthesis of novel 4(3H)-quinazolinones with 1,2,3-triazoles moiety conjugated by Schiff base. Asian Journal of Chemistry, 26(16), 5301–5304. https://doi.org/10.14233/ajchem.2014.17499

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