Synthesis and reactivity of [1,2,4]triazolo-annelated quinazolines

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Abstract

This paper reports the synthesis of phenyl-substituted 2- alkoxy(methylsulfanyl)- 1,2,4-triazolo[1,5-a]quinazolines starting from N-cyanoimidocarbonates and substituted hydrazinobenzoic acids as building blocks. Thionation or chlorination of the inherent lactam moiety in the target compounds followed by treatment with multifunctional nucleophiles provided access to a variety of derivatives. © 2010 by the authors.

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Al-Salahi, R. A. (2010). Synthesis and reactivity of [1,2,4]triazolo-annelated quinazolines. Molecules, 15(10), 7016–7034. https://doi.org/10.3390/molecules15107016

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