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Synthesis 2015; 47(21): 3385-3391
DOI: 10.1055/s-0034-1380455
DOI: 10.1055/s-0034-1380455
paper
Synthesis of Dibenzo[f,h][1,2,4]triazolo[3,4-b]quinazolines via a Two-Step Route with Water as the Only By-Product
Further Information
Publication History
Received: 31 March 2015
Accepted after revision: 07 May 2015
Publication Date:
23 July 2015 (online)
Abstract
Microwave-promoted cyclocondensation of isoflavones with 3-amino[1,2,4]triazole gave 6-phenyl-7-(2-hydroxyphenyl)-1,2,4triazolo[4,3-a]pyrimidines as intermediates. Subsequent photocyclization of these intermediates delivered dibenzo[f,h][1,2,4]triazolo[3,4-b]quinazolines as final products. Water was the only by-product in this two-step procedure. The products showed distinct fluorescence properties both in solution and in the solid state .
Supporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0034–1380455. Spectra for compounds 4a and 5a–n are included.
- Supporting Information
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