Synthesis and Heterocyclizations of 3,4-Dihydroquinazolin-2-yl Guanidine in the Search of New Anticancer Agents

The cyclocondensations of 3,4-dihydroquinazolin-2-yl guanidine with a variety of electrophilic reagents viz. aldehydes, ketones, triethyl orthoformate, diethyl ethoxymethylenemalonate, carbon disulfide and trichloroacetonitrile were found to afford 1,3,5-triazino[2,1-b]quinazolines. However, some un...

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Main Authors: Dolzhenko, Anton, Foo, M., Tan, B., Dolzhenko, A., Chiu, G., Chui, W.
Format: Journal Article
Published: The Japan Institute of Heterocyclic Chemistry 2009
Online Access:http://hdl.handle.net/20.500.11937/13442
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author Dolzhenko, Anton
Foo, M.
Tan, B.
Dolzhenko, A.
Chiu, G.
Chui, W.
author_facet Dolzhenko, Anton
Foo, M.
Tan, B.
Dolzhenko, A.
Chiu, G.
Chui, W.
author_sort Dolzhenko, Anton
building Curtin Institutional Repository
collection Online Access
description The cyclocondensations of 3,4-dihydroquinazolin-2-yl guanidine with a variety of electrophilic reagents viz. aldehydes, ketones, triethyl orthoformate, diethyl ethoxymethylenemalonate, carbon disulfide and trichloroacetonitrile were found to afford 1,3,5-triazino[2,1-b]quinazolines. However, some unexpected reactions were also observed. The structural properties such as tautomerism and hinderance to conformational rotation were also investigated. The results of biological testing suggested that the 1,3,5-triazino[2,1-b]quinazoline nucleus could be a new promising scaffold for the development of potential anticancer agents.
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institution Curtin University Malaysia
institution_category Local University
last_indexed 2025-11-14T07:03:37Z
publishDate 2009
publisher The Japan Institute of Heterocyclic Chemistry
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spelling curtin-20.500.11937-134422017-01-30T11:37:10Z Synthesis and Heterocyclizations of 3,4-Dihydroquinazolin-2-yl Guanidine in the Search of New Anticancer Agents Dolzhenko, Anton Foo, M. Tan, B. Dolzhenko, A. Chiu, G. Chui, W. The cyclocondensations of 3,4-dihydroquinazolin-2-yl guanidine with a variety of electrophilic reagents viz. aldehydes, ketones, triethyl orthoformate, diethyl ethoxymethylenemalonate, carbon disulfide and trichloroacetonitrile were found to afford 1,3,5-triazino[2,1-b]quinazolines. However, some unexpected reactions were also observed. The structural properties such as tautomerism and hinderance to conformational rotation were also investigated. The results of biological testing suggested that the 1,3,5-triazino[2,1-b]quinazoline nucleus could be a new promising scaffold for the development of potential anticancer agents. 2009 Journal Article http://hdl.handle.net/20.500.11937/13442 The Japan Institute of Heterocyclic Chemistry fulltext
spellingShingle Dolzhenko, Anton
Foo, M.
Tan, B.
Dolzhenko, A.
Chiu, G.
Chui, W.
Synthesis and Heterocyclizations of 3,4-Dihydroquinazolin-2-yl Guanidine in the Search of New Anticancer Agents
title Synthesis and Heterocyclizations of 3,4-Dihydroquinazolin-2-yl Guanidine in the Search of New Anticancer Agents
title_full Synthesis and Heterocyclizations of 3,4-Dihydroquinazolin-2-yl Guanidine in the Search of New Anticancer Agents
title_fullStr Synthesis and Heterocyclizations of 3,4-Dihydroquinazolin-2-yl Guanidine in the Search of New Anticancer Agents
title_full_unstemmed Synthesis and Heterocyclizations of 3,4-Dihydroquinazolin-2-yl Guanidine in the Search of New Anticancer Agents
title_short Synthesis and Heterocyclizations of 3,4-Dihydroquinazolin-2-yl Guanidine in the Search of New Anticancer Agents
title_sort synthesis and heterocyclizations of 3,4-dihydroquinazolin-2-yl guanidine in the search of new anticancer agents
url http://hdl.handle.net/20.500.11937/13442