<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lim FPL</submitter><funding>Ministry of Higher Education, Malaysia</funding><pagination>21495-21504</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9080918</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(38)</volume><pubmed_abstract>A highly selective, one-pot, three-component synthesis of novel 2-alkyl-substituted 4-aminoimidazo[1,2-&lt;i>a&lt;/i>][1,3,5]triazines has been developed. The scope of the method was explored in two dimensions, varying the structures of trialkyl orthoesters and 2-aminoimidazoles in their reactions with cyanamide. Conveniently performed under microwave irradiation, this method was also proved to be efficient under conventional heating. A library of 24 novel compounds was prepared in high purity using this multicomponent approach. Molecular and crystal structures of representative molecules were studied using X-ray crystallography.</pubmed_abstract><journal>RSC advances</journal><pubmed_title>A one-pot, multicomponent reaction for the synthesis of novel 2-alkyl substituted 4-aminoimidazo[1,2-&lt;i>a&lt;/i>][1,3,5]triazines.</pubmed_title><pmcid>PMC9080918</pmcid><funding_grant_id>FRGS/1/2015/SG01/MUSM/03/1</funding_grant_id><pubmed_authors>Lim FPL</pubmed_authors><pubmed_authors>Dolzhenko AV</pubmed_authors><pubmed_authors>Tan LY</pubmed_authors><pubmed_authors>Tiekink ERT</pubmed_authors></additional><is_claimable>false</is_claimable><name>A one-pot, multicomponent reaction for the synthesis of novel 2-alkyl substituted 4-aminoimidazo[1,2-&lt;i>a&lt;/i>][1,3,5]triazines.</name><description>A highly selective, one-pot, three-component synthesis of novel 2-alkyl-substituted 4-aminoimidazo[1,2-&lt;i>a&lt;/i>][1,3,5]triazines has been developed. The scope of the method was explored in two dimensions, varying the structures of trialkyl orthoesters and 2-aminoimidazoles in their reactions with cyanamide. Conveniently performed under microwave irradiation, this method was also proved to be efficient under conventional heating. A library of 24 novel compounds was prepared in high purity using this multicomponent approach. Molecular and crystal structures of representative molecules were studied using X-ray crystallography.</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Jun</publication><modification>2025-05-18T13:22:56.067Z</modification><creation>2025-02-19T04:21:54.089Z</creation></dates><accession>S-EPMC9080918</accession><cross_references><pubmed>35539915</pubmed><doi>10.1039/c8ra03703e</doi></cross_references></HashMap>