<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>71</viewCount><searchCount>0</searchCount></scores><additional><omics_type>Unknown</omics_type><volume>45(1)</volume><submitter>GUngOr T</submitter><pubmed_abstract>A series of novel imidazo[1,2- &lt;i>a&lt;/i> ]pyrimidine containing tri/tetrasubstituted imidazole derivatives (1-10) has been synthesized via sequential two-step, one-pot, multicomponent reaction using imidazo[1,2- &lt;i>a&lt;/i> ]pyrimidine-2-carbaldehyde, benzil, primary amines, and ammonium acetate catalyzed by &lt;i>p&lt;/i> -toluenesulfonic acid under microwave-assisted conditions. The results showed that target compounds can be obtained from a wide range of primary amines bearing different functional groups with moderate to good yields (46%-80%) under optimum reaction conditions. This method provides a green protocol for imidazo[1,2- &lt;i>a&lt;/i> ]pyrimidine containing tri/tetrasubstituted imidazole derivatives due to ethyl alcohol as a green solvent, microwave irradiation as a greener heating method and one-pot multicomponent reaction as a green technique. The synthesized compounds have been elucidated using various spectroscopic tools such as FT-IR, &lt;sup>1&lt;/sup>H NMR, &lt;sup>13&lt;/sup> C NMR, and MS.</pubmed_abstract><journal>Turkish journal of chemistry</journal><pagination>219-230</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7925308</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Microwave assisted, sequential two-step, one-pot synthesis of novel imidazo[1,2-a]pyrimidine containing tri/tetrasubstituted imidazole derivatives.</pubmed_title><pmcid>PMC7925308</pmcid><pubmed_authors>GUngOr T</pubmed_authors><view_count>71</view_count></additional><is_claimable>false</is_claimable><name>Microwave assisted, sequential two-step, one-pot synthesis of novel imidazo[1,2-a]pyrimidine containing tri/tetrasubstituted imidazole derivatives.</name><description>A series of novel imidazo[1,2- &lt;i>a&lt;/i> ]pyrimidine containing tri/tetrasubstituted imidazole derivatives (1-10) has been synthesized via sequential two-step, one-pot, multicomponent reaction using imidazo[1,2- &lt;i>a&lt;/i> ]pyrimidine-2-carbaldehyde, benzil, primary amines, and ammonium acetate catalyzed by &lt;i>p&lt;/i> -toluenesulfonic acid under microwave-assisted conditions. The results showed that target compounds can be obtained from a wide range of primary amines bearing different functional groups with moderate to good yields (46%-80%) under optimum reaction conditions. This method provides a green protocol for imidazo[1,2- &lt;i>a&lt;/i> ]pyrimidine containing tri/tetrasubstituted imidazole derivatives due to ethyl alcohol as a green solvent, microwave irradiation as a greener heating method and one-pot multicomponent reaction as a green technique. The synthesized compounds have been elucidated using various spectroscopic tools such as FT-IR, &lt;sup>1&lt;/sup>H NMR, &lt;sup>13&lt;/sup> C NMR, and MS.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2024-11-13T04:32:17.838Z</modification><creation>2021-03-12T08:19:48Z</creation></dates><accession>S-EPMC7925308</accession><cross_references><pubmed>33679165</pubmed><doi>10.3906/kim-2009-40</doi></cross_references></HashMap>