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Synthesis of Functionalized (2-Thienylcarbonyl)thiazoles and 4-(2-Thienyl)pyridines by Reaction of (2-Thienylcarbonyl)thioacetanilides and their Enamine Derivatives
Authors:Krystyna?Bogdanowicz-Szwed  mailto:bogdanow@chemia.uj.edu.pl"   title="  bogdanow@chemia.uj.edu.pl"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author,Jacek?Grochowski,Ma?gorzata?Krasodomska,Pawe??Serda
Affiliation:(1) Department of Organic Chemistry, Jagiellonian University, Pl-30060 Kraków, Poland;(2) Regional Laboratory, Jagiellonian University, Pl-30060 Kraków, Poland
Abstract:
Summary. The condensation of two molecules of 2-(2-thienylcarbonyl)thioacetanilides catalyzed by piperidine yielded thiazole derivatives as confirmed by X-ray crystal structure analysis. The reaction of malononitrile with 3-morpholino-3-(2-thienyl)acrylic acid thioanilides furnished 6-amino-1-aryl-4-(2-thienyl)-1,2-dihydro-2-thioxopyridine-5-carbonitriles. A similar reaction of malononitrile with 3-morpholino-3-(2-thienyl)acrylic acid anilides provided 2-oxopyridine-5-carbonitriles.
Keywords:. Michael addition   4-(2-Thienyl)pyridine   (2-Thienylcarbonyl)thioacetanilides   Thiazole   Crystal structure.
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