Regioselective Synthesis of Imidazo[4,5-e][1,3]Thiazino[3,2-b][1,2,4]Triazines as New Heterocyclic System Derivatives

IF 2 3区 化学 Q2 CHEMISTRY, ORGANIC
Alexei N. Izmest'ev, Vladimir V. Baranov, Natalya G. Kolotyrkina, Angelina N. Kravchenko, Galina A. Gazieva
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引用次数: 0

Abstract

A series of new 4a,7a-diarylperhydroimidazo[4,5-e][1,2,4]triazine-3-thiones were synthesized from 4,5-diaryl-4,5-dihydroxyimidazolidin-2-ones and thiosemicarbazide in high yields, and their interaction with ethyl phenylpropiolate was studied. An effective method for the regioselective synthesis of imidazo[4,5-e][1,3]thiazino[3,2-b][1,2,4]triazines as new heterocycic system derivatives was proposed based on the reaction of aforementioned imidazotriazinethiones with ethyl phenylpropiolate in the presence of MeONa in methanol. The reaction is initiated by a Michael-type addition of the imidazotriazinethiones to the triple bond of ethyl phenylpropiolate followed by intramolecular cyclization.

咪唑[4,5-e][1,3]噻唑[3,2-b][1,2,4]三嗪类杂环衍生物的区域选择性合成
以4,5-二芳基-4,5-二羟基咪唑烷-2-酮和硫代氨基脲为原料,高产地合成了一系列新的4a,7 -二芳基过氢咪唑[4,5-e][1,2,4]三嗪-3-硫酮,并研究了它们与苯基丙酸乙酯的相互作用。基于上述咪唑三嗪硫酮与苯基丙酸乙酯在甲醇中MeONa存在下的反应,提出了咪唑[4,5-e][1,3]噻嗪基[3,2-b][1,2,4]三嗪类杂环化合物的区域选择性合成方法。该反应是由咪唑三嗪硫酮在苯丙酸乙酯的三键上的迈克尔型加成引起的,然后是分子内环化。
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来源期刊
Journal of Heterocyclic Chemistry
Journal of Heterocyclic Chemistry 化学-有机化学
CiteScore
5.20
自引率
4.20%
发文量
177
审稿时长
3.9 months
期刊介绍: The Journal of Heterocyclic Chemistry is interested in publishing research on all aspects of heterocyclic chemistry, especially development and application of efficient synthetic methodologies and strategies for the synthesis of various heterocyclic compounds. In addition, Journal of Heterocyclic Chemistry promotes research in other areas that contribute to heterocyclic synthesis/application, such as synthesis design, reaction techniques, flow chemistry and continuous processing, multiphase catalysis, green chemistry, catalyst immobilization and recycling.
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