Title Triciklių heterosistemų, turinčių pirazolo[3,4-d]pirimidino fragmentą, sintezė. Intramolekulinės pirimidino azoto atomo reakcijos su O,O-acetaliais tyrimas /
Translation of Title Synthesis of tricyclic heterosystems based in pyrazolo[3,4-d]pyrimidine framework. Study of intramolecular reaction of pyrimidine nitrogen with O,O-acetals.
Authors Juškėnas, Robertas
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Pages 119
Keywords [eng] heterocycles ; cyclization ; acetals ; imidazo[1 ; 2-c]pyrimidines
Abstract [eng] The development of heterocyclic chemistry is important for various science areas and for the industry. The main task of this branch of chemistry is the search for the new, more effective synthetic methods for obtaining heterocyclic derivatives. That covers not only the formation of heterocycles, but also their functionalization, which leads to the creation of compounds having various chemical and physical properties. The accomplishments of this area are applied in biochemistry, pharmacochemistry, photophysics and other branches of science and industry. The creation of effective heterocycles synthesis methods, that may be applied for the formation of heterosystems based on pyrazolo[3,4-d]pyrimidine was the main aim in this work. During this work, three hitherto unknown peri-fused heterocyclic systems based on pyrazolo[3,4-d]pyrimidine scaffold were synthesized. The suitable conditions for the cyclization of 4-(2,2-diethoxyethyl)aminopyrimidines to 2,3-dihydroimidazo[1,2-c]pyrimidines were found. The influence of functional groups in pyrimidine moiety for the course of this reaction was investigated. It has been shown that functional groups including alkylthio, cyano, amino, formyl are tolerated in this type of reaction. The method for the replacement of ethoxy group with benzyl mercaptan in 3-ethoxy-2,3-dihydroimidazo[1,2-c]pyrazolo[4,3-e]pyrimidines has been found.
Type Doctoral thesis
Language Lithuanian
Publication date 2014