New heterocyclic scaffolds with thiophene and 1,2,4-triazole rings

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dc.citation.conference7th International youth science forum «Litteris et Artibus»
dc.citation.epage57
dc.citation.journalTitleLitteris et Artibus : матеріали
dc.citation.spage56
dc.contributor.affiliationIvan Franko National University of Lviv
dc.contributor.authorTupychak, Mykola
dc.contributor.authorShyyka, Olga
dc.contributor.authorPokhodylo, Nazariy
dc.contributor.authorObushak, Mykola
dc.coverage.placenameЛьвів
dc.coverage.placenameLviv
dc.coverage.temporal23–25 листопада 2017 року
dc.coverage.temporal23–25 November, 2017
dc.date.accessioned2018-04-12T13:06:10Z
dc.date.available2018-04-12T13:06:10Z
dc.date.created2017-12-23
dc.date.issued2017-12-23
dc.description.abstractSome chemical modifications of the Gewald 2- amino-thiophenes and 3-aminothiophenes were established. A number of new substituted thienotriazolopyrimidines, thienotriazoles and thiophenyl-triazolothiadiazine were obtained. This study provides new approaches to the construction of substituted 1H-1,2,4-triazoles bearing thiophene core and allows to use data in medical chemistry for further drug discover.
dc.format.extent56-57
dc.format.pages2
dc.identifier.citationNew heterocyclic scaffolds with thiophene and 1,2,4-triazole rings / Mykola Tupychak, Olga Shyyka, Nazariy Pokhodylo, Mykola Obushak // Litteris et Artibus : proceedings, 23–25 November, 2017. — Lviv : Lviv Polytechnic Publishing House, 2017. — P. 56–57. — (6th International academic conference «Chemistry & chemical technology 2017» (CCT-2017)).
dc.identifier.citationenNew heterocyclic scaffolds with thiophene and 1,2,4-triazole rings / Mykola Tupychak, Olga Shyyka, Nazariy Pokhodylo, Mykola Obushak // Litteris et Artibus : proceedings, 23–25 November, 2017. — Lviv : Lviv Polytechnic Publishing House, 2017. — P. 56–57. — (6th International academic conference «Chemistry & chemical technology 2017» (CCT-2017)).
dc.identifier.isbn978-966-941-108-2
dc.identifier.urihttps://ena.lpnu.ua/handle/ntb/40467
dc.language.isoen
dc.publisherВидавництво Львівської політехніки
dc.publisherLviv Polytechnic Publishing House
dc.relation.ispartofLitteris et Artibus : матеріали, 2017
dc.relation.ispartofLitteris et Artibus : proceedings, 2017
dc.relation.references[1]. R.M. Mohareb, A.E.M. Abdallah, M.H.E. Helal, S.M.H. Shaloof, “Synthesis and structure elucidation of some novel thiophene and benzothiophene derivatives as cytotoxic agents”, Acta Pharm., vol.66, pp. 53–68, 2016.
dc.relation.references[2]. N.B. Saidov, V.A Georgiyants, E.Yu. Lipakova, “Synthesis and pharmacological potential of new 3- mercapto-4-amino(pyrrolyl-1)-5-(thienyl-2)-1,2,4- triazole(4H) derivatives”, Pharm. Chem. J., vol. 51,no. 1, pp. 26−29, 2017.
dc.relation.references[3]. S. Botros, O.M. Khalil, M.M Kamel, Ya.S. El-Dash, “Synthesis, Characterization and Cytotoxicity of Substituted [1]Benzothieno[3,2-e][1,2,4]triazolo[4,3- a]pyrimidines”, Acta Chim. Slov., vol. 64, pp. 102–116, 2017.
dc.relation.references[4]. H.N. Hafez, S.A. Alsalaman, A-R.B.A. El-Gazzar, «Synthesis of thiophene and N-substituted thieno[3,2-d] pyrimidine derivatives as potent antitumor and antibacterial agents” Acta Pharm., vol.67, pp. 275–292, 2017.
dc.relation.references[5]. B. Zhang,, Y.-H. Li, Y. Liu, Y.-R. Chen, E.-S. Pan, W.-W. You, P.-L. Zhao, “Design, synthesis and biological evaluation of novel 1,2,4-triazolo[3,4-b][1,3,4]thiadiazines bearing furan and thiophene nucleus” Eur. J. Med. Chem., vol. 103, pp. 335−350, 2015.
dc.relation.references[6]. N.D. Obushak, N.T. Pokhodylo, I.I. Krupa, V.S. Matiichuk, “Synthesis of Substituted 4-([1,2,4] Triazolo[3,4-b]-[1,3,4]thiadiazol-6-yl)-quinolines”, Russ. Journ. of Org. Chem., vol. 43, no. 8,pp. 1223−1227, 2007.
dc.relation.references[7]. N.T. Pokhodylo, V. S. Matiychuk., M.D. Obushak, “New convenient synthesis of 2,3- diaminothieno[2,3-d]pyrimidin-4(3H)-one derivates from substituted alkyl 2-(1H-tetrazol-1-yl)thiophene-3-carboxylates”, Tetrahedron, vol. 64, no. 7, pp. 1430−1434, 2008.
dc.relation.referencesen[1]. R.M. Mohareb, A.E.M. Abdallah, M.H.E. Helal, S.M.H. Shaloof, "Synthesis and structure elucidation of some novel thiophene and benzothiophene derivatives as cytotoxic agents", Acta Pharm., vol.66, pp. 53–68, 2016.
dc.relation.referencesen[2]. N.B. Saidov, V.A Georgiyants, E.Yu. Lipakova, "Synthesis and pharmacological potential of new 3- mercapto-4-amino(pyrrolyl-1)-5-(thienyl-2)-1,2,4- triazole(4H) derivatives", Pharm. Chem. J., vol. 51,no. 1, pp. 26−29, 2017.
dc.relation.referencesen[3]. S. Botros, O.M. Khalil, M.M Kamel, Ya.S. El-Dash, "Synthesis, Characterization and Cytotoxicity of Substituted [1]Benzothieno[3,2-e][1,2,4]triazolo[4,3- a]pyrimidines", Acta Chim. Slov., vol. 64, pp. 102–116, 2017.
dc.relation.referencesen[4]. H.N. Hafez, S.A. Alsalaman, A-R.B.A. El-Gazzar, "Synthesis of thiophene and N-substituted thieno[3,2-d] pyrimidine derivatives as potent antitumor and antibacterial agents" Acta Pharm., vol.67, pp. 275–292, 2017.
dc.relation.referencesen[5]. B. Zhang,, Y.-H. Li, Y. Liu, Y.-R. Chen, E.-S. Pan, W.-W. You, P.-L. Zhao, "Design, synthesis and biological evaluation of novel 1,2,4-triazolo[3,4-b][1,3,4]thiadiazines bearing furan and thiophene nucleus" Eur. J. Med. Chem., vol. 103, pp. 335−350, 2015.
dc.relation.referencesen[6]. N.D. Obushak, N.T. Pokhodylo, I.I. Krupa, V.S. Matiichuk, "Synthesis of Substituted 4-([1,2,4] Triazolo[3,4-b]-[1,3,4]thiadiazol-6-yl)-quinolines", Russ. Journ. of Org. Chem., vol. 43, no. 8,pp. 1223−1227, 2007.
dc.relation.referencesen[7]. N.T. Pokhodylo, V. S. Matiychuk., M.D. Obushak, "New convenient synthesis of 2,3- diaminothieno[2,3-d]pyrimidin-4(3H)-one derivates from substituted alkyl 2-(1H-tetrazol-1-yl)thiophene-3-carboxylates", Tetrahedron, vol. 64, no. 7, pp. 1430−1434, 2008.
dc.rights.holder© Національний університет “Львівська політехніка”, 2017
dc.subject2-aminothiophene
dc.subject3-aminothiophene
dc.subject1 2 4- triazoles
dc.subjectaminohydrazones
dc.subjectthienotriazolopyrimidines
dc.subjecttriazolothiadiazines
dc.titleNew heterocyclic scaffolds with thiophene and 1,2,4-triazole rings
dc.typeConference Abstract

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