Запис Детальніше

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

Електронний науковий архів Науково-технічної бібліотеки Національного університету "Львівська політехніка"

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Поле Співвідношення
 
Title New heterocyclic scaffolds with thiophene and 1,2,4-triazole rings
 
Creator Tupychak, Mykola
Shyyka, Olga
Pokhodylo, Nazariy
Obushak, Mykola
 
Contributor Ivan Franko National University of Lviv
 
Subject 2-aminothiophene
3-aminothiophene
1 2 4- triazoles
aminohydrazones
thienotriazolopyrimidines
triazolothiadiazines
 
Description Some 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.
 
Date 2018-04-12T13:06:10Z
2018-04-12T13:06:10Z
2017-12-23
2017-12-23
 
Type Conference Abstract
 
Identifier New 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)).
978-966-941-108-2
http://ena.lp.edu.ua:8080/handle/ntb/40467
New 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)).
 
Language en
 
Relation Litteris et Artibus : матеріали, 2017
Litteris et Artibus : proceedings, 2017
[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.
[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.
[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.
[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.
[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.
[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.
[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.
[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.
[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.
[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.
[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.
[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.
[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.
[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.
 
Rights © Національний університет “Львівська політехніка”, 2017
 
Format 56-57
2
application/pdf
image/png
 
Coverage 23–25 листопада 2017 року
23–25 November, 2017
Львів
Lviv
 
Publisher Видавництво Львівської політехніки
Lviv Polytechnic Publishing House