1H-1,2,4-Triazolo-5-diazonium salts in the synthesis of new 6H-benzopyrano[4,3-e][1,2,4]triazolo[5,1-c]-[1,2,4]triazine-6-ones and [1,2,4]triazolo[5',1':3,4][1,2,4]-triazino[6,5-c]quinoline-6(7H)-ones
- 作者: Mawlood M.N.1, Potapov A.Y.1, Shikhaliev K.S.1
- 
							隶属关系: 
							- Voronezh State University
 
- 期: 卷 61, 编号 3 (2025)
- 页面: 240-245
- 栏目: ЭКСПЕРИМЕНТАЛЬНЫЕ СТАТЬИ
- URL: https://rjpbr.com/0514-7492/article/view/687774
- DOI: https://doi.org/10.31857/S0514749225030037
- EDN: https://elibrary.ru/ETSFZE
- ID: 687774
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A convenient synthetic approach to the synthesis of new 2-R-6Н-benzopyrano[4,3-е][1,2,4]triazolo[5,1-с][1,2,4]triazin-6-ones and 2-R-[1,2,4]triazolo[5',1':3,4][1,2,4]triazino[6,5-c]quinolin-6(7H)-ones based on 3-R-1H-1,2,4-triazolo-5-diazonium salts with 2H-1-benzopyran-2,4(3H)dione and 2,4(1H,3H)-quinolinedione.
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	                        作者简介
M. Mawlood
Voronezh State University
														Email: pistones@mail.ru
				                	ORCID iD: 0009-0007-7293-1823
				                																			                												                	俄罗斯联邦, 							pl. Universitetskaya, 1, Voronezh						
A. Potapov
Voronezh State University
							编辑信件的主要联系方式.
							Email: pistones@mail.ru
				                	ORCID iD: 0000-0001-8084-530X
				                																			                												                	俄罗斯联邦, 							pl. Universitetskaya, 1, Voronezh						
Kh. Shikhaliev
Voronezh State University
														Email: pistones@mail.ru
				                	ORCID iD: 0000-0002-6576-0305
				                																			                												                	俄罗斯联邦, 							pl. Universitetskaya, 1, Voronezh						
参考
- Viegas-Junior C., Danuello A., da Silva Bolzani V., Barreiro E.J., Manssour Fraga C.A. Curr. Med. Chem. 2007, 14, 1829–1852. doi: 10.2174/092986707781058805
- Gao F., Ye L., Wang Y., Kong F., Zhao Sh., Xiao J., Huang G. Eur. J. Med. Chem. 2019, 183, 111678. doi: 10.1016/j.ejmech.2019.111678
- Meunier B. Acc. Chem. Res. 2008, 41, 69–77. doi: 10.1021/ar7000843
- Kartsev V., Shikhaliev Kh.S., Geronikaki A., Medvedeva S.M., Ledenyova I.V., Krysin M.Yu., Petrou A., Ciric A., Glamoclija J., Sokovic M. Eur. J. Med. Chem. 2019, 175, 201–214. doi: 10.1016/j.ejmech.2019.04.046
- Gao J., Zhang, Z., Zhang B., Mao Q., Dai X., Zou Q., Lei Y., Feng Y., Wang S. Bioorg. Chem. 2020, 95, 103564. doi: 10.1016/j.bioorg.2019.103564
- Novichikhina N., Ilin I., Tashchilova A., Sulimov A., Kutov D., Ledenyova I., Krysin M., Shikhaliev Kh., Gantseva A., Gantseva E., Podoplelova N., Sulimov V. Molecules 2020, 25, 1889. doi: 10.3390/molecules25081889
- Djemoui A., Naouri A., Ouahrani M.R., Djemoui D., Lahcene S., Lahrech M.B., Boukenna L., Albuquerque H.M.T., Saher L., Rocha D.H.A., Monteiro F.L., Helguero L.A., Bachari K., Talhi O., Silva A.M.S. J. Mol. Struct. 2020, 1204, 127487. doi: 10.1016/j.molstruc.2019.127487
- Новичихина Н.П., Шестаков А.С., Потапов А.Ю., Кошелева Е.А., Шаталов Г.В., Вережников В.Н., Вандышев Д.Ю., Леденева И.В., Шихалиев Х.С. Изв. А.Н. Сер. хим. 2020, № 4, 787–792. [Novichikhina N.P., Shestakov A.S., Potapov A.Yu.,. Kosheleva E.A, Shatalov G.V., Verezhnikov V.N., Vandyshev D.Yu., Ledeneva I.V., Shikhaliev Kh.S. Russ. Chem. Bull. 2020, № 4, 787–792]
- Welsch M.E., Snyder S.A., Stockwell B.R. Curr. Opin. Chem. Biol. 2010, 14, 347–361. doi: 10.1016/j.cbpa.2010.02.018
- DeSimone R.W., Currie K.S., Mitchell S.A., Darrow J.W., Pippin D.A. Comb. Chem. High Throughput Screen 2004, 7, 473–494. doi: 10.2174/1386207043328544
- Sarveswari S., Vijayakumar V., Siva R., Priya R. Appl. Biochem. Biotechnol. 2015, 175 (1), 43–64. doi: 10.1007/s12010-014-1256-9
- Sabbah D.A., Hishmah B., Sweidan K., Bardaweel S., AlDamen M., Zhong H.A., Khalaf R.A., Ameerah (Hasan Ibrahim), Al-Qirim T., Sheikha G.A., Mubarak M.S. Anticancer Agents Med. Chem. 2018, 18, 263–276. doi: 10.2174/1871520617666170911171152
- Dodia N., Shah A. Indian J. Het. Chem. 1999, 9(2), 139–142.
- Tedesco R., Shaw A.N., Bambal R., Chai D., Concha N.O., Darcy M.G., Dhanak D., Fitch D.M., Gates A., Gerhardt W.G., Halegoua D.L., Han C., Hofmann G.A., Johnston V.K., Kaura A.C., Liu N., Keenan R.M., Lin-Goerke J., Sarisky R.T., Wiggall K.J., Zimmerman M.N., Duffy K.J. J. Med. Chem. 2006, 49, 971–983. doi: 10.1021/jm050855s
- Furugohri T., Isobe K., Honda Y., Kamisato-Matsumoto C., Sugiyama N., Nagahara T., Morishima Y., Shibano T.J. Thromb. Haemostasis. 2008, 6, 1542–1549. doi: 10.1111/j.1538-7836.2008.03064.x
- Fjellström O., Akkaya S., Beisel H.G., Eriksson P.O., Erixon K., Gustafsson D., Jurva U., Kang D., Karis D., Knecht W., Nerme V., Nilsson I., Olsson T., Redzic A., Roth R., Sandmark J., Tigerstrom A., Oster L. PLoS One. 2015, 10, 1–42. doi: 10.1371/journal.pone.0113705
- Obaidullah A.J., Al-Horani R.A. Cardiovasc. Hematol. Agents Med. Chem. 2017, 15, 40–48. doi.10.2174/1871525715666170529093938
- Amin K.M., Gawad N.M.A., Rahman D.E.A., El Ashry M.K.E. Bioorg. Chem. 2014, 52, 31–43. doi: 10.1016/j.bioorg.2013.11.002
- Verespy S., Mehta A.Y., Afosah, D., Al-Horani R.A., Desai U.R. Sci Rep. 2016, 6, 24043. doi: 10.1038/srep24043
- Riyadh S.M., Kheder N.A., Asiry A.M. Monatsh. Chem. 2013, 144, 1559–1567. doi: 10.1007/s00706-013-1028-1
- Abdelhamid A.O., Gomha S.M., El-Enany W.A.M.A. J. Heterocycl. Chem. 2019, 56, 426–432. doi: 10.1002/jhet.3415
- Уломский Е.Н., Деев У.Н., Шестакова Е.С., Руси-нов В.Л., Чупахин О.Н. Изв. АН, Сер. хим. 2002, 51, 1594–1600. [Ulomskii E.N., Deev S.L., Shestakova T.S., Rusinov V.L., Chupakhin O.N. Russ. Chem. Bull. 2002, 51, 1737–1743.] doi: 10.1023/A:1021320025860
- Abdelhamid A.O., Zohdy H.F., Zaida M.M. Ind. J. Chem. 2000, 39B, 202.
- Crespan E., Alexandrova L., Khandazhinskaya A., Jasko M., Kukhanova M., Villani G., Hübscher U., Spadari S., Maga G. Nucleic Acids Res. 2007, 35, 45–57. doi: 10.1093/nar/gkl1016
- Русинов В.Л., Уломский Е.Н., Чупахин О.Н., Забаиров М.М., Кпапустин А.В., Митин А.В., Жураветский М.И., Виноград И.А. Хим.-фарм. ж. 1990, 24, 41–44. [Rusinov V.L., Ulomskii E.N., Chupakhin O.N., Zubairov M.M., Kapustin A.B., Mitin N.I., Zhiravetskii M.I., Vinograd I.A. Pharm. Chem. J. 1990, 24, 646–650.] doi: 10.1007/BF00767030
- Русинов В.Л., Уломский Е.Н., Чупахин О.Н., Чарушин В.Н. Изв. АН, Сер. хим. 2008, 57, 967–996. [Rusinov V. L., Ulomskii E.N., Chupakhin O.N., Charushin V.N. Russ. Chem. Bull. 2008, 57, 985–1014.]. doi: 10.1007/s11172–008–0130–8
- Jashari A., Imeri F., Ballazhi L., Shabani A., Mikhova B., Drager G., Popovski E., Huwiler A. Bioorg. Med. Chem. 2014, 22, 2655–2661. doi: 10.1016/j.bmc.2014.03.026
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