Synthesis, sympatholytic and adrenolytic activity of aminoamides and aminоesters on the base of 1-(benzo[d][1,3]dioxol-5-yl)-cyclopentane- and 4-(benzo[d][1,3]dioxol-5-yl)tetrahydro-2H-pyrane-4-carboxylic acids
- Авторлар: Margaryan R.E.1, Stepanyan G.V.1, Aghekyan A.A.1, Panosyan H.A.1, Arutyunyan S.A.1, Tsatinyan A.S.1, Grigoryan M.S.1, Mkryan G.G.1
 - 
							Мекемелер: 
							
- The Scientific Technological Centre of Organic and Pharmaceutical Chemistry NAS RA
 
 - Шығарылым: Том 61, № 3 (2025)
 - Беттер: 293-301
 - Бөлім: ЭКСПЕРИМЕНТАЛЬНЫЕ СТАТЬИ
 - URL: https://vietnamjournal.ru/0514-7492/article/view/687813
 - DOI: https://doi.org/10.31857/S0514749225030095
 - EDN: https://elibrary.ru/EUDZPA
 - ID: 687813
 
Дәйексөз келтіру
Аннотация
By the reaction of 2-(benzo[d][1,3]dioxol-5-yl)acetonitrile with dibromobutane and 2,2'-dichlorodiethyl ether, nitriles of 1-(benzo[d][1,3]dioxol-5-yl)cyclopentane- and 4-(benzo[d][1,3]dioxol-5-yl)tetrahydro-2H-pyran-4-carboxylic acids were synthesized, converted into the corresponding acids by alkaline hydrolysis. Targeted (benzo[d][1,3]dioxol-5-yl)cyclopentane(tetrahydropyran)-carboxamides and (benzo[d][1,3]dioxol-5-yl)cyclopentane(tetrahydropyran)-carboxylates were synthesized by interaction of acid chlorides of isolated acids with N,N-dialkylaminoalkyl- and heterylalkylamines, as well as with N,N-dialkylaminoalkyl- and heterylalkylalcohols. The effect of the synthesized compounds on the cardiovascular system and blood hemodynamics was studied.
Негізгі сөздер
Толық мәтін
Авторлар туралы
R. Margaryan
The Scientific Technological Centre of Organic and Pharmaceutical Chemistry NAS RA
														Email: aaghekyan@mail.ru
				                	ORCID iD: 0000-0002-5066-0870
				                																			                												                	Армения, 							prosp. Azatutyana, 26, Yerevan, 0014						
G. Stepanyan
The Scientific Technological Centre of Organic and Pharmaceutical Chemistry NAS RA
														Email: aaghekyan@mail.ru
				                	ORCID iD: 0009-0006-6649-4439
				                																			                												                	Армения, 							prosp. Azatutyana, 26, Yerevan, 0014						
A. Aghekyan
The Scientific Technological Centre of Organic and Pharmaceutical Chemistry NAS RA
							Хат алмасуға жауапты Автор.
							Email: aaghekyan@mail.ru
				                	ORCID iD: 0000-0001-6151-4951
				                																			                												                	Армения, 							prosp. Azatutyana, 26, Yerevan, 0014						
H. Panosyan
The Scientific Technological Centre of Organic and Pharmaceutical Chemistry NAS RA
														Email: aaghekyan@mail.ru
				                	ORCID iD: 0000-0001-8311-6276
				                																			                												                	Армения, 							prosp. Azatutyana, 26, Yerevan, 0014						
S. Arutyunyan
The Scientific Technological Centre of Organic and Pharmaceutical Chemistry NAS RA
														Email: aaghekyan@mail.ru
				                	ORCID iD: 0000-0003-3748-6975
				                																			                												                	Армения, 							prosp. Azatutyana, 26, Yerevan, 0014						
A. Tsatinyan
The Scientific Technological Centre of Organic and Pharmaceutical Chemistry NAS RA
														Email: aaghekyan@mail.ru
				                	ORCID iD: 0000-0002-0923-2380
				                																			                												                	Армения, 							prosp. Azatutyana, 26, Yerevan, 0014						
M. Grigoryan
The Scientific Technological Centre of Organic and Pharmaceutical Chemistry NAS RA
														Email: aaghekyan@mail.ru
				                	ORCID iD: 0000-0002-6705-8536
				                																			                												                	Армения, 							prosp. Azatutyana, 26, Yerevan, 0014						
G. Mkryan
The Scientific Technological Centre of Organic and Pharmaceutical Chemistry NAS RA
														Email: aaghekyan@mail.ru
				                	ORCID iD: 0000-0001-9879-9524
				                																			                												                	Армения, 							prosp. Azatutyana, 26, Yerevan, 0014						
Әдебиет тізімі
- Коноваленко А.С., Шаблыкин О.В., Броваретс В.С., Шаблыкина О.В., Москвина В.С., Козитский А.В. ХГС. 2020, 56 (8), 1021–1029. [Konovalenko A.S., Shablykin O.V., Brovarets V.S., Shablykina O.V., Moskvina V.S., Kozytskiy A.V. Chem. Heterocycl. Compd. 2020, 56 (8), 1021–1029.] doi: 10.1007/s10593-020-02769-3
 - Hikichi Y. Jap. J. Phytopath. 1993, 59, 369–374. doi: 10.3186/jjphytopath.59.369
 - Nagate T., Kurashige S., Mitsuhashi S. Antimicrob. Agents Chemother. 1980, 17, 203–208. doi: 10.1128/AAC.17.2.203
 - сrestey F., Jensen A.A., Soerensen C., Magnus C.B., Andreasen J.T., Peters G.H. J., Kristensen J.L. J. Med. Chem. 2018, 61, 1719–1729. doi: 10.1021/acs.jmedchem.7601895
 - Davies S.G., Fletcher A.M., Frost A.B., Kennedy M.S., Roberts P.M., Thomson J.E. Tetrahedron. 2016, 72, 2139. doi: 10.1016/j.tet.2016.03.008
 - Bernard S., Kummerer N., Urgast D., Hack F., Ungelenk J., Frank A., Schollmeyer D., Dieter N. Synthesis. 2024, 56 (16), 2537–2548. doi: 10.1055/a-2328-2947
 - Yan X., Zheng J., Li W-D.Z. Tetrahedron Lett. 2023, 132, 154826. doi: 10.1016/j.tetlet.2023.154826
 - Попов А.A., Дряпак А.H., Буров О.Н., Клецкий М.Е., Загребаев А.Д., Ткачук А.В., Курбатов С.В., Алешукина А.В., Голошва Е.В., Маркова К.Г., Березинская И.С., Твердохлебова Т.И. ХГС. 2023, 59, 604–609. [Popov A.A., Dryapak A.N., Burov O.N., Kletskii M.E., Zagrebaev A.D., Tkachuk A.V., Kurbatov S.V., Aleshukina A.V., Goloshova E.V., Markova K.G., Berezinskaya I.S., Tverdokhlebova T.I. Chem. Hetероcycl. Compd. 2023, 59, 604–609.] doi: 10.1007/s10593-023-03239-2
 - Lacivita E., Schepetkin I.A., Stama M.L., Kirpotina L.N., Colabufo N.A., Perrone R., Khlebnikov A.I., Quinn M.T., Leopoldo M. Bioorg. Med. Chem. 2015, 23, 3913–3924. doi: 10.1016/j.bmc.2014.12.007
 - Marinovic M., Rimac H., Carvalho L.P., Rola C., Santana S., Pavic K., Prudencio M., Rajic Z. Bioorg. Med. Chem. 2023, 94, 117468. doi: 10.1016/j.bmc.2023.117468
 - Mашковский М.Д. Лекарственные средства, М.: Новая волна. 2010.
 - Агекян А.А., Мкрян Г.Г., Цатинян А.С., Нора-вян О.С., Гаспарян Г.В. ЖОрХ. 2016, 52, 226–230. [Aghekyan A.A., Mkryan G.G., Tsatinyan A.S., Noravyan O.S., Gasparyan G.V. Russ. J. Org. Chem. 2016, 52 (2), 209–213.] doi: 10.1134/S1070428016020081
 - Aгекян A.A., Мкрян Г.Г., Цатинян A.С., Гаспарян Г.В. ЖОХ. 2019, 89, 812–816. [Aghekyan A.A., Mkryan G.G., Tsatinyan A.S., Gasparyan G.V., Russ.J. Gen. Chem. 2019, 89, 1051–1054.] doi: 10.1134/S107036321905027X
 - Арустамян Ж.С., Маркарян Р.Э., Агекян А.А., Назарян И.М., Акобян А.Г., Пароникян Р.Г., Минасян Н.С. ЖОрХ, 2019, 55, 896–900. [Arustamyan Zh.S., Markaryan R.E., Aghekyan A.A., Nazaryan I.M., Hakobyan A.G., Paronikyan R.G., Minasyan N.S. Russ. J. Org. Chem. 2019, 55, 796–799.] doi: 10.1134/S1070428019060095
 - Krohs W., Ther L., Vogel G. Pat. 1124485. Germany, C.A. 1962, 57, 9738g.
 - Arustamyan Zh.S., Margaryan R.E., Mkryan G.G., Aghekyan A.A., Panosyan H.A., Buniatyan Zh.M., Muradyan R.E. Russ. J. Org. Chem. 2024, 60, 18–24. doi: 10.1134/S1070428024010032.
 - Авакян О.М. Симпато-адреналовая система. M.: Наука, 1977.
 - https://rat-house@neurobotics.ru, Россия, Зеленоград.
 
				
			
						
					
						
						
						





