Synthesis of hexa-substituted benzene derivative based on 4-pyridinecarboxaldehyde and malononitrile
- Autores: Mamedov I.G.1, Naghiyev F.N.1, Yakushev I.A.2, Khrustalev V.N.3,4
 - 
							Afiliações: 
							
- Baku State University
 - Kurnakov Institute of General and Inorganic Chemistry of RAS
 - Peoples’ Friendship University of Russia (RUDN University)
 - dZelinsky Institute of Organic Chemistry RAS
 
 - Edição: Volume 61, Nº 3 (2025)
 - Páginas: 308-312
 - Seção: ЭКСПЕРИМЕНТАЛЬНЫЕ СТАТЬИ
 - URL: https://vietnamjournal.ru/0514-7492/article/view/687712
 - DOI: https://doi.org/10.31857/S0514749225030113
 - EDN: https://elibrary.ru/EUFMTK
 - ID: 687712
 
Citar
Texto integral
Resumo
The present work reports the synthesis of a new compound 2-amino-4,6-di(pyridin-4-yl)benzene-1.3.5-tricarbonitrile as a result of the reaction of two moles of 2-(pyridin-4-ylmethylene)malononitrile with one mole of malononitrile in the presence of methylpiperazine as a catalyst. The structure of the obtained product was confirmed by NMR and X-ray. A plausible reaction mechanism is presented.
Palavras-chave
Texto integral
Sobre autores
I. Mamedov
Baku State University
							Autor responsável pela correspondência
							Email: bsu.nmrlab@gmail.com
				                	ORCID ID: 0000-0002-5757-9899
				                																			                								
химический факультет
Azerbaijão, ul. Z. Khalilova, 23, Baku, Az-1148F. Naghiyev
Baku State University
														Email: bsu.nmrlab@gmail.com
				                	ORCID ID: 0009-0003-9325-1756
				                																			                								
химический факультет
Azerbaijão, ul. Z. Khalilova, 23, Baku, Az-1148I. Yakushev
Kurnakov Institute of General and Inorganic Chemistry of RAS
														Email: bsu.nmrlab@gmail.com
				                					                																			                												                	Rússia, 							Leninsky prosp., 31, Moscow, 119071						
V. Khrustalev
Peoples’ Friendship University of Russia (RUDN University); dZelinsky Institute of Organic Chemistry RAS
														Email: bsu.nmrlab@gmail.com
				                	ORCID ID: 0000-0001-8806-2975
				                																			                												                	Rússia, 							ul. Miklukho-Maklaya, 6, Moscow, 117198; Leninsky prosp., 47, Moscow, 119991						
Bibliografia
- Freeman F. Chem. Rev. 1969, 69, 591–642. doi: 10.1021/cr60261a001
 - Fatiadi A.J. Synthesis. 1978, 165–204. doi: 10.1055/s-1978-24703
 - Wing L.K., Behanna H. A., Eldik L.J., Watterson D.M., Ralay R.H. Alzheimer Res. 2006, 3, 205–214. doi: 10.2174/156720506777632844
 - Rozsa E., Obotka H., Nagy D, Farkas T., Saa K., Vecsei L., Toldi J. Brain Res. Bull. 2008, 76, 474–479. doi: 10.1016/j.brainresbull.2007.12.001
 - Odlo K., Hentzen J., Chabert J. F., Ducki S., Gani O.A. Sylte I., Skrede M., Florenes V.A., Hanse T.V. Bioorgan. Med. Chem. 2008, 16, 4829–4838. doi: 10.1016/j.bmc.2008.03.049
 - Zhao H., Serby M.D., Xin Z., Szczepankiewicz B.G., Liu,M., Kosogof C., Liu L., Nelson T., Johnson E.F., Wang S., Terry P., Rebecca J.G., Jill E.C., Deanna L.H., Cele A.Z., Elizabeth H. F., Cristina R., James M.T., Hing L.S., Gang L. J. Med. Chem. 2006, 26, 4455–4458. doi: 10.1021/jm060465l
 - Muranaka K., Sano A., Ichikawa S., Mastsuda A. Bioorgan. Med. Chem. 2008, 16, 5862–5870. doi: 10.1016/j.bmc.2008.04.070
 - Burguete A., Pontiki D., Litina H., Villar R., Vicente E., Solano B., Ancizu S., Silanes S., Aldana I., Monge A. Bioorg. Med. Chem. Lett. 2007, 17, 6439–6443. doi: 10.1016/j.bmcl.2007.10.002
 - Hirokawa Y., Kinoshita H., Tanaka T., Nakamura T., Fujimoto K., Kashimoto S., Kojima T., Kato S. Bioorg. Med. Chem. Lett. 2008, 18, 3556–3561. doi: 10.1016/j.bmcl.2008.05.011
 - Palmer A.M., Grobbel B., Brehm C., Zimmermann P.J., Buhr W., Feth M.O., Holst H.C., Simon W.A. Bioorgan. Med. Chem. 2007, 15, 7647–7660. doi: 10.1016/j.bmc.2007.08.065
 - Leon R., Rois C., Contelles J.M., Lopez M.G., Barcia, A.G., Villaroya M. Eur. J. Med. Chem. 2008, 43, 668–674. doi: 10.1016/j.ejmech.2007.06.001
 - Mamedov I.G., Mamedova Y.V. Russ. J. Org. Chem. 2021, 57 (6), 942–949. doi: 10.1134/S1070428021060099
 - Mamedov I.G., Shikhaliyeva I.M., Mamedova Y.V., Abdurahmanli S.G., Maharramov A.M. Indian J. Chem. 2019, 58B, 930–934.
 - Rafat M.M., Amr S.A., Nermeen S.A. Anticanc. Agents Med. Chem. 2018, 17, 1951–1962. doi: 10.2174/1871520617666170725153523
 - Amal A.A., Huda M. ACS Omega. 2020, 5, 10160–10166. doi: 10.1021/acsomega.0c01001
 - Magerramov A.M., Naghiyev F.N., Mamedova G.Z., Asadov Kh.A., Mamedov I.G. Russ. J. Org. Chem. 2018, 54 (11), 1731–1734. doi: 10.1134/S1070428018110192
 - Naghiyev F.N., Mamedov I.G., Asadov Kh.A., Dorovatovskii P.V., Khrustalev V.N., Maharramov A.M. Russ. J. Org. Chem. 2019, 55 (12), 1967–1970. doi: 10.1134/S1070428019120273
 - Nesterov, V.N., Struchkov, Yu.T., Khoroshilov, G.E., Sharanin, Yu.A., Shklover, V.E., Russ. Chem. Bull. 1989, 38 (12), 2537. doi: 10.1007/BF00962440
 - Maryasov M.A., Davydova V.V., Nasakin O.E., Shteingolts S.A., Lodochnikova O.A. Russ. J. Gen. Chem. 2020, 90 (8), 1573–1577. doi: 10.1134/S1070363220080289
 - Khalilov A.N. Rev. Roum. de Chim. 2021, 66 (8–9), 719–723. doi: 10.33224/rrch.2021.66.8-9.04
 - Askerov R.K., Maharramov A.M. Khalilov A.N., Akkurt M., Akobirshoeva A.A., Osmanov V.K., Borisov A.V. Acta Cryst. 2020, E76, 1007–1011. doi: 10.1107/S2056989020007033
 - Rzayev R., Khalilov A. Chem. Rev. Lett. 2024, 7(3), 479–490. doi: 10.22034/crl.2024.465900.1371
 
Arquivos suplementares
				
			
						
						
					
						
						
									




