Synthesis of ethyl-4-aryl-2-imino-1-(2-methoxyphenyl)-5-(2-methoxyphenylcarbamoyl)-6-oxopiperidine-3-carboxylates
- Authors: Khachatryan A.K.1,2, Avagyan K.A.1, Sargsyan A.A.1, Badasyan A.E.1
- 
							Affiliations: 
							- Scientific Technological Centre of Organic and Pharmaceutical Chemistry NAS RA
- Crisis Management State Academy, MIA RA
 
- Issue: Vol 60, No 4 (2024)
- Pages: 533-536
- Section: Articles
- URL: https://ruspoj.com/0514-7492/article/view/672188
- DOI: https://doi.org/10.31857/S0514749224040163
- EDN: https://elibrary.ru/RXPDXJ
- ID: 672188
Cite item
Abstract
The reaction of ethyl 3-aryl-2-cyanoprop-2-enoates with N1,N3-bis(2-methoxyphenyl)propanediamide afforded previously unknown products of intramolecular heterocyclization of the primary Michael adducts, ethyl 4-aryl-2-imino-1-(2-methoxyphenyl)-5-[(2-methoxyphenyl)carbamoyl]-6-oxopiperidine-3-carboxylates, in 73–90% yields. The product structure was determined by IR and NMR (1H, 13C) spectroscopy.
Full Text
 
												
	                        About the authors
A. Kh. Khachatryan
Scientific Technological Centre of Organic and Pharmaceutical Chemistry NAS RA; Crisis Management State Academy, MIA RA
							Author for correspondence.
							Email: khachatryan-ax@mail.ru
				                	ORCID iD: 0000-0003-1210-9903
				                																			                												                	Armenia, 							prosp. Azatutyan, 26, Yerevan, 0014; ul. Acharyana, 1, Yerevan, 0040						
K. A. Avagyan
Scientific Technological Centre of Organic and Pharmaceutical Chemistry NAS RA
														Email: khachatryan-ax@mail.ru
				                	ORCID iD: 0000-0002-5370-041X
				                																			                												                	Armenia, 							prosp. Azatutyan, 26, Yerevan, 0014						
A. A. Sargsyan
Scientific Technological Centre of Organic and Pharmaceutical Chemistry NAS RA
														Email: khachatryan-ax@mail.ru
				                	ORCID iD: 0000-0002-0303-0710
				                																			                												                	Armenia, 							prosp. Azatutyan, 26, Yerevan, 0014						
A. E. Badasyan
Scientific Technological Centre of Organic and Pharmaceutical Chemistry NAS RA
														Email: khachatryan-ax@mail.ru
				                	ORCID iD: 0000-0003-3574-5443
				                																			                												                	Armenia, 							prosp. Azatutyan, 26, Yerevan, 0014						
References
- Пулатова Н.У., Максумова О. С. Universum: химия и биология. 2021, 6, 5–8. doi: 10.32743/UniChem.2021.84.6.11853
- Василюк А.А., Козловский В. И. Вестник ВГМУ. 2021, 20, 8–17. doi: 10.22263/2312–4156.2021.2.8
- Дьяченко В.Д., Ткачев Р. П., Битюкова О. С. ЖОрХ. 2008, 44, 1591–1604. [Dyachenko V.D., Tkachiov R.P., Bityukova O.S. Russ. J. Org. Chem. 2008, 44, 1565.] doi 10.1134 /S1070428008110018
- Bertuzzi G., Silvestrini F., Moimare P., Pecorari D., Mazzanti A., Bernardi L., Fochi M. Advanced Synthesis Catal. 2020, 362, 1167–1175. doi. 10.1002/adsc.201901500
- Дьяченко В.Д., Ткачев Р. П. ЖОрХ. 2006, 42, 167–188. [Dyachenko V.D., Tkachev R.P. Russ. J. Org. Chem. 2006, 42, 149.] doi: 10.1134/S1070428002120011
- Ткачев Р.П., Битюкова О. С., Дьяченко В. Д., Ткачева В. П., Дьяченко А. Д. ЖОХ. 2007, 77, 125–132. [Tkachev R.P., Bityukova O.S., Dyachenko V.D., Tkacheva V.P., Dyachenko A.D. Russ. J. Gen. Chem. 2007, 77, 116.] doi 10.1134 /S1070363207010161
- Vereshchagin A.N., Karpenko K. A., Elinson M. N., Goloveshkin A. S., Ushakov I. E., Egorov M. P. Res. Chem. Intermed. 2018, 44, 5623–5634. doi: 10.1007/s11164–018–3444–7
- Саргсян М.С., Айоцян С. С., Хачатрян А. Х., Бадасян А. Э., Конькова С. Г. ЖОХ. 2013, 83, 1217–1218. [Sargsyan M.S., Hayotsyan S.S., Khachatryan A.Kh., Badasyan A.E., Kon’kova S.G. Russ. J. Gen. Chem. 2013, 83, 1463.] doi: 10.1134/s107036321307030x
- Саргсян М.С., Авагян К. А., Саргсян А. А., Бадасян А. Э., Хачатрян А. Х., Айвазян A. Г., Балян А. А., Конькова С. Г., Айоцян С. С. Хим. ж. Армении 2019, 72, 304–312.
- Авагян К.А., Саргсян М.С, Бадасян А. Э., Саргсян А. А., Манукян А. Г., Паносян Г. А., Айвазян А. Г., Хачатрян А. Х. ЖОХ. 2023, 93, 516–524. [Avagyan K.A., Sargsyan M.S., Badasyan A.E., Sargsyan A.A., Manukyan A.G., Panosyan H.A., Ayvazyan A.G., Khachatryan A.Кh. Russ. J. Gen. Chem. 2023, 93, 4, 787.] doi: 10.31857/S0044460X23040030
- Краузе А., Дубур Г. ХГС. 1999, 35, 506–509. doi 10. 1007/BF02319332 [Krauze A., Duburs G. Chem. Heterocycl. Compd. 1999, 35, 446.]
 
				
			 
					 
						 
						 
						 
						 
									

 
  
  
  Email this article
			Email this article 
 Open Access
		                                Open Access Access granted
						Access granted

