INTERACTION OF 2-AMINO-(4-ARYL)-SUBSTITUTED THIA- AND OXAZOLES WITH 5-CYANO-1,2,4-TRIAZINES
- 作者: Krinochkin A.P.1,2, Matern A.I.1, Zyryanov G.V.1,2, Taniya O.S.1,2, Sharafieva E.R.1,3, Ladin E.D.1, Kopchuk D.S.1,2, Shtaitz Y.K.1, Rammohan A.1, Chupakhin O.N.1,2
- 
							隶属关系: 
							- Ural Federal University
- I.Ya. Postovsky Institute of Organic Synthesis of the Ural Branch of the Russian Academy of Sciences
- Ural State Medical University, Ministry of Healthcare of the Russian Federation
 
- 期: 卷 508, 编号 1 (2023)
- 页面: 55-58
- 栏目: CHEMISTRY
- URL: https://rjeid.com/2686-9535/article/view/651993
- DOI: https://doi.org/10.31857/S2686953522600295
- EDN: https://elibrary.ru/EVQNUQ
- ID: 651993
如何引用文章
详细
An interaction of 6-aryl-1,2,4-triazine-5-carbonitriles with 2‑amino-substituted thiazoles and oxazoles has been studied. The difference in the reactivity of these aminoheterocycles depending on the presence of an oxygen or sulfur atom in their composition has been demonstrated. Previously, the 4-aryl-3-hydroxy-2,2'-bipyridines were obtained as products of aza-Diels–Alder reaction between 6-aryl-3-(2-pyridyl)-1,2,4-triazine-5-carbonitriles and 2-amino-4-aryloxazoles. In the present work we have shown that the reaction of 6-aryl-1,2,4-triazine-5-carbonitriles with 2-aminothiazoles led to the products of ipso-substitution of cyano-group. The aza-Diels–Alder reaction of these compounds with 2,5-norbornadiene allowed to obtain (2,2'-bi)pyridines with the thiazol-2-amine moiety at alpha-position.
作者简介
A. Krinochkin
Ural Federal University; I.Ya. Postovsky Institute of Organic Synthesis of the Ural Branch of the Russian Academy of Sciences
														Email: iaroslav.shtaits@urfu.ru
				                					                																			                												                								Russian, 620002, Yekaterinburg; Russian, 
620219, Yekaterinburg						
A. Matern
Ural Federal University
														Email: iaroslav.shtaits@urfu.ru
				                					                																			                												                								Russian, 620002, Yekaterinburg						
G. Zyryanov
Ural Federal University; I.Ya. Postovsky Institute of Organic Synthesis of the Ural Branch of the Russian Academy of Sciences
														Email: iaroslav.shtaits@urfu.ru
				                					                																			                												                								Russian, 620002, Yekaterinburg; Russian, 
620219, Yekaterinburg						
O. Taniya
Ural Federal University; I.Ya. Postovsky Institute of Organic Synthesis of the Ural Branch of the Russian Academy of Sciences
														Email: iaroslav.shtaits@urfu.ru
				                					                																			                												                								Russian, 620002, Yekaterinburg; Russian, 
620219, Yekaterinburg						
E. Sharafieva
Ural Federal University; Ural State Medical University, Ministry of Healthcare of the Russian Federation
														Email: iaroslav.shtaits@urfu.ru
				                					                																			                												                								Russian, 620002, Yekaterinburg; Russian, 620028, Yekaterinburg						
E. Ladin
Ural Federal University
														Email: iaroslav.shtaits@urfu.ru
				                					                																			                												                								Russian, 620002, Yekaterinburg						
D. Kopchuk
Ural Federal University; I.Ya. Postovsky Institute of Organic Synthesis of the Ural Branch of the Russian Academy of Sciences
														Email: iaroslav.shtaits@urfu.ru
				                					                																			                												                								Russian, 620002, Yekaterinburg; Russian, 
620219, Yekaterinburg						
Ya. Shtaitz
Ural Federal University
							编辑信件的主要联系方式.
							Email: iaroslav.shtaits@urfu.ru
				                					                																			                												                								Russian, 620002, Yekaterinburg						
A. Rammohan
Ural Federal University
														Email: iaroslav.shtaits@urfu.ru
				                					                																			                												                								Russian, 620002, Yekaterinburg						
O. Chupakhin
Ural Federal University; I.Ya. Postovsky Institute of Organic Synthesis of the Ural Branch of the Russian Academy of Sciences
														Email: iaroslav.shtaits@urfu.ru
				                					                																			                												                								Russian, 620002, Yekaterinburg; Russian, 
620219, Yekaterinburg						
参考
- Atwood J.L., Davies J.E.D., MacNicol D.D., Vögtle F., Lehn J.-M. Comprehensive Supramolecular Chemistry. Oxford: Pergamon, 1996.
- Kaes C., Katz A., Hosseini M.W. // Chem. Rev. 2000. V. 100. P. 3553–3590. https://doi.org/10.1021/cr990376z
- Hancock R.D. // Chem. Soc. Rev. 2013. V. 42. P. 1500–1524. https://doi.org/10.1039/C2CS35224A
- Constable E.C., Housecroft C.E. // Molecules. 2019. V. 24. P. 3951. https://doi.org/10.3390/molecules24213951
- Prokhorov A.M., Kozhevnikov D.N. // Chem. Heterocycl. Compd. 2012. V. 48. P. 1153–1176. https://doi.org/10.1007/s10593-012-1117-9
- Anderson E.D., Boger D.L. // J. Am. Chem. Soc. 2011. V. 133. P. 12285–12292. https://doi.org/10.1021/ja204856a
- Charushin V.N., Chupakhin O.N. Metal Free C–H Functionalization of Aromatics, Nucleophilic Displacement of Hydrogen, in Topics in Heterocyclic Chemistry. Maes B.U.W., Cossy J., Polanc S. (Eds.). Springer, 2014. V. 37. P. 1–50.
- Kozhevnikov D.N., Rusinov V.L., Chupakhin O.N. // Adv. Heterocycl. Chem. 2002. V. 82. P. 261–305. https://doi.org/10.1016/S0065-2725(02)82029-3
- Huang J.J. // J. Org. Chem. 1985. V. 50. P. 2293–2298. https://doi.org/10.1021/jo00213a019
- Kozhevnikov D.N., Kozhevnikov V.N., Kovalev I.S., Rusinov V.L., Chupakhin O.N., Aleksandrov G.G. // Russ. J. Org. Chem. 2002. V. 38. P. 744–750. https://doi.org/10.1023/A:1019631610505
- Rykowski A., Branowska D., Makosza M., Van Ly P. // J. Heterocycl. Chem. 1996. V. 33. P. 1567–1571. https://doi.org/10.1002/jhet.5570330603
- Savchuk M.I., Starnovskaya E.S., Shtaitz Y.K., Kop-chuk D.S., Nosova E.V., Zyryanov G.V., Rusinov V.L., Chupakhin O.N. // Russ. J. Gen. Chem. 2018. V. 88. P. 2213–2215. https://doi.org/10.1134/S1070363218100316
- Ohba S., Konno S., Yamanaka H. // Chem. Pharm. Bull. 1991. V. 39. P. 486–488. https://doi.org/10.1248/cpb.39.486
- Kopchuk D.S., Chepchugov N.V., Kovalev I.S., Santra S., Rahman M., Giri K., Zyryanov G.V., Majee A., Charu-shin V.N., Chupakhin O.N. // RSC Adv. 2017. V. 7. P. 9610–9619. https://doi.org/10.1039/c6ra26305d
- Kopchuk D.S., Krinochkin A.P., Starnovskaya E.S., Shtaitz Y.K., Khasanov A.F., Taniya O.S., Santra S., Zyryanov G.V., Majee A., Rusinov V.L., Chupakhin O.N. // ChemistrySelect. 2018. V. 3. P. 4141–4146. https://doi.org/10.1002/slct.201800220
- Krinochkin A.P., Guda M.R., Kopchuk D.S., Sloves-nova N.V., Kovalev I.S., Savchuk M.I., Shtaitz Ya.K., Starnovskaya E.S., Zyryanov G.V., Chupakhin O.N. // Russ. J. Org. Chem. 2021. V. 57. P. 1753–1756. https://doi.org/10.1134/S1070428021100262
- Krinochkin A.P., Guda M.R., Kopchuk D.S., Shtaitz Ya.K., Savateev K.V., Ulomsky E.N., Zyryanov G.V., Rusinov V.L., Chupakhin O.N. // Russ. J. Org. Chem. 2022. V. 58. P. 188–191. https://doi.org/10.1134/S1070428022020051
- Krinochkin A.P., Reddy G.M., Kopchuk D.S., Slepu-khin P.A., Shtaitz Ya.K., Khalymbadzha I.A., Kovalev I.S., Kim G.A., Ganebnykh I.N., Zyryanov G.V., Chupa-khin O.N., Charushin V.N. // Mendeleev Commun. 2021. V. 31. P. 542–544. https://doi.org/10.1016/j.mencom.2021.07.035
- Rammohan A., Krinochkin A.P., Kopchuk D.S., Shtaitz Ya.K., Savchuk M.I., Starnovskaya E.S., Zyrya-nov G.V., Rusinov V.L., Chupakhin O.N. // Russ. J. Org. Chem. 2022. V. 58. P. 180–183. https://doi.org/10.1134/S1070428022020038
- Kozhevnikov V.N., Kozhevnikov D.N., Nikitina T.V., Rusinov V.L., Chupakhin O.N., Zabel M., König B. // J. Org. Chem. 2003. V. 68. P. 2882–2888. https://doi.org/10.1021/jo0267955
- Krayushkin M.M., Sedishev I.P., Yarovenko V.N., Zavarzin I.V., Kotovskaya S.K., Kozhevnikov D.N., Charu-shin V.N. // Russ. J. Org. Chem. 2008. V. 44. P. 407–411. https://doi.org/10.1134/S1070428008030160
- Shafikov M.Z., Kozhevnikov D.N., Bodensteiner M., Brandl F., Czerwieniec R. // Inorg. Chem. 2016. V. 55. P. 7457–7466. https://doi.org/10.1021/acs.inorgchem.6b00704
- Krinochkin A.P., Shtaitz Y.K., Rammohan A., Butorin I.I., Savchuk M.I., Khalymbadzha I.A., Kopchuk D.S., Slepukhin P.A., Melekhin V.V., Shcheglova A.V., Zyrya-nov G.V., Chupakhin O.N. // Eur. J. Org. Chem. 2022. e202200227. https://doi.org/10.1002/ejoc.202200227
- Kozhevnikov D.N., Kozhevnikov V.N., Prokhorov A.M., Ustinova M.M., Rusinov V.L., Chupakhin O.N., Aleksandrov G.G., König B. // Tetrahedron Lett. 2006. V. 47. P. 869–872. https://doi.org/10.1016/j.tetlet.2005.12.006
- Krinochkin A.P., Kopchuk D.S., Kozhevnikov D.N. // Polyhedron. 2015. V. 102. P. 556–561. https://doi.org/10.1016/j.poly.2015.09.055
- Kopchuk D.S., Krinochkin A.P., Khasanov A.F., Kova-lev I.S., Slepukhin P.A., Starnovskaya E.S., Mukherjee A., Rahman M., Zyryanov G.V., Majee A., Rusinov V.L., Chupakhin O.N., Santra S. // Synlett. 2018. V. 29. P. 483–488. https://doi.org/10.1055/s-0036-1590961
 
				
			 
						 
						 
						 
						 
					

 
  
  
  电邮这篇文章
			电邮这篇文章 
 开放存取
		                                开放存取 ##reader.subscriptionAccessGranted##
						##reader.subscriptionAccessGranted## 订阅或者付费存取
		                                							订阅或者付费存取
		                                					
