Synthesis and conversions of benzo-substituted 1-[2-methyl4-(methyltio)quinolin-3-yl]propan-2-ones
- Autores: Aleksanyan I.L.1, Hambardzumyan L.P.1
 - 
							Afiliações: 
							
- Yerevan State University
 
 - Edição: Volume 60, Nº 6 (2024)
 - Páginas: 62-68
 - Seção: Articles
 - URL: https://vietnamjournal.ru/0514-7492/article/view/676673
 - DOI: https://doi.org/10.31857/S0514749224060051
 - EDN: https://elibrary.ru/QZUNQZ
 - ID: 676673
 
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Resumo
New derivatives of Schiff bases were synthesized using 1-[2-methyl-4-mercaptoquinolin-3-yl]propan-2-ones and 1-[2-methyl-4-(methylthio)quinoline substituted in the benzene ring-3- yl]propan-2-ones as starting materials. To obtain the 4-methylthio derivatives of the Schiff base, the corresponding 4-mercaptoquinoline-propan-2-ones and 3-(2-chloroallyl)-4-mercaptoquinolines were first methylated, followed by acid hydrolysis of the chloro allyl group in the latter samples.
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Sobre autores
I. Aleksanyan
Yerevan State University
							Autor responsável pela correspondência
							Email: ialeksanyan@ysu.am
				                	ORCID ID: 0000-0002-4039-2323
				                																			                												                	Armênia, 							ul. Aleka Manukyana, 1, Yerevan, 375025						
L. Hambardzumyan
Yerevan State University
														Email: ialeksanyan@ysu.am
				                	ORCID ID: 0000-0003-1210-0052
				                																			                												                	Armênia, 							ul. Aleka Manukyana, 1, Yerevan, 375025						
Bibliografia
- Teja C., Khan F.R.N. Chem.-Asian J. 2020, 15 (24), 4153–4167. doi: 10.1002/asia.202001156
 - Matada B.S., Pattanashettar R., & Yernale, N.G. Bioorg. Med. Chem. 2021, 32, 115973. https://doi.org/10.1016/j.bmc.2020.115973
 - Yadav V., Reang, J., Sharma V., Majeed J., Sharma P.C., Sharma K., Giri N., Kumar A., Tonk R.K. Chem. Biol. Drug. Des. 2022, 100 (3), 389–418. doi: 10.1111/cbdd.14099.
 - Kaur T., Bhandari D.D. Biointerface Res. Appl. Chem. 2023, 13 (4), 355–374. https://doi.org/10.33263/BRIAC134.355
 - Patel A., Patel S., Mehta M., Patel Y., Patel R., Shah D., Patel D., Shah U., Patel M., Patel S., Solanki N., Bambharoliya T., Patel S., Nagani A., Patel H., Vaghasiya J., Shah H., Prajapati B., Rathod M., Bhimani B., Patel R., Bhavsar V., Rakholiya B., Patel M., and Patel P. Green Chem. Lett. Rev. 2022, 15 (2), 337–372. https://doi.org/10.1080/17518253.2022.2064194
 - Mokhtar M., Alghamdi K.S., Ahmed N.S., Bakhotmah D., Saleh T.S.J. Enzyme Inhib. Med. Chem. 2021, 36 (1), 1454–1471. https://doi.org/10.1080/14756366.2021.1944126.
 - Desai N.C., Maheta A.S., Rajpara K.M., Joshi V.V., Vaghani H.V., Satodiya H.M.J. Saudi Chem. Soc. 2014, 18 (6), 963–971. https://doi.org/10.1016/j.jscs.2011.11.021.
 - Yadav P., Bhalla A. Chemistry Select. 2022, 7, e202201721. https://doi.org/10.1002/slct.202201721
 - Shivangi S., Kuldeep S., Shivendra S. Curr. Org. Synthes. 2023, 20 (6), 606–629. https://doi.org/10.2174/1570179420666221004143910
 - Govindarao K., Srinivasan N., Suresh R., Raheja R.K., Annadurai S., Bhandare R.R., Shaik A.B.J. Saudi Chem. Soc. 2022, 26 (3), 101471. https://doi.org/10.1016/j.jscs.2022.101471.
 - Li K., Li Y., Zhou D., Fan Y., Guo H., Ma T., Wen J., Liu D., Zhao L. Bioorg. Med. Chem. 2016, 24 (8), 1889–1897. https://doi.org/10.1016/j.bmc.2016.03.016.
 - Batista V.f., Pinto D.C.G.A. and Silva A.M.S. ACS Sustainable Chem. Engineering. 2016, 4 (8), 4064–4078. https://doi.org/10.1021/acssuschemeng.6b01010
 - Аветисян А.А., Алексаиян И.Л., Саргсян К.С. ЖОрХ. 2007 43 (3) 423–426. [Avetisyan A.A., Aleksanyan I.L., Sargsyan K.S. Russ. J. Org. Chem. 2007, 43 (3) 422–425.] https://doi.org/10.1134/S1070428007030165
 - Алексанян И.Л., Амбарцумян Л.П. ЖОрХ. 2021, 57 (8), 1170–1176. [Aleksanyan I.L., Hambardzumyan L.P. Russ. J. Org. Chem. 2021, 57 (8) 1289–1294.] https://doi.org/10.1134/S107042802108008X
 
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