Synthesis and conversions of benzo-substituted 1-[2-methyl4-(methyltio)quinolin-3-yl]propan-2-ones
- Авторлар: Aleksanyan I.L.1, Hambardzumyan L.P.1
-
Мекемелер:
- Yerevan State University
- Шығарылым: Том 60, № 6 (2024)
- Беттер: 62-68
- Бөлім: Articles
- URL: https://modernonco.orscience.ru/0514-7492/article/view/676673
- DOI: https://doi.org/10.31857/S0514749224060051
- EDN: https://elibrary.ru/QZUNQZ
- ID: 676673
Дәйексөз келтіру
Аннотация
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.
Авторлар туралы
I. Aleksanyan
Yerevan State University
Хат алмасуға жауапты Автор.
Email: ialeksanyan@ysu.am
ORCID iD: 0000-0002-4039-2323
Армения, ul. Aleka Manukyana, 1, Yerevan, 375025
L. Hambardzumyan
Yerevan State University
Email: ialeksanyan@ysu.am
ORCID iD: 0000-0003-1210-0052
Армения, ul. Aleka Manukyana, 1, Yerevan, 375025
Әдебиет тізімі
- 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
Қосымша файлдар
