Synthesis and Biological Properties of 4-Chloro-N¹-(5-Chloro-1H-Indol-1-yl)-N²-(2-Chlorophenyl) benzene-1,2-Diamine Derivatives.

Autor: Andhale, Nikita Shridhar, Bhor, Rohit Jaysing, Kolhe, Mahesh Hari, Pawar, Tanishka Anil, Tambe, Pornima Ramdas, Ghule, Rupali Mahadev, Bhange, Sarthak Anil, Thete, Bhakti Sharad, Kute, Pruthviraj Vijay, Malvade, Pratik Vijay, Bhagat, Jyoti Ramkisan, Waykar, Poonam Prakash
Předmět:
Zdroj: Journal of Young Pharmacists; Jul-Sep2024, Vol. 16 Issue 3, p498-505, 8p
Abstrakt: Background: Five-membered heterocycle with one neighbouring nitrogen atoms is present in the indole nucleus. Heterocyclic substances feature two adjacent benzene and pyrrole ring atoms. Indole are heterocyclic compounds with one oxygen ring that have a benzoannelated - pyrrole ring. Indole derivatives are highly valuable chemical synthesis and medicinal intermediates. Recent years have seen a surge in interest in the effective synthesis of indole blocks and associated functionalization's, particularly the alkylation of indoles. The two following factors will be the main emphasis of this review: i) Recent advancements in the alkylation of indoles, namely those involving the N1-, C2- and C3-positions and the synthesis of indoles, which was facilitated by transition metals. Materials and Methods: Benzoic acid and ethanoic acid, propionic acid, hydroxylamine, 2,5 Dichloro aniline are used for the synthesis of indole derivatives were used for the synthesis of indole. Results: Compared to indomethacin, the anti-inflammatory results for the substances or their derivatives like N2-(biphenyl-2-yl)-4-chloro-N1-(5-chloro-1H-indol-1-yl)-4-am inobenzene-1,2-diamine NA5 (Scheme 1B); N2-(biphenyl-2-yl)-4-chloro-N1-(5-chloro-1H-ind ol-1-yl)-3-aminobenzene-1,2-diamine NA6 (Scheme 1B) and N2-(biphenyl-2-yl)-4-chloro-N1-(5-chloro-1H-indol-1-yl)-2-aminobenzene-1,2-diamine NA7 (Scheme 1B). Conclusion: Examined were the anti-inflammatory properties of the substances in the title and their derivatives. The compounds containing indole derivatives with an electron-withdrawing group have a higher activity than those containing an electron-donating group, according to research on the link between structure and activity. Summarising the data from the previously reviewed literature, we can say that indole has a broad spectrum of biological activity. Numerous opportunities exist to investigate indole for new therapeutic uses. Researchers worldwide will benefit from this study's coverage of the chemistry of indole derivatives in the design and synthesis of new pharmaceuticals that might be utilised to treat a range of diseases. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index