Issue 30, 2022, Issue in Progress

Coupling of acceptor-substituted diazo compounds and tertiary thioamides: synthesis of enamino carbonyl compounds and their pharmacological evaluation

Abstract

This paper describes the synthesis of enamino carbonyl compounds by the copper(I)-catalyzed coupling of acceptor-substituted diazo compounds and tertiary thioamides. We plan to use this method to synthesize indolizidine (−)-237D analogs to find α6-selective antismoking agents. Therefore, we also performed in silico α6-nAchRs binding studies of selected products. Compounds with low root-mean-square deviation values showed more favorable binding free energies. We also report preliminary pharmacokinetic data on indolizidine (−)-237D and found it to have weak activity at CYP3A4. In addition, as enamino carbonyl compounds are also known for antimicrobial properties, we screened previously reported and new enamino carbonyl compounds for antibacterial, antimicrobial, and antifungal properties. Eleven compounds showed significant antimicrobial activities.

Graphical abstract: Coupling of acceptor-substituted diazo compounds and tertiary thioamides: synthesis of enamino carbonyl compounds and their pharmacological evaluation

Supplementary files

Article information

Article type
Paper
Submitted
14 Apr 2022
Accepted
25 Jun 2022
First published
05 Jul 2022
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2022,12, 19431-19444

Coupling of acceptor-substituted diazo compounds and tertiary thioamides: synthesis of enamino carbonyl compounds and their pharmacological evaluation

J. Secka, A. Pal, F. A. Acquah, B. H. M. Mooers, A. B. Karki, D. Mahjoub, M. K. Fakhr, D. R. Wallace, T. Okada, N. Toyooka, A. Kuta, N. Koduri, D. Herndon, K. P. Roberts, Z. Wang, B. Hileman, N. Rajagopal and S. R. Hussaini, RSC Adv., 2022, 12, 19431 DOI: 10.1039/D2RA02415B

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