Bis-indolylation of aldehydes and ketones using silica-supported FeCl3: molecular docking studies of bisindoles by targeting SARS-CoV-2 main protease binding sites. Issue 49 (16th September 2021)

• Record Type: Journal Article
• Authors: Deb, Barnali; Debnath, Sudhan; Chakraborty, Ankita; Majumdar, Swapan
• Is Part Of: RSC advances. Volume 11:Issue 49(2021)
• Page Start: 30827
• Page End: 30839
• Publication Date: 2021-09-16
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d1ra05679d
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : Silica supported FeCl3 catalyzed simple protocol for the synthesis of bis-indolylmethanes was explored via grindstone chemistry. Synthesized compounds were screened virtually as inhibitor by targeting the binding site of SARS-CoV-2 main protease enzyme. Abstract : We report herein an operationally simple, efficient and versatile procedure for the synthesis of bis-indolylmethanes via the reaction of indoles with aldehydes or ketones in the presence of silica-supported ferric chloride under grindstone conditions. The prepared supported catalyst was characterized by SEM and EDX spectroscopy. The present protocol has several advantages such as shorter reaction time, high yield, avoidance of using harmful organic solvents during the reaction and tolerance of a wide range of functional groups. Molecular docking studies targeted toward the binding site of SARS-CoV-2 main protease (3CL pro or M pro ) enzymes were investigated with the synthesized bis-indoles. Our study revealed that some of the synthesized compounds have potentiality to inhibit the SARS-CoV-2 M pro enzyme by interacting with key amino acid residues of the active sites via hydrophobic as well as hydrogen bonding interactions.