Issue 42, 2018

Synthesis and anticholinesterase activity of 2-substituted-N-alkynylindoles

Abstract

In this paper, we report a protocol for the preparation of 2-substituted-N-alkynylindoles via metalation of N-alkynylindoles followed by the capture of a 2-indolyl lithium intermediate with different electrophiles. The reactivity of the indoles prepared was also demonstrated through the reaction with CBr4/Ph3P for the preparation of 2-gem-dibromovinyl N-alkynylindoles and the hydrotelluration reaction of N-alkynylindoles, which led to vinylic tellurides. Some compounds prepared showed AChE inhibitory potential in the low micromolar range similar to that obtained with donepezil, a commercially available cholinesterase inhibitor.

Graphical abstract: Synthesis and anticholinesterase activity of 2-substituted-N-alkynylindoles

Supplementary files

Article information

Article type
Paper
Submitted
03 Sep 2018
Accepted
04 Oct 2018
First published
04 Oct 2018

Org. Biomol. Chem., 2018,16, 7926-7934

Synthesis and anticholinesterase activity of 2-substituted-N-alkynylindoles

T. Prochnow, A. Maroneze, D. F. Back, N. S. Jardim, C. W. Nogueira and G. Zeni, Org. Biomol. Chem., 2018, 16, 7926 DOI: 10.1039/C8OB02165A

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