Microwave-assisted, acetic acid-catalyzed, metal-free synthesis of 5H-pyrazino[2,3-b]indoles via sequential C–C and C–N bond formation

Abstract

This study introduces a synthetic method to obtain 5H-pyrazino[2,3-b]indoles through acetic acid catalyzed C–C coupling under microwave irradiation. This technique offers mild conditions as well as short reaction times and efficient product formation. A sustainable process for the production of diverse complicated nitrogen-containing heterocycles is highlighted, which paves the way for further developments in synthetic organic chemistry.

Graphical abstract: Microwave-assisted, acetic acid-catalyzed, metal-free synthesis of 5H-pyrazino[2,3-b]indoles via sequential C–C and C–N bond formation

Supplementary files

Article information

Article type
Paper
Submitted
20 Jan 2026
Accepted
09 Mar 2026
First published
21 Mar 2026

Org. Biomol. Chem., 2026, Advance Article

Microwave-assisted, acetic acid-catalyzed, metal-free synthesis of 5H-pyrazino[2,3-b]indoles via sequential C–C and C–N bond formation

T. Dhar, D. Bera, S. Halder and C. Mukhopadhyay, Org. Biomol. Chem., 2026, Advance Article , DOI: 10.1039/D6OB00100A

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