Issue 32, 2024

Synthesis of tetrahydroquinazolines from 2-aminobenzonitriles and alkylidene malonates via 1,4-conjugate addition and an unprecedented rearrangement reaction

Abstract

An efficient methodology for the synthesis of highly diverse tetrahydroquinazoline scaffolds from 2-aminobenzonitriles and alkylidene malonates via 1,4-conjugate addition followed by an unprecedented rearrangement has been demonstrated. The methodology is further applicable for the synthesis of quinazolines and tetracyclic compounds. Some of the synthesized compounds exhibit photophysical properties.

Graphical abstract: Synthesis of tetrahydroquinazolines from 2-aminobenzonitriles and alkylidene malonates via 1,4-conjugate addition and an unprecedented rearrangement reaction

Supplementary files

Article information

Article type
Communication
Submitted
16 Jan 2024
Accepted
19 Mar 2024
First published
21 Mar 2024

Chem. Commun., 2024,60, 4358-4361

Synthesis of tetrahydroquinazolines from 2-aminobenzonitriles and alkylidene malonates via 1,4-conjugate addition and an unprecedented rearrangement reaction

B. Porashar, B. K. Behera, H. Phukon and A. K. Saikia, Chem. Commun., 2024, 60, 4358 DOI: 10.1039/D4CC00240G

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