Issue 11, 2023

I2-mediated coupling of quinazolinone enamines with 2-aminopyridines: a new strategy to access spiroquinazolinones

Abstract

Herein, we report a novel, rapid and efficient route to the spiroquinazolinone framework via an umpolung strategy mediated by molecular iodine. A library of functionalized spiroquinazolinone iodide salts was synthesized in moderate to good yields under ambient, metal-free and mild conditions. The current methodology opens up a new efficient and concise strategy for the construction of spiroquinazolinones.

Graphical abstract: I2-mediated coupling of quinazolinone enamines with 2-aminopyridines: a new strategy to access spiroquinazolinones

Supplementary files

Article information

Article type
Paper
Submitted
15 Jan 2023
Accepted
14 Feb 2023
First published
16 Feb 2023

Org. Biomol. Chem., 2023,21, 2355-2360

I2-mediated coupling of quinazolinone enamines with 2-aminopyridines: a new strategy to access spiroquinazolinones

J. Fang, Z. Pan, T. Liu, Y. Rao, H. Jiang and Y. Ma, Org. Biomol. Chem., 2023, 21, 2355 DOI: 10.1039/D3OB00083D

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