Asymmetric synthesis of 1H-pyrazolo[3,4-b]pyridine analogues catalyzed by chiral-at-metal Rh(iii) complexes

Abstract

An efficient asymmetric Friedel–Crafts-type alkylation/cyclization of 5-aminopyrazoles with α,β-unsaturated 2-acyl imidazoles has been developed, affording corresponding pyrazolo[3,4-b]pyridine analogues in 81–98% yield with 85–99% enantioselectivity. Remarkably, this protocol exhibits extraordinary advantages in terms of reactivity and enantioselectivity, given the fact that chiral Rh(III) complex at an amount as low as 0.05 mol% can promote the title reaction on the gram scale to afford the desired product, with excellent enantioselectivity (96% ee). Application of the methodology in the efficient synthesis of pyrazolo[3,4-b]pyridine via dehydrogenation is reported.

Graphical abstract: Asymmetric synthesis of 1H-pyrazolo[3,4-b]pyridine analogues catalyzed by chiral-at-metal Rh(iii) complexes

Supplementary files

Article information

Article type
Research Article
Submitted
18 Jun 2024
Accepted
09 Jul 2024
First published
10 Jul 2024

Org. Chem. Front., 2024, Advance Article

Asymmetric synthesis of 1H-pyrazolo[3,4-b]pyridine analogues catalyzed by chiral-at-metal Rh(III) complexes

X. Ji, S. Zhu, Y. Li, Z. Zhao and S. Li, Org. Chem. Front., 2024, Advance Article , DOI: 10.1039/D4QO01100G

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