Copper-catalysed site-selective arylation of pyrazoles

作者：Minghao Wang, Xintong Hou, Stephanie A. Corio, Lori Digal, Jennifer S. Hirschi, Vy M. Dong · 发表于：Nature Chemistry · 年份：2026 · DOI：10.1038/s41557-026-02148-z · 被引用次数：1 · 研究领域：Cyclization and Aryne Chemistry、Catalytic Cross-Coupling Reactions、Chemical Reactions and Mechanisms

A major challenge in late-stage functionalization is the selective N-arylation of unsymmetric pyrazoles, five-membered heterocycles with two adjacent nitrogen atoms, which are prevalent in blockbuster medicines and bioactive molecules. Traditional cross-coupling methods usually favour one type of regioisomer, limiting access to complementary structures that could accelerate drug discovery and streamline structure-activity relationship studies. Here we show that copper catalysis harnesses arynes to achieve switchable arylation of pyrazoles under mild conditions. By tuning Cu-pyrazole coordination, we direct arylation to either nitrogen atom, unlocking selectivity between two similar sites. Mechanistic studies reveal how steric and electronic effects govern regioselectivity, transforming an inherently unpredictable process into a blueprint for selective recognition of N-N linkages. This approach establishes a general strategy for controlling site selectivity in nitrogen-rich heterocycles and highlights the use of strained intermediates in late-stage diversification.