This work reveals efficient C3-selective nitration in pyrazolo compounds, suggesting its potential in materials science and product diversification.
Nitro‐functionalized pyrazolo[1,5‐ a ]pyrimidines are valuable in materials science and energetics, but traditional methods typically require a mixture of sulfuric and nitric acids. This work presents a mild, iron‐complex‐mediated strategy for efficient C3‐selective nitration of pyrazolo[1,5‐ a ]pyrimidin‐7‐amines, providing direct access to these important scaffolds. The utility of this versatile method is highlighted by its successful application in late‐stage modification, gram‐scale synthesis, and further product diversification.
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Pang et al. (2025) studied this question.
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