. 2024 Feb 15;14(9):5975–5980. doi: 10.1039/d4ra00517a

Table 2. Scope of N-aryl pyrazoles in C–H bond amidation^a^,^b.

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Reaction conditions: N-aryl pyrazoles 1 (0.25 mmol), N-hydroxybenzamide 2a (0.25 mmol), [Cp*IrCl₂]₂ (4 mol%), and AgNTf₂ (40 mol%) in PhCl (3 mL) were stirred at 120 °C under air for 8 h.

Isolated yields.

Table 2. Scope of N-aryl pyrazoles in C–H bond amidationa,b.

Table 2. Scope of N-aryl pyrazoles in C–H bond amidation^a^,^b.