This Randomized trial demonstrates the conversion of isothiazoles to pyrazoles, highlighting its potential in medicinal chemistry.
We report a Tf 2 O-promoted skeletal editing of 4-substituted isothiazoles to pyrazoles via a two-atom N–S to N–N swap. The reaction proceeds via activation of the isothiazole ring by Tf 2 O, followed by a nucleophilic addition/Dimroth rearrangement cascade in a one-pot process under mild conditions. A range of 4-substituted isothiazoles bearing various electronic and steric substituents are compatible, affording the corresponding pyrazoles in moderate to good yields. The method is scalable to gram-scale synthesis and allows late-stage modification of drug-derived isothiazole derivatives, demonstrating its utility for scaffold hopping in medicinal chemistry. This work establishes Tf 2 O activation as a viable platform for skeletal editing of five-membered heteroarenes, providing a mild and modular entry to pyrazoles from isothiazoles.
No takes yet. Share an insight, caveat, or question.
Huang et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: