Reveals an efficient synthesis method for benzothiophene-fused pyridazinone, indicating significant potential for diverse chemical applications.
Skeletal editing has emerged as a highly valuable strategy for the precise and efficient modification of cyclic frameworks. However, its application in divergent synthesis and domino reactions remains underexplored. In this study, we report an efficient domino reaction for the synthesis of benzothiophene-fused pyridazinone. These domino reactions encompass both skeletal editing and pyridine migration. Moreover, by modulating the substrate structure, we can achieve pyridine 1,2-migration, which proceeds through a ring-opening/ring-closing skeletal editing process rather than a direct shift between two nitrogen atoms, a conclusion supported by both controlled experiments and DFT calculations. Furthermore, based on DFT calculations, we can also achieve a potential pyridine 1,5-migration.
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Guo et al. (2026) studied this question.
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