Demonstrates a novel method to synthesize hydrazine derivatives, highlighting its practicality and eco-friendliness.
We developed a facile visible-light-induced radical C–N coupling reaction to synthesize hydrazine derivatives. The reaction between azodicarboxylates and 2,3-dihydroquinazolin-4(1 H )-ones can be carried out readily at room temperature and is free of any extra photosensitizers and additives. The yields of the target products ranged from 54% to 99%. This method is compatible with a wide range of substrates and functional groups. The practicality of the method is demonstrated through gram-scale synthesis and further product elaboration. Radical trapping experiments are consistent with a radical pathway. Taken together, this method provides a mild and environmentally friendly way to prepare hydrazines and valuable nitrogen-containing intermediates used in medicine.
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Han et al. (2026) studied this question.
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