We investigated the S‐arylation of 5,4‐disubstituted 2,4‐dihydro‐3 H ‐1,2,4‐triazole‐3‐thiones under ligand‐free Cu(0) catalysis employing Ullmann‐type reaction conditions. We determined optimal reaction conditions and assessed the impact of substituents in the arylating agent on the reaction progress. Notably, the presence of an electron‐withdrawing group (EWG) in the aryl halide facilitated the reaction even without a catalyst. In particular, an EWG in the para position of the aromatic ring exerted a directing effect on the leaving group, regardless of the halogen present.
No takes yet. Share an insight, caveat, or question.
Petrosyan et al. (2024) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: