Synthesis reports 6-aryl-9-phenyl-5H-imidazo compounds from phenacyl bromides, indicating new chemical methods.
2-(2-Benzoyl-1H-imidazol-1-yl)-1-arylethanones were obtained by alkylation of 2-benzoylimidazole with phenacyl bromides; their cyclization with hydrazine hydrate leads to the formation of previously undescribed 6-aryl-9-phenyl-5H-imidazo[2,1-d][1,2,5]triazepines. The reduction of the latter with sodium borohydride in a dioxane medium leads to the production of 6-aryl-9-phenyl-6,7-dihydro-5H-imidazo[2,1-d][1,2,5]triazepines.
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D.A. LOMOV (2025) studied this question.
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