化学
哒嗪
吡啶
环加成
掉期(金融)
组合化学
分子
小分子
立体化学
咪唑吡啶
支化(高分子化学)
衍生工具(金融)
核嬗变
呋喃
化学合成
作者
Malte Haring,Debkanta Bhattacharya,Pengwei Xu,David Ben Fadhla,Constantin G. Daniliuc,Armido Studer
摘要
Skeletal editing has emerged as a powerful strategy for the late-stage diversification of drug molecules. Recently, transmutation of widely available pyridine motifs into less explored pyridazines via C-to-N single-atom swaps has garnered attention. Here, we report a CN-to-NN atom-pair swap to transmute pyridopyrimidones, dienamines that are generated by temporary dearomatization of pyridines, into pyridazines in a one- or two-pot dearomatization-[4 + 2]-retro-[4 + 2]-cycloaddition-aromatization sequence with 4-phenyl-1,2,4-triazoline-3,5-dione as the N═N dienophile. Crucially, this transformation only works with pyridopyrimidones and not with the previously established oxazinopyridine-based temporary dearomatization strategy; for the latter, the driving force for the retro-[4 + 2] cycloaddition is insufficient, since the formation of the target product itself does not facilitate a gain in arene resonance energy. Pyridopyrimidones provide such a driving force through the formation of an aromatic pyrimidone byproduct. The synthetic utility of the method is demonstrated through late-stage skeletal editing of complex molecules and a 7-mmol large-scale reaction.
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