Molecular Design and Synthesis, Department of Chemistry, KU Leuven, 3001 Leuven, Belgium.
Molecules. 2021 Jan 22;26(3):581. doi: 10.3390/molecules26030581.
4-Sulfonyl-1,2,3-triazole scaffolds possess promising bioactivities and applications as anion binders. However, these structures remain relatively unexplored and efficient synthetic procedures for their synthesis remain desirable. A practical room-temperature, aerobic copper-catalyzed three-component reaction of aromatic ketones, sodium sulfinates, and azides is reported. This procedure allows for facile access to 4-sulfonyl-1,5-disubstituted-1,2,3-triazoles in yields ranging from 34 to 89%. The reaction proceeds via a sequential aerobic copper(II)chloride-catalyzed oxidative sulfonylation and the Dimroth azide-enolate cycloaddition.
4-磺酰基-1,2,3-三唑骨架具有有前途的生物活性和作为阴离子结合物的应用。然而,这些结构仍然相对未被探索,并且需要有效的合成方法来合成它们。本文报道了一种实用的室温、有氧条件下铜催化的芳香酮、亚磺酸钠和叠氮化物的三组分反应。该方法可以方便地得到 4-磺酰基-1,5-二取代-1,2,3-三唑,产率为 34%至 89%。反应通过顺序有氧氯化铜(II)催化的氧化磺酰化和 Dimroth 叠氮化物烯醇化物环加成进行。