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Efficient Syntheses of 123-Triazoloamide Derivatives Using Solid- and Solution-Phase Synthetic Approaches

机译:使用固相和固相合成方法高效合成123-三唑酰胺衍生物

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摘要

Efficient synthetic routes for the preparation of secondary and tertiary 1,2,3-triazoloamide derivatives were developed. A secondary α-1,2,3-triazoloamide library was constructed and expanded by a previously developed solid-phase synthetic route and a tertiary 1,2,3-triazoloamide library was constructed by a parallel solution-phase synthetic route. The synthetic routes rely on amide formation with secondary amines and chloro-acid chlorides; SN2 reaction with sodium azide; and the selective [3 + 2] Hüisgen cycloaddition with appropriate terminal alkynes. The target secondary and tertiary 1,2,3-triazoloamide derivatives were obtained with three-diversity points in excellent overall yields and purities using the reported solid- and solution-phase synthetic routes, respectively.
机译:开发了用于制备仲和叔1,2,3-三唑酰胺衍生物的有效合成途径。通过先前开发的固相合成方法构建并扩展了第二个α-1,2,3-三唑酰胺库,并通过并行溶液相合成方法构建了叔1,2,3-三唑酰胺库。合成途径依赖于与仲胺和氯酰氯形成酰胺。 SN2与叠氮化钠反应;以及带有适当末端炔烃的选择性[3 + 2]Hüisgen环加成反应。使用已报道的固相和溶液相合成路线,分别以三个多样性点获得了优异的总收率和纯度的目标二,1,2,3-三唑酰胺二级和三级衍生物。

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