首页> 外文期刊>Molecules >Efficient Syntheses of 1,2,3-Triazoloamide Derivatives Using Solid- and Solution-Phase Synthetic Approaches
【24h】

Efficient Syntheses of 1,2,3-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1,2,3-三唑酰胺衍生物

获取原文
           

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1,2,3-三唑酰胺叔库。合成途径依赖于与仲胺和氯酰氯形成酰胺。 S N 2与叠氮化钠的反应;以及带有适当末端炔烃的选择性[3 + 2]Hüisgen环加成反应。使用所报道的固相和溶液相合成路线,分别以优异的总收率和纯度获得具有三个多样性点的目标1,2,3-三唑酰胺二级和三级衍生物。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号