4.6 Article

Efficient Syntheses of 1,2,3-Triazoloamide Derivatives Using Solid- and Solution-Phase Synthetic Approaches

Journal

MOLECULES
Volume 20, Issue 11, Pages 19984-20013

Publisher

MDPI AG
DOI: 10.3390/molecules201119673

Keywords

1,2,3-triazoloamide; solid-phase synthesis; solution-phase synthesis

Funding

  1. National Research Foundation of Korea (NRF) from the Basic Science Research Program, the Ministry of Science, ICT and Future Planning, Republic of Korea [NRF-2014R1A1A1037635, NRF-2014R1A2A1A11052798]
  2. Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI) - Ministry of Health & Welfare, Republic of Korea [HI11C1300(A111345)]

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Efficient synthetic routes for the preparation of secondary and tertiary 1,2,3-triazoloamide derivatives were developed. A secondary -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; S(N)2 reaction with sodium azide; and the selective [3 + 2] Huisgen 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.

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