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Molecules ; 20(11): 19984-20013, 2015 Nov 05.
Article in English | MEDLINE | ID: mdl-26556332

ABSTRACT

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.


Subject(s)
Amines/chemistry , Chemistry Techniques, Synthetic , Amines/chemical synthesis , Nuclear Magnetic Resonance, Biomolecular , Solid-Phase Synthesis Techniques , Spectroscopy, Fourier Transform Infrared
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