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In this paper the synthesis of a library of new 1, 4-disubstituted 1, 2, 3-triazoles 1, with a variety of additional functional groups on its structure, from an in situ generated benzyl azide 2 and different alkynes and dialkynes 3 is reported. Optimal experimental conditions were established for the conventional click chemistry and for the microwave-assisted synthesis of these 1, 2, 3-triazoles. Comparing the results it was concluded that under microwave-assisted conditions the products are obtained in higher yields in shorter times.