One-pot multicomponent click synthesis of some novel 1,4-disubstituted-1H-1,2,3-triazoles from alkenes

A facile and one-pot multicomponent synthesis of novel 1,4-disubstituted-1H-1,2,3-triazoles from alkenes at room temperature is reported. At the first step, in the presence of I2/NaN3 reagents, various alkenes were converted to the corresponding azido iodides and in the next step, the reaction of these compounds with phenylacetylene in the presence of catalytic amount of sodium ascorbate/ CuSO4 afforded regioselective synthesis of 1,4-disubstituted-1H-1,2,3-triazoles in short times and at good to high yields. This greenapproach has several advantages such as short reaction times, clean reaction profiles, and simple experimental and workupprocedures. All the products were fully characterized by 1HNMR, 13CNMR, IR and CHN analysis

Keywords:

Click chemistry , styrene , regioselective , sodium azide , triazole , azido iodination