Approach to the synthesis of new analogue of sildenafil towards palladium-catalyzed 3-methylsulfanyl-1,2,4-triazine - boronic acid cross coupling
Abstract
In the search for more potent and selective PDE5 inhibitors, approach to the synthesis of new sildenafil analogue 2 characterized by the presence of the pyrazolo[4,3-e][1,2,4]triazine core and ethylamino group in the 2’ position on the phenyl ring was designed.
Keywords
sulfonamides, 1H-pyrazolo[4,3-e][1,2,4]triazine, biological activity, PDE5 inhibitor
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