Alkoxide-catalyzed ring-opening of a novel homosaccharin derivative: Synthesis of potent, selective P3-lactam thrombin inhibitors containing P4- o-alkoxycarbonylbenzylsulfonamide residues

Article abstract of DOI:10.1016/S0960-894X(98)00667-2

A series of lactam derivatives 1b-g featuring P₄-o- alkoxycarbonylbenzylsulfonamide residues along with the potential P₄- homosaccharin prodrug candidate 1h was prepared in order to probe the thrombin S₃ specificity pocket. The synthesis and alkoxide-catalyzed ring opening of the novel homosaccharin intermediate 7 followed by subsequent elaboration delivered the targets 1b-h which were potent and selective thrombin inhibitors. The design, synthesis, and biological activity of these targets will be presented.