Abstract
A series of S-substituted 2-thioadenines (VII) and S, 9-di-substituted 2-thioadenines (VIII) were prepared by direct alkylation of 2-thioadenine (IV). Among the compounds synthesized, 2-cyclopentylthio-9-methyladenine (VIII7), 2-cyclopentylthio-9-cyclopentyl-adenine (VIII20) and 2-[2-(4-benzylpiperazino) ethyl] thio-9-[2-(4-benzylpiperazino) ethyl]-adenine (VIII22) were inhibitory against adenosine 5'-diphosphate induced platelet aggregation but these were less potent than adenosine.