| abstract |
Procedure for preparing amidoxime derivatives, of the general formula I and their pharmaceutically acceptable salts ***(See formula I), in which R2 is hydrogen or alkyl having from one to five carbon atoms; R3 is alkyl having from one to five carbon atoms, cycloalkyl, or phenyl optionally substituted with hydroxyl or phenyl; or R2 and R3 together form a five to eight membered ring optionally also containing other heteroatoms and/or fused to another ring. |