A series of eleven butanediamine analogues, of which nine were new, were synthesized by the nucleophilic substitution of aromatic amines and benzylamines with maleic anhydride and tested on four yeast strains ofCandidaspecies using the broth microdilution method. Compounds3aand3cwith an unsubstituted phenyl ring and a 3-methoxyphenyl ring, respectively, are the most active against the fungal species with MIC values ranging from 20.2 to 80.6 μM forC. albicansandC. parapsilosisand 178.5 and 161.2 μM forC. krusei, respectively.