The synthesis of some impurities of the cephalosporin antibiotics cefa
lexin and cefradine is described. These impurities which may be presen
t in commercial samples are formed during the semi-synthetic preparati
on of these antibiotics or upon their degradation. The preparation of
these compounds enables the validation of selective quantitative analy
tical methods, such as column liquid chromatography and thin layer chr
omatography.