The synthesis of the protected glycopeptide Z-Thr(tBu)-Ala-Thr-[α-D-Gal(Bzl)4 ]-Thr(tBu)-NHNH-Boc was performed in solution by a stepwise coupling strategy. Fmoc-Thr[(α+β)-D- Gal(Bzl)4]-0Su, obtained from the reducing sugar and the protected aminoacid by the trifluoromethanesulfonic anhydride procedure, was reacted with H-Thr(tBu)-NHNH-Boc. The two diastereoisomers of the resulting glycosylated dipeptide