The protected hexapeptide sequence (5-10) of human fibrinopeptide-A, BOC-Glu(OBzl)-Gly-Asp(OBzl)-Phe-Leu-Ala-OMe (BOC = Me3CO2C, Bzl = PhCH2) (I), was synthesized using the mixed anhydride (MA), dicyclohexylcarbodiimide (DCC), 2,4,5-trichlorophenyl ester (OCP) and pentachlorophenyl ester (OPCP) methods. The OCP method was applicable only after the tripeptide stage. The overall yield of I from the DCC, MA and OPCP methods was 23.2, 20.5 and 18.7%, resp