The synthesis of amide prodrugs of some 2-arylpropionic acids (ibuprof
en, naproxen, diclofenac and ketorolac) and the enantiomeric separatio
n of these compounds are reported in this paper. The compounds were pr
epared from the corresponding 2-arylpropionic acids and (R-(-)-2-amino
-1-butanol in the presence of N,N'-dicyclohexylcarbodiimide (DCC). Ena
ntiomers were separated by preparative chromatography or crystallisati
on. The structure were confirmed by infrared, nuclear magnetic resonan
ce and elementary analysis. The compounds prepared in the study have s
ignificant analgesic activity.