The reactions of 1-Amino-pyrimidine derivatives (1) and some 1,3-dicarbonyl compounds (2) were realized in the presence of p-toluensulfonic acid catalyst to give convenient enamine (3) and/or imine derivatives (4). In the same way, the enamine (5) and/or imine derivatives (6) were synthesized using (1) and 1,3-indanedione which is one of the different 1,3-dicarbonyl compounds. The molecular structures of all the prepared compounds were determined by H-1-nmr, C-13-nmr, i.r. spectra and elemental analyses, and were drawn by taking imine-enamine tautomerism into account.