Abstract
The quinazoline derivatives (1–6) are potential antitumour preparations. The selectivity of the TLC parameters of six new quinazoline derivatives (1–6) has been investigated on silica gel 60 F 254. Optimisation of the retention and efficiency of these compounds was performed by changing the mixture of eluents and the concentration of modifier in organic diluent (v/v). Chromatograms were developed in the DS chamber and the substances were detected using UV light (λ 254 nm). The best separation parameters for compounds 1–3 were obtained with chloroform:ethyl acetate [5% (v/v)] as a mobile phase and for compounds 4–6 with ethyl acetate:acetonitrile [65% (v/v)] as a mobile phase.
Acknowledgment
Analytical research is supported by Medical University of Łódź, Poland (grant no. 507 13 028).