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Synthesis of new compounds of the aryloxyaminopropanol type and their HPLC enantioseparation Cover

Synthesis of new compounds of the aryloxyaminopropanol type and their HPLC enantioseparation

Open Access
|Dec 2013

Abstract

This article describes a preparation of some new compounds of the aryloxyaminopropanol type derived from 4-hydroxyphenylpropan- 1-one with phenylamino, cyclohexylamino and isobutylamino group in the hydrophilic part and methoxymethyl or ethoxymethyl substituent in the lipophilic part of the molecule. The purity of the prepared compounds was checked by thinlayer chromatography and the structure was confirmed on the basis of interpretation of the IR, UV, 1H NMR and 13C NMR spectra. An enantioseparation of the prepared compounds was performed by using high-performance liquid chromatography on an amylase tris(3,5-dimethylphenylcarbamate) (Chiralpak AD) and native teicoplanin (Chirobiotic T). The chromatographic results such as retention, separation and resolution factors have shown that Chiralpak AD is more suitable for enantioseparation of some of the prepared compounds.

Language: English
Page range: 37 - 42
Published on: Dec 31, 2013
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
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© 2013 Čižmáriková R., Némethy A., Valentová J., Hroboňová K., Adamcová K., published by Comenius University in Bratislava, Faculty of Pharmacy
This work is licensed under the Creative Commons License.