TLC and HPLC Separation of Positional Isomers of Alkylesters of 2-, 3-, 4- {2-Hydroxy-3-
-[(4-diphenylmethyl)piperazine-1-yl]propoxy}phenylcarbamic Acid and Their Lipo-Hydrophilic
Properties
OPATŘILOVÁ R., BLEŠOVÁ M., CSÖLLEI J.
Ústav chemických léčiv Farmaceutické fakulty Veterinární a farmaceutické univerzity, Brno |
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Summary:
The paper deals with chromatographic separations of newly prepared substances, aryloxyaminopropanol
derivatives. The derivatives represent three homological series of four carbons and four
groups of positional isomers (methyl- to butyl- in positions 2-, 3, and 4-). Thin-layer adsorption
chromatography employed the foil Silufol® UV 254 as the stationary phase and partition chromatography,
commercially produced glass plates DC Fertigplatten MERCK RP-8 F254 S. High-performance
liquid chromatography was used to separate positional isomers on the column SupelkosilTM
ABZ+PLUS. The mobile phase was methanol and acetonitrile in graded rations with water and
various flow rates of the mobile phase were tested. Partition chromatography, determination of
partition coefficient in the system octanol-water, and the values of capacity factors k’ of the
substances was employed to evaluate their lipophilicity.
Key words:
HPLC – TLC – positional isomers – aryloxyaminopropanol – lipophilicity
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