Publication details

Evaluation of the stability of biologically active chlorinated arylcarbamoylnaphthalenylcarbamates by RP-HPLC

Authors

PINDJAKOVÁ Dominika HEGEDUŠ Marina VRÁBLOVÁ Lucia GONĚC Tomáš JAMPÍLEK Josef

Year of publication 2022
Type Article in Proceedings
Conference Proceedings of the 18th International Students Conference “Modern Analytical Chemistry”
MU Faculty or unit

Faculty of Pharmacy

Citation
Web http://web.natur.cuni.cz/analchem/isc/isc18.pdf
Keywords carbamates; HPLC; phenyl-based stationary phases; stability
Description The original carbamates with excellent antimicrobial activity derived from 1-hydroxy-N-(2,4,5-trichlorophenyl)-2-naphthamide were investigated for their stability. 2-[N-(2,4,5-Trichlorophenyl)- carbamoyl]naphthalen-1-yl ethyl carbamate with the weakest steric protection, i.e., with the expected highest degradability and two other carbamates with a more sterically protected carbamate bond (2-[N-(2,4,5-trichlorophenyl)carbamoyl]naphthalen-1-yl 2-phenylethyl carbamate and 2-[N-(2,4,5-trichlorophenyl)carbamoyl]- naphthalen-1-yl isopropyl carbamate), i.e., with the expected lower degradability, were chosen. The developed HPLC methods using chromatographic columns with phenyl-based stationary phases and acetonitrile:phosphate buffer (pH = 2.5) as the mobile phases provided sufficient resolution between the studied carbamates and expected degradant, pattern anilide.

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