The synthesis and characterization of some novel 5-chloro-2-(substituted alkoxy)-N-phenylbenzamide derivatives

To obtain biologically active compounds, the synthesis of some new derivatives with an o-hydroxybenzamide structure was performed. The ethyl esters 4–6 were obtained by the reaction of 5-chloro-2-hydroxy-N-phenylbenzamide and chloro-substituted acid ethyl esters 1–3 in ethyl methyl ketone. The obtai...

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Main Authors: IOANA M. C. IENAŞCU, ALFA X. LUPEA, IULIANA M. POPESCU, MIRABELA A. PĂDURE, ALINA D. ZAMFIR
Format: Article
Language:English
Published: Serbian Chemical Society 2009-08-01
Series:Journal of the Serbian Chemical Society
Subjects:
Online Access:http://www.shd.org.rs/JSCS/Vol74/No8/01_3881_4027.pdf
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spelling doaj-c8b2a17fc65b4168be7449e83ff7bdad2020-11-24T20:47:06ZengSerbian Chemical Society Journal of the Serbian Chemical Society0352-51392009-08-01748-9846855The synthesis and characterization of some novel 5-chloro-2-(substituted alkoxy)-N-phenylbenzamide derivativesIOANA M. C. IENAŞCUALFA X. LUPEAIULIANA M. POPESCUMIRABELA A. PĂDUREALINA D. ZAMFIRTo obtain biologically active compounds, the synthesis of some new derivatives with an o-hydroxybenzamide structure was performed. The ethyl esters 4–6 were obtained by the reaction of 5-chloro-2-hydroxy-N-phenylbenzamide and chloro-substituted acid ethyl esters 1–3 in ethyl methyl ketone. The obtained ethyl esters were condensed with hydrazine yielding the hydrazides 7–8. The hydrazones 11–14 were obtained by the reaction of the hydrazides and the chloro-substituted benzaldehydes 9–10. All the newly synthesized compounds were characterized by FTIR, 1H-NMR, 13C-NMR, MS and elemental analyses.http://www.shd.org.rs/JSCS/Vol74/No8/01_3881_4027.pdf5-chloro-2-(substituted alkoxy)-N-phenylbenzamide derivativesethyl estershydrazideshydrazonesO-substituted salicylanilides
collection DOAJ
language English
format Article
sources DOAJ
author IOANA M. C. IENAŞCU
ALFA X. LUPEA
IULIANA M. POPESCU
MIRABELA A. PĂDURE
ALINA D. ZAMFIR
spellingShingle IOANA M. C. IENAŞCU
ALFA X. LUPEA
IULIANA M. POPESCU
MIRABELA A. PĂDURE
ALINA D. ZAMFIR
The synthesis and characterization of some novel 5-chloro-2-(substituted alkoxy)-N-phenylbenzamide derivatives
Journal of the Serbian Chemical Society
5-chloro-2-(substituted alkoxy)-N-phenylbenzamide derivatives
ethyl esters
hydrazides
hydrazones
O-substituted salicylanilides
author_facet IOANA M. C. IENAŞCU
ALFA X. LUPEA
IULIANA M. POPESCU
MIRABELA A. PĂDURE
ALINA D. ZAMFIR
author_sort IOANA M. C. IENAŞCU
title The synthesis and characterization of some novel 5-chloro-2-(substituted alkoxy)-N-phenylbenzamide derivatives
title_short The synthesis and characterization of some novel 5-chloro-2-(substituted alkoxy)-N-phenylbenzamide derivatives
title_full The synthesis and characterization of some novel 5-chloro-2-(substituted alkoxy)-N-phenylbenzamide derivatives
title_fullStr The synthesis and characterization of some novel 5-chloro-2-(substituted alkoxy)-N-phenylbenzamide derivatives
title_full_unstemmed The synthesis and characterization of some novel 5-chloro-2-(substituted alkoxy)-N-phenylbenzamide derivatives
title_sort synthesis and characterization of some novel 5-chloro-2-(substituted alkoxy)-n-phenylbenzamide derivatives
publisher Serbian Chemical Society
series Journal of the Serbian Chemical Society
issn 0352-5139
publishDate 2009-08-01
description To obtain biologically active compounds, the synthesis of some new derivatives with an o-hydroxybenzamide structure was performed. The ethyl esters 4–6 were obtained by the reaction of 5-chloro-2-hydroxy-N-phenylbenzamide and chloro-substituted acid ethyl esters 1–3 in ethyl methyl ketone. The obtained ethyl esters were condensed with hydrazine yielding the hydrazides 7–8. The hydrazones 11–14 were obtained by the reaction of the hydrazides and the chloro-substituted benzaldehydes 9–10. All the newly synthesized compounds were characterized by FTIR, 1H-NMR, 13C-NMR, MS and elemental analyses.
topic 5-chloro-2-(substituted alkoxy)-N-phenylbenzamide derivatives
ethyl esters
hydrazides
hydrazones
O-substituted salicylanilides
url http://www.shd.org.rs/JSCS/Vol74/No8/01_3881_4027.pdf
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