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A convenient synthesis of new NSAID esters containing amino acid, urea and amide moieties Cover

A convenient synthesis of new NSAID esters containing amino acid, urea and amide moieties

Open Access
|Oct 2013

Abstract

A convenient synthetic method for the preparation of novel NSAID twin esters 6a-i containing amino acid residue, urea and amide moieties has been developed. The synthetic pathway applied for the preparation of target compounds and key intermediates 1-benzotriazolecarboxylic acid chloride (1), NSAID benzotriazolides 2a-c and N-(1-benzotriazolecarbonyl)-amino acids 3a-d involved benzotriazole as a synthetic auxiliary. The final preparation step of esters 6a-i included the solvent-free reaction of compounds 2a-c with amino acid derivatives 5a-g, bearing two hydroxyl groups, one at each terminal, beside urea and amide functionalities.

DOI: https://doi.org/10.2478/acph-2013-0023 | Journal eISSN: 1846-9558 | Journal ISSN: 1330-0075
Language: English
Page range: 409 - 418
Published on: Oct 22, 2013
Published by: Croatian Pharmaceutical Society
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year
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© 2013 Ivana Perković, Zrinka Rajić Džolić, Branka Zorc, published by Croatian Pharmaceutical Society
This work is licensed under the Creative Commons License.