Acta Pharmaceutica, Vol. 63 No. 3, 2013.
Kratko priopćenje
https://doi.org/10.2478/acph-2013-0023
A convenient synthesis of new NSAID esters containing amino acid, urea and amide moieties
IVANA PERKOVIĆ
; Faculty of Pharmacy and Biochemistry, University of Zagreb, Zagreb, Croatia
ZRINKA RAJIĆ DŽOLIĆ
; Faculty of Pharmacy and Biochemistry, University of Zagreb, Zagreb, Croatia
BRANKA ZORC
orcid.org/0000-0003-4355-8816
; Faculty of Pharmacy and Biochemistry, University of Zagreb, Zagreb, Croatia
Sažetak
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.
Ključne riječi
NSAID; ester; amino acid; benzotriazole; urea; amide
Hrčak ID:
102049
URI
Datum izdavanja:
30.9.2013.
Posjeta: 2.188 *