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Synthesis, Chiral Resolution and Enantiomers Absolute Configuration of 4-Nitropropranolol and 7-Nitropropranolol.

Authors :
Sparaco, Rosa
Scognamiglio, Antonia
Corvino, Angela
Caliendo, Giuseppe
Fiorino, Ferdinando
Magli, Elisa
Perissutti, Elisa
Santagada, Vincenzo
Severino, Beatrice
Luciano, Paolo
Casertano, Marcello
Aiello, Anna
De Nucci, Gilberto
Frecentese, Francesco
Source :
Molecules; Jan2023, Vol. 28 Issue 1, p57, 15p
Publication Year :
2023

Abstract

We recently identified 6-nitrodopamine and other nitro-catecholamines (6-nitrodopa, 6-nitroadrenaline), indicating that the endothelium has the ability to nitrate the classical catecholamines (dopamine, noradrenaline, and adrenaline). In order to investigate whether drugs could be subject to the same nitration process, we synthesized 4-nitro- and 7-nitropropranolol as probes to evaluate the possible nitration of the propranolol by the endothelium. The separation of the enantiomers in very high yields and excellent enantiopurity was achieved by chiral HPLC. Finally, we used Riguera's method to determine the absolute configuration of the enantiomers, through double derivatization with MPA and NMR studies. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14203049
Volume :
28
Issue :
1
Database :
Complementary Index
Journal :
Molecules
Publication Type :
Academic Journal
Accession number :
161186937
Full Text :
https://doi.org/10.3390/molecules28010057