Analyses by GC-MS and GC-MS-MS of the hantzsch synthesis products using hydroxy- and methoxy-aromatic aldehydes

Nunez-Vergara, LJ; Navarrete-Encina, PA; SALAS, S.; Conde, B; Carbajo, J; Squella, JA; Camargo C.

Abstract

EI mass spectra of products of the dihydropyridine Hantzsch synthesis using hydroxy and methoxy aldehydes as starting materials are reported. The reaction products (C-4 hydroxy- and methoxyphenyl-1,4-dihydropyridines and chromeno[3,4,c]-pyridines) were derivatized with N-methyl-N-(trimethylsilyl)-trifluoracetamide to be analyzed by gas chromatographic techniques. Fragmentation pathways for 1,4-dihydropyridines and chromeno-pyridines are proposed. The study provides (mainly through MS-MS technique) useful data for the confirmation of the structure of the compounds and also is a valuable tool for further analytical purposes to follow both photostability and reactivity studies with free radicals for these types of compounds. © 2007.

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Título según WOS: Analyses by GC-MS and GC-MS-MS of the hantzsch synthesis products using hydroxy- and methoxy-aromatic aldehydes
Título según SCOPUS: Analyses by GC-MS and GC-MS-MS of the hantzsch synthesis products using hydroxy- and methoxy-aromatic aldehydes
Título de la Revista: JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS
Volumen: 44
Número: 1
Editorial: Elsevier
Fecha de publicación: 2007
Página de inicio: 236
Página final: 242
Idioma: English
URL: http://linkinghub.elsevier.com/retrieve/pii/S0731708507000647
DOI:

10.1016/j.jpba.2007.01.025

Notas: ISI, SCOPUS