Acetylation of methyl 5-amino-1H-[1,2,4]triazole-3-carboxylate

Autor:	A, Dzygiel, E, Masiukiewicz, B, Rzeszotarska
Rok vydání:	2002
Předmět:	Bromides Magnetic Resonance Spectroscopy Nitrogen Potassium Compounds Carboxylic Acids Temperature Acetylation Triazoles Gas Chromatography-Mass Spectrometry Kinetics Models Chemical Spectroscopy Fourier Transform Infrared Dimethyl Sulfoxide Chromatography High Pressure Liquid
Zdroj:	Acta biochimica Polonica. 48(4)
ISSN:	0001-527X
Popis:	Acetylation with acetic anhydride of methyl 5-amino-1H-[1,2,4]triazole-3-carboxylate, one of the hetareneamino acids, was studied using HPLC, H NMR, FTIR and GC-MS. The compound has a significantly decreased susceptibility to acetylation compared to 5-amino-1H-[1,2,4]triazole itself. Two isomeric diacetylated products were found.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=pmid________::e5e27cbf2ac8778bcb81e076fbfa2d9d https://pubmed.ncbi.nlm.nih.gov/11995987 Zobrazit plný text záznamu