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The Use of 4-(Bromomethylene)-5,5-dimethyl-1,3-dioxolan-2-one as “Masked” α-Bromo-α'-Hydroxy Ketone in the Synthesis of Heterocyclic Systems
Authors:A A Bogolyubov  N B Chernysheva  V V Semenov
Institution:(1) N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Russia
Abstract:4-(Bromomethylene)-5,5-dimethyl-1,3-dioxolan-2-one was obtained on the basis of the readily obtainable 4-methylene-5,5-dimethyl-1,3-dioxolan-2-one. It forms 2-imidazo1,2-a]pyridin-2-yl-2-propanol with 2-aminopyridine, 11a-hydroxy-1,1-dimethyl-3-oxo-1,5,11,11a-tetrahydro1,3]oxazolo3,4-a]pyrido1,2-d]-10-pyrazinium bromide with 2-(aminomethyl)pyridine, and the corresponding derivative of 4-hydroxyoxazolidin-2-one with 2-(3,4-dimethoxyphenyl)ethylamine. The last product was converted by intramolecular amidoalkylation without isolation into 10b-(bromomethyl)-8,9-dimethoxy-1,1-dimethyl-1,5,6,10b-tetrahydro1,3]oxazolo3,4-a]isoquinolin-3-one.
Keywords:4-bromo-4-(bromomethyl)-5  5-dimethyl-1  3-dioxolan-2-one  11a-hydroxy-1  1-dimethyl-3-oxo-1  5  11  11a-tetrahydro[1  3]oxazolo[3  4-a]pyrido[1  2-d]-10-pyrazinium bromide  4-(bromomethylene)-5  5-dimethyl-1  3-dioxolan-2-one  10b-(bromomethyl)-8  9-dimethoxy-1  1-dimethyl-1  5  6  10b-tetrahydro[1  3]oxazolo[4  3-a]isoquinolin-3-one  2-imidazo[1  2-a]pyridin-2-yl-2-propanol  intramolecular amidoalkylation
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