FACILE SYNTHESIS OF CARBOXAMIDE-SUBSTITUTED 1,3,4-THIADIAZINES AND 5,6-DIHYDRO-4<i>H</i>-1,3,4-THIADIAZIN-5-OLS
DOI:
https://doi.org/10.1007/5019Ключевые слова:
5, 6-dihydro-4H-[1, 3, 4]thiadiazin-5-ols, oxamic acid thiohydrazides, phenacyl bromide, 1, 4-thiadiazines, cyclocondensationАннотация
Novel 2-carboxamide-substituted 1,3,4-thiadiazines and 5,6-dihydro-4H-1,3,4-thiadiazin-5-ols were synthesized by the reaction of oxamic acid thiohydrazides with phenacyl bromides. This reaction was performed using an equimolar mixture of thiohydrazide and α-bromoacetophenones in methanol under basic conditions. The ratio of products obtained in the cyclocondensation was found to be strongly dependent on the substitution pattern and reaction conditions.
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Опубликован
2019-07-23
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Оригинальные статьи