Анелювання 1,2,4-триазинового ядра до 2,3-бензодіазепіну

A one-pot, stepwise method for the annelation of the 1,2,4-triazine core to the seven-membered 2,3-benzodiazepine ring via the interaction of the corresponding 2,3-benzodiazepin-1-yl- or 2,3-benzodiazepin-4-ylhydrazines with α-ketoesters has been developed. It has been found that a stepwise formatio...

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Збережено в:
Бібліографічні деталі
Дата:2025
Автори: Bohdan, Natalia M., Shuvakin, Serhii I., Nechaieva, Diana S., Suikov, Sergii Yu., Bohza, Serhii L.
Формат: Стаття
Мова:Англійська
Опубліковано: National University of Pharmacy 2025
Теми:
Онлайн доступ:https://ophcj.nuph.edu.ua/article/view/327856
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Назва журналу:Journal of Organic and Pharmaceutical Chemistry

Репозитарії

Journal of Organic and Pharmaceutical Chemistry
Опис
Резюме:A one-pot, stepwise method for the annelation of the 1,2,4-triazine core to the seven-membered 2,3-benzodiazepine ring via the interaction of the corresponding 2,3-benzodiazepin-1-yl- or 2,3-benzodiazepin-4-ylhydrazines with α-ketoesters has been developed. It has been found that a stepwise formation of an azomethine intermediate followed by solvent replacement and subsequent cyclization enables the desired compounds to be obtained in high yields. Derivatives of a new heterocyclic system of [1,2,4]triazino[3,4-a][2,3]benzodiazepine have been synthesized.