Synthesis and reactivity of 2-(furan-2-yl)benzo[e][1,3]benzothiazole
- Авторы: Aleksandrov А.1, El’chaninov М.1
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Учреждения:
- Platov South-Russian State Polytechnic University
- Выпуск: Том 87, № 8 (2017)
- Страницы: 1716-1720
- Раздел: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/220972
- DOI: https://doi.org/10.1134/S1070363217080138
- ID: 220972
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Аннотация
N-(1-Naphthyl)furan-2-carboxamide was synthesized by the coupling of naphthalen-1-amine with furan-2-carbonyl chloride in propan-2-ol and then treated with excess P2S5 in anhydrous toluene to obtain the corresponding thioamide. The latter was oxidized with potassium ferricyanide in an alkaline medium by the Jakobson procedure to synthesize 2-(furan-2-yl)benzo[e][1,3]benzothiazole which was subjected to electrophilic substitution reactions: nitration, bromination, formylation, and acylation.
Об авторах
А. Aleksandrov
Platov South-Russian State Polytechnic University
Автор, ответственный за переписку.
Email: aaanet1@yandex.ru
Россия, pr. Prosveshcheniya 132, Novocherkassk, 346428
М. El’chaninov
Platov South-Russian State Polytechnic University
Email: aaanet1@yandex.ru
Россия, pr. Prosveshcheniya 132, Novocherkassk, 346428
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