Synthesis and reactivity of 2-(furan-2-yl)benzo[e][1,3]benzothiazole
- Авторлар: Aleksandrov А.1, El’chaninov М.1
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Мекемелер:
- Platov South-Russian State Polytechnic University
- Шығарылым: Том 87, № 8 (2017)
- Беттер: 1716-1720
- Бөлім: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/220972
- DOI: https://doi.org/10.1134/S1070363217080138
- ID: 220972
Дәйексөз келтіру
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.
Авторлар туралы
А. Aleksandrov
Platov South-Russian State Polytechnic University
Хат алмасуға жауапты Автор.
Email: aaanet1@yandex.ru
Ресей, pr. Prosveshcheniya 132, Novocherkassk, 346428
М. El’chaninov
Platov South-Russian State Polytechnic University
Email: aaanet1@yandex.ru
Ресей, pr. Prosveshcheniya 132, Novocherkassk, 346428