Synthesis and reactivity of 2-(furan-2-yl)benzo[e][1,3]benzothiazole
- 作者: Aleksandrov А.1, El’chaninov М.1
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隶属关系:
- Platov South-Russian State Polytechnic University
- 期: 卷 87, 编号 8 (2017)
- 页面: 1716-1720
- 栏目: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/220972
- DOI: https://doi.org/10.1134/S1070363217080138
- ID: 220972
如何引用文章
详细
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.
作者简介
А. Aleksandrov
Platov South-Russian State Polytechnic University
编辑信件的主要联系方式.
Email: aaanet1@yandex.ru
俄罗斯联邦, pr. Prosveshcheniya 132, Novocherkassk, 346428
М. El’chaninov
Platov South-Russian State Polytechnic University
Email: aaanet1@yandex.ru
俄罗斯联邦, pr. Prosveshcheniya 132, Novocherkassk, 346428
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