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首页> 外文期刊>Journal of sulfur chemistry >A convenient [hydroxy(tosyloxy)iodo]benzene-mediated one-pot synthesis of 2-arylimidazo[2,1-b]benzothiazoles
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A convenient [hydroxy(tosyloxy)iodo]benzene-mediated one-pot synthesis of 2-arylimidazo[2,1-b]benzothiazoles

机译:方便的[羟基(甲苯磺酰氧基)碘]苯介导的一锅合成2-芳基咪唑[2,1-b]苯并噻唑

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摘要

Several 2-arylimidazo[2,1-b]benzothiazoles (4) have been conveniently synthesized in one-pot reactions via alpha-tosyloxylation of enolizable ketones (1) using [hydroxy(tosyloxy)iodo]benzene 2 in acetonitrile, followed by treatment with 2-amino-6-(substituted)benzothiazoles (3). The present protocol offers several advantages towards general access of 2-arylimidazo[2,1-b]benzothiazoles, including an intriguing alternative to the literature protocols, a readily available nontoxic reagent, operational simplicity and an environmentally benign procedure.
机译:通过在乙腈中使用[羟基(甲苯磺酰基氧基)碘]苯2进行可烯化酮(1)的α-甲苯磺酰氧基化反应,可以在一锅反应中方便地合成了几种2-芳基咪唑[2,1-b]苯并噻唑(4),然后进行处理用2-氨基-6-(取代的)苯并噻唑(3)。本方案为2-芳基咪唑并[2,1-b]苯并噻唑的普遍使用提供了若干优点,包括对文献方案的一种吸引人的选择,一种容易获得的无毒试剂,操作简便和对环境有益的程序。

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