首页> 外文期刊>Green Processing and Synthesis >Synthesis of pyrazolopyrldine and pyrazoloquinoline derivatives by one-pot, three-component reactions of arylglyoxals, 3-methyl-l-aryl-1H-pyrazol-5-amines and cyclic 1,3-dicarbonyl compounds in the presence of tetrapropylammonium bromide
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Synthesis of pyrazolopyrldine and pyrazoloquinoline derivatives by one-pot, three-component reactions of arylglyoxals, 3-methyl-l-aryl-1H-pyrazol-5-amines and cyclic 1,3-dicarbonyl compounds in the presence of tetrapropylammonium bromide

机译:用一锅,三组分反应的芳基唑吡ld喹啉和吡唑喹啉衍生物在四丙基溴化铵存在下通过芳基甘氨酸,3-甲基-1-芳基-1H-吡唑-5-胺和环1,3-二羰基化合物的三分反应

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摘要

Pyrazolopyridine and pyrazoloquinoline derivatives were obtained by a one-pot, three-component reaction of arylglyoxals, 3-methyl-l-aryl-lH-pyrazol-5-amines and cyclic 1,3-dicarbonyl compounds in the presence of tetrapropylammonium bromide at 80°C in water through Knoevenagel and Micheal reactions, followed by intramolecular condensation, unexpected dearoylation and oxidation. Mild reaction conditions, high yields, simplicity of work up procedure, starting materials availability and clean product formation are some of the main advantages of this synthetic strategy.
机译:通过在80℃下通过芳基甘氨酸,3-甲基-1-芳基-1H-吡唑-5-胺和环状1,3-二羰基化合物的单罐,三分组分反应获得吡唑吡啶和吡唑喹啉衍生物。 ℃通过Knoevenagel和Micheal反应,然后进行分子内缩合,意外的亲脂和氧化。 温和的反应条件,高收益率,工作过程简单,起始材料可用性和清洁产品形成是这种合成策略的一些主要优点。

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