首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >Facile and Convenient Syntheses of Fluorine-Containing Pyrido(2,3-h)-quinazolines and 1,7-Phenanthrolines by Condensation Reactions of 6,8-Bis(trifluoroacetyl)quinoIin-5-amine with Carbonyl Compounds
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Facile and Convenient Syntheses of Fluorine-Containing Pyrido(2,3-h)-quinazolines and 1,7-Phenanthrolines by Condensation Reactions of 6,8-Bis(trifluoroacetyl)quinoIin-5-amine with Carbonyl Compounds

机译:通过6,8-双(三氟乙酰基)喹啉-5-胺与羰基化合物的缩合反应轻松合成含氟的吡啶并(2,3-h)-喹唑啉和1,7-菲咯啉

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摘要

6,8-Bis(trifluoroacetyl)quinolin-5-amine reacted easily with various aldehydes in the presence of aqueous ammonia to afford trifluoromethylated pyrido[2,3-h]quinazoline derivatives and 1,7-phenanthroline derivatives in good to excellent yields. Under almost the same conditions, the use of ketones instead of aldehydes gave 1,7-phenanthroline derivatives selectively, except in the case of cyclohexanone.
机译:在氨水存在下,6,8-双(三氟乙酰基)喹啉-5-胺容易与各种醛反应,以良好的收率获得了三氟甲基化的吡啶并[2,3-h]喹唑啉衍生物和1,7-菲咯啉衍生物。在几乎相同的条件下,使用酮代替醛可选择性地得到1,7-菲咯啉衍生物,但环己酮除外。

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