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Efficient Synthesis Of Enaminones And Cyclic Imides Using Ammonium Acetate Under Microwave Conditions

机译:微波条件下乙酸铵高效合成烯胺酮和环酰亚胺

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Enaminones are versatile intermediates for the synthesis of many natural and pharmaceutical compounds. We have developed an efficient method for their synthesis under microwave irradiation. A number of these enaminones were synthesized in 73-91% yields within few minutes from 1,3-diones and ammonium acetate. Further, reactions of the enaminones with anhydrides under microwave conditions resulted in the formation of enone-imides in very good yields. The process is simple, quick, and high yielding. Cyclic Imides were also obtained in high yields under similar conditions, upon reactions of ammonium acetate with various anhydrides. A library of the cyclic imides was synthesized; the process was applied for the synthesis of thalidomide analogues.
机译:烯胺酮是用于合成许多天然和药物化合物的通用中间体。我们已经开发了一种在微波辐射下合成它们的有效方法。这些烯胺酮中的许多都是在1,几分钟内由1,3-二酮和乙酸铵以73-91%的产率合成的。此外,在微波条件下烯胺酮与酸酐的反应导致烯酮酰亚胺的形成,产率很高。该过程简单,快速且产率高。乙酸铵与各种酸酐反应后,在相似条件下也可以高收率获得环状酰亚胺。合成了环状酰亚胺的文库;该方法用于沙利度胺类似物的合成。

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