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Efficient solid-phase synthesis of a library of imidazo[1,2-a]pyridine-8-carboxamides

机译:咪唑并[1,2-a]吡啶-8-羧酰胺库的高效固相合成

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摘要

A versatile method for the solid-phase synthesis of imidazo[1,2-a]pyridine-based derivatives, imidazo[1,2-a]pyridine-8-carboxamides, has been developed. They were obtained by treatment of the amino group of the polymer-bound 2-aminonicotinate with different alpha-haloketones, followed by halogenation at the 3-position of the polymer-bound imidazo[1,2-a]pyridine. The derived polymer-bound imidazo[1,2-a]pyridines 5, 6, and 7 were finally cleaved from the solid-support with an excess of primary or secondary amines. The final crude products were purified from excess amines by solid-supported liquid-liquid extraction (SLE).
机译:已开发出一种用于固相合成咪唑并[1,2-a]吡啶的衍生物咪唑并[1,2-a]吡啶-8-羧酰胺的通用方法。通过用不同的α-卤代酮处理聚合物结合的2-氨基烟酸酯的氨基,然后在聚合物结合的咪唑并[1,2-a]吡啶的3-位卤化,得到它们。最后,用过量的伯胺或仲胺从固相载体上裂解衍生的与聚合物结合的咪唑并[1,2-a]吡啶5、6和7。最终的粗产物通过固相支持的液-液萃取(SLE)从过量的胺中纯化。

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