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Iodine Mediated Annulation of Triethylamine, Aldehydes and 2-Aminopyridines for the Synthesis of 3-Formyl-Imidazo [1,2-a]pyridine Derivatives
Advanced Synthesis & Catalysis ( IF 4.4 ) Pub Date : 2024-06-27 , DOI: 10.1002/adsc.202400473 Wenqing Zhang 1 , Lihong Shen 2 , Jun Zhang 1
中文翻译:
碘介导的三乙胺、醛和 2-氨基吡啶环化用于合成 3-甲酰基-咪唑并[1,2-a]吡啶衍生物
更新日期:2024-06-27
Advanced Synthesis & Catalysis ( IF 4.4 ) Pub Date : 2024-06-27 , DOI: 10.1002/adsc.202400473 Wenqing Zhang 1 , Lihong Shen 2 , Jun Zhang 1
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With triethylamine as a synthon, an alternative method for the synthesis of 3-formyl imidazo[1,2-a]pyridines has been accomplished from aldehydes, and 2-aminopyridines. The reaction proceeded via iodine-catalyzed C−N bond cleavage of triethylamine, generation of α,β-unsaturated aldehyde in situ, and oxidative cyclization with air as the oxygen source. This protocol may facilitate the synthesis of imidazo[1,2-a]pyridine derivatives and provide a reference for the usage of triethylamine as a synthon.
中文翻译:
碘介导的三乙胺、醛和 2-氨基吡啶环化用于合成 3-甲酰基-咪唑并[1,2-a]吡啶衍生物
以三乙胺为合成子,从醛和2-氨基吡啶合成3-甲酰基咪唑并[1,2-a]吡啶的替代方法已经完成。该反应通过碘催化三乙胺的CN键断裂,原位生成α , β-不饱和醛,并以空气为氧源进行氧化环化。该方案可促进咪唑并[1,2-a]吡啶衍生物的合成,并为三乙胺作为合成子的使用提供参考。