The Mannich Reaction in Imidazo [1,2-a] Pyridine Series Assisted by Microwave

O. Cheham, S. Ghezali, A. Derdor
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Abstract

A comparative studying for the preparation of new compounds in series Imidazo [1,2-a] pyridine via the Mannich reaction which was carried out. Mannich bases, 3 to 6, were synthesized under standard conditions (conventional heating) or microwave irradiation (MW), by action of secondary amines on 2-methyl imidazo [1,2-a] pyridine 1 in the presence of formaldehyde. The results show synthesis under different conditions, for the first time, the training side of Mannich bases of 7 dimer resulting from the condensation of two moles of compound 1 and a mole of formaldehyde with very variable yields. For compound 3, for example,it is about 100%. Our study shows, whenthat we are preparing the initial substrate under MW irradiation, the presence of a compound 2 of the same molecular weight in the trace
咪唑[1,2-a]吡啶系微波辅助下的Mannich反应
采用曼尼希反应对咪唑[1,2- A]吡啶系列化合物的制备进行了比较研究。在标准条件下(常规加热)或微波辐照(MW)下,仲胺在甲醛存在下作用于2-甲基咪唑[1,2-a]吡啶1,合成了曼尼希碱3 ~ 6。结果表明,在不同条件下,首次合成了由2摩尔化合物1和1摩尔甲醛缩合而成的7二聚体的曼尼希碱的训练侧,其产率变化很大。以化合物3为例,它大约是100%。我们的研究表明,当我们在毫瓦辐射下制备初始底物时,痕量存在相同分子量的化合物2
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