Facile Synthesis of Novel Hexahydroimidazo[1,2-a]pyridine Derivatives by One-Pot, Multicomponent Reaction under Ambient Conditions

IF 3.784 3区 化学 Q1 Chemistry ACS Combinatorial Science Pub Date : 2020-07-07 DOI:10.1021/acscombsci.0c00105
Hongbo Tan*, Yinfeng Wang
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引用次数: 11

Abstract

An efficient one-pot multicomponent reaction for the synthesis of novel tetrasubstituted hexahydroimidazo[1,2-a]pyridines starting from readily available cinnamaldehydes, ethylenediamines, and 1,3-dicarbonyl compounds catalyzed by AcOH is described. Two new cycles and four new bonds are constructed with all reactants being efficiently utilized in this transformation. The products could be obtained in 1–3 h under ambient conditions exclusively as a single isomer (trans). Single-crystal X-ray analysis confirmed the trans derivative as the only isomer.

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环境条件下一锅多组分反应简便合成新型六氢咪唑[1,2-a]吡啶衍生物
介绍了一种高效的一锅多组分反应,以易得的肉桂醛、乙二胺和1,3-二羰基化合物为原料,在AcOH催化下合成新型四取代六氢咪唑[1,2-a]吡啶。两个新循环和四个新键被构建,所有的反应物都被有效地利用。在环境条件下1-3小时内,产物完全以单一异构体(反式)形式得到。单晶x射线分析证实反式衍生物是唯一的异构体。
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ACS Combinatorial Science
ACS Combinatorial Science CHEMISTRY, APPLIED-CHEMISTRY, MEDICINAL
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审稿时长
1 months
期刊介绍: The Journal of Combinatorial Chemistry has been relaunched as ACS Combinatorial Science under the leadership of new Editor-in-Chief M.G. Finn of The Scripps Research Institute. The journal features an expanded scope and will build upon the legacy of the Journal of Combinatorial Chemistry, a highly cited leader in the field.
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