Synthesis of N-alkyl-3- (1H-benzimidazolyl) -2-chloroquinoline derivatives potential candidates against infectious organisms

Gbè Gondo Didier Diomandé, Sagne Jacques Akpa, D. Zon, A. Adjou
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Abstract

In the search for new drugs possessing the activities we have sought to synthesize new quinoline derivatives which constitute a basic heterocyclic support of some drugs such as quinine, chloroquine marketed under the name Nivaquine®, Mefloquine®, used in the treatment of malaria. The objective of this work is to contribute to the synthesis of new derivatives of quinoline. It consists in introducing heterocycles such as benzimidazole in its 3-position. The introduction of heterocyclics, aryls or alkyls on the pyrrolic nitrogen of benzimidazole, allowed us to obtain compounds 3a-f. The chemical structures of all these compounds were determined by NMR (1H, 13C) and electron impact mass spectrometry. Key words: Quinoline, benzimidazole, aryls, alkyls.
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n -烷基-3- (1h -苯并咪唑)-2-氯喹啉衍生物的合成
在寻找具有这些活性的新药的过程中,我们试图合成新的喹啉衍生物,这些衍生物构成一些药物的基本杂环支撑,如奎宁、氯喹,以尼瓦奎®、甲氟喹®的名称销售,用于治疗疟疾。本工作的目的是为合成新的喹啉衍生物作出贡献。它包括在3位上引入杂环,如苯并咪唑。在苯并咪唑的吡咯氮上引入杂环、芳基或烷基,使我们得到化合物3a-f。所有化合物的化学结构均通过核磁共振(1H, 13C)和电子冲击质谱测定。关键词:喹啉,苯并咪唑,芳基,烷基。
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