A Novel Synthesis of N-substituted Glutarimides using ZnCl2 Catalyst: A green approach

A. P. Rajput, D. V. Nagarale
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引用次数: 3

Abstract

The glutarimides containing piperidine ring is a structural feature of many alkaloids and starting material for drug synthesis. Many piperidine type of compounds are mentioned in clinical and preclinical analysis. The piperidine ring system is one of the commonest structural sub units in natural compounds. Several substituted piperidines display important biological properties like antiviral activity. We have optimised and used a simple ZnCl 2 catalysed and highly efficient method for the synthesis of 1-(4-chlorophenyl) piperidine-2,6-diones(Glutarimides) using ethanol solvent. The synthesized compounds are used as precursor for 2,6-dichlorodialdehydes 1, 4-DHP[1-2]. All the synthesized glutarimides are characterized by analytical and modern spectral methods such as FTIR, 1 H-NMR, GC-MS. The resulting compounds possess symmetrical structures and have high yields.
用ZnCl2催化剂合成n -取代戊二酰亚胺的新方法:绿色途径
含哌啶环的戊二酰亚胺是许多生物碱的结构特征,也是药物合成的起始原料。许多哌啶类化合物在临床和临床前分析中被提及。哌啶环系是天然化合物中最常见的结构亚基之一。几种取代的哌啶具有重要的生物学特性,如抗病毒活性。我们优化并使用了一种简单的氯化锌催化合成1-(4-氯苯基)哌啶-2,6-二酮(戊二酰亚胺)的高效方法。合成的化合物被用作2,6-二氯二醛1,4 - dhp的前体[1-2]。用FTIR、1h - nmr、GC-MS等分析和现代光谱方法对合成的戊二酰亚胺进行了表征。所得化合物具有对称结构,产率高。
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