O, S, n-含氮杂环化合物在水、聚乙二醇和生物基溶剂中的绿色合成

J. F. Campos, Sabine Berteina‐Raboin
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引用次数: 4

摘要

化学中使用的溶剂是企业和学术实验室过程环境绩效的基本要素。它们对成本、健康安全和自然的影响不容忽视。从数量上讲,溶剂是化学转化中最丰富的成分;因此,作用于溶剂和用更安全的产品替代标准溶剂会产生很大的生态影响。然而,并不是所有的绿色溶剂都适用于范围广泛的有机化学反应。第二点需要考虑的是,50%的药物是氮杂环化合物。因此,对合成这类化合物的更生态的方法进行概述显得很重要。在这篇综述中,考虑了自2000年以来所有描述使用安全溶剂形成氮杂环的绿色反应的出版物。我们选择了水、聚乙二醇和生物基溶剂,因为它们的毒性可以忽略不计。本文描述了利用绿色反应合成五元、六元和七元芳香氮杂环的方法。我们描述了生物基溶剂,已报道为n -杂环合成的有效替代品,它们是;甲氨胺,葡萄糖酸,乳酸乙酯和乳酸。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Greener Synthesis of O, S, N-Nitrogen-Containing Heterocycles in Water, PEG, and Bio-Based Solvents
The solvents used in chemistry are a fundamental element of the environmental performance of processes in corporate and academic laboratories. Their influence on costs, health safety, and nature cannot be neglected. Quantitatively, solvents are the most abundant constituents of chemical transformations; therefore, acting on solvents and replacing standard solvents with safer products can have a great ecological impact. However, not all green solvents are suitable for the wide scope of organic chemistry reactions. A second point to consider is that 50% of pharmaceutical drugs are nitrogen heterocycles compounds. It therefore appeared important to provide an overview of the more ecological methodologies for synthesizing this class of compounds. In this review, all publications since 2000 that describe green reactions leading to the formation of nitrogen heterocycles using safe solvents were considered. We chose water, PEG, and bio-based solvents for their negligible toxicity. The synthesis of five-, six-, and seven-membered aromatic nitrogen heterocycles using green reactions reported in the literature to date is described. We describe biologically based solvents that have been reported as valid alternatives in the synthesis of N-heterocycles, which are; Meglumine, Gluconic acid, Ethyl lactate and Lactic acid.
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