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机械化学促进杂环化合物:无溶剂路线合成三唑碳水化合物作为糖原磷酸化酶抑制剂。

Mechanochemical Promoted Heterocycles: A Solvent-free Route to Triazole Carbohydrates as Glycogen Phosphorylase Inhibitors.

机构信息

Chemistry Department, College of Science, IMSIU (Imam Mohammad Ibn Saud Islamic University), Riyadh 11432, Saudi Arabia.

Textile Engineering Laboratory, Higher Institute of Technological Studies of Ksar, University of Monastir, Hellal, Tunisia.

出版信息

Curr Org Synth. 2022;19(8):930-936. doi: 10.2174/1570179419666220420133644.

Abstract

AIMS

This study aimed to recommend a novel way for the preparation of carbohydrates containing triazole derivatives.

BACKGROUND

Triazoles containing derivatives have numerous biological activities. Ball milling is a fast, modest, green process with massive potential. One of the greatest interesting applications of this technique is in the arena of heterocycles.

OBJECTIVE

Solvent-free click reactions are facilitated via the activation of copper powder using a ball milling mechanochemical procedure. An optimization study of parameters affecting the reaction rate, such as reaction time, size, and milling ball number, has been conducted. Different substrates have been tested using this adopted procedure considering in all cases, in high yields and purity, the corresponding chiral optically pure five-membered glycoconjugates containing 1,2,3-triazole.

METHODS

Three milling balls of 10 mm in diameter were placed in the milling jar (50 mL; stainless steel). 1 mmol of alkyne, 2 mmol of azide, and 1 mmol of Cu powder (63 mg) were added, respectively, in the presented order. Milling was assured for 25 min at 650 rpm deprived of solvent.

RESULTS

The cycloaddition results and the deprotection of the cycloadducts were affected by the selection of the protective groups. Cleavage of the acetyl protecting groups provided water-soluble triazoles. The four 1,4-di-substituted 1,2,3-triazoles synthesized via deacetylation were tested against glycogen phosphorylase. The best inhibitor of rabbit muscle glycogen phosphorylase was 2-Amino-3-{2-[1-(3,4,5,6-tetrahydroxytetrahydro- pyran-2-ylmethyl)-1H-[1,2,3]triazol-4-yl]-ethylsulfanyl}-propionic acid b (Ki = 40.8 ± 3.2 μM). This novel procedure affords an eco-friendly reaction profile (catalyst-free) affording high yields and short reaction times.

CONCLUSION

In this work, acetyl protective groups were used to the corresponding deprotected watersoluble triazole analogous to recognizing glycogen phosphorylase inhibitors. Triazole 6a was the most effective inhibitor of RMGP b with a Ki value of 40.8 μM.

摘要

目的

本研究旨在为含三唑衍生物的碳水化合物的制备推荐一种新方法。

背景

含三唑衍生物具有多种生物活性。球磨是一种快速、温和、绿色的过程,具有巨大的潜力。该技术最有趣的应用之一是在杂环领域。

目的

通过使用球磨机械化学程序激活铜粉,促进无溶剂点击反应。已经对影响反应速率的参数(例如反应时间、大小和球磨球数量)进行了优化研究。使用该方法对不同的底物进行了测试,在所有情况下,都以高收率和纯度得到了相应的手性光学纯五元糖基缀合物,其中含有 1,2,3-三唑。

方法

将三个 10 毫米直径的球磨球放入球磨罐(50 毫升;不锈钢)中。分别按以下顺序加入 1 毫摩尔炔烃、2 毫摩尔叠氮化物和 1 毫摩尔铜粉(63 毫克)。在无溶剂的情况下以 650 rpm 研磨 25 分钟。

结果

环加成结果和环加成产物的脱保护受保护基的选择影响。乙酰基保护基团的裂解提供了水溶性三唑。通过脱乙酰化合成的四个 1,4-二取代 1,2,3-三唑被测试对糖原磷酸化酶的抑制作用。对兔肌肉糖原磷酸化酶抑制作用最强的是 2-氨基-3-{2-[1-(3,4,5,6-四羟基四氢-吡喃-2-基甲基)-1H-[1,2,3]三唑-4-基]-乙基硫基}-丙酸 b(Ki = 40.8 ± 3.2 μM)。该新方法提供了一种环保的反应概况(无催化剂),可获得高产率和短反应时间。

结论

在这项工作中,使用乙酰基保护基团来制备相应的水溶性三唑类似物,以识别糖原磷酸化酶抑制剂。三唑 6a 是对 RMGP b 抑制作用最强的抑制剂,Ki 值为 40.8 μM。

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