Comprehensive review on green methods: Synthesis of benzothiazoles

IF 4.2 Q2 CHEMISTRY, MULTIDISCIPLINARY Results in Chemistry Pub Date : 2025-03-24 DOI:10.1016/j.rechem.2025.102212
V.V.K. Vasu Juthiga , S.N. Murthy Boddapati , Megha Balha , Ramana Tamminana
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Abstract

The study of heterocyclic compounds has consistently attracted the attention of chemists working on both synthetic and natural products. Benzothiazole (BTZ) is one of the most important fused heterocyclic motifs among the heterocyclic scaffolds containing nitrogen and sulfur. In recent times, medicinal chemists have focused more on the structurally distinct benzothiazole motifs with remarkable bioactivity in order to continuously develop new drug moieties. In recent decades, many methodologies have been developed for the construction benzothiazole derivatives as desired molecules and they have illustrated diverse biological activities, however, a lot of real synthetic techniques are not sustainable, necessitating the use of eco-friendly tactics. Therefore, to support future advancements in the quantity of benzothiazole-based lead molecules, understanding the green synthetic pathways towards the benzothiazole is very crucial. Accordingly, this review focused on the results of published work on the green methods for the synthesis of benzothiazoles. In this review, the latest developments in different green synthetic approaches of benzothiazole and its derivatives over the last ten years (2014–2024) were compiled.

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绿色方法综述:苯并噻唑的合成
杂环化合物的研究一直吸引着从事合成和天然产物研究的化学家的注意。苯并噻唑(BTZ)是氮硫杂环支架中最重要的融合杂环基序之一。近年来,药物化学家越来越关注结构独特、生物活性显著的苯并噻唑基序,以不断开发新的药物基序。近几十年来,人们已经开发了许多方法来构建苯并噻唑衍生物作为所需的分子,并展示了多种生物活性,然而,许多真正的合成技术是不可持续的,需要使用环保策略。因此,为了支持苯并噻唑基铅分子数量的未来发展,了解苯并噻唑的绿色合成途径是非常重要的。因此,本文主要对已发表的绿色合成苯并噻唑方法的研究结果进行综述。本文综述了近十年来(2014-2024年)苯并噻唑及其衍生物的各种绿色合成方法的最新进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Results in Chemistry
Results in Chemistry Chemistry-Chemistry (all)
CiteScore
2.70
自引率
8.70%
发文量
380
审稿时长
56 days
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