A synthetic strategy for the preparation of alkoxy-functionalized bis-1,2,4-triazinyl-2,6-pyridines

IF 2 3区 化学 Q2 CHEMISTRY, ORGANIC Journal of Heterocyclic Chemistry Pub Date : 2024-05-23 DOI:10.1002/jhet.4828
Mariah L. Tedder, Jesse D. Carrick
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Abstract

Heteroaryl-1,2,4-triazine complexants are commonly utilized in separation science for the selective chelation of minor An from Ln in simulated high-level waste. To facilitate access to relevant chemical entities for hypothesis-driven inquiry toward improved separations performance, a synthetic method to construct various alkoxy-complexant derivatives was required. In this work, a convergent synthetic strategy for the production of 3,3′- and 4,4′-tetraalkoxy-bis-1,2,4-triazinyl-2,6-pyridines from readily available starting materials via a dealkylation/alkylation/condensation approach is described. Synthetic method development, substrate scope, preliminary solubility, and hydrolytic stability data in various process-relevant diluents are reported herein.

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制备烷氧基官能化双-1,2,4-三嗪基-2,6-吡啶的合成策略
杂芳基-1,2,4-三嗪络合剂是分离科学中常用的螯合剂,用于选择性地螯合模拟高浓度废物中锰的微量鞍。为便于获取相关化学实体,以进行假设驱动的研究,从而提高分离性能,需要一种合成方法来构建各种烷氧基络合剂衍生物。在这项工作中,介绍了一种通过脱烷基化/烷基化/缩合方法,从容易获得的起始材料中生产 3,3′- 和 4,4′- 四烷氧基双-1,2,4-三嗪基-2,6-吡啶的聚合合成策略。本文报告了合成方法的开发、底物范围、初步溶解度以及在各种工艺相关稀释剂中的水解稳定性数据。
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
Journal of Heterocyclic Chemistry
Journal of Heterocyclic Chemistry 化学-有机化学
CiteScore
5.20
自引率
4.20%
发文量
177
审稿时长
3.9 months
期刊介绍: The Journal of Heterocyclic Chemistry is interested in publishing research on all aspects of heterocyclic chemistry, especially development and application of efficient synthetic methodologies and strategies for the synthesis of various heterocyclic compounds. In addition, Journal of Heterocyclic Chemistry promotes research in other areas that contribute to heterocyclic synthesis/application, such as synthesis design, reaction techniques, flow chemistry and continuous processing, multiphase catalysis, green chemistry, catalyst immobilization and recycling.
期刊最新文献
Issue Information Issue Information Synthetic Strategies for C-Amino 1,2,3-Triazoles and Their Oxides: A Review Coumarin Derivatives: Microwave Synthesis and Biological Properties—A Review Lewis Base Promoted [4+2] Annulation of o-Acylamino-Aryl Morita-Baylis-Hillman Carbonates With Isatylidene Malononitriles: Facile Access to Spiro[Indolin-3,2′-Quinoline] Frameworks
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