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重水和超重水中非定向钯催化 C-H 活化对药物的氘化和氚化。

Deuteration and Tritiation of Pharmaceuticals by Non-Directed Palladium-Catalyzed C-H Activation in Heavy and Super-Heavy Water.

机构信息

Department of Chemistry, Indian Institute of Technology Bombay Powai, Mumbai, 400076, India.

Albert-Ludwigs University Freiburg, Institute of Organic Chemistry, Albertstr. 21, 79104, Freiburg, Germany.

出版信息

Angew Chem Int Ed Engl. 2024 Nov 25;63(48):e202410162. doi: 10.1002/anie.202410162. Epub 2024 Oct 17.

Abstract

Deuterated and tritiated analogs of drugs are valuable compounds for pharmaceutical and medicinal chemistry. In this work, we present a novel hydrogen isotope exchange reaction of drugs using non-directed homogeneous Pd-catalysis. Aromatic C-H activation is achieved by a commercially available pyridine ligand. Using the most convenient and cheapest deuterium source, DO, as the only solvent 39 pharmaceuticals were labelled with clean reaction profiles and high deuterium uptakes. Additionally, we describe the first application of non-directed homogeneous Pd-catalysis for H/T exchange on three different pharmaceuticals by using TO as isotopic source, demonstrating the applicability to the synthesis of radiotracers.

摘要

氘代和氚代类似物是药物的重要化合物,在药物和医药化学领域具有重要价值。在这项工作中,我们提出了一种使用非定向均相 Pd 催化的药物新型氢同位素交换反应。通过商业可得的吡啶配体实现芳香族 C-H 活化。使用最方便和最便宜的氘源 DO 作为唯一的溶剂,39 种药物在干净的反应谱和高氘摄取率下进行标记。此外,我们还描述了首次使用 TO 作为同位素源,通过非定向均相 Pd 催化对三种不同药物进行 H/T 交换的应用,证明了其在放射性示踪剂合成中的适用性。

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