RORγt 抑制剂 JNJ-61803534 的碳 14 标记合成。

IF 0.9 4区 医学 Q4 BIOCHEMICAL RESEARCH METHODS Journal of labelled compounds & radiopharmaceuticals Pub Date : 2024-05-27 DOI:10.1002/jlcr.4114
Fengbin Song, Rhys Salter, Lu Chen
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引用次数: 0

摘要

RORγt 抑制剂 JNJ-61803534 (1) 的碳 14 标记合成分四个步骤完成,C14 标记位于噻唑-2-甲酰胺碳原子上。该合成方法的特点是在温和条件下通过亚胺中间体将腈[14C]-12 高效转化为酯[14C]-17,克服了腈12在酸性或碱性条件下直接水解不成功的问题。由于通过安装[14C]-腈并随后转化为[14C]-羧酸衍生物进行碳-14标记是一种常见的标记策略,因此在温和条件下将腈有效转化为酯可用于未来的 C14 标记合成。
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Carbon-14 Labeling Synthesis of RORγt Inhibitor JNJ-61803534

Carbon-14 labeling synthesis of RORγt inhibitor JNJ-61803534 (1) was accomplished in four steps with the C14 label located at the thiazole-2-carboxamide carbon. The synthesis featured a highly efficient conversion of nitrile [14C]-12 to ester [14C]-17 under mild conditions via an imidate intermediate, overcoming the unsuccessful direct hydrolysis of nitrile 12 under either acidic or basic conditions. Since carbon-14 labeling via [14C]-nitrile installation and subsequent conversion to [14C]-carboxylic acid derivatives is a common labeling strategy, an efficient conversion of a nitrile to an ester under mild conditions could be of use for the future C14 labeling syntheses.

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来源期刊
CiteScore
3.30
自引率
0.00%
发文量
57
审稿时长
1 months
期刊介绍: The Journal of Labelled Compounds and Radiopharmaceuticals publishes all aspects of research dealing with labeled compound preparation and applications of these compounds. This includes tracer methods used in medical, pharmacological, biological, biochemical and chemical research in vitro and in vivo. The Journal of Labelled Compounds and Radiopharmaceuticals devotes particular attention to biomedical research, diagnostic and therapeutic applications of radiopharmaceuticals, covering all stages of development from basic metabolic research and technological development to preclinical and clinical studies based on physically and chemically well characterized molecular structures, coordination compounds and nano-particles.
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