磺胺
化学
同位素
脱氨基
试剂
组合化学
小学(天文学)
降级(电信)
体内
同位素标记
分子
立体化学
有机化学
酶
生物
天文
物理
计算机科学
生物技术
电信
作者
Sean W. Reilly,Frank Bennett,Patrick S. Fier,Sumei Ren,Neil A. Strotman
标识
DOI:10.1002/chem.202000484
摘要
A late-stage 18 O labeling approach of sulfonamides that employs the corresponding unlabeled molecule as the starting material was developed. Upon deamination of the sulfonamide, a sulfinate intermediate was isotopically enriched using eco-friendly reagents H2 18 O and 15 NH3 (aq) to afford a M+5 isotopologue of the parent compound. This degradation-reconstruction approach afforded isolated yields of up to 96 % for the stable isotope labeled (SIL) sulfonamides, and was compatible with multiple marketed therapeutics, including celecoxib, on a gram scale. The SIL products also exhibited no 18 O/16 O back exchange under extreme conditions, further validating the utility of this green strategy for drug labeling for both in vitro and in vivo use. This procedure was also adapted to include pharmaceutically relevant methyl sulfones by using 13 CH3 , affording M+5 isotopic enrichment, thereby illustrating the broad utility of this methodology.
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