Reddy Rajarathnam E, Chen Yon-Yih, Johnson Donald D, Beligere Gangamani S, Rege Sushil D, Pan You, Thottathil John K
Core R&D Chemistry Group (Department 09MD, Building AP20), Diagnostics Division, Abbott Laboratories, 100 Abbott Park Road, Abbott Park, Illinois 60064-6016, USA.
Bioconjug Chem. 2005 Sep-Oct;16(5):1323-8. doi: 10.1021/bc040259x.
An efficient synthesis of 4-[(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)methyl]-N-(6-[[6-([6-[(2,5-dioxopyrrolidin-1-yl)oxy]-6-oxohexyl]amino)-6-oxohexyl]amino]-6-oxohexyl)cyclohexanecarboxamide (12), a heterobifunctional coupling agent, was developed, which is critical for chemoselective conjugation of proteins and enzymes. The synthesis involved seven steps starting from 6-{[(benzyloxy)carbonyl]amino}hexanoic acid (1), and multigram quantities of coupling agent (12) were prepared using this protocol in excellent overall yield and 99.6% purity by reversed phase HPLC. The new method is suitable for the synthesis of coupling agent 12, consistently with purity >99%, and is useful for the preparation of other analogous coupling agents.
开发了一种4-[(2,5-二氧代-2,5-二氢-1H-吡咯-1-基)甲基]-N-(6-[[6-([6-[(2,5-二氧代吡咯烷-1-基)氧基]-6-氧代己基]氨基)-6-氧代己基]氨基]-6-氧代己基)环己烷甲酰胺(12)的有效合成方法,其为一种异双功能偶联剂,对蛋白质和酶的化学选择性缀合至关重要。该合成从6-{[(苄氧基)羰基]氨基}己酸(1)开始涉及七个步骤,并且使用该方案以优异的总收率和通过反相HPLC测定的99.6%纯度制备了多克量的偶联剂(12)。该新方法适用于合成纯度>99%的偶联剂12,并且可用于制备其他类似的偶联剂。