为 ABBV-154 开发和实施免疫 ADC 药物连接剂的可扩展路线

IF 3.1 3区 化学 Q2 CHEMISTRY, APPLIED Organic Process Research & Development Pub Date : 2024-06-25 DOI:10.1021/acs.oprd.4c00142
Nathan B. Bennett, Xiaoqiang Shen, Bradley D. Gates, Dennie S. Welch, Mark A. Servos, Justin A. Simanis, Ryan G. Ellis, Haixiao Qiu, Eric G. Moschetta, Jiajie Feng, Moussa Boukerche, Michael Rasmussen, Laura A. McKee, Laurie B. Mlinar, Shuang Chen, Zhe Wang
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引用次数: 0

摘要

溴乙酰胺1是一种磷酸化糖皮质激素药物连接剂,用于与单克隆抗体(mAb)阿达木单抗(adalimumab)结合生产抗体药物结合剂ABBV-154。我们开发出了一种可扩展的药物连接剂 1 生产工艺,它改进了第一代工艺,可生产数百克材料。新路线首先是乙缩醛的形成,其中包含结晶过程,省去了以前需要用反相色谱法剔除不需要的乙缩醛非对映异构体的过程。链接片段的二肽部分在一次转化中完成。随后的产物直接进入磷酸化过程,使用的是一锅磷酰胺置换和氧化顺序。在对 Fmoc 基团进行脱保护的同时,还要进行连续萃取以去除相关副产物。胺与溴乙酸偶联,最后通过反相纯化对三个 t-丁基进行整体脱保护,得到药物连接剂。
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Development and Execution of a Scalable Route to an Immunology ADC Drug-Linker for ABBV-154
Bromoacetamide 1 is a phosphorylated glucocorticoid drug-linker used in conjugation with the monoclonal antibody (mAb) adalimumab to produce the antibody-drug conjugate ABBV-154. A scalable route to drug-linker 1 has been developed that improves upon the first-generation sequence and allows the production of hundreds of grams of material. The new route begins with an acetal formation that incorporates a crystallization eliminating the previous need for reversed-phase chromatography to reject the undesired acetal diastereomer. The dipeptide portion of the linker fragment is then installed in a single transformation. The subsequent product is taken directly into a phosphorylation using a one-pot phosphoramidite displacement and oxidation sequence. Deprotection of a Fmoc group is accompanied by a continuous extraction to remove associated byproducts. The amine is coupled with bromoacetic acid, and a final global deprotection of three t-butyl groups with a reversed-phase purification yields drug-linker.
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来源期刊
CiteScore
6.90
自引率
14.70%
发文量
251
审稿时长
2 months
期刊介绍: The journal Organic Process Research & Development serves as a communication tool between industrial chemists and chemists working in universities and research institutes. As such, it reports original work from the broad field of industrial process chemistry but also presents academic results that are relevant, or potentially relevant, to industrial applications. Process chemistry is the science that enables the safe, environmentally benign and ultimately economical manufacturing of organic compounds that are required in larger amounts to help address the needs of society. Consequently, the Journal encompasses every aspect of organic chemistry, including all aspects of catalysis, synthetic methodology development and synthetic strategy exploration, but also includes aspects from analytical and solid-state chemistry and chemical engineering, such as work-up tools,process safety, or flow-chemistry. The goal of development and optimization of chemical reactions and processes is their transfer to a larger scale; original work describing such studies and the actual implementation on scale is highly relevant to the journal. However, studies on new developments from either industry, research institutes or academia that have not yet been demonstrated on scale, but where an industrial utility can be expected and where the study has addressed important prerequisites for a scale-up and has given confidence into the reliability and practicality of the chemistry, also serve the mission of OPR&D as a communication tool between the different contributors to the field.
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