Bcl抑制剂Obatoclax的可扩展合成工艺

IF 3.5 3区 化学 Q2 CHEMISTRY, APPLIED
Kenza Daïri*, Yuxing Yao, Michael Faley, Sasmita Tripathy, Elise Rioux, Xavier Billot, Daniel Rabouin, Gerson Gonzalez, Jean-François Lavallée, Giorgio Attardo
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引用次数: 23

摘要

最近,我们创造了一种新的吲哚酰prodigiosin衍生物2 (obatoclax),并证明了它能够拮抗b细胞淋巴瘤(Bcl)抗凋亡蛋白家族的多种成员。该化合物在几种动物肿瘤模型中显示出强大的抗癌活性。Obatoclax目前正处于针对多种血液学和实体肿瘤恶性肿瘤的1b期和2期临床试验。为了支持其临床开发,需要一种新的可扩展的合成方法。从市售的4-甲氧基-3-吡咯啉-2- 1开始,采用三步合成方法制备了Obatoclax。反应顺序包括一个卤代甲酰化反应,然后是与吲哚-2-硼酸的铃木交叉偶联反应。由酸介导的2,4-二甲基- 1h -吡咯缩合完成合成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Scalable Process for the Synthesis of the Bcl Inhibitor Obatoclax

A Scalable Process for the Synthesis of the Bcl Inhibitor Obatoclax

Recently we created the novel indolylprodigiosin derivative 2 (obatoclax) and demonstrated its ability to antagonize multiple members of the B-cell lymphoma (Bcl) family of antiapoptotic proteins. The compound has shown potent anticancer activity in several animal tumor models. Obatoclax is now in Phase 1b and 2 clinical trials directed against multiple hematologic and solid tumor malignancies. To support its clinical development, a new scalable synthesis was required. Obatoclax has been prepared using a three-step synthesis, starting from commercially available 4-methoxy-3-pyrrolin-2-one. The reaction sequence involves a haloformylation reaction followed by a Suzuki cross-coupling reaction with an indole-2-boronic acid. The synthesis is completed by an acid-mediated condensation with 2,4-dimethyl-1H-pyrrole.

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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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