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Small-Volume Continuous Manufacturing of Merestinib. Part 1. Process Development and Demonstration

机译:小批量连续制造氟尿。 第1部分。过程开发和示范

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摘要

Development of a small volume continuous process that used a combination of batch and flow unit operations to manufacture the small molecule oncolytic candidate merestinib is described. Continuous processing was enabled following the identification and development of suitable chemical transformations and unit operations. Aspects of the nascent process control strategy were evaluated in the context of a 20 kg laboratory demonstration campaign, executed in walk-in fume hoods at a throughput of 5-10 kg of active pharmaceutical ingredient per day. The process comprised an automated Suzuki-Miyaura cross-coupling reaction, a nitro-group hydrogenolysis, a continuous amide bond formation, and a continuous deprotection. Three of the four steps were purified using mixed-suspension, mixed-product removal crystallizations. Process analytical technology enabled real-time or nearly real-time process diagnostics. Findings from the demonstration campaign informed a second process development cycle as well as decision making for what steps to implement using continuous processing in a proximate manufacturing campaign, which will be described in part 2 of this series.
机译:描述了使用批次和流动单元操作的组合制造小分子的小体积连续过程,以制造小分子溶解候选掠夺性掠夺性掠夺。在识别和开发合适的化学转换和单位操作后,能够连续处理。在20公斤实验室示范运动的背景下评估了新入门过程控制策略的方面,以每天5-10kg活性药物成分的吞吐量在步入式通量罩中执行。该方法包括自动铃木 - 霉龙交叉偶联反应,硝基氢解,连续酰胺键形成和连续脱保护。使用混合悬浮液,混合产物去除结晶纯化四个步骤中的三个。过程分析技术启用了实时或几乎实时的过程诊断。演示活动的调查结果了解第二个过程开发周期以及在近似制造活动中使用连续处理实施的步骤的决策,这将在本系列的第2部分中描述。

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