连续流动
危险废物
序列(生物学)
流动化学
批处理
试剂
可扩展性
化学
叠氮化物
有机化学
组合化学
计算机科学
工艺工程
生化工程
数据库
工程类
生物化学
程序设计语言
废物管理
作者
Hansjörg Lehmann,Thomas Ruppen,Thomas Knoepfel
标识
DOI:10.1021/acs.oprd.2c00016
摘要
Rapid synthesis and scale-up of active molecules to support the development process of new drug candidates is key in the pharmaceutical industry. Herein, we describe the development of a scalable continuous flow procedure for three key steps in the synthesis of 2H-indazoles, which were identified as highly potent and selective TLR7 and TLR8 antagonists. Transformation of hazardous diazonium salt and azide chemistries from the batch mode to continuous flow mode helped mitigate and limit the risks associated with the handling of large amounts of hazardous reagents and intermediates in the batch mode. In a two-step approach, we first screened and optimized the reaction parameter for a diazotization─azidation─cyclization three-step sequence using a commercial research-scale plug flow reactor. In the second step, we demonstrated the robustness and scalability of this reaction sequence, which finally enabled us to rapidly prepare and deliver the required amount of material in high quality.
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