Self-optimisation of the final stage in the synthesis of EGFR kinase inhibitor AZD9291 using an automated flow reactor

被引:87
作者
Holmes, Nicholas [1 ]
Akien, Geoffrey R. [1 ,2 ]
Blacker, A. John [1 ,3 ]
Woodward, Robert L. [4 ]
Meadows, Rebecca E. [4 ]
Bourne, Richard A. [1 ,3 ,4 ]
机构
[1] Univ Leeds, Sch Chem, Inst Proc Res & Dev, Leeds LS2 9JT, W Yorkshire, England
[2] Univ Lancaster, Dept Chem, Faraday Bldg, Lancaster LA1 4YB, England
[3] Univ Leeds, Sch Chem & Proc Engn, Leeds LS2 9JT, W Yorkshire, England
[4] AstraZeneca Pharmaceut Dev, Silk Rd Business Pk, Macclesfield SK10 2NA, Cheshire, England
来源
REACTION CHEMISTRY & ENGINEERING | 2016年 / 1卷 / 04期
基金
英国工程与自然科学研究理事会;
关键词
MICROFLUIDIC SYSTEM; CHEMICAL-SYNTHESIS; ORGANIC-SYNTHESIS; SIMPLEX; SPECTROSCOPY; PERFORMANCE; ANTAGONIST; RECEPTOR; POTENT;
D O I
10.1039/c6re00059b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Self-optimising flow reactors combine online analysis with evolutionary feedback algorithms to rapidly achieve optimum conditions. This technique has been applied to the final bond-forming step in the synthesis of AZD9291, an irreversible epidermal growth factor receptor kinase inhibitor developed by AstraZeneca. A four parameter optimisation of a telescoped amide coupling followed by an elimination reaction was achieved using at-line high performance liquid chromatography. Optimisations were initially carried out on a model compound (2,4-dimethoxyaniline) and the data used to track the formation of various impurities and ultimately propose a mechanism for their formation. Our protocol could then be applied to the optimisation of the 2-step telescoped reaction to synthesise AZD9291 in 89% yield.
引用
收藏
页码:366 / 371
页数:6
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