Large-scale Negishi coupling as applied to the synthesis of PDE472, an inhibitor of phosphodiesterase type 4D

被引:45
作者
Manley, PW
Acemoglu, M
Marterer, W
Pachinger, W
机构
[1] Novartis Pharma AG, Preclin Res, CH-4002 Basel, Switzerland
[2] Novartis Pharma AG, Chem & Analyt Dev, Proc R&D, CH-4002 Basel, Switzerland
关键词
D O I
10.1021/op025615q
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
5-[2-Methoxy-5-(4-pyridinyl)phenyl]-2,1,3-benzoxadiazole (PDE472) is a selective inhibitor of the phosphodiesterase PDE4D isoenzyme, which is a recognised drug target for the treatment of asthma. Different synthetic routes to PDE472 were investigated, and the research synthesis was optimised to prepare a phase I batch on pilot-plant scale with the focus on the elimination or minimization of inherent process risks. An important refinement of the key Negishi aryl-aryl coupling involved preforming the arylpalladium complex, which was then added to the arylzinc intermediate. Residual palladium was removed from PDE472 via crystallization of the hemi-maleate salt, which afforded drug-substance containing < 2 ppm Pd.
引用
收藏
页码:436 / 445
页数:10
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