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Separation and identification of an impurity from the istradefylline intermediate

Istradefylline is a selective adenosine antagonist for the A(2a) receptor, and it is used to treat the Parkinson's disease and improve dyskinesia in the early stage of the Parkinson's disease. An impurity in the istradefylline intermediate A(1) (6-amino-1,3-diethyl-2,4-(1H,3H)-pyrimidinedi...

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Detalles Bibliográficos
Autores principales: Xu, Haojie, Wang, Yiyun, Wang, Hongyi, Zheng, Zhonghui, Meng, Zihui, Xue, Min, Xu, Zhibin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052088/
https://www.ncbi.nlm.nih.gov/pubmed/35497116
http://dx.doi.org/10.1039/c9ra09074f
Descripción
Sumario:Istradefylline is a selective adenosine antagonist for the A(2a) receptor, and it is used to treat the Parkinson's disease and improve dyskinesia in the early stage of the Parkinson's disease. An impurity in the istradefylline intermediate A(1) (6-amino-1,3-diethyl-2,4-(1H,3H)-pyrimidinedione) was identified by high performance liquid chromatography (HPLC); it was separated by preparative HPLC and further characterized by UV, IR, MS, NMR, 2D NMR and single-crystal XRD analyses. The impurity was identified as (E)-N-ethyl-2-cyano-3-ethylamino-2-butenamide, which originated from the synthetic process of the intermediate A(1). The structure of this impurity might affect the efficiency and safety of istradefylline; therefore, the research and control of this impurity are necessary for ensuring the quality of istradefylline.