化学
癫痫
药品
溶剂
组合化学
有机化学
药理学
精神科
心理学
医学
作者
Saurabh Kumar Singh,Partha Ghosh,Rajendra Prasad
标识
DOI:10.2174/0115701786350134241220173948
摘要
Abstract: Brivaracetam is a relatively new racetam drug for the treatment of epilepsy, synthesis of which with proper stereocontrol remains challenging. Herein we describe a solvent-free lactamization method for the development of two efficient synthetic routes to brivaracetam. The key method is a one-step condensation of amines with chiral α-carboxyethyl-β-propyl butyrolactone under neat conditions that proceed through tandem decarboxylation and lactamization. The lactam obtained using benzylamine was converted to (S)-3-propyl pyrrolidinone, a key intermediate to brivaracetam. Whereas, the lactam obtained from the condensation of (S)-2-amino butanol was further transformed into brivaracetam. objective: Efficient synthesis of the epilepsy drug brivaracetam method: a solvent free lactamization method
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