Attrition-Enhanced Deracemization in the Synthesis of Clopidogrel - A Practical Application of a New Discovery

Maarten W. van der Meijden, Michel Leeman, Edith Gelens, Wim L. Noorduin, Hugo Meekes, W.J.P. van Enckevort, Bernard Kaptein, Elias Vlieg, Richard M. Kellogg

Organic Process Research & Development · 2009 · 126 citations · 16 references

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Abstract

The recently discovered technique of deracemization by means of attrition-induced grinding of a solid conglomerate in contact with a solution wherein racemization occurs has been used with a derivative of 2-chlorophenyl glycine, the key chiral component in the synthesis of Clopidogrel (Plavix). Deracemization of the racemate proceeds to a single enantiomer and in essentially absolute enantiomeric excess. Further conversion of enantiomerically pure material to Clopidogrel was achieved in 88% yield.

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