A new processdeveloped for the synthesis of enantiomerically pure R-(+)-N-propargyl-1- aminoindan mesylate(Rasagiline mesylate) by using K2HPO4/Triethylbenzylammonium chloride (TEBAC) as a reagent. This approach controls the formation of other isomerS-(-)-N-propargyl- 1-aminoindane. This new process may be useful for the preparation of enantiomerically pure Rasagiline mesylatein commercial scale with good yields.
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