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  • Practical resolution of 3-aminopyrrolidine via diastereomeric salt formation with (S)-2-methoxy-2-phenylacetic acid
  • Add time:07/17/2019         Source:sciencedirect.com

    The resolution of 3-aminopyrrolidine 1, a versatile key intermediate for chiral pharmaceuticals, via diastereomeric salt formation was investigated. The resolution conditions were optimized focusing on an industrial-scale production to afford enantiopure (R)-1, while (S)-methoxy-2-phenylacetic acid 5 was found to be a suitable resolving agent. The less-soluble diastereomeric salt, 1:2 (R)-1:(S)-5, was obtained with high resolution efficiency (E) (yield 44%, 98% de, E 86%) under the best resolution conditions; (RS)-1/(S)-5/HCl molar ratio = 1.0/1.0/1.0 in water solvent in the presence of sodium chloride. The optimized resolution process was scaled up to a pilot-scale production using 50 kg of (RS)-1 dihydrochloride as a starting racemate, and the resolution efficiency successfully reproduced the laboratory results.

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    Prev:Phase II Study of Pyrazine Diazohydroxide (NSC 361456) for Advanced Non–Small-Cell Lung Cancer
    Next: Chiral 3-aminopyrrolidines as a rigid diamino scaffold for organocatalysis and organometallic chemistry)

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