Fremgangsmåde til fremstilling af enantiomert rene 3-methyl-5-(1-alkyl-2(S)-pyrrolidinyl)isoxazoler

A novel process for preparing enantiomerically-pure 3-methyl-5-(1-(C1-C3-alkyl)-2-pyrrolidinyl)isoxazole in high yield, wherein a protected pyrrolidine or 2-oxo-pyrrolidine starting material is reacted with a suitable organic anion and a resulting beta-keto oxime intermediate is cyclized and dehydra...

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Hauptverfasser: BUNNELLE, WILLIAM, H, WITZIG, CHRISTIAN, C, LIN, NAN-HORNG, ESCH, THOMAS, K., J, NARAYANAN, BIKSHANDAR, A, SINGAM, PULLA R, ELLIOTT, RICHARD, L, BEER, DIETER, O, RAO, ALLA, V. RAMA, RESIDENCE OF DIRECTOR, CHORGHADE, MUKUND, S, HE, YUN, HERZIG, THOMAS, C, WITTENBERGER, STEVEN, J
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Sprache:dan
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Zusammenfassung:A novel process for preparing enantiomerically-pure 3-methyl-5-(1-(C1-C3-alkyl)-2-pyrrolidinyl)isoxazole in high yield, wherein a protected pyrrolidine or 2-oxo-pyrrolidine starting material is reacted with a suitable organic anion and a resulting beta-keto oxime intermediate is cyclized and dehydrated, as well as intermediates useful in the preparation thereof.