<i>N</i>-TOSYL-(<i>S</i>)-PROLYL CHLORIDE IN KINETIC RESOLUTION OF RACEMIC HETEROCYCLIC AMINES
DOI:
https://doi.org/10.1007/988Keywords:
amines, (3R)-7, 8-difluoro-3-methyl-3, 4-dihydro-2H-[1, 4]benzoxazine, N-tosyl-(S)-proline, acylation, diastereoisomers, kinetic resolution, stereoselectivityAbstract
The kinetic resolution of racemic heterocyclic amines via acylation with N-tosyl-(S)-prolyl chloride was systematically investigated. It was established that racemic mixtures of aromatic amines could be resolved with high efficiency, while the acylation of 2- and 3-methylpiperidines occurred with low diastereoselectivity. A method for the preparation of enantiomerically pure (3R)-7,8-difluoro-3-methyl-3,4‑dihydro-2H-[1,4]benzoxazine was developed.
How to Cite
Gruzdev, D. A.; Vakarov, S. A.; Levit, G. L.; Krasnov, V. P. Chem. Heterocycl. Compd. 2014, 49, 1795. [Khim. Geterotsikl. Soedin. 2013, 1936.]
For this article in the English edition see DOI 10.1007/s10593-014-1432-4