(R)-camphorsulfonic acid → (2S,3R)-3-(2,5-difluorophenyl)-3-hydroxy-2-methyl-4-(1H-1,2,4-triazol-1-yl)butanenitrile (1R)-10-camphorsulfonate

To a solution of racemic 3-(2,5-difluorophenyl)-3-hydroxy-2-methyl-4-(1H-1,2,4-triazol-1-yl)butanenitrile (2.7 g) in acetone (40 ml) a solution of (1R)-10-camphorsulfonic acid (2 g) in methanol (30 ml) was added and the mixture was heated under reflux until a solution was obtained. The solution was slowly cooled to rt, seeded with crystals of the desired enantiomeric salt and let overnight. The solid was collected by filtration, washed with small amount of cold acetone and dried to provide (2S,3R)-3-(2,5-difluorophenyl)-3-hydroxy-2-methyl-4-(1H-1,2,4-triazol-1-yl)butanenitrile-(1R)-10-camphorsulfonate as white solid. This salt was taken up in methylenechloride (20 ml) and water (ca. 30 ml) and the mixture was basified with aqueous sodium hydroxide solution. The organic layer was separated and the aqueous phase washed twice with methylenechloride (50 ml) and combined. The organic phases were then washed with water (2×30 ml), dried with sodium sulfate, filtrated and the solvent removed under reduced pressure. The crude product was then mixed with isopropanol (20 ml), heated for 10 min, cooled to 0° C. and stirred for ca. 2 hrs. The product was collected, washed with aqueous isopropanol and dried under reduced pressure to provide the enantiomerically pure title compound (1.05 g, 38% yield, 99% ee). The analytical data were identical with published: U.S. Pat. No. 6,300,353 and WO 99/45008.

1. temperaturethe mixture was heated
2. temperatureunder reflux until a solution
3. customwas obtained
4. filtrationThe solid was collected by filtration
5. washwashed with small amount of cold acetone
6. customdried

ORD record

ord-f4dd8385f9d24efa85e526d058bea327

Source dataset

uspto-grants-2012_06

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08207352B2