Pyridine → HCID 23071197, compound

To a solution of bis(trichloromethyl)carbonate (0.48 g) in tetrahydrofuran (20 mL) was added dropwise a solution of pyridine (0.39 mL) in tetrahydrofuran (1 mL) under ice-cooling. The reaction solution was stirred for 20 minutes under ice-cooling, and 2-(methylamino)ethyl tetrahydropyran-4-yl carbonate hydrochlride (0.96 g) obtained in Reference Synthetic Example 17 was added. A solution of triethylamine (0.67 mL) in tetrahydrofuran (1 mL) was added dropwise, and stirred at room temperature for 2 hrs. The reaction solution was concentrated under reduced pressure, and to the residue was added water (50 mL), and extracted with ethyl acetate (50 mL). The ethyl acetate layer was washed with 0.2 N hydrocloric acid (20 mL), and saturated brine (50 mL), and dried over anhydrous magnesium sulfate. The solution was concentrated under reduced pressure, and the residue was dissolved in tetrahydrofuran (20 mL). To the solution were added (R)-2-[[[3-methyl-4-(2,2,2-trifluoroethoxy)-2-pyridyl]methyl]sulfinyl]-1H-benzimidazole (1.26 g), triethylamine (0.71 mL) and 4-dimethylaminopyridine (0.042 g), and stirred at 60° C. for 6 hrs, and then at room temperature for 8 hrs. The reaction solution was concentrated under reduced pressure, and to the residue was added water (50 mL), and extracted with ethyl acetate (50 mL). The ethyl acetate layer was washed with saturated saline (50 mL), and dried over anhydrous magnesium sulfate. After concentrating under reduced pressure, the residue was purified with basic silica gel column chromatography (eluted with ethyl acetate:hexane=3:7, then ethyl acetate). The purified material was crystallized from diethyl ether, and further recrystallized from acetone-diisopropyl ether to give title compound as colorless solid (1.45 g).

1. temperaturecooling
2. temperaturecooling

ORD record

ord-f1ad48486317404baa98e2020eedad32

Source dataset

uspto-grants-2013_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08449911B2