Dimethyl Sulfoxide → HCID 136063915, compound

Temperature

50 °C

A mixture of hydroxylammonium chloride (1.3 g), sodium hydrogen carbonate (2.1 g) and dimethyl sulfoxide (10 mL) was stirred at 50° C. for 30 min, 4′-{[4-(2-{[tert-butyl(dimethyl)silyl]oxy}-2-cyclohexylethyl)-2-methyl-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]methyl}biphenyl-2-carbonitrile (0.76 g) was added, and the mixture was stirred at 90° C. for 20 hr. After allowing to cool to room temperature, ethyl acetate and water were added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and then with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography, and dissolved in tetrahydrofuran (15 mL). N,N′-Carbonyldiimidazole (0.24 g) and then 1,8-diazabicyclo[5.4.0]undec-7-ene (0.2 mL) were added, and the mixture was stirred at room temperature for 2 hr. The reaction mixture was diluted with ethyl acetate, washed with 1 N hydrochloric acid and then with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was dissolved in tetrahydrofuran (10 mL). Tetrabutylammonium fluoride (1 M tetrahydrofuran solution, 3.1 mL) was added and the mixture was stirred at 70° C. for 5 hr. The reaction mixture was extracted with ethyl acetate and water, and the organic layer was washed with water and then with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to give the title compound as a colorless amorphous solid (0.6 g, 86%).

1. stirringthe mixture was stirred at 90° C. for 20 hr
2. temperatureto cool to room temperature
3. extractionthe mixture was extracted with ethyl acetate
4. washThe organic layer was washed with water
5. dry with materialwith saturated brine, and dried over anhydrous magnesium sulfate
6. customThe solvent was evaporated under reduced pressure
7. customthe residue was purified by silica gel column chromatography
8. dissolutiondissolved in tetrahydrofuran (15 mL)
9. additionN,N′-Carbonyldiimidazole (0.24 g) and then 1,8-diazabicyclo[5.4.0]undec-7-ene (0.2 mL) were added
10. stirringthe mixture was stirred at room temperature for 2 hr
11. additionThe reaction mixture was diluted with ethyl acetate
12. washwashed with 1 N hydrochloric acid
13. dry with materialwith saturated brine, and dried over anhydrous magnesium sulfate
14. customThe solvent was evaporated under reduced pressure
15. dissolutionthe residue was dissolved in tetrahydrofuran (10 mL)
16. additionTetrabutylammonium fluoride (1 M tetrahydrofuran solution, 3.1 mL) was added
17. stirringthe mixture was stirred at 70° C. for 5 hr
18. extractionThe reaction mixture was extracted with ethyl acetate and water
19. washthe organic layer was washed with water
20. dry with materialwith saturated brine, and dried over anhydrous magnesium sulfate
21. customThe solvent was evaporated under reduced pressure
22. customThe obtained residue was purified by silica gel column chromatography

ORD record

ord-bec2da8e092f4d6f9d4e728509617983

Source dataset

uspto-grants-2014_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08921379B2