Triethylamine → (2R)-3-bromo-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide

Thionyl chloride (46.02 g, 0.39 mol) was added dropwise to a cooled solution (less than 4° C.) of (R)-3-bromo-2-hydroxy-2-methylpropanoic acid (51.13 g, 0.28 mol) in 300 mL of THF under an argon atmosphere. The resulting mixture was stirred for 3 h under the same condition. To this was added Et3N (39.14 g, 0.39 mol) and stirred for 20 min under the same condition. After 20 min, 5-amino-2-cyanobenzotrifluoride (40.0 g, 0.21 mol), 400 mL of THF were added and then the mixture was allowed to stir overnight at room temperature. The solvent was removed under reduced pressure to give a solid which was treated with 300 mL of H2O, extracted with EtOAc (2×400 mL). The combined organic extracts were washed with saturated NaHCO3 solution (2×300 mL) and brine (300 mL). The organic layer was dried over MgSO4 and concentrated under reduced pressure to give a solid which was purified from column chromatography using CH2Cl2/EtOAc (80:20) to give a solid. This solid was recrystallized from CH2Cl2/hexane to give 55.8 g (73.9%) of (2R)-3-bromo-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide as a light-yellow solid.

1. stirringstirred for 20 min under the same condition
2. waitAfter 20 min
3. stirringto stir overnight at room temperature
4. customThe solvent was removed under reduced pressure
5. customto give a solid which
6. extractionextracted with EtOAc (2×400 mL)
7. washThe combined organic extracts were washed with saturated NaHCO3 solution (2×300 mL) and brine (300 mL)
8. dry with materialThe organic layer was dried over MgSO4
9. concentrationconcentrated under reduced pressure
10. customto give a solid which
11. customwas purified from column chromatography
12. customto give a solid
13. customThis solid was recrystallized from CH2Cl2/hexane

ORD-Eintrag

ord-b9c92c87bdda4e3895793ac57064295a

Quelldatensatz

uspto-grants-2016_03

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US09278914B2