Ammonium Chloride → 5-Bromo-2-{4-[2-(trifluoromethyl)phenoxy]piperidin-1-yl}pyrimidine

Into a 100-mL flask equipped with a magnetic stirbar was added 5-bromo-2-chloropyrimidine (3.80 g, 19.5 mmol), 4-[2-(trifluoromethyl)phenoxy]piperidine hydrochloride (6.90 g, 24.5 mmol) and 2-propanol (25 mL). The suspension was treated with N,N-diisopropylethylamine (8.6 mL, 49 mmol) and stirred at room temperature for 10 min and then heated to 100° C. for 16 h. After this time, the mixture was cooled to room temperature, poured into a 250-mL separatory funnel containing saturated aqueous NH4Cl (125 mL) and the mixture was extracted with ethyl acetate (3×50 mL). The combined organic layers were washed with brine, dried over MgSO4, filtered and the solvent was evaporated under reduced pressure. The crude solid was triturated in diethyl ether to yield the title compound as an off-white solid. MS (ESI, Q+) m/z 403, 405 (M+1 for 35Br and 37Br).

1. customInto a 100-mL flask equipped with a magnetic stirbar
2. temperatureheated to 100° C. for 16 h
3. temperatureAfter this time, the mixture was cooled to room temperature
4. additionpoured into a 250-mL separatory funnel
5. extractionthe mixture was extracted with ethyl acetate (3×50 mL)
6. washThe combined organic layers were washed with brine
7. dry with materialdried over MgSO4
8. filtrationfiltered
9. customthe solvent was evaporated under reduced pressure
10. customThe crude solid was triturated in diethyl ether

ORD record

ord-a135bc66c4d943d3b416eb19094344b7

Source dataset

uspto-grants-2009_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07582633B2