Hydrochloric Acid → 2-(3-Chloro-5-fluorophenyl)-5-pentylpyrimidine

Temperature

-60 °C

A solution of 3-chloro-5-fluorophenylmagnesium bromide [prepared from 22.7 g (108.3 mmol) of 3-chloro-5-fluoro-bromobenzene and 2.7 g (111.0 mmol) of magnesium, and 100 ml of diethyl ether] in diethyl ether was added by drops to a mixture of 10 g (54.1 mmol) of 2-chloro-5-pentylpyrimidine, 0.4 g (0.5 mmol) of dichloro[1,1′-bis(diphenylphosphino) ferrrocene]palladium, and 300 ml of diethyl ether while being maintained at a temperature lower than −60° C., stirred at the same temperature for 1 hour, and then stirred at 10° C. for 10 hours. A diluted hydrochloric acid in an amount of 300 ml was added to the reaction mixture and extracted with 250 ml of heptane. The organic layer thus obtained was washed with a diluted aqueous sodium bicarbonate solution thrice and water thrice, and then dried over anhydrous magnesium sulfate. The solvent was distilled off under a reduced pressure and the residue was subjected to silica gel column chromatography (eluent: heptane/toluene=1/1) to obtain 11.0 g of a crude 2-(3-chloro-5-fluorophenyl)-5-pentylpyrimidine. (Yield: 72.8%)

1. stirringstirred at 10° C. for 10 hours
2. extractionextracted with 250 ml of heptane
3. customThe organic layer thus obtained
4. washwas washed with a diluted aqueous sodium bicarbonate solution thrice and water thrice
5. dry with materialdried over anhydrous magnesium sulfate
6. distillationThe solvent was distilled off under a reduced pressure

ORD record

ord-5c99b135cf264570a5f6fc5e5a77e261

Source dataset

uspto-grants-2001_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06329027B1