Tributyltin Chloride → 5-Tri-n-butylstannyl-2-dimethylaminopyrimidine

n-Butyl lithium (1.5 M n-hexane solution; 6.06 ml, 9.09 mmol) was added dropwise to a solution of 5-bromo-2-dimethylaminopyrimidine (1.75 g, 8.66 mmol) in tetrahydrofuran (18 ml) at −78° C. under argon atmosphere in 15 min. The mixture was stirred at the same temperature for 2 hrs. and then tri-n-butyltin chloride (2.5 ml) was added dropwise thereto. The mixture was stirred at the same temperature for 0.5 hrs. and then at room temperature for 1 hr. To the reaction mixture were added 10% aqueous potassium fluoride (50 ml) and ethyl acetate (50 ml) in turn and the mixture was stirred at room temperature for 0.5 hrs. The organic layer was separated and washed with water and brine in turn and dried. The solvent was distilled off under reduced pressure and the residue was purified by column chromatography on amine silica gel (Chromatolex (trademark) NH) (n-hexane) to give 5-tri-n-butylstannyl-2-dimethylaminopyrimidine (2.65 g, 74%) as a colorless oil.

1. stirringThe mixture was stirred at the same temperature for 0.5 hrs
2. waitand then at room temperature for 1 hr
3. stirringthe mixture was stirred at room temperature for 0.5 hrs
4. customThe organic layer was separated
5. washwashed with water and brine in turn
6. customdried
7. distillationThe solvent was distilled off under reduced pressure
8. customthe residue was purified by column chromatography on amine silica gel (Chromatolex (trademark) NH) (n-hexane)

ORD record

ord-d52ae36bfec84961b378fa88d68338d7

Source dataset

uspto-grants-2008_03

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07345068B2