Reacción #1596987

Ecuación de reacción

2-aminopyrimidine

bromobenzene

BuLi

→

47

Rendimiento 10.0%

4-Phenyl-pyrimidin-2-ylamine

Rendimiento 10.0%

Disolventes

toluene

THF

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.WAITthe mixture left
2. 2
   TemperaturaThe mixture was refluxed for 16 h
3. 3
   Temperaturato cool to room temperature
4. 4
   Otrocarefully quenched with aqueous NaHCO3
5. 5
   FiltraciónThe mixture was filtered
6. 6
   Concentraciónthe filtrate concentrated under vacuum
7. 7
   workup.DISSOLUTIONThe residue was then dissolved in DCM
8. 8
   Lavadowashed with aqueous NaHCO3, brine
9. 9
   Secadodried (MgSO4)
10. 10
    OtroThe solvent was removed

Procedimiento

To a solution of bromobenzene (4.43 mL, 42.06 mmol) in dry THF (100 mL) at −78° C. was added BuLi (394 mL, 63.08 mmol) and the mixture left to stir at −78° C. for 2 h. To this was added 2-aminopyrimidine (2.0 g, 21.03 mmol) in hot toluene (80 mL) over a 15 minutes period. The mixture was refluxed for 16 h and allowed to cool to room temperature and carefully quenched with aqueous NaHCO3. The mixture was filtered and the filtrate concentrated under vacuum. The residue was then dissolved in DCM and washed with aqueous NaHCO3, brine and dried (MgSO4). The solvent was removed to afford 350 mg of 47 (10%) as a pale yellow solid: 1H NMR (400 MHz, CDCl3) δ 8.32 (d, J=4.8 Hz, 1H), 7.97 (m, 2H), 7.45 (m, 3H), 7.02 (J=4.8 Hz, 1H). 5.27 (br s, 2H); MS (+)-ES [M+H]+ 172.2 m/z.

Fuente