Reacción #59157

Ecuación de reacción

3-(4-bromo-benzoyl)-cyclohexanecarboxylic acid methyl ester

4-aminophenyl boronic acid

→

3-(4′-amino-biphenyl-4-carbonyl)-cyclohexanecarboxylic acid methyl ester

Disolventes

toluene

dioxane

Na2CO3

Condiciones de reacción

Tratamiento posterior

1. 1
   Otrothe mixture was degassed
2. 2
   Otroby bubbling with a flow of argon for 45 minutes
3. 3
   TemperaturaThe reaction mixture was cooled to rt
4. 4
   Filtraciónfiltered through a pad of Celite®
5. 5
   Lavadorinsing with ethyl acetate
6. 6
   OtroThe organic layer was separated
7. 7
   Lavadowashed with water and brine
8. 8
   Secadodried (Na2SO4)
9. 9
   OtroThe solvent was removed by rotary evaporation
10. 10
    Otrothe solid residue was purified

Procedimiento

To a solution of 3-(4-bromo-benzoyl)-cyclohexanecarboxylic acid methyl ester (500 mg, 1.54 mmol) and 4-aminophenyl boronic acid (252 mg, 1.85 mmol) in toluene (40 mL) and dioxane (10 mL), 2 N aqueous Na2CO3 (10 mL) was added, and the mixture was degassed by bubbling with a flow of argon for 45 minutes. (1,1-Bis(diphenylphosphino)ferrocene)-dichloropalladium (63 mg, 0.08 mmol) was added to the mixture, which was then heated at 80° C. overnight. The reaction mixture was cooled to rt, and then filtered through a pad of Celite®, rinsing with ethyl acetate. The organic layer was separated, washed with water and brine, and dried (Na2SO4). The solvent was removed by rotary evaporation, and the solid residue was purified by using a Biotage QuadUV flash chromatography system (eluant: 3:1 hexane/EtOAc). The product 3-(4′-amino-biphenyl-4-carbonyl)-cyclohexanecarboxylic acid methyl ester was obtained as a brown solid (200 mg, yield 38.5%). 1H NMR (300 MHz, DMSO) δ 7.90 (d, 2H), 7.60 (d, 2H), 7.45 (d, 2 H), 6.80 (d, 2H), 3.70 (s, 3H), 3.25 (m, 1H), 2.50 (m, 1H), 2.20-1.90 (m, 4 H), 1.70-1.50 (m, 4H); LC-MS ret. time 3.80 min (method 2), m/z 338.17 (MH+).

Fuente