Reacción #706797

Ecuación de reacción

ethyl 4-[(2,2-dimethyl-4-trifluoromethanesulfonyloxy-7-fluoro-(2H)-thiochromen-6-yl)ethynyl]-benzoate

Compound 211

ethyl 4-[(2,2-dimethyl-4-trifluoromethanesulfonyloxy-7-fluoro-(2H)-thiochromen-6-yl)ethynyl]-benzoate

2-methylthiophene

n-butyllithium

→

title compound

Ethyl 4-[[4-(5-methyl-thiophen-2yl)-2,2-dimethly-7-fluoro-(2H)-thiochromen-6-yl]-ethynyl]-benzoate

Disolventes

THF

THF

—

hexanes

THF

Condiciones de reacción

Tratamiento posterior

1. 1
   TemperaturaThe resulting solution was warmed to room temperature
2. 2
   TemperaturaThis solution was heated to 50° C. for 2 hours
3. 3
   Temperaturacooled to room temperature
4. 4
   Otrothe reaction quenched by the addition of saturated aqueous NH4Cl
5. 5
   ExtracciónThei solution was extracted with EtOAc
6. 6
   Lavadothe combined organic layers washed with H2O and saturated aqueous NaCl
7. 7
   Secadobefore being dried (MgSO4)
8. 8
   Concentraciónconcentrated under reduced pressure

Procedimiento

A solution of 2-methylthiophene (130.0 mg, 1.30 mmol) in 2.0 mL of THF was cooled to -78° C. and n-butyllithium (83.3 mg, 1.30 mmol, 0.84 ml of a 1.6M solution in hexanes) was added and the solution warmed to 0° C. during 1.5 hours. A solution of ZnCl2 (341.0 mg, 2.50 mmol) in 3.0 mL THF was slowly added via cannula. The resulting solution was warmed to room temperature, stirred for 40 minutes, and transferred via cannula to a solution of ethyl 4-[(2,2-dimethyl-4-trifluoromethanesulfonyloxy-7-fluoro-(2H)-thiochromen-6-yl)ethynyl]-benzoate (Compound 211, 158.0 mg, 0.31 mmol) and tetrakis(triphenylphosphine) palladium(0) (24.0 mg, 0.02 mmol) in 2.0 mL THF. This solution was heated to 50° C. for 2 hours, cooled to room temperature, and the reaction quenched by the addition of saturated aqueous NH4Cl. Thei solution was extracted with EtOAc and the combined organic layers washed with H2O and saturated aqueous NaCl before being dried (MgSO4) and concentrated under reduced pressure. The title compound, 70.0 mg (50%), was isolated by column chromatography (3% EtOAc/hexanes) as a waxy solid. 1H NMR (300 MHz, CDCl3) δ:8.01 (2H, d, J=8.3 Hz), 7.61 (1H, d, J=7.5 Hz), 7.58 (2H, d, J=8.3 Hz), 7.13 (1H, d, J=7.2 Hz), 6.82 (1H, d, J=4.4 Hz), 6.73 1H, d, J=4.4 Hz), 5.96 (1H, s), 4.39 (2H, q, J=7.1 Hz), 2.52 (3H, s), 1.46 (6H, s), 1.41 (3H, t, J=7.1 Hz).

Fuente