Reacción #42396

Ecuación de reacción

n-butyllithium

oxazole

3-iodo-5-(methoxycarbonyl)benzoic acid

→

title compound

3-(Methoxycarbonyl)-5-(1,3-oxazol-2-yl)benzoic acid

Disolventes

tetrahydrofuran

tetrahydrofuran

Condiciones de reacción

Tratamiento posterior

1. 1
   TemperaturaThe reaction mixture is heated
2. 2
   Temperaturaat reflux for 15 h
3. 3
   TemperaturaThe reaction mixture is cooled
4. 4
   Filtraciónfiltered through diatomaceous earth
5. 5
   workup.ADDITIONdiluted with ethyl acetate (50 mL)
6. 6
   Lavadowashed with water, and brine
7. 7
   Secadodried (sodium sulfate)
8. 8
   Filtraciónfiltered
9. 9
   Concentraciónconcentrated under reduced pressure
10. 10
    OtroPurification by flash column chromatography (silica gel, 5% methanol/methylene chloride)

Procedimiento

To a −70° C. stirred solution of oxazole (432 mg, 6.3 mmol) in tetrahydrofuran (10 mL) is added n-butyllithium (2.5 M in hexanes, 2.75 mL, 6.9 mmol). After 30 min, zinc chloride (1 M in diethyl ether, 18.75 mL, 18.75 mmol) is added and the reaction mixture is warmed to 0° C. for 1 h. To this mixture is added a solution of 3-iodo-5-(methoxycarbonyl)benzoic acid prepared by the method in Example SP-281, step 1 (1.8 g, 6 mmol) in anhydrous tetrahydrofuran (10 mL) followed by palladium(0)tetrakis(triphenylphosphine) (291 mg, 0.25 mmol). The reaction mixture is heated at reflux for 15 h. The reaction mixture is cooled, filtered through diatomaceous earth, diluted with ethyl acetate (50 mL), washed with water, and brine, dried (sodium sulfate), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica gel, 5% methanol/methylene chloride) provides the title compound in pure form. ESI MS m/z 246.1 [M−H]−.

Fuente