Réaction #42580

Équation de réaction

n-butyllithium

oxazole

methyl 3-{[ethyl(propyl)amino]carbonyl}-5-iodobenzoate

→

title compound

Methyl 3-{[ethyl(propyl)amino]carbonyl}-5-(1,3-oxazol-2-yl)benzoate

Solvants

ethyl acetate

tetrahydrofuran

tetrahydrofuran

Conditions de réaction

Traitement

1. 1
   TempératureThe reaction mixture is heated
2. 2
   Températureat reflux for 2 h
3. 3
   TempératureThe reaction mixture is cooled
4. 4
   Lavagewashed with water, and saturated sodium chloride
5. 5
   Séchagedried (sodium sulfate)
6. 6
   Filtrationfiltered
7. 7
   Concentrationconcentrated under reduced pressure
8. 8
   AutrePurification by flash column chromatography (silica gel, 60% ethyl acetate/hexane)

Mode opératoire

To a −70° C. stirred solution of oxazole (106 mg, 1.5 mmol) in tetrahydrofuran (4 mL) is added n-butyllithium (1.6 M in hexanes, 1.0 mL, 1.7 mmol). After 30 min, zinc chloride (1 M in diethyl ether, 4.6 mL, 4.6 mmol) is added and the reaction mixture is warmed to 0° C. for 1 h. To this mixture is added a solution of methyl 3-{[ethyl(propyl)amino]carbonyl}-5-iodobenzoate (535 mg, 1.45 mmol) in anhydrous tetrahydrofuran (1.8 mL) followed by palladium(0)tetrakis(triphenylphosphine) (120 mg, 0.10 mmol). The reaction mixture is heated at reflux for 2 h. The reaction mixture is cooled, diluted with ethyl acetate, washed with water, and saturated sodium chloride, dried (sodium sulfate), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica gel, 60% ethyl acetate/hexane) provides the title compound. ESI MS m/z 317.1 [M+H]+.

Source