Reacción #6239

Ecuación de reacción

4-(3-aminopropyloxy)pyridine

triethylamine

thenoyl chloride

→

desired compound

Rendimiento 70.4%

4-[3-(2-thenoylamino)propyloxy]pyridine

Rendimiento 70.4%

Disolventes

methylene chloride

Condiciones de reacción

Tratamiento posterior

1. 1
   Temperaturacooling
2. 2
   workup.STIRRINGThe mixture was stirred at room temperature for 1.5 hours
3. 3
   LavadoThe reaction mixture was washed successively with a saturated aqueous solution of sodium bicarbonate and brine
4. 4
   Secadodried over anhydrous magnesium sulfate
5. 5
   workup.DISTILLATIONthe solvent was distilled off
6. 6
   OtroThe residue was purified by column chromatography (eluent: ethyl acetate)

Procedimiento

To a solution of 700 mg (4.60 mmol) of 4-(3-aminopropyloxy)pyridine and 0.77 ml (5.52 mmol) of triethylamine in 30 ml of methylene chloride, 0.50 ml (4.68 mmol) of thenoyl chloride was added under ice-cooling with stirring. The mixture was stirred at room temperature for 1.5 hours. The reaction mixture was washed successively with a saturated aqueous solution of sodium bicarbonate and brine and dried over anhydrous magnesium sulfate, and the solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate) to obtain 850 mg of the desired compound (yield: 70.0%, colorless crystals).

Fuente