Reacción #325764

Ecuación de reacción

sodium sulfite

sodium bicarbonate

2-chloroacetic acid

sodium hydroxide

5-bromo-6-chloropyridine-3-sulfonyl chloride

→

3-bromo-2-chloro-5-methanesulfonyl-pyridine

Rendimiento 19.3%

Disolventes

water

water

Condiciones de reacción

Tratamiento posterior

1. 1
   Temperaturaat room temperature overnight under a nitrogen atmosphere, the mixture was heated to 40° C.
2. 2
   workup.STIRRINGThe resulting mixture was stirred
3. 3
   Temperaturaat reflux for 48 hours
4. 4
   Temperaturacooled to room temperature
5. 5
   FiltraciónThe precipitated product was collected by filtration
6. 6
   Lavadowashed with water (50 mL)
7. 7
   Otropurified by column chromatography (gradient elution with 15-20% ethyl acetate in petroleum ether)

Procedimiento

A stirred solution of sodium sulfite (4.80 g, 38.1 mmol) and sodium bicarbonate (6.10 g, 72.6 mmol) in water (100 mL) was cooled to 15° C., and 5-bromo-6-chloropyridine-3-sulfonyl chloride (10.00 g, 34.4 mmol) was added. After being stirred at 15° C. for 3 hours and then at room temperature overnight under a nitrogen atmosphere, the mixture was heated to 40° C., and a solution of 2-chloroacetic acid (3.80 g, 40.2 mmol) and sodium hydroxide (1.90 g. 47.5 mmol) in water (20 mL) was added. The resulting mixture was stirred at reflux for 48 hours and then cooled to room temperature. The precipitated product was collected by filtration, washed with water (50 mL) and purified by column chromatography (gradient elution with 15-20% ethyl acetate in petroleum ether) to afford 3-bromo-2-chloro-5-methanesulfonyl-pyridine (1.80 g, 6.65 mmol) as a white solid. A solution of 2-chloroacetic acid (1.90 g, 20.1 mmol) and sodium hydroxide (0.80 g, 20.0 mmol) in water (10 mL) was added to the filtrate. The mixture was heated at reflux overnight, and then evaporated to remove most of the water (about 100 mL). The residue was cooled to room temperature, and then extracted with dichloromethane (80 mL×3). The combined organic layers were dried over sodium sulfate and concentrated in vacuo. The residue was purified by flash column chromatography (gradient elution with 15-20% ethyl acetate in petroleum ether) to afford another batch of 3-bromo-2-chloro-5-methanesulfonyl-pyridine (1.30 g, 4.8 mmol, yield of two batches 35.5%) as a white solid (reference: U.S. Pat. No. 5,424,481).

Fuente