Reacción #45394

Ecuación de reacción

NaN3

dioxane

(2E)-3-(4-bromo-2-thienyl)acrylic acid

SOCl2

→

desired product

3-bromothieno[3,2-c]pyridin-4(5H)-one

Disolventes

water

dichloromethane

Condiciones de reacción

Tratamiento posterior

1. 1
   Temperaturaheated
2. 2
   Temperaturato reflux for 2 hours
3. 3
   Concentraciónconcentrated
4. 4
   workup.DISSOLUTIONThe residue was dissolved in dioxane (100 mL)
5. 5
   workup.STIRRINGThe resulting mixture was stirred at room temperature for 2.5 hours
6. 6
   Extracciónextracted twice with 150 mL of ethyl acetate
7. 7
   LavadoThe combined organics were washed with water and brine
8. 8
   Secadodried (Na2SO4)
9. 9
   Filtraciónfiltered
10. 10
    Concentraciónconcentrated
11. 11
    workup.ADDITIONA solution of the residue in dichloromethane (150 mL) was added dropwise over 5 hours
12. 12
    Otrofitted with 2 air-cooled condensers
13. 13
    workup.STIRRINGThe mixture was stirred
14. 14
    Temperaturaat reflux for an additional 1 hour
15. 15
    Temperaturacooled to room temperature
16. 16
    Concentraciónconcentrated
17. 17
    Temperaturahexanes (200 mL), cooled
18. 18
    Filtraciónfiltered
19. 19
    LavadoThe filter cake was washed with additional diethyl ether/hexanes
20. 20
    Otrodried

Procedimiento

A suspension of (2E)-3-(4-bromo-2-thienyl)acrylic acid (commercially available, 50.2 g, 0.215 mol) in dichloromethane (150 mL) was treated with DMF (2 drops) and SOCl2 (23 mL, 0.315 mol), stirred at room temperature for 48 hours, heated to reflux for 2 hours, and concentrated. The residue was dissolved in dioxane (100 mL) and added to a vigorously stirred solution of NaN3 (25 g, 0.384 mol) in water (100 mL) and dioxane (100 mL) over 10 minutes. The resulting mixture was stirred at room temperature for 2.5 hours and extracted twice with 150 mL of ethyl acetate. The combined organics were washed with water and brine, dried (Na2SO4), filtered, and concentrated. A solution of the residue in dichloromethane (150 mL) was added dropwise over 5 hours to boiling diphenyl ether (150 mL) in a 3-neck flask fitted with 2 air-cooled condensers. The mixture was stirred at reflux for an additional 1 hour, cooled to room temperature, and concentrated. The residue was suspended in diethyl ether (100 mL) and hexanes (200 mL), cooled, and filtered. The filter cake was washed with additional diethyl ether/hexanes and dried to provide 37.4 g of the desired product. MS (ESI(+)) m/e 231 (M+H)+.

Fuente