Reacción #48017

Ecuación de reacción

ethyl ether

sodium hydride

ethyl 5-fluoro-1H-indole-2-carboxylate

sodium hydride

3-bromomethylpyridine hydrobromide

3-bromomethylpyridine hydrobromide

→

expected product

Rendimiento 35.4%

Ethyl 5-fluoro-1-[(pyrid-3-yl)methyl]-1H-indole-2-carboxylate

Rendimiento 35.4%

Disolventes

dimethylformamide

dimethylformamide

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.STIRRINGThe mixture is stirred for 30 minutes at 0° C.
2. 2
   TemperaturaThe reaction mixture is cooled
3. 3
   workup.STIRRINGThe mixture is stirred for 30 minutes at 0° C.
4. 4
   workup.WAITfor 30 minutes at 20° C
5. 5
   TemperaturaThe reaction mixture is cooled again to 0° C.
6. 6
   workup.WAITAfter 30 minutes at 0° C.
7. 7
   workup.STIRRINGThe reaction mixture is stirred for 58 hours at 20° C
8. 8
   OtroThe organic phase is separated out
9. 9
   Extracciónthe aqueous phase is re-extracted with 100 ml of ethyl ether
10. 10
    Lavadowashed with 50 ml of water
11. 11
    Secadodried over sodium sulfate
12. 12
    Filtraciónfiltered
13. 13
    Concentraciónconcentrated under reduced pressure
14. 14
    OtroThe residue is purified by preparative chromatography (eluent: dichloromethane/acetone)

Procedimiento

A solution of 1 g (4.73 mmol) of ethyl 5-fluoro-1H-indole-2-carboxylate is added dropwise to a suspension of 0.38 g (9.45 mmol) of 60% sodium hydride in 10 ml of dimethylformamide, stirred at 0° C. under argon. The mixture is stirred for 30 minutes at 0° C. and then for 30 minutes at 20° C. The reaction mixture is cooled and 1.24 g (4.8 mmol) of 3-bromomethylpyridine hydrobromide are added portionwise. The mixture is stirred for 30 minutes at 0° C. and then for 30 minutes at 20° C. The reaction mixture is cooled again to 0° C. and a further 0.38 g (9.45 mmol) of 60% sodium hydride in 10 ml of dimethylformamide is added. After 30 minutes at 0° C., 1.24 g (4.8 mmol) of 3-bromomethylpyridine hydrobromide are added portionwise. The reaction mixture is stirred for 58 hours at 20° C. The mixture is then poured into a solution of 100 ml of ice-water and 100 ml of ethyl ether. The organic phase is separated out and the aqueous phase is re-extracted with 100 ml of ethyl ether. The organic phases are combined, washed with 50 ml of water and then dried over sodium sulfate, filtered and then concentrated under reduced pressure. The residue is purified by preparative chromatography (eluent: dichloromethane/acetone). 0.5 g of expected product is obtained in the form of a solid, which is used without further purification in the subsequent synthesis.

Fuente