Reacción #75193

Ecuación de reacción

1-(3-chloropropyl)-1,3-dihydro-3-(1-methylethenyl)-2H-benzimidazol-2-one

1-(1-methylethyl)-3-(4-piperidinyl)-2H-benzimidazol-2-one

sodium carbonate

potassium iodide

→

1-{1-[3-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)propyl]-4-piperidinyl}-1,3-dihydro-3-(1-methylethyl)-2H-benzimidazol-2-one

Rendimiento 64.0%

Disolventes

4-methyl-2-pentanone

water

Condiciones de reacción

Tratamiento posterior

1. 1
   Temperaturarefluxed overnight
2. 2
   Otrothe layers are separated
3. 3
   OtroThe organic phase is dried
4. 4
   Filtraciónfiltered
5. 5
   Otroevaporated
6. 6
   workup.STIRRINGThe residue is stirred for 30 minutes with a solution of 12 parts of a concentrated hydrochloric acid solution in 40 parts of ethanol
7. 7
   OtroThe solvent is evaporated
8. 8
   Extracciónthe product is extracted with trichloromethane
9. 9
   OtroThe extract is dried
10. 10
    Filtraciónfiltered
11. 11
    Otroevaporated
12. 12
    OtroThe residue is purified by column-chromatography over silica gel using
13. 13
    workup.ADDITIONa mixture of trichloromethane and methanol (95:5 by volume) as eluent
14. 14
    OtroThe pure fractions are collected
15. 15
    Otrothe eluent is evaporated
16. 16
    OtroThe residue is crystallized from 4-methyl-2-pentanone
17. 17
    FiltraciónThe product is filtered off
18. 18
    Otrodried

Procedimiento

A mixture of 4.15 parts of 1-(3-chloropropyl)-1,3-dihydro-3-(1-methylethenyl)-2H-benzimidazol-2-one, 3.9 parts of 1-(1-methylethyl)-3-(4-piperidinyl)-2H-benzimidazol-2-one, 3.2 parts of sodium carbonate, 0.1 parts of potassium iodide and 120 parts of 4-methyl-2-pentanone is stirred and refluxed overnight. The reaction mixture is cooled to room temperature, water is added and the layers are separated. The organic phase is dried, filtered and evaporated. The residue is stirred for 30 minutes with a solution of 12 parts of a concentrated hydrochloric acid solution in 40 parts of ethanol. The solvent is evaporated and the residue is suspended in water. The suspension is alkalized with a diluted ammonium hydroxide solution and the product is extracted with trichloromethane. The extract is dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from 4-methyl-2-pentanone. The product is filtered off and dried, yielding 4.2 parts (64%) of 1-{1-[3-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)propyl]-4-piperidinyl}-1,3-dihydro-3-(1-methylethyl)-2H-benzimidazol-2-one; mp. 174.3° C.

Fuente