Réaction #75164
ord-49cd37f1118140bb940d3bc8aa2a4093
Équation de réaction
Réactifs
Réactifs
Solvants
Conditions de réaction
Traitement
- 1Températureheated at 50°-60° C. for 1.50 hours
- 2workup.ADDITIONThe reaction mixture is poured onto ice-water
- 3FiltrationThe precipitated product is filtered off
- 4workup.DISSOLUTIONdissolved in trichloromethane
- 5LavageThe solution is washed with water
- 6Autredried
- 7Filtrationfiltered
- 8Autreevaporated
- 9AutreThe solid residue is purified by column-chromatography over silica gel using
- 10workup.ADDITIONa mixture of trichloromethane and 10% of methanol as eluent
- 11AutreThe pure fractions are collected
- 12Autrethe eluent is evaporated
- 13workup.STIRRINGThe solid residue is stirred in a small amount of trichloromethane
- 14FiltrationThe product is filtered off
- 15Autrecrystallized from 4-methyl-2-pentanone
Mode opératoire
A mixture of 6.7 parts of 5-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one methanesulfonate, 4.2 parts of 4-(4-chlorophenyl)-4-piperidinol, 3.2 parts of sodium carbonate and 32 parts of 4-methyl-2-pentanone is stirred and heated at 50°-60° C. for 1.50 hours. The reaction mixture is poured onto ice-water. The precipitated product is filtered off and dissolved in trichloromethane. The solution is washed with water, dried, filtered and evaporated. The solid residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and 10% of methanol as eluent. The pure fractions are collected and the eluent is evaporated. The solid residue is stirred in a small amount of trichloromethane. The product is filtered off and crystallized from 4-methyl-2-pentanone, yielding 2 parts (24%) of 5-chloro-1-{3-[4-(4-chlorophenyl)-4-hydroxy-1-piperidinyl]propyl}-1,3-dihydro-2H-benzimidazol-2-one; mp. 190.8° C.