Réaction #75164

ord-49cd37f1118140bb940d3bc8aa2a4093

Équation de réaction

CS(=O)(=O)O.O=c1[nH]c2cc(Cl)ccc2n1CCCO
5-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one methanesulfonate
OC1(c2ccc(Cl)cc2)CCNCC1
4-(4-chlorophenyl)-4-piperidinol
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
O=c1[nH]c2cc(Cl)ccc2n1CCCN1CCC(O)(c2ccc(Cl)cc2)CC1
5-chloro-1-{3-[4-(4-chlorophenyl)-4-hydroxy-1-piperidinyl]propyl}-1,3-dihydro-2H-benzimidazol-2-one
Rendement 24.0%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températureheated at 50°-60° C. for 1.50 hours
  2. 2
    workup.ADDITIONThe reaction mixture is poured onto ice-water
  3. 3
    FiltrationThe precipitated product is filtered off
  4. 4
    workup.DISSOLUTIONdissolved in trichloromethane
  5. 5
    LavageThe solution is washed with water
  6. 6
    Autredried
  7. 7
    Filtrationfiltered
  8. 8
    Autreevaporated
  9. 9
    AutreThe solid residue is purified by column-chromatography over silica gel using
  10. 10
    workup.ADDITIONa mixture of trichloromethane and 10% of methanol as eluent
  11. 11
    AutreThe pure fractions are collected
  12. 12
    Autrethe eluent is evaporated
  13. 13
    workup.STIRRINGThe solid residue is stirred in a small amount of trichloromethane
  14. 14
    FiltrationThe product is filtered off
  15. 15
    Autrecrystallized 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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US04175129uspto-grants-1979_11