Реакция #75149

ord-469b644151a9415fbfd03bf85b206a76

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThe reaction mixture is cooled
  2. 2
    Другоеthe layers are separated
  3. 3
    СушкаThe 4-methyl-2-pentanone-phase is dried
  4. 4
    Фильтрацияfiltered
  5. 5
    Другоеevaporated
  6. 6
    ДругоеThe residue is purified by column-chromatography over silica gel using
  7. 7
    workup.ADDITIONa mixture of trichloromethane and 5% of methanol as eluent
  8. 8
    ДругоеThe pure fractions are collected
  9. 9
    Другоеthe eluent is evaporated
  10. 10
    ДругоеThe residue is triturated in 4-methyl-2-pentanone
  11. 11
    ФильтрацияThe solid product is filtered off
  12. 12
    Другоеdried

Методика

A mixture of 4.8 parts of 1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-one, 5.6 parts of 3-methyl-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one hydrochloride, 7.4 parts of sodium carbonate and 200 parts of 4-methyl-2-pentanone is stirred and refluxed overnight with water-separator. The reaction mixture is cooled, water is added and the layers are separated. The 4-methyl-2-pentanone-phase is dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and 5% of methanol as eluent. The pure fractions are collected and the eluent is evaporated. The residue is triturated in 4-methyl-2-pentanone. The solid product is filtered off and dried, yielding 4.0 parts (50%) of 8-[3-(1,3-dihydro-2-oxo-2H-benzimidazol-1-yl)propyl]-3-methyl-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one; mp. 186° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04175129uspto-grants-1979_11