Реакция #75184

ord-e14ae101c17d401ab38a545c8ba86135

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураrefluxed overnight
  2. 2
    ТемператураThe reaction mixture is cooled
  3. 3
    Другоеthe layers are separated
  4. 4
    ДругоеThe organic phase is dried
  5. 5
    Фильтрацияfiltered
  6. 6
    Другоеevaporated
  7. 7
    ДругоеThe residue is crystallized from 4-methyl-2-pentanone

Методика

A mixture of 9 parts of 1-(3-chloropropyl)-1H-benzimidazole, 10 parts of 5-chloro-1,3-dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-one, 7.4 parts of sodium carbonate and 200 parts of 4-methyl-2-pentanone is stirred and refluxed overnight. The reaction mixture is cooled, water is added and the layers are separated. The organic phase is dried, filtered and evaporated. The residue is crystallized from 4-methyl-2-pentanone, yielding 2.9 parts (14%) of 1-{1-[3-(1H-benzimidazol-1-yl)propyl]-4-piperidinyl}-5-chloro-1,3-dihydro-2H-benzimidazol-2-one; mp. 224° C.

Источник

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