Reacción #64954

ord-43d0b048f05b4c92bf685f0b8d64e2b7

Ecuación de reacción

CN1CCCC2CN(Cc3ccccc3)CC21
6-benzyl-1-methyl-octahydropyrrolo[3,4-b]pyridine
Cl.Cl.Nc1c(F)c(N)c(F)c(F)c1F
dihydrochloride
CN1CCCC2CNCC21
1-Methyl-octahydropyrrolo[3,4-b]pyridine

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.DISTILLATIONWorking up by distillation
  2. 2
    Otrogives 2.6 g (34% of theory) of a colorless oil of boiling point 83°-85°/12 mbar)

Procedimiento

11.7 g (54 retool) of 6-benzyl-1-methyl-octahydropyrrolo[3,4-b]pyridine as the dihydrochloride are hydrogenated in 100 ml of methanol over palladium-on-active charcoal in accordance with the working instructions of Example Id. Working up by distillation gives 2.6 g (34% of theory) of a colorless oil of boiling point 83°-85°/12 mbar).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05416096uspto-grants-1995_05