Reacción #487567

ord-1255f5b7c872423bb3640fca0206620b

Ecuación de reacción

CN(c1ccnc2[nH]ccc12)C1CCCN(Cc2ccccc2)C1
N-(1-benzylpiperidin-3-yl)-N-methyl-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)-amine
CCO
ethanol
Cl
hydrogen chloride
CN(c1ccnc2[nH]ccc12)C1CCCNC1.Cl.Cl.Cl
orange oil
CN(c1ccnc2[nH]ccc12)C1CCCNC1.Cl.Cl.Cl
N-methyl-N-piperidin-3-yl-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)-amine trihydrochloride

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónThe reaction mixture was filtered
  2. 2
    Lavadowashed with MeOH
  3. 3
    ConcentraciónThe filtrate was concentrated under vacuum

Procedimiento

A degassed mixture of N-(1-benzylpiperidin-3-yl)-N-methyl-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)-amine (0.17 g, 0.00053 mol) and palladium hydroxide (0.15 g, 0.00011 mol) in ethanol (3.5 mL, 0.060 mol) and 3.0 M of hydrogen chloride in water (0.40 mL) was stirred under an atmosphere of hydrogen over 2.5 days. The reaction mixture was filtered and washed with MeOH. The filtrate was concentrated under vacuum to give 92 mg of orange oil.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08741895B2uspto-grants-2014_06