Реакция #487567

ord-1255f5b7c872423bb3640fca0206620b

Уравнение реакции

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

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ФильтрацияThe reaction mixture was filtered
  2. 2
    Промывкаwashed with MeOH
  3. 3
    КонцентрированиеThe filtrate was concentrated under vacuum

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08741895B2uspto-grants-2014_06