反応 #487567

ord-1255f5b7c872423bb3640fca0206620b

反応方程式

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

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過The reaction mixture was filtered
  2. 2
    洗浄washed with MeOH
  3. 3
    濃縮The filtrate was concentrated under vacuum

実験手順

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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08741895B2uspto-grants-2014_06