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1-Benzyloxycarbonylamino3-([1,8]naphthyridin-2-yl)-propane → 3-(5,6,7,8-Tetrahydro-1,8-naphthyridin-2-yl)propan-1-amine

HRID 617902
Notes
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Reaction equation

HRID 617902 reaction equation
C(OC([NH:11][CH2:12][CH2:13][CH2:14][C:15]1[CH:24]=[CH:23][C:22]2[C:17](=[N:18][CH:19]=[CH:20][CH:21]=2)[N:16]=1)=O)C1C=CC=CC=1.[H][H]>CCO.[Pd].[C]>[N:16]1[C:17]2[NH:18][CH2:19][CH2:20][CH2:21][C:22]=2[CH:23]=[CH:24][C:15]=1[CH2:14][CH2:13][CH2:12][NH2:11]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 2

HCID 218500091-Benzyloxycarbonylamino3-([1,8]naphthyridin-2-yl)-propaneHCID 178418361HCID 178418361, compound

Product 1

HCID 98775993-(5,6,7,8-Tetrahydro-1,8-naphthyridin-2-yl)propan-1-amine

Reagents, catalysts & solvents 2

HCID 178418390HCID 178418390, compoundCatalystHCID 702EthanolSolvent

Procedure

A mixture of 1-7 (0.40 g, 1.24 mmol) and 10% Pd/carbon (0.08 g) in EtOH (12 mL) was stirred under a balloon of hydrogen for 20 h. Filtration through a celite pad and then evaporative removal of the filtrate solvent gave 1-8 as a colorless oil.

Workup

  1. filtrationFiltration through a celite pad
  2. customremoval of the filtrate solvent

Sources & evidence

ORD record
ord-b76cde09736546e88cde543518f2299b
Source dataset
uspto-grants-1999_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05952341

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes