Reaktion #438830

ord-c07c0ab157704ac0969a79d74be51adb

Reaktionsgleichung

CC(=O)C1CCN(C(=O)OC(C)(C)C)CC1
1-tert-butoxycarbonyl-4-acetyl-piperidine
Nc1ncccc1C=O
2-amino-3-formyl-pyridine
O=C(O)[C@@H]1CCCN1
L-proline
CC(C)(C)OC(=O)N1CCC(c2ccc3cccnc3n2)CC1
title compound
Ausbeute 24.9%
CC(C)(C)OC(=O)N1CCC(c2ccc3cccnc3n2)CC1
4-([1,8]Naphthyridin-2-yl)-piperidine-1-carboxylic acid tert-butyl ester
Ausbeute 24.9%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeAfter removing the solvent in vacuo the residue
  2. 2
    Sonstigeobtained in an identical reaction
  3. 3
    Sonstigechromatographed on silica gel with ethyl acetate/n-heptane (1:1)

Vorschrift

3.14 g of 1-tert-butoxycarbonyl-4-acetyl-piperidine and 1.83 g of 2-amino-3-formyl-pyridine were refluxed with 0.25 g of L-proline in n-butanol for 72 hours. After removing the solvent in vacuo the residue was combined with the residue obtained in an identical reaction and chromatographed on silica gel with ethyl acetate/n-heptane (1:1) to give 1.08 g of the title compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06743800B1uspto-grants-2004_06