Reaktion #8482

ord-838a0f414b414d4bad70479de4331dc3

Reaktionsgleichung

Cc1cccn2cc(-c3ccc(OCC4CO4)cc3)nc12
product
Cc1cccn2cc(-c3ccc(OCC4CO4)cc3)nc12
2-[4-[(2,3-Epoxy)propoxy]phenyl]-8-methylimidazo[1,2-a]pyridine
CCCNCC(O)COc1ccc(-c2cn3cccc(C)c3n2)cc1
title compound
CCCNCC(O)COc1ccc(-c2cn3cccc(C)c3n2)cc1
2-[4-(2-hydroxy-3-propylaminopropoxy)phenyl]-8-methylimidazo[1,2-a]pyridine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeevaporated
  2. 2
    Sonstigethe residue purified via silica gel chromatography (dichloromethane/methanol)

Vorschrift

The product of Step C (5.0 g) and propylamine (20 mL) was heated at 40° C. for 18 hours. The reaction was cooled to ambient temperature evaporated and the residue purified via silica gel chromatography (dichloromethane/methanol) to give the title compound which was converted to a HCl salt upon treatment with HCl/methanol.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07087757B2uspto-grants-2006_08