Reacción #63199
ord-4bfa4c33e2054304a26c369a1db80481
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1OtroThe solvent was removed in vacuo
- 2workup.DISSOLUTIONthe residue was dissolved in chloroform
- 3Otrochromatographed on silica in chloroform and later chloroform/methanol 4:1
- 4workup.ADDITIONThe fractions containing the product
- 5Concentraciónwere concentrated
Procedimiento
A mixture of 3-(5,6,7,8-tetrahydroquinol-8-yl)propylamine (4.5 g), 2-chloro-3-nitro-5-(pyrid-3-ylmethyl)pyridine hydrochloride (5 g) and triethylamine (10 ml) was refluxed in ethanol (200 ml) for 7.5 hours. The solvent was removed in vacuo, the residue was dissolved in chloroform and chromatographed on silica in chloroform and later chloroform/methanol 4:1. The fractions containing the product were concentrated to give the title compound as an oil (6.1 g).