Reaktion #969906

ord-b943579a3553441aa21192e72e2503a9

Reaktionsgleichung

C1CN2CCC(CC2)N1
1,4-diazabicyclo[3.2.2]nonane
O=[N+]([O-])c1cccnc1Cl
2-chloro-nitropyridine
C1COCCO1
dioxane
O=[N+]([O-])c1ccc(N2CCN3CCC2CC3)nc1
title compound
O=[N+]([O-])c1ccc(N2CCN3CCC2CC3)nc1
4-(5-Nitro-pyridin-2-yl)-1,4-diaza-bicyclo[3.2.2]nonane

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    ExtraktionThe mixture was extracted with dichloromethane (3×50 ml)

Vorschrift

1,4-diazabicyclo[3.2.2]nonane (6.3 g, 50 mmol) was added to a mixture of 2-chloro-nitropyridine (11.9, 75 mmol), and dioxane (250 ml) at 0° C. The reaction mixture was allowed to reach room-temperature. Water (100 ml) was added. The mixture was extracted with dichloromethane (3×50 ml). Chromatography on silica gel with dichloromethane and 10% methanol as solvent gave the title compound as an oil. Yield 8.1 g (65%). Mp. 143-146° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08236793B2uspto-grants-2012_08