Reaktion #1010

ord-ee77b780e0524603be88a42bd2c29021

Reaktionsgleichung

Cl
hydrochloride
Clc1nccc2c1ncn2Cc1ccccc1
1-benzyl-4-chloro-1H-imidazo[4,5-c]pyridine
OC1CN2CCC1CC2
3-quinuclidinol
c1ccc(Cn2cnc3c(OC4CN5CCC4CC5)nccc32)cc1
title compound
Ausbeute 48.6%
c1ccc(Cn2cnc3c(OC4CN5CCC4CC5)nccc32)cc1
3-(1-Benzyl-1H-imidazo[4,5-c]pyridin-4-yloxy)-1-aza-bicyclo[2,2,2]octane
Ausbeute 48.6%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

Following the procedure of Example 1, 1-benzyl-4-chloro-1H-imidazo[4,5-c]pyridine (0.78 g, 3.2 mmol) was treated with 3-quinuclidinol (0.44 g, 3.5 mmol) to give 0.52 g (39%) of the title compound as the hydrochloride, 2.5 hydrate: mp 162°-183° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05723468uspto-grants-1998_03