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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411526Generated: October 25, 2026

Potassium Carbonate → 4-({3-[3-Azabicyclo[3.2.1]oct-8-yl(methyl)amino]propyl}amino)benzonitrile

https://huagongshe.com/reaction/411526

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-benzyl-N-methyl-3-azabicyclo[3.2.1]octan-8-amineHCID 18541030—
Reactant3-(4-Cyanoanilino)propyl 4-methylbenzenesulfonateHCID 21867652—
SolventDimethylformamideHCID 6228—
Product4-({3-[3-Azabicyclo[3.2.1]oct-8-yl(methyl)amino]propyl}amino)benzonitrileHCID 1854090765.5%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 3-benzyl-N-methyl-3-azabicyclo[3.2.1]octan-8-amine (Preparation B; 4.0 g, 17.4 mmol), 3-(4-cyanoanilino)propyl 4-methyl-benzenesulfonate (Preparation G(ii); 5.74 g, 17.4 mmol), and potassium carbonate (2.40 g, 17.4 mmol) in DMF (85 mL) was heated at 90° C. under nitrogen overnight. The mixture was partitioned with water (200 mL) and diethyl ether (150 mL). The aqueous layer was extracted with ethyl acetate (2×50 mL). The combined organic extracts were washed with brine (2×30 mL), dried (Na2SO4), filtered and then concentrated in vacuo. The residue was chromatographed on silica gel, eluting with dichloromethane:methanol (98:2), to afford 3.40 g (50%) of the sub-title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559162B2
Source datasetuspto-grants-2003_05
ORD IDord-159d2fdcc8c34753ace01f967dbd9955
Source noteuspto-grants-2003_05