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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411534Generated: October 30, 2026

Potassium Carbonate → Tert-butyl 3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl-(methyl)carbamate

https://huagongshe.com/reaction/411534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-(2-Bromoethoxy)benzonitrileHCID 2452212—
ReactantTert-butyl 3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamateHCID 18541001—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl-(methyl)carbamateHCID 1854089876%

Reaction Steps

A mixture of 4-(2-bromoethoxy)benzonitrile (see step (i) above; 0.94 g, 4.2 mmol), tert-butyl 3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate (Preparation D; 0.91 g, 3.8 mmol) and K2CO3 (0.79 g, 5.7 mmol) in 15 mL of dry DMF was stirred at 90° C. overnight before additional K2CO3 (1 g) was added. The mixture was diluted with 300 mL of DCM, and the mixture was washed with water. The organic layer was separated, dried with Na2SO4 and then evaporated. The crude product was purified by flash chromatography on silica gel, eluting with DCM:MeOH (10:1) containing 0.1% TEA, to yield 1.1 g (76%) of the sub-tide compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559162B2
Source datasetuspto-grants-2003_05
ORD IDord-af45229c152d45d1a6f430ab5e88bbd5
Source noteuspto-grants-2003_05