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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899147Generated: October 28, 2026

Potassium Carbonate → 7-(2-{[2-(4-Cyanophenoxy)ethyl]methanesulfonylamino}ethyl)-9-oxa-3,7-diazabicyclo[3.3.1]nonane-3-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/899147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Boc-9-oxa-3,7-diazabicyclo[3.3.1]nonaneHCID 18540412—
ReactantN-(2-Bromoethyl)-N-[2-(4-cyanophenoxy)ethyl]methanesulfonamideHCID 69075823—
SolventAcetonitrileHCID 6342—
Product7-(2-{[2-(4-Cyanophenoxy)ethyl]methanesulfonylamino}ethyl)-9-oxa-3,7-diazabicyclo[3.3.1]nonane-3-carboxylic acid tert-butyl esterHCID 69074760—

Reaction Steps

To a suspension of N-(2-bromoethyl)-N-[2-(4-cyanophenoxy)ethyl]methane-sulfonamide (6 g, 0.019 mol; see Preparation C above) and anhydrous potassium carbonate (3.6 g, 0.026 mol) in dry acetonitrile (100 mL) was added 9-oxa-3,7-diaza-bicyclo[3.3.1]nonane-3-carboxylic acid tert-butyl ester (4.35 g, 0.019 mol; see WO 01/28992), and the resultant mixture was then stirred at 50-55° C. overnight. After completion of the reaction (as determined by TLC), the mixture was filtered and concentrated. The crude product was further purified by column chromatography (silica gel: 60-120 mesh, eluent: chloroform-methanol, 99:1). Yield: 4.2 g (46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07354917B2
Source datasetuspto-grants-2008_04
ORD IDord-a11bcff4278344f384a6615848989c30
Source noteuspto-grants-2008_04