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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899118Generated: October 29, 2026

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

https://huagongshe.com/reaction/899118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Boc-9-oxa-3,7-diazabicyclo[3.3.1]nonaneHCID 18540412—
ReactantMethanesulfonic acid 2-{[3-(4-cyanophenyl)propyl]methanesulfonylamino}ethyl esterHCID 86616240—
SolventAcetonitrileHCID 6342—
Product7-(2-{[3-(4-Cyanophenyl)propyl]methanesulfonylamino}ethyl)-9-oxa-3,7-diazabicyclo[3.3.1]nonane-3-carboxylic acid tert-butyl esterHCID 69072053—

Reaction Conditions

Temperature57.5 °C

Reaction Steps

A mixture of 9-oxa-3,7-diaza-bicyclo[3.3.1]nonane-3-carboxylic acid tert-butyl ester (2.35 g, 0.01 mol; see WO 01/28992), methanesulfonic acid 2-{[3-(4-cyanophenyl)propyl]methanesulfonylamino}ethyl ester (3.7 g, 0.01 mol; see Preparation A above) and anhydrous K2CO3 (2.1 g, 0.015 mol) in dry acetonitrile (70 mL) was stirred under nitrogen atmosphere at 55-60° C. for 3 days. After filtration and concentration, the crude product was purified by column chromatography (silica gel: 60-120 mesh, eluent: petroleum ether-ethyl acetate, 50:50). Yield: 3.25 g (66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07354917B2
Source datasetuspto-grants-2008_04
ORD IDord-21dcb69662c547549377bfcaa064083f
Source noteuspto-grants-2008_04