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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469460Generated: October 26, 2026

2-Bromo-1-(thiophen-2-yl)ethan-1-one → (3R)-3-(2-(benzo[b]thiophen-3-yl)-2-(phenylamino)acetoxy)-1-(2-oxo-2-(thiophen-2-yl)ethyl)-1-azoniabicyclo[2.2.2]octane bromide

https://huagongshe.com/reaction/469460

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-1-(thiophen-2-yl)ethan-1-oneHCID 2776372—
Reactant(R)-quinuclidin-3-yl 2-(benzo[b]thiophen-3-yl)-2-(phenylamino)acetateHCID 58556957—
SolventEthyl AcetateHCID 8857—
Product(3R)-3-(2-(benzo[b]thiophen-3-yl)-2-(phenylamino)acetoxy)-1-(2-oxo-2-(thiophen-2-yl)ethyl)-1-azoniabicyclo[2.2.2]octane bromideHCID 5476507936.5%

Reaction Steps

(R)-quinuclidin-3-yl 2-(benzo[b]thiophen-3-yl)-2-(phenylamino)acetate (C19) (90 mg, 0.23 mmol) was dissolved in EtOAc (3 ml), and 2-bromo-1-(thiophen-2-yl)ethanone (51.7 mg, 0.25 mmol) was added. The reaction mixture was stirred at room temperature overnight. The crude was purified by flash chromatography (DCM/MeOH=9/1) to obtain (3R)-3-(2-(benzo[b]thiophen-3-yl)-2-(phenylamino)acetoxy)-1-(2-oxo-2-(thiophen-2-yl)ethyl)-1-azoniabicyclo[2.2.2]octane bromide (50 mg, 36.5% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629160B2
Source datasetuspto-grants-2014_01
ORD IDord-2a993f0564b44601ac1b8708e2b87f6d
Source noteuspto-grants-2014_01