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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469456Generated: October 31, 2026

2-Bromo-1-(thiophen-3-yl)ethan-1-one → HCID 54764990, compound

https://huagongshe.com/reaction/469456

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-1-(thiophen-3-yl)ethan-1-oneHCID 2776379—
ReactantHCID 46840422HCID 46840422—
SolventEthyl AcetateHCID 8857—
ProductHCID 54764990HCID 5476499061%

Reaction Steps

2-Bromo-1-(thiophen-3-yl)ethanone (25.6 mg, 0.12 mmol) was added to a solution of methyl 3-(2-oxo-1-phenyl-2-((R)-quinuclidin-3-yloxy)ethylamino)thiophene-2-carboxylate (C11) (50 mg, 0.12 mmol) in EtOAc (2 ml). The reaction mixture was stirred at room temperature overnight, and then the solvent was evaporated under vacuum. The residue was triturated with Et2O and then purified by preparative HPLC (Eluent: CH3CN/H2O) to obtain (3R)-3-(2-(2-(methoxycarbonyl)thiophen-3-ylamino)-2-phenylacetoxy)-1-(2-oxo-2-(thiophen-3-yl)ethyl)-1-azoniabicyclo[2.2.2]octane bromide (44.3 mg, 58.6% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629160B2
Source datasetuspto-grants-2014_01
ORD IDord-a175476e8e2149b3a8a1c891f352d0c6
Source noteuspto-grants-2014_01