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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734979Generated: October 30, 2026

Potassium Carbonate → N-{2-(methyloxy)-5-[3-(4-{[2-(methyloxy)phenyl]sulfonyl}-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}cyclopropanesulfonamide

https://huagongshe.com/reaction/734979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium AcetateHCID 517044—
ReactantBis(pinacolato)diboraneHCID 2733548—
ReactantN-(5-Bromo-2-methoxypyridin-3-yl)cyclopropanesulfonamideHCID 57843318—
Reactant7-Bromo-2-(4-{[2-(methyloxy)phenyl]sulfonyl}-1-piperazinyl)quinoxalineHCID 68501552—
Solvent1,4-DioxaneHCID 31275—
ProductN-{2-(methyloxy)-5-[3-(4-{[2-(methyloxy)phenyl]sulfonyl}-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}cyclopropanesulfonamideHCID 5784340738%

Reaction Steps

A slurry of 7-bromo-2-(4-{[2-(methyloxy)phenyl]sulfonyl}-1-piperazinyl)quinoxaline (0.54 mmol), bis(pinacolato)diboron (0.81 mmol), potassium acetate (2.15 mmol), and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) dichloromethane complex (1:1) (0.05 mmol) in 1,4-dioxane (4 ml) was heated at 100° C. After the reaction stirred for 1 hour, N-[5-bromo-2-(methyloxy)-3-pyridinyl]cyclopropanesulfonamide (0.81 mmol) and 2M solution potassium carbonate (2 ml) was added and continued to stir for 1 hour. The reaction was cooled to ambient temperature, separated the organic layer and purified directly on silica by column chromatography (30-100% ethyl acetate/hexanes). The desired fractions were combined and concentrated to give the title compound (125 mg, 38% yield) as a pale tan solid. MS(ES)+ m/e 611.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592342B2
Source datasetuspto-grants-2009_09
ORD IDord-e80c496dbd144289b5a0811a7904a78a
Source noteuspto-grants-2009_09