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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359918Generated: November 1, 2026

Acetyl chloride → N-[(6-Bromopyridin-2-yl)sulphonyl]acetamide

https://huagongshe.com/reaction/2359918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Bromopyridine-2-sulfonamideHCID 57345816—
SolventAcetonitrileHCID 6342—
ProductN-[(6-Bromopyridin-2-yl)sulphonyl]acetamideHCID 86667250—

Reaction Steps

6-Bromopyridine-2-sulphonamide (0.5 g, 2.11 mmol, prepared by the methods described in WO2005/058299) and potassium carbonate (2.92 g, 21.1 mmol) were initially charged in acetonitrile (10 ml). While cooling with ice, acetyl chloride (1.16 g, 14.8 mmol) was added dropwise and the reaction mixture was stirred at room temperature for 16 h. The solvent was removed under reduced pressure, and the residue was taken up in water and acidified with dilute hydrochloric acid solution. It was extracted with ethyl acetate and the solvent was removed under reduced pressure. This gave 0.54 g (85% of theory) of N-[(6-bromopyridin-2-yl)sulphonyl]-acetamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08686004B2
Source datasetuspto-grants-2014_04
ORD IDord-e4177b39fa5f40ca9af2143ba7806818
Source noteuspto-grants-2014_04