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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366273Generated: November 1, 2026

Potassium Carbonate → 2-(5-bromo-2-chloro-pyrimidin-4-ylamino)-N-methyl-benzenesulfonamide

https://huagongshe.com/reaction/1366273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-Bromo-2,4-dichloropyrimidineHCID 289973—
Reactant2-amino-N-methylbenzene-1-sulfonamideHCID 1132840—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-(5-bromo-2-chloro-pyrimidin-4-ylamino)-N-methyl-benzenesulfonamideHCID 58748399—

Reaction Steps

A suspension of 5-bromo-2,4-dichloropyrimidine (684 mg, 3.0 mmol) and 2-amino-N-methyl-benzenesulfonamide (559 mg, 3.0 mmol) in N,N-dimethylformamide (10 mL) containing potassium carbonate (830 mg, 6.0 mmol) is stirred at room temperature for 23 hours. Saturated aqueous ammonium chloride is added and the mixture is poured into water and extracted twice with ethyl acetate. The organic layer is washed with brine, dried over sodium sulfate, and evaporated in vacuo. The residue is purified by silica gel column chromatography (n-hexane-ethyl acetate gradient) to afford the title compound as a slightly yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893074B2
Source datasetuspto-grants-2011_02
ORD IDord-af3e9384b1144ccda743240f15326d78
Source noteuspto-grants-2011_02