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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251812Generated: October 26, 2026

Citric Acid → N-(6-Chloropyrimidin-4-yl)-4-isopropylbenzenesulfonamide

https://huagongshe.com/reaction/2251812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantSodium hydrideHCID 24758—
Reactant4,6-DichloropyrimidineHCID 70943—
ReactantHCID 19098635HCID 19098635—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductN-(6-Chloropyrimidin-4-yl)-4-isopropylbenzenesulfonamideHCID 86003781—

Reaction Steps

996 mg (5.0 mmol) of isopropylbenzenesulfonamide were dissolved in 20 ml of dimethyl sulfoxide, after which 288 mg (6.0 mmol) of 50% sodium hydride were added and the mixture was stirred at room temperature for 30 minutes. 819 mg (5.5 mmol) of 4,6-dichloropyrimidine were then added and the reaction mixture was stirred overnight at room temperature. Subsequently, the mixture was heated at 90° C. for 3 hours and, after that, stirred at 120° C., in a microwave oven, for 30 minutes. After the reaction mixture had cooled down to room temperature, it was diluted with 150 ml of water, neutralized with citric acid and extracted three times with diethyl ether. The residue, which was obtained after drying with sodium sulfate and after removing the solvent, was dissolved in 100 ml of diethyl ether and extracted with an aqueous solution of sodium hydrogen carbonate. The aqueous phase was acidified and extracted with diethyl ether. The organic phase was dried, filtered and evaporated down to dryness, with 440 mg (28% of theory) of the title compound being obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07320979B2
Source datasetuspto-grants-2008_01
ORD IDord-345670760c40476ba526a2868a4cf0a9
Source noteuspto-grants-2008_01