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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1082303Generated: October 27, 2026

Sodium hydride → 4-tert-butyl-N-(6-chloropyrimidin-4-yl)benzenesulfonamide

https://huagongshe.com/reaction/1082303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4,6-DichloropyrimidineHCID 70943—
Reactant4-tert-ButylbenzenesulfonamideHCID 222872—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-tert-butyl-N-(6-chloropyrimidin-4-yl)benzenesulfonamideHCID 1087107869.4%

Reaction Steps

To a solution of 4,6-dichloropyrimidine (1.33 g) and 4-tertbutylbenzenesulfonamide (1.96 g) in dimethylformamide (20 ml) is added sodium hydride (60% dispersion-type, 714 mg). The mixture is stirred at room temperature for two hours, and the reaction solution is diluted with 10% hydrochloric acid and water. The mixture is extracted with ethyl acetate, and the ethyl acetate layer is washed, dried, and evaporated to remove the solvent. The residue is recrystallized from ethyl acetate to give 4-tert-butyl-N-(6-chloropyrimidin-4-yl)benzenesulfonamide (2.02 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05589478
Source datasetuspto-grants-1996_12
ORD IDord-31127bca4c4c420e81a16e253c1c48ea
Source noteuspto-grants-1996_12