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HRID 1082303생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1082303

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물4,6-DichloropyrimidineHCID 70943—
반응물4-tert-ButylbenzenesulfonamideHCID 222872—
용매Hydrochloric AcidHCID 313—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물4-tert-butyl-N-(6-chloropyrimidin-4-yl)benzenesulfonamideHCID 1087107869.4%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05589478
출처 데이터셋uspto-grants-1996_12
ORD IDord-31127bca4c4c420e81a16e253c1c48ea
출처 메모uspto-grants-1996_12