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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2309생성일: 2026년 10월 24일

N-bromobutanimide → N-[5-bromo-6-(2-hydroxyethoxy)pyrimidin-4-yl]-4-tert-butylbenzenesulfonamide

https://huagongshe.com/ko/reaction/2309

반응식

참여 물질

역할이름HCID투입량
반응물N-bromobutanimideHCID 67184—
반응물4-tert-butyl-N-[6-(2-hydroxyethoxy)pyrimidin-4-yl)benzenesulfonamideHCID 11783102—
반응물Sodium BisulfiteHCID 23665763—
용매DimethylformamideHCID 6228—
생성물N-[5-bromo-6-(2-hydroxyethoxy)pyrimidin-4-yl]-4-tert-butylbenzenesulfonamideHCID 1102637465.7%

반응 단계

To a solution of 4-tert-butyl-N-[6-(2-hydroxyethoxy)pyrimidin-4-yl)benzenesulfonamide (210 mg) in dimethylformamide (4 ml) is added N-bromosuccinimide (116 mg), and the mixture is stirred at room temperature for one hour. The mixture is treated with aqueous sodium hydrogen sulfite solution, and extracted with ethyl acetate. The ethyl acetate layer is washed, dried and evaporated to remove the solvent. The residue is purified by silica gel column chromatography (solvent; chloroform/methanol=40:1), and recrystallized from hexane/ethyl acetate to give N-[5-bromo-6-(2-hydroxyethoxy)pyrimidin-4-yl]-4-tert-butylbenzenesulfonamide (169 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728706
출처 데이터셋uspto-grants-1998_03
ORD IDord-da9e15d8493a44cfbbae58022cf084ac
출처 메모uspto-grants-1998_03