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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1366269생성일: 2026년 10월 27일

2-Aminobenzenesulfonamide → 2-(5-Bromo-2-chloropyrimidin-4-ylamino)benzenesulfonamide

https://huagongshe.com/reaction/1366269

반응식

참여 물질

역할이름HCID투입량
반응물2-AminobenzenesulfonamideHCID 72894—
반응물5-Bromo-2,4-dichloropyrimidineHCID 289973—
반응물Sodium BicarbonateHCID 516892—
용매Hydrochloric AcidHCID 313—
용매IsopropanolHCID 3776—
생성물2-(5-Bromo-2-chloropyrimidin-4-ylamino)benzenesulfonamideHCID 85997992—

반응 조건

온도90 °C

반응 단계

To a solution of 5-bromo-2,4-dichloropyrimidine (300 mg, 1.32 mmol) and 2-amino-benzenesulfonamide (340 mg, 1.97 mmol) in 2-propanol (3 mL), concentrated hydrochloric acid (0.06 mL) is added and the mixture is stirred at 90° C. for 4.5 hours. The mixture is poured into aqueous sodium hydrogen carbonate and extracted with ethyl acetate three times. The organic layer is washed with water, dried over sodium sulfate, and evaporated in vacuo. The residue is purified by column chromatography (hexane:ethyl acetate=2:1) to afford the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07893074B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-0a38286668a24c23a8428189c674cb6b
출처 메모uspto-grants-2011_02