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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46363생성일: 2026년 10월 24일

Dabco → 5-chloro-2,4-difluoro-N-pyrimidin-4-ylbenzenesulfonamide

https://huagongshe.com/ko/reaction/46363

반응식

참여 물질

역할이름HCID투입량
반응물DabcoHCID 9237—
반응물4-AminopyrimidineHCID 68958—
반응물5-Chloro-2,4-difluorobenzenesulphonyl chlorideHCID 2773527—
용매AcetonitrileHCID 6342—
생성물5-chloro-2,4-difluoro-N-pyrimidin-4-ylbenzenesulfonamideHCID 594365455%

반응 단계

A mixture of 4-aminopyrimidine (1.30 g, 13.7 mmol) and 1,4-diazabicyclo[2.2.2]octane (1.54 g, 13.7 mmol) were added concurrently to a solution of 5-chloro-2,4-difluorobenzenesulfonyl chloride (3.4 g, 14 mmol) in anhydrous acetonitrile (63 mL). The reaction mixture immediately turned yellow and a precipitate formed. The reaction mixture was stirred under argon. After 72 hours, the reaction mixture was filtered and the filtrate was concentrated in vacuo to give a residue. The residue was partitioned between 1M hydrochloric acid and ethyl acetate. The organic phase was separated, dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue was partially purified by automated flash column chromatography using an 80 g silica gel ISCO™ column using hexanes to 1% v/v acetic acid in ethyl acetate gradient elution. The product was purified a second time by reverse phase HPLC to give the title compound (193 mg, 5%) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541588B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-e411c3715dc34aff853b7427251500dc
출처 메모uspto-grants-2013_09