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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 75992생성일: 2026년 10월 23일

Cesium carbonate → 4-tert-butyl-N-[5-chloro-2-(4-nitro-pyrazol-1-yl)-pyridin-3-yl]-benzenesulfonamide

https://huagongshe.com/ko/reaction/75992

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물4-nitro-1H-pyrazoleHCID 16376—
반응물trans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
반응물N-(2-bromo-5-chloro-pyridin-3-yl)-4-tert-butyl-benzenesulfonamideHCID 57942597—
촉매Copper iodideHCID 83717—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
용매DimethylacetamideHCID 31374—
생성물4-tert-butyl-N-[5-chloro-2-(4-nitro-pyrazol-1-yl)-pyridin-3-yl]-benzenesulfonamideHCID 68464085—

반응 단계

A solution of N-(2-bromo-5-chloro-pyridin-3-yl)-4-tert-butyl-benzene sulfonamide (534 mg, 1.32 mmol), 4-nitropyrazole (224 mg, 1.98 mmol), trans-N,N′-dimethyl-cyclohexane-1,2-diamine (42 μL, 0.264 mmol), copper iodide (51 mg, 0.264 mmol), and cesium carbonate (903 mg, 2.77 mmol) in 5 mL of N,N-dimethylacetamide was heated at 130° C. for 2 hours. Ethyl acetate and water were added and the layers were separated. The organic layer was washed with brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. The crude reside was subsequently purified by flash column chromatography (0-100% ethyl acetate in hexanes) to afford 4-tert-butyl-N-[5-chloro-2-(4-nitro-pyrazol-1-yl)-pyridin-3-yl]-benzenesulfonamide as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835468B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-f9f0f6399497473a809f2b5cef77dd9d
출처 메모uspto-grants-2014_09