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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 218195생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/218195

반응식

참여 물질

역할이름HCID투입량
반응물4-tert-butyl-N-[5-chloro-2-(4-nitro-pyrazol-1-yl)-pyridin-3-yl]-benzenesulfonamideHCID 68464085—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물N-[2-(4-amino-pyrazol-1-yl)-5-chloro-pyridin-3-yl]-4-tert-butyl-benzenesulfonamideHCID 59428137—

반응 단계

To a solution of 4-tert-butyl-N-[5-chloro-2-(4-nitro-pyrazol-1-yl)-pyridin-3-yl]-benzenesulfonamide (100 mg, 0.229 mmol) in 2 mL of ethanol was added 10% Pd/C and the heterogeneous solution was stirred under an atmosphere of hydrogen. After two hours, the reaction was filtered through celite and concentrated in vacuo. The crude reside was subsequently purified by flash column chromatography (0-100% ethyl acetate in hexanes) to afford N-[2-(4-amino-pyrazol-1-yl)-5-chloro-pyridin-3-yl]-4-tert-butyl-benzene sulfonamide as a white solid: MS (ES) M+H expected 406.1, found 406.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198309B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-a019efc9ed394466846f301594301252
출처 메모uspto-grants-2012_06