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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72678생성일: 2026년 10월 25일

1-(5-Nitropyridin-2-yl)piperazine → HCID 25004371, 화합물

https://huagongshe.com/reaction/72678

반응식

참여 물질

역할이름HCID투입량
반응물1-(5-Nitropyridin-2-yl)piperazineHCID 2928799—
반응물3-[6-Chloro-5-phenyl-2-(trifluoromethyl)pyrimidin-4-yl]benzenesulfonamideHCID 86613621—
용매PyridineHCID 1049—
생성물HCID 25004371HCID 25004371—

반응 단계

The solution of 3-[6-chloro-5-phenyl-2-(trifluoromethyl)pyrimidin-4-yl]benzenesulfonamide (0.1 g, 0.242 mmol) in pyridine (2 ml) was treated with 1-(5-nitropyridin-2-yl)piperazine (0.075 g, 0.363 mmol) and stirred for 11 hours. Subsequently the reaction mixture was poured onto ice-cold water and extracted with ethyl acetate (25 ml). The organic layer was washed with brine and evaporated to give the crude material. Purification by column chromatography (elution with 70% ethyl acetate in hexane) yielded the title compound. 1H-NMR (CDCl3) δ: 3.45-3.46 (m, 4H), 3.72 (m, 4H), 6.52-6.54 (d, 1H), 7.08-7.11 (d, 2H), 7.21-7.26 (m, 2H), 7.32-7.34 (d, 1H), 7.40-7.42 (d, 1H), 7.50 (m, 1H), 7.68 (s, 1H), 7.84-7.89 (m, 1H), 8.21-8.23 (d, 1H), 8.99 (s, 1H); MS m/z: 585.8 (M+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08828999B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-c71cebf072604b6681de1c00a59ebdd7
출처 메모uspto-grants-2014_09