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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 574767생성일: 2026년 10월 26일

4-Chloro-3-nitrobenzenesulfonamide → 4-(4-Methylpiperazin-1-ylamino)-3-nitrobenzenesulfonamide

https://huagongshe.com/reaction/574767

반응식

참여 물질

역할이름HCID투입량
반응물4-Chloro-3-nitrobenzenesulfonamideHCID 7324—
반응물N,N,N',N'-TetramethylethylenediamineHCID 8037—
반응물4-Methylpiperazin-1-ylamine dihydrochloride hydrateHCID 198221—
용매1,4-DioxaneHCID 31275—
생성물4-(4-Methylpiperazin-1-ylamino)-3-nitrobenzenesulfonamideHCID 4737741—

반응 단계

A 50 mL round-bottomed flask was charged with 4-chloro-3-nitrobenzenesulfonamide (1 g, 4.23 mmol), 4-methylpiperazin-1-amine dihydrochloride (1 g, 5.32 mmol), and N1,N1,N2,N2-tetramethylethane-1,2-diamine (3 mL, 20.01 mmol) in dioxane (10 mL). The reaction mixture was refluxed for 12 hours. After this time, the reaction mixture was cooled to room temperature, the salt filtered off via a Buchner funnel, and the solvent removed in vacuo. The crude product was added to a silica gel column (Analogix, SF65-200 g) and purified by eluting with 0-5% methanol in dichloromethane.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09034875B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-254c940763bb446c9c0bf28987f0e297
출처 메모uspto-grants-2015_05