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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50235생성일: 2026년 10월 27일

Benzenesulfonyl chloride, 4-chloro-3-nitro- → 4-Chloro-3-nitrobenzenesulfonic acid-n-(1-methylpiperidin-4-yl)-n-methylamide

https://huagongshe.com/reaction/50235

반응식

참여 물질

역할이름HCID투입량
반응물Benzenesulfonyl chloride, 4-chloro-3-nitro-HCID 7323—
반응물1-Methyl-4-(methylamino)piperidineHCID 566323—
용매PyridineHCID 1049—
생성물4-Chloro-3-nitrobenzenesulfonic acid-n-(1-methylpiperidin-4-yl)-n-methylamideHCID 11371456—

반응 단계

To a solution of 2.2 mL (15 mmol) of 1-methyl-4-methylaminopiperidine in 60 mL pyridine, 3.8 g (15 mmol) of 4-chloro-3-nitrobenzenesulfonic acid chloride were added, in batches, whilst cooling with ice. The mixture was then stirred for two hours with cooling, then evaporated to dryness, the residue was mixed with about 50 mL of water and made alkaline with concentrated ammonia whilst stirring vigorously. The crude product precipitated was suction filtered and purified by column chromatography (250 g silica gel, eluant: dichloromethane with 1.5% ethanol). Yield: 1.6 g (31% of theory), C13H18ClN3O4S (347.8); Rf value: 0.19 (silica gel; dichloromethane/ethanol=19:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710055B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-a4b92adeb6194e9899e79b37a3d3ec15
출처 메모uspto-grants-2004_03