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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1294714생성일: 2026년 10월 26일

Pyridine → 2,4-Dinitrobenzenesulfonamide

https://huagongshe.com/reaction/1294714

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Trifluoroacetic acidHCID 6422—
반응물Sulfuryl chlorideHCID 24648—
반응물Benzenesulfonyl chloride, 2,4-dinitro-HCID 74255—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물2,4-DinitrobenzenesulfonamideHCID 10911854—

반응 단계

A solution of Part A compound (1.01 g, 2.37 mmol) and TFA (8 mL) in CH2Cl2 (30 mL) was stirred at RT for 4.5 h. The solution was concentrated in vacuo, and the residue was dissolved in CH2Cl2 and filtered through a pad of solid K2CO3. The filtrate was concentrated in vacuo to give the corresponding crude amine. To a solution of the crude amine in THF (11.9 mL) were added pyridine (0.383 mL, 4.74 mmol) and 2,4-dinitrobenzenesulfonyl chloride (0.85 g, 3.19 mmol) and the solution was stirred at RT for 15 h. Since some starting material still remained at this point, more sulfonyl chloride (0.32 g, 1.2 mmol) was then added. After a further 4 h, HPLC analysis indicated that all starting material had been consumed. The reaction mixture was diluted with Et2O, washed with 1N aq HCl, saturated aq NaHCO3 and brine, dried (MgSO4), filtered and concentrated in vacuo to provide the crude 2,4-dinitrobenzenesulfonamide

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07241780B2
출처 데이터셋uspto-grants-2007_07
ORD IDord-9a6f3c68a27c48d99b239b56849d49a4
출처 메모uspto-grants-2007_07