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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 424176생성일: 2026년 10월 24일

Pyridine → 2-Amino-5-[(methylsulfonyl)amino]benzenesulfonamide

https://huagongshe.com/ko/reaction/424176

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Methanesulfonyl chlorideHCID 31297—
반응물2,5-DiaminobenzenesulfonamideHCID 21888765—
용매DichloromethaneHCID 6344—
생성물2-Amino-5-[(methylsulfonyl)amino]benzenesulfonamideHCID 2495065773.7%

반응 조건

온도23 °C

반응 단계

2,5-Diamino-benzenesulfonamide (4.20 kg, 22.4 mol) was dissolved in dichloromethane (120 L) and pyridine (8.00 kg, 89.9 mol), and the resulting solution was cooled to 0° C. Methanesulfonyl chloride (2.80 kg, 24.4 mol) was added slowly, and the resulting mixture was allowed to warm to 23° C. and stirred for 2 days. The mixture was filtered and the resulting solid was washed with dichloromethane (2×20 L). The solid was diluted with water (100 L) and 1.0 M aqueous hydrochloric acid solution (25 L), and was then stirred at 23° C. for 1 h. The mixture was filtered and the resulting solid was washed with water (20 L) and then with methyl-tert-butyl ether (2×10 L). The solid was further dried in vacuo at 45° C. to afford the desired product, 2-amino-5-methanesulfonylamino-benzenesulfonamide (4.39 kg, 16.5 mol, 73%) as a pale pink solid. 1H NMR (400 MHz, CD3OD) δ: 2.89 (3H, s), 6.82 (1H, d, J=8.5 Hz), 7.20 (1H, dd, J1=8.5 Hz, J2=2.5 Hz), 7.58 (1H, d, J=2.5 Hz). LC-MS (ESI) calcd for C7H11N3O4S2 265.02, found 266.0 [M+H+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08101800B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-b29eb93d59ee4a5a8e224f7ae9eb8f2c
출처 메모uspto-grants-2012_01