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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 446665생성일: 2026년 10월 25일

Tin tetrachloride → 3-amino-N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)benzenesulfonamide

https://huagongshe.com/reaction/446665

반응식

참여 물질

역할이름HCID투입량
반응물Tin tetrachlorideHCID 24287—
반응물N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)-3-nitrobenzenesulfonamideHCID 57448443—
촉매WaterHCID 962—
용매DimethylacetamideHCID 31374—
생성물3-amino-N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)benzenesulfonamideHCID 57448448—

반응 조건

온도80 °C

반응 단계

A flask was charged with N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)-3-nitro-benzenesulfonamide (3.4 g, 7.06 mmol), prepared using procedures similar to those in Example 14, tin chloride solvate (6.4 g, 28.2 mmol), and 30 mL of DMA. A few drops of water were added and the reaction mixture was stirred at 80° C. for 3 hours, after which time, solvent was removed on a rotary evaporator, and 50 mL of water and 10 mL of Methanol were added. The slurry was filtered, and the filtrate was washed with MeOH, water, and diethyl ether (20 mL of each), resulting in 3.25 g 3-amino-N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide. 1H NMR (400 MHz, DMSO) δ 12.2 (br s, 1H), 8.85 (s, 1H), 7.90 (br s, 1H), 7.50-7.60 (m, 1H), 7.3-7.4 (m, 4H), 7.2 (m, 3H), 6.74 (m, 1H), 6.24 (m, 1H), 5.56 (br s, 2H), 3.76 (s, 6H). MS (EI) m/z for C22H21N5O4S: 452.0 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481001B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-b4191081e6af4864a7f3a35b5d5bb534
출처 메모uspto-grants-2013_07