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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 446672생성일: 2026년 10월 24일

P-Xylene → N-{3-[(2,6-dichloropyridin-4-yl)amino]quinoxalin-2-yl}-3-nitrobenzenesulfonamide

https://huagongshe.com/ko/reaction/446672

반응식

참여 물질

역할이름HCID투입량
반응물P-XyleneHCID 7809—
반응물4-Amino-2,6-dichloropyridineHCID 137652—
반응물N-(3-chloroquinoxalin-2-yl)-3-nitrobenzenesulfonamideHCID 5007601—
용매DichloromethaneHCID 6344—
생성물N-{3-[(2,6-dichloropyridin-4-yl)amino]quinoxalin-2-yl}-3-nitrobenzenesulfonamideHCID 57448672—

반응 조건

온도135 °C

반응 단계

A mixture of N-(3-chloroquinoxalin-2-yl)-3-nitrobenzenesulfonamide (1 g), 2,6-dichloropyridin-4-amine (760 mg) and p-xylene (10 mL) was heated at 135° C. with stirring overnight. Upon cooling to room temperature, the mixture was dissolved in dichloromethane, washed with 2 N HCl (2×) and brine, concentrated in vacuo to give a crude product of N-{3-[(2,6-dichloropyridin-4-yl)amino]quinoxalin-2-yl}-3-nitrobenzenesulfonamide. A small portion of this crude product was purified by HPLC to give N-{3-[(2,6-dichloropyridin-4-yl)amino]quinoxalin-2-yl}-3-nitro-benzenesulfonamide. 1H NMR (400 MHz, DMSO) δ 9.71 (s, 1H), 8.90 (s, 1H), 8.50 (d, 2H), 8.8.41 (d, 1H), 8.30 (s, 2H), 7.88-7.78 (m, 27.65 (d, 1H), 7.47-7.37 (m, 2H); MS (EI) m/z for C19H12C12N6O4S: 491.1, 493.1 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481001B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-da48f2f4c03d4794bc2192b78051f167
출처 메모uspto-grants-2013_07