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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 336801생성일: 2026년 10월 24일

Acetic Acid → HCID 57448664, 화합물

https://huagongshe.com/ko/reaction/336801

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Dimethyl SulfoxideHCID 679—
반응물Sodium MethoxideHCID 10942334—
반응물N-{3-[(2,6-dichloropyridin-4-yl)amino]quinoxalin-2-yl}-3-nitrobenzenesulfonamideHCID 57448672—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물HCID 57448664HCID 57448664—

반응 조건

온도100 °C

반응 단계

To a crude product of N-{3-[(2,6-dichloropyridin-4-yl)amino]quinoxalin-2-yl}-3-nitrobenzenesulfonamide (1.24 g) prepared using procedures similar to those for Example 151, was added anhydrous DMSO (10 mL), followed by sodium methoxide (273 mg). The resulting mixture was heated at 100° C. for 3 days. The mixture was diluted with EtOAc and water, and the pH was adjusted to about 4 by adding acetic acid. The product was extracted with EtOAc (3×). The combined extracts were washed with brine to give the crude product. A portion of the crude product was purified by prep HPLC to give N-(3-{[2-chloro-6-(methyloxy)pyridin-4-yl]amino}quinoxalin-2-yl)-3-nitrobenzenesulfonamide. 1H NMR (400 MHz, DMSO) δ 9.44 (s, 1H), 8.90 (s, 1H), 8.50 (d, 1H), 8.42 (d, 1H), 7.88-7.84 (m, 2H), 7.77 (s, 1H), 7.74 (s, 1H), 7.64 (d, 1H), 7.45-7.38 (m, 2H), 3.82 (s, 3H); MS (EI) m/z for C20H15ClN6O5S: 496.94 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889664B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-0d21021e536941e5b5037f602f3446df
출처 메모uspto-grants-2014_11