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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1267000생성일: 2026년 10월 27일

Methane → 3-Nitro-(quinoxalinylamino)benzoic acid

https://huagongshe.com/reaction/1267000

반응식

참여 물질

역할이름HCID투입량
반응물MethaneHCID 297—
반응물EthylmorpholineHCID 7525—
반응물2-Bromo-3-nitrobenzoic acidHCID 68452—
반응물5-AminoquinoxalineHCID 85494—
용매AmmoniaHCID 222—
용매IsopropanolHCID 3776—
생성물3-Nitro-(quinoxalinylamino)benzoic acidHCID 1854544442%

반응 조건

온도67.5 °C

반응 단계

A mixture of 5-aminoquinoxaline (1.0 g, 6.89 mmol), 2-bromo-3-nitrobenzoic acid (4.0 g, 13.78 mmol), Cu/CuI (catalytic) and N-ethylmorpholine (5 mL) in isopropanol (5 mL) was heated at 65-70° C. overnight. The mixture was then dissolved in aqueous ammonia, treated with charcoal/Celite, and filtered. The filtrate was acidified with conc. HCl, and the resulting precipitate was collected while the mixture was still warm and washed with water (to remove unreacted 2-bromo-3-nitrobenzoic acid). It was then dried and chromatographed on silica gel, eluting with CH2Cl2/MeOH (19:1), to give 3-nitro-(quinoxalinylamino)benzoic acid (0.9 g, 42%): mp (MeOH) 232-237° C.; 1H NMR [(CD3)2SO] δ 6.92-6.97 (m, 1 H, ArH), 7.30 (t, J=8.0 Hz, 1 H, ArH), 7.62-7.66 (m, 2 H, 2xArH), 8.23 (dd, J=8.2, 1.6 Hz, 1 H, ArH), 8.29 (dd, J=7.8, 1.6 Hz, 1 H, ArH), 8.97 (d, J=1.7 Hz, 1 H, H-2′ or H-3′), 9.03 (d, J=1.9 Hz, 1 H, H-2′ or H-3′), 10.73 (br s, 1 H, NH), 13.8 (br s, 1 H, CO2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06552021B2
출처 데이터셋uspto-grants-2003_04
ORD IDord-86d5a59d56cc4c9c93605e5cfd06affe
출처 메모uspto-grants-2003_04