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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1272471생성일: 2026년 10월 26일

1,2,4-Benzenetriamine, hydrochloride (1:2) → 2,3-Bis(3-hydroxyphenyl)quinoxalin-6-ylamine dihydrochloride salt

https://huagongshe.com/reaction/1272471

반응식

참여 물질

역할이름HCID투입량
반응물1,2,4-Benzenetriamine, hydrochloride (1:2)HCID 94179—
반응물Bis(3-hydroxyphenyl)ethane-1,2-dioneHCID 13158606—
용매1,4-Dioxane--water (1/1)HCID 21886435—
생성물2,3-Bis(3-hydroxyphenyl)quinoxalin-6-ylamine dihydrochloride saltHCID 18455688168.5%

반응 단계

40.4 mg (0.206 mmol) of 1,2,4-benzenetriamine dihydrochloride and 50 mg (0.20 mmol) of 3,3′-dihydroxybenzil were dissolved in 2 mL of 1:1 mixture of dioxane-water. The reaction was refluxed for 3 hours. Then solvent was removed in vacuo. The residue was dissolved in 2 mL of methanol and this solution was added dropwise to 40 mL of diethyl ether. The formed dark-red precipitate was collected, washed with ether and dried in vacuo to give 69.8 mg (92.6% yield) of the product. 97.6% purity by LC/MS (230 DAD). Mass-spec [ES+]=330.8. 1H NMR (500 MHz, MeOH-d4) 6.81–6.87 (2H, m), 6.96–6.98 (4H, m), 7.10 (1H, m), 7.13–7.16 (1H, t), 7.28–7.31 (1H, t), 7.56–7.58 (1H, m), 8.04–8.06 (1H, d).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07208493B2
출처 데이터셋uspto-grants-2007_04
ORD IDord-d6cbecb797184468a35cd63732610dec
출처 메모uspto-grants-2007_04