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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16252생성일: 2026년 10월 23일

3-Aminophenylboronic acid → 2-(3,4,5-Trimethoxyphenylamino)-6-(3-aminophenyl)pyrazine

https://huagongshe.com/ko/reaction/16252

반응식

참여 물질

역할이름HCID투입량
반응물3-Aminophenylboronic acidHCID 92269—
반응물2-(3,4,5-Trimethoxyphenylamino)-6-chloropyrazineHCID 11609049—
생성물2-(3,4,5-Trimethoxyphenylamino)-6-(3-aminophenyl)pyrazineHCID 1155940338.6%

반응 단계

Using Method C with 1.0 g (3.4 mmol) 2a and 635 mg (4.1 mmol) 3-aminophenyl boronic acid, 463 mg pure title compound were obtained. The filtrate was submitted to purification by preparative HPLC (eluent:AcOEt) and another fraction of 412 mg was obtained. A total of 875 mg CJS 364 (72.9%) were obtained. Reaction time: 28 hours. 1H-NMR (DMSO), δ (ppm), J (Hz): 3.64 (s, 3H, CH3O(4′)), 3.81 (s, 6H, CH3O(3′+5′)), 5.19 (s, 2H, NH2), 6.66 (d, 1H, Harom 4′, J=7.70), 7.13 (t, 1H, Harom 5′, J=7.77), 7.22 (d, 1H, Harom 6′), 7.26 (s, 2H, Harom(2+6)), 7.29 (s, 1H, Harom 2′), 8.11 (s, 1H, HP5), 8.33 (s, 1H, HP3), 9.51 (s, 1H, NHamine);

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737152B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-7453702616c54593bf58545c50d6c240
출처 메모uspto-grants-2010_06