돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1489590생성일: 2026년 10월 27일

N4-(3-bromophenyl)-4,6,7-Quinazolinetriamine → N-(3-bromophenyl)pyrazino[2,3-g]quinazolin-4-amine

https://huagongshe.com/reaction/1489590

반응식

참여 물질

역할이름HCID투입량
반응물N4-(3-bromophenyl)-4,6,7-QuinazolinetriamineHCID 2426—
반응물1,4-Dioxane-2,3-diolHCID 96170—
용매MethanolHCID 887—
생성물N-(3-bromophenyl)pyrazino[2,3-g]quinazolin-4-amineHCID 532824684.1%

반응 단계

A mixture of 4-(3-bromoanilino)-6,7-diaminoquinazoline (90 mg, 0.27 mmol) and 1,4-dioxane-2,3-diol (0.2 g, 1.6 mmol) [Venuti, M. C.; Synthesis, 1982, 61-63] in MeOH (20 mL) is stirred at room temperature overnight to give a precipitate of 4-(3-bromoanilino)pyrazino[2,3-g]quinazoline (80 mg, 83%). 1H NMR (DMSO) δ10.45 (1H, brs), 9.52 (1H, s), 9.09 (1H, d, J=1.6 Hz), 9.06 (1H, d, J=1.6 Hz), 8.71 (1H, s), 8.44 (1H, s), 8.32 (1H, brs), 7.99 (1H, m), 7.45-7.34 (2H, m). ##STR24##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05679683
출처 데이터셋uspto-grants-1997_10
ORD IDord-c68c5321e34a4300ad340cb262690622
출처 메모uspto-grants-1997_10