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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 353043생성일: 2026년 10월 24일

2,4-Dichloro-6,7-dimethoxyquinazoline → 2,4-Dichloro-6,7-dimethoxy-5-nitroquinazoline

https://huagongshe.com/ko/reaction/353043

반응식

참여 물질

역할이름HCID투입량
반응물2,4-Dichloro-6,7-dimethoxyquinazolineHCID 520327—
반응물Nitronium tetrafluoroborateHCID 11073463—
용매AcetonitrileHCID 6342—
생성물2,4-Dichloro-6,7-dimethoxy-5-nitroquinazolineHCID 2270704874%

반응 단계

To a suspension of 2,4-dichloro-6,7-dimethoxyquinazoline (30.0 g, 0.12 mol) in acetonitrile (550 ml) at 0° C. was added nitronium tetrafluoroborate (25.9 g, 0.19 mol) portionwise over 15 min. The reaction was stirred for 0.75 h and then evaporated under reduced pressure. The resulting solid was suspended in a mixture of saturated aqueous sodium bicarbonate and EtOAc and the solid filtered, dissolved in CH2Cl2, dried over MgSO4 and evaporated to give the subtitle compound as a pale yellow solid (27 g). Further material was obtained by separating the organic layer of the filtrate, washing with H2O (1×), saturated brine (1×), drying over MgSO4 and filtering through a pad of silica. Subsequent evaporation under reduced pressure, trituration with EtOAc and filtration gave the subtitle compound as a pale yellow solid (3.9 g, overall yield 88%). Rf 0.24 (ether/hexane 1/1, v/v).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06750214B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-1d53f366d6aa40a38022f11709a45a87
출처 메모uspto-grants-2004_06