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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 217137생성일: 2026년 10월 25일

Chloranil → 6-Nitro-2-(1,3-benzodioxole-5-yl)-quinazoline

https://huagongshe.com/reaction/217137

반응식

참여 물질

역할이름HCID투입량
반응물ChloranilHCID 8371—
반응물1,3-Benzodioxole-5-carbonyl chlorideHCID 2734749—
반응물2-(Aminomethyl)-4-nitroaniline hydrochlorideHCID 23085707—
용매TolueneHCID 1140—
용매DichloromethaneHCID 6344—
생성물6-Nitro-2-(1,3-benzodioxole-5-yl)-quinazolineHCID 5786315682.5%

반응 단계

To a suspension of 5-nitro-2-amino-benzylamine hydrochloride (31 g, 0.152 mol) in DCM (450 ml) was added at 0° C. TEA (52.6 ml, 0.38 mol) and a solution of piperonyloyl chloride (27.3 g, 0.16 mol) in DCM (80 ml). The mixture was stirred for 2 hours at r.t. The solvent was removed i.v. and the residue triturated with ethanol/water 1/9, then with diisopropyl ether. The obtained solid was dried and suspended in toluene (900 ml) and POCl3 (670 ml). The mixture was heated at reflux for 2 hours, then the solvent was removed i.v. and the residue was triturated with water/ammonia, washed with water, dried over P2O5. A mixture of the obtained product and chloranil (32.7 g, 0.129 mol) in toluene (500 ml) was heated at reflux for 2 hours. The mixture was concentrated i.v. and the residue was triturated with NaOH 1M, washed with water and with methanol. The obtained solid was dried i.v. (37 g, 82.5% yield). C15H9N3O4, MW: 295.26, mp 220-222° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08193353B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-808266bd50b44deb9e23ca3d7e66ac90
출처 메모uspto-grants-2012_06