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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 523272생성일: 2026년 10월 26일

Water → 3-(3-bromo-2-chlorophenyl)-8-fluoroquinazoline-2,4(1H,3H)-dione

https://huagongshe.com/reaction/523272

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TriphosgeneHCID 94429—
반응물amino-N-(3-bromo-2-chlorophenyl)-3-fluorobenzamideHCID 117761114—
용매TetrahydrofuranHCID 8028—
생성물3-(3-bromo-2-chlorophenyl)-8-fluoroquinazoline-2,4(1H,3H)-dioneHCID 11776111285%

반응 단계

Triphosgene (453 mg, 1.53 mmol) was added in one portion to a solution of amino-N-(3-bromo-2-chlorophenyl)-3-fluorobenzamide (350 mg, 1.019 mmol) in THF (10 mL) at 0° C. The mixture was stirred at room temperature for 1 h, then was cooled to 0° C. and treated with water until no more gas evolution was observed. The mixture was concentrated and the residue was dissolved in EtOAc, washed sequentially with saturated aqueous NaHCO3, water and brine, and dried and concentrated. The residue was purified by column chromatography on silica gel (24 g), eluting with EtOAc-hexanes (gradient from 0-50%), to provide 3-(3-bromo-2-chlorophenyl)-8-fluoroquinazoline-2,4(1H,3H)-dione as a yellow solid (320 mg, 85% yield). Mass spectrum m/z 369, 371 (M+H)+. 1H NMR (400 MHz, chloroform-d) δ 8.54 (br. s., 1H), 7.97 (d, J=8.1 Hz, 1H), 7.77 (dd, J=6.8, 2.6 Hz, 1H), 7.46 (ddd, J=9.8, 8.3, 1.2 Hz, 1H), 7.36-7.29 (m, 2H), 7.24 (td, J=8.0, 4.8 Hz, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09334290B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-e2c0956b32fe4fac962701c7e532cfc7
출처 메모uspto-grants-2016_05