戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 523272作成日:2026年10月26日

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

https://huagongshe.com/reaction/523272

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物TriphosgeneHCID 94429—
反応物amino-N-(3-bromo-2-chlorophenyl)-3-fluorobenzamideHCID 117761114—
溶媒TetrahydrofuranHCID 8028—
生成物3-(3-bromo-2-chlorophenyl)-8-fluoroquinazoline-2,4(1H,3H)-dioneHCID 11776111285%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09334290B2
出典データセットuspto-grants-2016_05
ORD IDord-e2c0956b32fe4fac962701c7e532cfc7
出典メモuspto-grants-2016_05