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HRID 545637作成日:2026年10月26日

Methyl chloroformate → 6-bromo-1-(2-morpholinoethyl)quinazolin-2(1H)-one

https://huagongshe.com/reaction/545637

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl chloroformateHCID 6586—
反応物TetrahydrofuranHCID 8028—
反応物5-Bromo-2-(2-morpholinoethylamino)benzonitrileHCID 18367607—
反応物DiisobutylaluminumhydrideHCID 21225700—
反応物Potassium tert-butoxideHCID 23665647—
生成物6-bromo-1-(2-morpholinoethyl)quinazolin-2(1H)-oneHCID 67187682—

反応条件

温度0 °C

反応手順

To a stirred solution of 5-bromo-2-(2-morpholinoethylamino)benzonitrile (0.5521 g, 1.8 mmol) in THF (0.13 g, 1.8 mmol) was added bis(iso-butyl)aluminum hydride (2.4 ml, 3.6 mmol) at 0° C. and the resulting bright yellow-orange solution was stirred at 0° C. for 1 h. Methyl chloroformate (0.17 ml, 2.1 mmol) was added to the reaction at 0° C. The mixture was stirred at RT for 2 h, then treated with potassium tert-butoxide 1M THF (3.6 ml, 3.6 mmol) and heated to 60° C. for 5 h. After cooling, the reaction was quenched with NH4Cl(aq) and water (10 mL each) and the separated aqueous layer was extracted with EtOAc (3×10 mL). The combined organic phases were washed with brine, dried (Na2SO4), and concentrated to give a crude residue. Flash column chromatographic purification (eluting with 100% DCM to 3% MeOH in DCM gradient) provided 6-bromo-1-(2-morpholinoethyl)quinazolin-2(1H)-one as a sticky colorless oil. MS m/e 338 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07935709B2
出典データセットuspto-grants-2011_05
ORD IDord-bb83f0a2b7414dffb55e579ea6dcf4a9
出典メモuspto-grants-2011_05