돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 545637생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/545637

반응식

참여 물질

역할이름HCID투입량
반응물Methyl chloroformateHCID 6586—
반응물TetrahydrofuranHCID 8028—
반응물5-Bromo-2-(2-morpholinoethylamino)benzonitrileHCID 18367607—
반응물DiisobutylaluminumhydrideHCID 21225700—
반응물Potassium tert-butoxideHCID 23665647—
생성물6-bromo-1-(2-morpholinoethyl)quinazolin-2(1H)-oneHCID 67187682—

반응 조건

온도0 °C

반응 단계

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)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07935709B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-bb83f0a2b7414dffb55e579ea6dcf4a9
출처 메모uspto-grants-2011_05