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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 241163생성일: 2026년 10월 26일

4-Chloroquinoline → 7-Bromo-4-quinolin-4-yl-2,3,4,5-tetrahydro-1,4-benzoxazepine

https://huagongshe.com/reaction/241163

반응식

참여 물질

역할이름HCID투입량
반응물4-ChloroquinolineHCID 69140—
반응물DiisopropylethylamineHCID 81531—
반응물7-Bromo-2,3,4,5-tetrahydro-1,4-benzoxazepine hydrochlorideHCID 66820137—
용매1-ButanolHCID 263—
용매Ethyl AcetateHCID 8857—
생성물7-Bromo-4-quinolin-4-yl-2,3,4,5-tetrahydro-1,4-benzoxazepineHCID 6682078284.6%

반응 단계

A solution of 7-bromo-2,3,4,5-tetrahydro-1,4-benzoxazepine hydrochloride (1.50 g, 5.67 mmol) (example 2, step 1), 4-chloroquinoline (0.973 g, 5.95 mmol), diisopropylethylamine (2.93 g, 22.7 mmol) in 1-butanol (15 mL) was stirred at 170° C. for 1 hour in a microwave synthesizer. The reaction mixture was diluted with ethyl acetate (100 mL), washed with saturated sodium bicarbonate (50 mL) and brine (50 mL), dried over sodium sulfate. Filtration and concentration afforded a crude brown oil that was purified by silica gel chromatography (9:1 dichloromethane/methanol) to provide 7-bromo-4-quinolin-4-yl-2,3,4,5-tetrahydro-1,4-benzoxazepine (1.70 g, 84.6% yield) as a yellow oil. MS (EI) for C18H15BrN2O: 356 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08648066B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-d7389744bcd647fc8245228d7df8eec0
출처 메모uspto-grants-2014_02