Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-Chloroquinoline → 7-Bromo-4-quinolin-4-yl-2,3,4,5-tetrahydro-1,4-benzoxazepine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-Chloroquinoline | HCID 69140 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 7-Bromo-2,3,4,5-tetrahydro-1,4-benzoxazepine hydrochloride | HCID 66820137 | — |
| 용매 | 1-Butanol | HCID 263 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 7-Bromo-4-quinolin-4-yl-2,3,4,5-tetrahydro-1,4-benzoxazepine | HCID 66820782 | 84.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08648066B2 |
| 출처 데이터셋 | uspto-grants-2014_02 |
| ORD ID | ord-d7389744bcd647fc8245228d7df8eec0 |
| 출처 메모 | uspto-grants-2014_02 |