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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 459711생성일: 2026년 10월 25일

3-Ethoxy-2-propenoyl chloride → 1,6,7,8,9,10-Hexahydro-2h-azepino[3,2-g]quinolin-2-one

https://huagongshe.com/reaction/459711

반응식

참여 물질

역할이름HCID투입량
반응물3-Ethoxy-2-propenoyl chlorideHCID 3014429—
반응물2,3,4,5-tetrahydro-1H-benzo[b]azepin-8-amineHCID 18444221—
용매DichloromethaneHCID 6344—
용매Sodium HydroxideHCID 14798—
생성물1,6,7,8,9,10-Hexahydro-2h-azepino[3,2-g]quinolin-2-oneHCID 9899244—

반응 조건

온도50 °C

반응 단계

A solution of 2,3,4,5-tetrahydro-1H-1-benzazapin-8-amine (0.6 g, 3.4 mmol) and 3-ethoxyacryloyl chloride (0.45 g, 3.4 mmol) in CH2Cl2 (50 mL) and 3N NaOH (10 mL) was stirred for 1 h at ambient temperature. The reaction was partitioned between CH2Cl2 and water. The organic layer was concentrated and the remaining brown oil was dissolved in 70% aq. H2SO4 (20 mL) and heated gently (50° C.) for 2 h. The reaction was cooled and neutralized with aq. NH4OH and partitioned between water and EtOAc. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated. The residue was dissolved in DMF (1 mL) and purified on a GILSON automated system affixed with a YMC COMBIFLASH 50 mm×20 mm reverse phase column eluted 5–95% CH3CN in water at 30 mL/min over 10.5 min to provide pure desired product. HRMS m/z (M+1) calcd 215.1179; found 215.1186.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07196076B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-f67beddc9b33443db36a36f7388ba7e4
출처 메모uspto-grants-2007_03