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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1247521생성일: 2026년 10월 24일

Sodium hydride → Methyl (3-amino-2-oxo-3,4-dihydroquinolin-1(2H)-yl)acetate

https://huagongshe.com/ko/reaction/1247521

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Methyl bromoacetateHCID 60984—
반응물3-Amino-3,4-dihydroquinolin-2(1H)-one--hydrogen chloride (1/1)HCID 13499428—
용매DimethylformamideHCID 6228—
생성물Methyl (3-amino-2-oxo-3,4-dihydroquinolin-1(2H)-yl)acetateHCID 21974597100%

반응 단계

Sodium hydride (60% in oil, 2.52 g, 63.0 mmol) was added to 3-amino-3,4-dihydroquinolin-2(1H)-one hydrochloride (J. Med. Chem., 28, 1985, 1511–16; 5.0 g, 25.2 mmol), in anhydrous DMF (100 mL) at 0° C. over a period of 5 min keeping the internal temperature at <10° C. The reaction was stirred for a further 30 min before addition of methyl bromoacetate (2.85 mL, 30.2 mmol), then stirred for a further 60 min. The reaction was quenched by addition of 1M aqueous HCl (5 mL) and the volatiles were removed by evaporation. The residue was dissolved in DCM (250 mL) and washed with sat. aqueous NaHCO3 (100 mL) and the organic layer was dried (MgSO4), filtered and evaporated to yield the title compound (5.89 g, 25.2 mmol) as yellow paste which was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07129249B2
출처 데이터셋uspto-grants-2006_10
ORD IDord-9e68bece12e24000b7aff4e9a80ad1fe
출처 메모uspto-grants-2006_10