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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1247522생성일: 2026년 10월 25일

Sodium hydride → 3-Amino-1-[(2,2-dimethyl-1,3-dioxolan-4-yl)methyl]-3,4-dihydroquinolin-2(1H)-one

https://huagongshe.com/reaction/1247522

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물3-Amino-3,4-dihydroquinolin-2(1H)-one--hydrogen chloride (1/1)HCID 13499428—
반응물(2,2-Dimethyl-1,3-dioxolan-4-yl)methyl methanesulfonateHCID 15570840—
용매DimethylformamideHCID 6228—
생성물3-Amino-1-[(2,2-dimethyl-1,3-dioxolan-4-yl)methyl]-3,4-dihydroquinolin-2(1H)-oneHCID 2190682153%

반응 조건

온도80 °C

반응 단계

Sodium hydride (60% in oil, 191 mg, 4.70 mmol) was added to 3-amino-3,4-dihydroquinolin-2(1H)-one hydrochloride (J. Med. Chem., 28, 1985; 1511–16,450 mg, 2.27 mmol), in anhydrous DMF (6 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 (2,2-dimethyl-1,3-dioxolan-4-yl)methyl methanesulfonate (J. Med. Chem. 35, 1992, 1650–62; 528 mg, 2.50 mmol) and the reaction has then heated to 80° C. for a period of 5 h. The reaction was then cooled and evaporated before addition of sat. aqueous NaHCO3 (20 mL) and EtOAc (50 mL). The organic layer was then dried (MgSO4), filtered and evaporated and the residue was purified by column chromatography (MeOH:DCM 1:19) to afford the title compound (330 mg, 53%) as colourless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07129249B2
출처 데이터셋uspto-grants-2006_10
ORD IDord-c9898cd3b4694b7ca5f894223eb35679
출처 메모uspto-grants-2006_10