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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1178439생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/1178439

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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 번호US07276517B2
출처 데이터셋uspto-grants-2007_10
ORD IDord-e675a1ddeb784d15bcbac73ce4beb6cd
출처 메모uspto-grants-2007_10