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HRID 1178439作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物3-Amino-3,4-dihydroquinolin-2(1H)-one--hydrogen chloride (1/1)HCID 13499428—
反応物(2,2-Dimethyl-1,3-dioxolan-4-yl)methyl methanesulfonateHCID 15570840—
溶媒DimethylformamideHCID 6228—
生成物3-Amino-1-[(2,2-dimethyl-1,3-dioxolan-4-yl)methyl]-3,4-dihydroquinolin-2(1H)-oneHCID 2190682153%

反応条件

温度80 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07276517B2
出典データセットuspto-grants-2007_10
ORD IDord-e675a1ddeb784d15bcbac73ce4beb6cd
出典メモuspto-grants-2007_10