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HRID 1247525作成日:2026年10月26日

Sodium hydride → 3-amino-1-(2-methoxyethyl)-3,4-dihydroquinolin-2(1H)-one

https://huagongshe.com/reaction/1247525

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2-Bromoethyl methyl etherHCID 80972—
反応物3-Amino-3,4-dihydroquinolin-2(1H)-one--hydrogen chloride (1/1)HCID 13499428—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物3-amino-1-(2-methoxyethyl)-3,4-dihydroquinolin-2(1H)-oneHCID 2190683778%

反応手順

Sodium hydride (60% in oil, 321 mg, 8.03 mmol) was added to 3-amino-3,4-dihydroquinolin-2(1H)-one hydrochloride (J. Med. Chem., 28, 1985; 1511–16; 759 mg, 3.82 mmol) in anhydrous DMF (10 mL) at 0° C. over a period of 5 min. After 1 hour 2-bromoethyl methyl ether (0.40 mL, 4.20 mmol) was added and stirring maintained for 18 hours. The reaction was diluted with EtOAc (100 mL) and washed with sat. aqueous K2CO3 (20 mL). The aqueous was extracted with DCM (3×50 mL) and the combined organics dried (Na2SO4), filtered and evaporated. The residue was purified by column chromatography (DCM to DCM:MeOH (4:1)) to afford the title compound (654 mg, 78%) as a brown oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07129249B2
出典データセットuspto-grants-2006_10
ORD IDord-8cdf941be0934c8e8835f9631b9965f6
出典メモuspto-grants-2006_10