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HRID 384493作成日:2026年10月27日

1-Hexanesulfonyl chloride → N-[(3-methyl-4-oxo-1,4-dihydroquinolin-2-yl)methyl]hexane-1-sulfonamide

https://huagongshe.com/reaction/384493

反応式

関与物質

役割名称HCID仕込み量
反応物1-Hexanesulfonyl chlorideHCID 84504—
反応物2-(aminomethyl)-3-methylquinolin-4(1H)-one dihydrochlorideHCID 68510759—
溶媒Dimethylformamide pyridineHCID 21954950—
生成物N-[(3-methyl-4-oxo-1,4-dihydroquinolin-2-yl)methyl]hexane-1-sulfonamideHCID 5952742520.5%

反応手順

To a solution of 2-(aminomethyl)-3-methylquinolin-4(1H)-one dihydrochloride (212 mg) in pyridine-DMF (8:1, 9 mL) was added hexanesulfonyl chloride (180 mg) under ice-cooling, and the mixture was stirred at room temperature for 12 hours. The reaction mixture was concentrated under reduced pressure, and water (50 mL) was added to the residue, followed by extraction with ethyl acetate (100 mL). The organic layer was washed sequentially with water and saturated brine, and then dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and then the residue was purified by silica gel column chromatography (eluent: chloroform/methanol=20/1) to obtain N-[(3-methyl-4-oxo-1,4-dihydroquinolin-2-yl)methyl]hexane-1-sulfonamide (56 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367702B2
出典データセットuspto-grants-2013_02
ORD IDord-7b5755018290426fbfa3f308eead003a
出典メモuspto-grants-2013_02