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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 384493생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/384493

반응식

참여 물질

역할이름HCID투입량
반응물1-Hexanesulfonyl chlorideHCID 84504—
반응물2-(aminomethyl)-3-methylquinolin-4(1H)-one dihydrochlorideHCID 68510759—
용매Dimethylformamide pyridineHCID 21954950—
생성물N-[(3-methyl-4-oxo-1,4-dihydroquinolin-2-yl)methyl]hexane-1-sulfonamideHCID 5952742520.5%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367702B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-7b5755018290426fbfa3f308eead003a
출처 메모uspto-grants-2013_02