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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Hexanesulfonyl chloride | HCID 84504 | — |
| 반응물 | 2-(aminomethyl)-3-methylquinolin-4(1H)-one dihydrochloride | HCID 68510759 | — |
| 용매 | Dimethylformamide pyridine | HCID 21954950 | — |
| 생성물 | N-[(3-methyl-4-oxo-1,4-dihydroquinolin-2-yl)methyl]hexane-1-sulfonamide | HCID 59527425 | 20.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08367702B2 |
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| 출처 데이터셋 | uspto-grants-2013_02 |
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| ORD ID | ord-7b5755018290426fbfa3f308eead003a |
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| 출처 메모 | uspto-grants-2013_02 |
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