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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384493Generated: October 25, 2026

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

https://huagongshe.com/reaction/384493

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Hexanesulfonyl chlorideHCID 84504—
Reactant2-(aminomethyl)-3-methylquinolin-4(1H)-one dihydrochlorideHCID 68510759—
SolventDimethylformamide pyridineHCID 21954950—
ProductN-[(3-methyl-4-oxo-1,4-dihydroquinolin-2-yl)methyl]hexane-1-sulfonamideHCID 5952742520.5%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367702B2
Source datasetuspto-grants-2013_02
ORD IDord-7b5755018290426fbfa3f308eead003a
Source noteuspto-grants-2013_02