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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290731Generated: October 30, 2026

N-Acetylsulfanilyl chloride → HCID 18918200, compound

https://huagongshe.com/reaction/1290731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Acetylsulfanilyl chlorideHCID 8481—
Reactant3-Quinolinecarboxylic acid, 1,4-dihydro-6,8-difluoro-1-ethyl-4-oxo-7-(1-piperazinyl)-HCID 113523—
SolventBenzeneHCID 241—
SolventPyridineHCID 1049—
ProductHCID 18918200HCID 1891820092.4%

Reaction Steps

2.80 g of 1-ethyl-6,8-difluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid is suspended in 100 ml of pyridine. To this suspension is slowly added 7.76 g of 4-acetamidobenzenesulfonyl chloride in 20 ml of benzene under ice-cooling while stirring. Stirring is continued for 1 hour under ice-cooling and then for further 3 hours at room temperature. The reaction mixture is concentrated under reduced pressure. To the residue is added 1N sodium hydroxide solution to dissolve. The pH of the solution is then adjusted to 4 with acetic acid. Precipitating crystals are collected by filtration, washed with water and recrystallized from dimethylformamide (DMF)-ethanol to give 4.10 g of the titled compound. Melting point: 276°-277° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753658
Source datasetuspto-grants-1998_05
ORD IDord-5f868b0b3d1e4eb4a6837624acfb27d8
Source noteuspto-grants-1998_05