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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290734Generated: October 29, 2026

Methane → 1-Ethyl-6,8-difluoro-1,4-dihydro-4-oxo-7-[3-(4-acetamidobenzenesulfonamido)-1-pyrrolidinyl]-3-quinolinecarboxylic acid

https://huagongshe.com/reaction/1290734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantN-Acetylsulfanilyl chlorideHCID 8481—
ReactantHCID 11724607HCID 11724607—
SolventBenzeneHCID 241—
SolventPyridineHCID 1049—
SolventDimethylformamideHCID 6228—
Product1-Ethyl-6,8-difluoro-1,4-dihydro-4-oxo-7-[3-(4-acetamidobenzenesulfonamido)-1-pyrrolidinyl]-3-quinolinecarboxylic acidHCID 1891820332.7%

Reaction Steps

2.80 g of 1-ethyl-6,8-difluoro-1,4-dihydro-4-oxo-7-(3-amino-1-pyrrolidinyl)-3-quinolinecarboxylic acid (see REFERENCE SYNTHESIS EXAMPLE hereinafter) is suspended in 100 ml of pyridine. To this is slowly added 3.88 g of 4-acetamidobenzenesulfonyl chloride in 20 ml of benzene. The mixture is stirred for 1 hour under ice-cooling and then overnight at room temperature. After evaporating off the solvent from the reaction mixture, the residue is added water and then adjusted to pH 12 with 2N sodium hydroxide solution. Any undissolved matter, if present, is filtered off. The filtrate is adjusted to pH 7 with acetic acid. The precipitated crystals are collected by filtration and washed. The crystals are then suspended in 100 ml of water. The suspension is adjusted to pH 4 with acetic acid, stirred and then filtered to recover the crystals, which are then thoroughly washed with water. The crude crystals thus obtained are dissolved in dimethylformamide (DMF), treated with activated charcoal, and recrystallized from DMF-methanol to give 1.45 g of the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753658
Source datasetuspto-grants-1998_05
ORD IDord-00ecf782a6eb4c62b73d4b91c84051fe
Source noteuspto-grants-1998_05