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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469216Generated: October 30, 2026

Ethyl ((5-chlorothiophen-2-yl)sulfonyl)carbamate → 5-chloro-N-({[7-(cyclohexylamino)-6-fluoro-1-isopropyl-4-oxo-1,4-dihydroquinolin-3-yl]amino}carbonyl)thiophene-2-sulfonamide

https://huagongshe.com/reaction/469216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl ((5-chlorothiophen-2-yl)sulfonyl)carbamateHCID 24778122—
Reactant3-amino-7-(cyclohexylamino)-6-fluoro-1-isopropylquinolin-4(1H)-oneHCID 66637023—
SolventTolueneHCID 1140—
Product5-chloro-N-({[7-(cyclohexylamino)-6-fluoro-1-isopropyl-4-oxo-1,4-dihydroquinolin-3-yl]amino}carbonyl)thiophene-2-sulfonamideHCID 6663691065.7%

Reaction Conditions

Temperature110 °C

Reaction Steps

287 mg of ethyl [(5-chloro-2-thienyl)sulfonyl]carbamate was dissolved in 5.0 ml of toluene, and 250 mg of 3-amino-7-(cyclohexylamino)-6-fluoro-1-isopropylquinolin-4(1H)-one was added, followed by overnight stirring at 110° C. The reaction mixture was cooled to room temperature and concentrated under a reduced pressure. Then, ethyl acetate was added and the insoluble materials were collected by filtration, thereby obtaining 280 mg of 5-chloro-N-({[7-(cyclohexylamino)-6-fluoro-1-isopropyl-4-oxo-1,4-dihydroquinolin-3-yl]amino}carbonyl)thiophene-2-sulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629126B2
Source datasetuspto-grants-2014_01
ORD IDord-0a8b436641284b6fac22c6372ae31dee
Source noteuspto-grants-2014_01