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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl ((5-chlorothiophen-2-yl)sulfonyl)carbamate | HCID 24778122 | — |
| Reactant | 3-amino-7-(cyclohexylamino)-6-fluoro-1-isopropylquinolin-4(1H)-one | HCID 66637023 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-chloro-N-({[7-(cyclohexylamino)-6-fluoro-1-isopropyl-4-oxo-1,4-dihydroquinolin-3-yl]amino}carbonyl)thiophene-2-sulfonamide | HCID 66636910 | 65.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08629126B2 |
|---|
| Source dataset | uspto-grants-2014_01 |
|---|
| ORD ID | ord-0a8b436641284b6fac22c6372ae31dee |
|---|
| Source note | uspto-grants-2014_01 |
|---|