HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853436Generated: October 30, 2026
Thioanisole → N-(4-(6-Cyano-7-hydroxy-4-quinolyl)oxyphenyl)-N'-(4-fluorophenyl)urea
https://huagongshe.com/reaction/853436
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thioanisole | HCID 7520 | — |
| Reactant | N-(4-(7-(benzyloxy)-6-cyano-4-quinolyl)oxyphenyl)-N'-(4-fluorophenyl)urea | HCID 22936525 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | N-(4-(6-Cyano-7-hydroxy-4-quinolyl)oxyphenyl)-N'-(4-fluorophenyl)urea | HCID 135829395 | 94.8% |
Reaction Steps
After dissolving N-(4-(7-(benzyloxy)-6-cyano-4-quinolyl)oxyphenyl)-N′-(4-fluorophenyl)urea (6.20 g, 12.3 mmol) in trifluoroacetic acid (60 ml) and thioanisole (3.6 ml, 30.7 mmol) under a nitrogen atmosphere, the solution was stirred at 60° C. overnight. The reaction solution was concentrated under reduced pressure, and after adding water (100 ml) to the obtained residue, sodium bicarbonate was added to neutralization, diethylether (200 ml) was added, the mixture was stirred, and the precipitated crystals were filtered out, washed with water and diethyl ether and dried at 70° C. to obtain the title compound (4.816 g, 11.6 mmol, 94.8%) as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07253286B2 |
|---|
| Source dataset | uspto-grants-2007_08 |
|---|
| ORD ID | ord-553ebde18b974dd8b2da82cd732e5769 |
|---|
| Source note | uspto-grants-2007_08 |
|---|