HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853554Generated: October 29, 2026
Dimethylformamide → HCID 86591478, compound
https://huagongshe.com/reaction/853554
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Glycidyl tosylate, (R)- | HCID 154187 | — |
| Reactant | N-(2-chloro-4-(6-cyano-7-hydroxyquinolin-4-yloxy)phenyl)-N'-methylurea | HCID 135829408 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86591478 | HCID 86591478 | 94% |
Reaction Steps
N-[2-Chloro-4-(6-cyano-7-hydroxyquinolin-4-yloxy) phenyl]-N′-methylurea (600 mg) was added to dimethylformamide (4 ml), and then (2R)-(−)-glycidyl p-toluenesulfonate (484 mg) and potassium carbonate (450 mg) were added thereto and the mixture was heated at 50° C. for 4 hours. Water was added to the reaction solution, extraction was performed with ethyl acetate, the organic layer was washed with water and saturated brine in that order and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained crude product was recrystallized with ethyl acetate to obtain the title compound (650 mg) as light yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07253286B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-f133ff9e1c53477ea0121e187ae04164 |
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| Source note | uspto-grants-2007_08 |
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