HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1008474Generated: October 30, 2026
Water → N-(2,4-Difluorophenyl)-N'-[4-({6-methoxy-7-[2-(1H-1,2,3-triazol-1-yl)ethoxy]-4-quinolyl}oxy)-2,5-dimethylphenyl]urea
https://huagongshe.com/reaction/1008474
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(1H-1,2,3-triazol-1-yl)ethyl 4-methyl-1-benzenesulfonate | HCID 22667111 | — |
| Reactant | N-(2,4-difluorophenyl)-N'-{4-[(7-hydroxy-6-methoxy-4-quinolyl)oxy]-2,5-dimethylphenyl}urea | HCID 135674215 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(2,4-Difluorophenyl)-N'-[4-({6-methoxy-7-[2-(1H-1,2,3-triazol-1-yl)ethoxy]-4-quinolyl}oxy)-2,5-dimethylphenyl]urea | HCID 22667214 | 30% |
Reaction Steps
A starting compound (N-(2,4-difluorophenyl)-N′-{4-[(7-hydroxy-6-methoxy-4-quinolyl)oxy]-2,5-dimethyl-phenyl}urea, 93 mg), potassium carbonate (138 mg), and 2-(1H-1,2,3-triazol-1-yl)ethyl 4-methyl-1-benzene-sulfonate (52 mg) were dissolved in N,N-dimethylformamide (1 ml), and the solution was stirred at 80° C. for 5 hr. Water was added to the reaction mixture, and the mixture was extracted with chloroform-propanol (3/1). The organic layer was dried over anhydrous sodium sulfate, and the solvent was removed by distillation under the reduced pressure. The residue was purified by HPLC by development with chloroform/methanol to give 33 mg (yield 30%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06797823B1 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-c932c5acee7a469d8a9c2f7e27b7f5ee |
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| Source note | uspto-grants-2004_09 |
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