HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375810Generated: November 2, 2026
Potassium Carbonate → HCID 17819617, compound
https://huagongshe.com/reaction/1375810
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Morpholine, 4-(2-chloroethyl)-, hydrochloride (1:1) | HCID 77210 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 135674213 | HCID 135674213 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 17819617 | HCID 17819617 | 57% |
Reaction Steps
N-(2,4-Difluorophenyl)-N′-{2-fluoro-4-[(7-hydroxy-6-methoxy-4-quinolyl)oxy)phenyl}urea (20 mg), potassium carbonate (7 mg), tetra-n-butylammonium iodide (2 mg), and N-(2-chloroethyl)morpholine hydrochloride (10 mg) were dissolved in N,N-dimethylformamide (1 ml), and the solution was stirred at 70° C. overnight. A saturated aqueous sodium hydrogencarbonate solution was added to the reaction solution, and the mixture was extracted with chloroform. The chloroform layer was dried over anhydrous magnesium sulfate. The solvent was removed by distillation under the reduced pressure. The residue was purified by thin-layer chromatography on silica gel by development with chloroform/methanol (30/1) to give 14 mg (yield 57%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07169789B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-8f733c70b9ec4182a97eb5d3c049bf40 |
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| Source note | uspto-grants-2007_01 |
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