HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228959Generated: October 26, 2026
Dimethylformamide → HCID 23078599, compound
https://huagongshe.com/reaction/228959
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 7-(2-Chloro-ethoxy)-6-methoxy-4-(2-methyl-quinolin-3-yloxy)-quinoline | HCID 23078272 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 23078599 | HCID 23078599 | 89% |
Reaction Steps
N,N-Dimethylformamide (1 ml) was added to 7-(2-chloro-ethoxy)-6-methoxy-4-(2-methyl-quinolin-3-yloxy)-quinoline (compound 353) (35 mg), potassium carbonate (37 mg), and piperidine (23 mg), and the mixture was stirred at 75° C. overnight. The reaction solution was cooled to room temperature, water was added to the reaction solution, and the mixture was extracted with chloroform. The chloroform layer was washed with water and was then dried over anhydrous magnesium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by thin layer chromatography using chloroform-methanol to give the title compound (35 mg, yield 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560558B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-8ed2625226c14ea4afdb1b6bc42a90fe |
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| Source note | uspto-grants-2009_07 |
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