HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228963Generated: October 29, 2026
4-Piperidinecarboxamide → HCID 57756555, compound
https://huagongshe.com/reaction/228963
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Piperidinecarboxamide | HCID 3772 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| 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 57756555 | HCID 57756555 | 32.5% |
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) (50 mg), potassium carbonate (53 mg), and piperidine-4-carboxamide (49 mg), and the mixture was stirred at 80° 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 sodium 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 (20 mg, yield 32%).
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-3e6b7f4d12eb4f73aff9c2d25bfe4650 |
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| Source note | uspto-grants-2009_07 |
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