HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911744Generated: November 1, 2026
Potassium Carbonate → 2-[(Cyclopentylmethyl)(ethyl)amino]quinoline-3-carbaldehyde
https://huagongshe.com/reaction/1911744
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloro-3-quinolinecarboxaldehyde | HCID 690958 | — |
| Reactant | HCID 21965446 | HCID 21965446 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[(Cyclopentylmethyl)(ethyl)amino]quinoline-3-carbaldehyde | HCID 57444439 | 179.6% |
Reaction Steps
2-Chloroquinoline-3-carbaldehyde (0.27 grams, 1.40 mmol) and potassium carbonate (0.579 grams, 1.4 mmol) were added to a 25 mL two-necked round bottomed flask. To this flask was added 3 mL of N,N-dimethylformamide (DMF), followed by the drop-wise addition of a dimethylformamide solution of cyclopentyl methyl ethyl amine (0.214 grams, 1.69 mmol). The resulting mixture was refluxed for 2 hours and then cooled to 25-35° C., after which the mixture was poured onto crushed ice (10 mL), and extracted with ethyl acetate (3×50 mL). The organic layer was washed with brine and dried over sodium sulfate. The solvent was evaporated in vacuo to provide the product as yellow oil (0.355 g, yield: 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08604055B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-f97eb6f42714425890b1195e7a19aff9 |
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| Source note | uspto-grants-2013_12 |
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