HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577779Generated: October 23, 2026
Potassium Carbonate → 2-[4-(Cyclohexylmethyl)piperazin-1-yl]quinoline-3-carbaldehyde
https://huagongshe.com/en/reaction/577779
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloro-3-quinolinecarboxaldehyde | HCID 690958 | — |
| Reactant | 1-(Cyclohexylmethyl)piperazine | HCID 2735885 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[4-(Cyclohexylmethyl)piperazin-1-yl]quinoline-3-carbaldehyde | HCID 57486817 | 86% |
Reaction Steps
1-(Cyclohexylmethyl)piperazine (0.42 mL, 2.2 mmol) was added to a mixture of 2-chloro-3-quinolinecarboxaldehyde (0.383 g, 2.0 mmol) and potassium carbonate (0.7 g, 5.0 mmol) in anhydrous DMF (4 mL) at ambient temperature under a nitrogen atmosphere. After being stirred for 20 minutes, the reaction mixture was heated at 110° C. for 4.5 h. After cooling to room temperature this mixture was diluted with water (40 mL) and extracted with ethyl acetate (3×30 mL). The combined organic extracts were washed with brine, dried over sodium sulfate, filtered, and then concentrated under vacuum to give a pale brown crude product. Purification by silica gel column chromatography and eluting with 2.5% methanol in dichloromethane afforded the title compound (0.56 g), yield: 86%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040558B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-596641ef58e540a4a5d550a7168db462 |
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| Source note | uspto-grants-2015_05 |
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