HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295568Generated: October 30, 2026
Hydrochloric Acid → 2-Methyl-5-(2-piperazin-1-ylethoxy)quinoline
https://huagongshe.com/reaction/1295568
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | tert-Butyl 4-[2-(2-methylquinolin-5-yloxy)ethyl]piperazine-1-carboxylate | HCID 11394642 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Methyl-5-(2-piperazin-1-ylethoxy)quinoline | HCID 11254267 | 91% |
Reaction Steps
tert-Butyl 4-[2-(2-methylquinolin-5-yloxy)ethyl]piperazine-1-carboxylate (1.04 g, 2.8 mmol) was dissolved in ethanol (60 mL) and treated with 1 M hydrochloric acid in diethyl ether (16 mL, 16 mmol) and stirred at 40° C. for 17 h. The reaction mixture was filtered and the white solid was collected and dried in vacuo. The hydrochloride salt precipitate was dissolved in water (25 mL) and potassium carbonate was added until the pH reached 10. The aqueous layer was washed with 5% methanol in dichloromethane (4×100 mL) then 10% methanol in dichloromethane (4×100 mL). The organic layers were combined, dried (Na2SO4) and concentrated in vacuo, affording the title compound as a brown oil (0.69 g, 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07244726B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-2f53d0bbd9f543a299506b8d11dd627e |
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| Source note | uspto-grants-2007_07 |
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