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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
Reactanttert-Butyl 4-[2-(2-methylquinolin-5-yloxy)ethyl]piperazine-1-carboxylateHCID 11394642—
SolventEthanolHCID 702—
Product2-Methyl-5-(2-piperazin-1-ylethoxy)quinolineHCID 1125426791%

Reaction Conditions

Temperature40 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244726B2
Source datasetuspto-grants-2007_07
ORD IDord-2f53d0bbd9f543a299506b8d11dd627e
Source noteuspto-grants-2007_07