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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577793Generated: October 28, 2026

Potassium Carbonate → 2-(Cyclopentylmethyl-ethyl-amino)-5,6,7,8-tetrahydro-quinoline-3-carbonitrile

https://huagongshe.com/reaction/577793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,2-Diaminocyclohexane, trans-HCID 43806—
ReactantN-EthylcyclopentanamineHCID 558581—
Reactant2-Chloro-5,6,7,8-tetrahydroquinoline-3-carbonitrileHCID 3779818—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
Product2-(Cyclopentylmethyl-ethyl-amino)-5,6,7,8-tetrahydro-quinoline-3-carbonitrileHCID 57486829135.8%

Reaction Steps

Dry dioxane (15 mL) was added to a mixture of 2-chloro-5,6,7,8-tetrahydro-quinoline-3-carbonitrile (3.0 g, 15.62 mmol), potassium carbonate (8.6 g, 62.5 mmol), CuI (5 mol %, 0.064 g), and trans-1,2-cyclohexanediamine (5 mol %, 0.089 g) under an argon atmosphere. A solution of N-cyclopentyl-ethylamine (2.3 g, 18.75 mmol) in dioxane was them added to the stirred reaction mixture, which was then refluxed for 24 h. After this time, the solvent was evaporated under vacuum, and the residue was purified by column chromatography over silica gel (100-200 mesh), eluted with 2% ethyl acetate and petroleum ether, to afford 2-(cyclopentylmethyl-ethyl-amino)-5,6,7,8-tetrahydro-quinoline-3-carbonitrile (0.3 g), yield: 10%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040558B2
Source datasetuspto-grants-2015_05
ORD IDord-9db5cea5f67b4f37828ca260e40adb5e
Source noteuspto-grants-2015_05