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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043785Generated: October 25, 2026

Triethylamine → 3-Amino-6-(2-(pyrrolidin-1-yl)ethoxy)quinoline

https://huagongshe.com/reaction/1043785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Nitro-6-(2-(pyrrolidin-1-yl)ethoxy)quinolineHCID 59507599—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product3-Amino-6-(2-(pyrrolidin-1-yl)ethoxy)quinolineHCID 59507982—

Reaction Steps

3-Nitro-6-(2-(pyrrolidin-1-yl)ethoxy)quinoline (134 mg, 0.46 mmol) was dissolved in EtOAc (10 mL) and the solution was sparged with N2 for several minutes. Triethylamine (0.065 mL, 0.46 mmol) was then added followed by a catalytic amount of 10% Pd/C. Sparging with N2 was repeated after each addition. A balloon of H2 was connected to the reaction flask and the reaction mixture was stirred at room temperature under H2 atmosphere for 48 hours. The mixture was then filtered through a Celite pad and concentrated to obtain crude 3-amino-6-(2-(pyrrolidin-1-yl)ethoxy)quinoline, which was used as is in the next reaction. LC/MS (m/z): 258.1 (MH+), Rt 0.33 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563549B2
Source datasetuspto-grants-2013_10
ORD IDord-1260b52ca94a471592548e362ef93802
Source noteuspto-grants-2013_10