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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503156Generated: October 30, 2026

Ammonia → 2-(Acetamido)-6-(2-aminoethyl)quinoline

https://huagongshe.com/reaction/1503156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantNinhydrinHCID 10236—
Reactant2-(Acetamido)-6-(cyanomethyl)quinolineHCID 118252190—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
Product2-(Acetamido)-6-(2-aminoethyl)quinolineHCID 118252183—

Reaction Steps

Compound 47 (0.060 g, 0.266 mmol) was diluted in absolute EtOH (7 mL) and methanolic ammonia (7 N, 7 mL) was added. Raney nickel (˜1.5 g, washed with H2O and MeOH) was added, and the mixture was degassed and hydrogenated with a balloon at room temperature for 30 min while stirring rapidly. The clear solution was decanted away from the nickel and was filtered through a Pall 0.2 μm syringe filter to remove fine particulate matter. The solution was concentrated and dried in vacuo to yield a colorless gum that became a white semisolid upon standing (0.050 g, 82%). Conversion to this amine was confirmed by 1H NMR spectrometry, TLC, MS, and ninhydrin staining, and it was used crude without any further characterization or purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212144B2
Source datasetuspto-grants-2015_12
ORD IDord-e227a6b8e231457492184a031fe6837e
Source noteuspto-grants-2015_12