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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192562Generated: November 2, 2026

Ammonium Acetate → 1-[8-(3-Fluorophenyl)-5-methylquinolin-7-yl]ethanamine

https://huagongshe.com/reaction/1192562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-[8-(3-Fluorophenyl)-5-methylquinolin-7-yl]ethanoneHCID 58368662—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
Product1-[8-(3-Fluorophenyl)-5-methylquinolin-7-yl]ethanamineHCID 58368628—

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 1-[8-(3-fluorophenyl)-5-methylquinolin-7-yl]ethanone (50 mg, 0.2 mmol) and ammonium acetate (138 mg, 1.79 mmol) in methanol (1.0 mL) and acetonitrile (1.0 mL) was heated at 65° C. in a sealed tube for 30 minutes. After cooling to room temperature, sodium cyanoborohydride (22.5 mg, 0.358 mmol). The reaction was heated at 65° C. for another 4 hours, then cooled to room temperature and quenched with sat. sodium bicarbonate, extracted with dichloromethane. The combined extracts were dried over magnesium sulfate and evaporated to dryness. The residue was used directly in the next step. LCMS calculated for C18H18FN2 (M+H)+: m/z=281.1; Found: 281.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680108B2
Source datasetuspto-grants-2014_03
ORD IDord-df7050142b4740a19076534e87656050
Source noteuspto-grants-2014_03