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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75934Generated: October 29, 2026

Potassium Carbonate → (S)-6-chloro-N-(1-(4-fluorophenyl)ethyl)-3-nitropyridin-2-amine

https://huagongshe.com/reaction/75934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2,6-Dichloro-3-nitropyridineHCID 85239—
Reactant(S)-1-(4-Fluorophenyl)-ethylamineHCID 2779063—
SolventAcetonitrileHCID 6342—
Product(S)-6-chloro-N-(1-(4-fluorophenyl)ethyl)-3-nitropyridin-2-amineHCID 8662061282%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a mixture of 2,6-dichloro-3-nitropyridine (2.26 g, 10.8 mmol) and potassium carbonate (1.29 g, 9.34 mmol) in anhydrous CH3CN (20 ml), was added (S)-1-(4-fluoro-phenyl)-ethylamine (1.00 g, 7.19 mmol) dropwise at 0° C. The reaction mixture was stirred at 25° C. for 17 hours. The solid was removed by filtration and the resulted cake was washed with EtOAc (20 ml). The combined filtrate was concentrated and purified by column chromatography (hexane-EtOAc=10:1) to give the title compound as a yellow solid (1.74 g, 82%). 1H NMR (400 MHz) δ 8.65 (d, J=7.6 Hz, 1H), 8.43 (d, J=8.4 Hz, 1H), 7.51 (m, 2H), 7.16 (m, 2H), 6.81 (d, J=8.8 Hz, 1H), 5.37 (m, 1H), 1.59 (d, J=6.8 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835465B2
Source datasetuspto-grants-2014_09
ORD IDord-152266fa1625419c8348840528701070
Source noteuspto-grants-2014_09