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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243257Generated: November 1, 2026

HCID 68157042, compound → HCID 68157586, compound

https://huagongshe.com/reaction/243257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68157042HCID 68157042—
SolventEthyl AcetateHCID 8857—
ProductHCID 68157586HCID 68157586107%

Reaction Steps

(3-Fluoro-6-nitro-2-pyridin-2-yl-phenyl)isopropylamine (0.49 g, 1.79 mmol) was dissolved in EtOAc (10 mL). The flask was evacuated and purged with N2. Pd/C (10%) was added and the mixture was hydrogenated at atmospheric pressure under a H2 atmosphere. The mixture was stirred overnight. The flask was evacuated and purged with N2. The catalyst was removed by filtration and the filtrate was concentrated in vacuo and the resulting residue was purified by chromatography (Si—PPC, gradient 0-50% EtOAc/cyclohexane) to afford the title compound as a yellow oil (0.47 g, 99%). 1H NMR (CDCl3, 400 MHz): δ 8.71 (1H, ddd, J=6.6, 2.4, 1.3 Hz), 7.78 (1H, ddd, J=10.6, 10.2, 2.5 Hz), 7.57 (1H, ddt, J=10.6, 5.2, 1.4 Hz), 7.26 (1H, ddd, J=10.0, 6.6, 1.6 Hz), 6.76-6.66 (2H, m), 5.34 (1H, br s), 3.80 (2H, br s), 3.19 (1H, sept, J=8.5 Hz), 7.63 (6H, d, J=8.5 Hz)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653089B2
Source datasetuspto-grants-2014_02
ORD IDord-2d50151022ac4a90b5c6ae2d76191166
Source noteuspto-grants-2014_02