HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243257Generated: November 1, 2026
HCID 68157042, compound → HCID 68157586, compound
https://huagongshe.com/reaction/243257
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 68157042 | HCID 68157042 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 68157586 | HCID 68157586 | 107% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653089B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-2d50151022ac4a90b5c6ae2d76191166 |
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| Source note | uspto-grants-2014_02 |
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