HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042036Generated: October 27, 2026
Potassium Carbonate → 5-(5-Chloropyridin-3-yloxy)-2,4-difluorobenzenamine
https://huagongshe.com/reaction/2042036
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,5-Dichloropyridine | HCID 17153 | — |
| Reactant | 5-Amino-2,4-difluorophenol | HCID 2782999 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(5-Chloropyridin-3-yloxy)-2,4-difluorobenzenamine | HCID 67253056 | 66% |
Reaction Steps
To a solution of 5-amino-2,4-difluorophenol (0.3 g, 2.07 mmol) in DMSO (2 mL) was added potassium t-butoxide (0.23 g, 2.07 mmol) at RT. After stirring for 1 h, 3,5-dichloropyridine (0.37 g, 2.5 mmol) and potassium carbonate (0.14 g, 1 mmol) were added and the mixture was heated to 190° C. for 1 h in microwave reactor. Water (30 mL) was added, and the product was extracted with EtOAc (2×35 mL) and the combined organic layers were washed with brine solution, dried (Na2SO4), concentrated in vacuo and purified by chromatography (EtOAc/hexane) to afford 5-(5-chloropyridin-3-yloxy)-2,4-difluorobenzenamine (0.35 g, 66% yield) as a solid. 1H NMR (400 MHz, Acetone-d6) δ 8.33-8.30 (m, 2H), 7.44 (t, J=2.4 Hz, 1H), 7.13 (t, J=10.8 Hz, 1H), 6.78 (t, J=8.4 Hz, 1H), 4.85 (brs, 2H); MS (ESI) m/z: 257.0 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08586565B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-5c561e707be64f3fb7ebfceeb6d08926 |
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| Source note | uspto-grants-2013_11 |
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