HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1517446Generated: November 3, 2026
Potassium Carbonate → 3-Amino-6-(4-fluorophenyl)picolinamide
https://huagongshe.com/reaction/1517446
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Fluorophenylboronic acid | HCID 285645 | — |
| Reactant | 3-Amino-6-chloropyridine-2-carboxamide | HCID 10749704 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-Amino-6-(4-fluorophenyl)picolinamide | HCID 59647906 | 85% |
Reaction Steps
To a solution of 3-amino-6-chloropyridine-2-carboxylic acid amide (2.57 g, 15 mmol) in dioxane (200 ml) and water (50 ml) was added 4-fluorophenylboronic acid (2.1 g, 15 mmol), K2CO3 (6.2 g, 45 mmol), and tetrakis(triphenylphosphine) palladium(0) (860 mg, 0.75 mmol). The mixture was heated at reflux for 3 hours. After cooling to room temperature, the reaction mixture was concentrated to a small volume, filtrated and washed with water to yield a crude product. The residue was purified by silica gel flash chromatography, the mobile phase being a mixture of methanol and dichloromethane, in a volume ratio of 1:80, yielding the title compound (2.9 g, yield 85%) as a white solid. The mass spectrum characterising data was as follows: MS (m/z): 232 ([M+H]+, 100).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08232278B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-76546f6eda764381aad07a2b3d4d8508 |
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| Source note | uspto-grants-2012_07 |
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