HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733149Generated: October 30, 2026
Potassium Phosphate, Tribasic → 1-[6-fluoro-2'-(trifluoromethoxy)-1,1'-biphenyl-3-yl]-5-methyl-1H-pyrazole-3-carboxamide
https://huagongshe.com/reaction/733149
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2-(Trifluoromethoxy)phenylboronic Acid (contains varying amounts of Anhydride) | HCID 2777204 | — |
| Reactant | 1-(3-Chloro-4-fluorophenyl)-5-methyl-1H-pyrazole-3-carboxamide | HCID 57839541 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-[6-fluoro-2'-(trifluoromethoxy)-1,1'-biphenyl-3-yl]-5-methyl-1H-pyrazole-3-carboxamide | HCID 49866119 | 11.9% |
Reaction Steps
To a solution of the carboxamide (from step 2) (0.063 g, 0.2 mmol) and 2-trifluromethoxyphenyl boronic acid (0.076 g, 0.37 mmol) in dioxane (1 mL) were added NiCl2(dppf)2 (0.002 g, 1 mole %) and potassium phosphate (0.158 g, 0.74 mmol) and the mixture was stirred at 95° C. for 16 hours. After cooling, the reaction was partitioned between EtOAc and water. The organic phase was washed with saturated sodium bicarbonate, brine and then dried over sodium sulfate. The crude product, obtained upon concentration of the organic phase, was purified by reverse phase HPLC (acetonitrile/water system) (gradient: 10% to 90% acetonitrile over 10 minutes) to yield the titled product (0.009 g, 9.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07589116B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-3a43a05f902d4f589d5cd50b77abe14a |
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| Source note | uspto-grants-2009_09 |
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