HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83550Generated: October 30, 2026
Potassium Carbonate → 1-(4-Fluorophenyl)-5-[3-fluoro-5-((R)-2,2,2-trifluoro-1-methylethoxymethyl)phenyl]-1H-pyrazol-3-ylamine
https://huagongshe.com/reaction/83550
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Tricyclohexylphosphine | HCID 75806 | — |
| Reactant | HCID 71287745 | HCID 71287745 | — |
| Reactant | HCID 86680375 | HCID 86680375 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-(4-Fluorophenyl)-5-[3-fluoro-5-((R)-2,2,2-trifluoro-1-methylethoxymethyl)phenyl]-1H-pyrazol-3-ylamine | HCID 71287864 | — |
Reaction Steps
To a solution of 1-(4-fluorophenyl)-5-iodo-1H-pyrazol-3-ylamine (84 mg) prepared according to the same procedures as Preparation 18 in 1,4-dioxane (1.0 ml) were sequentially added 2-[3-fluoro-5-((R)-2,2,2-trifluoro-1-methylethoxymethyl)phenyl]-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (106 mg) prepared according to the same procedures as Preparation 15, palladium (II) acetate (7 mg), tricyclohexylphosphine (17 mg) and a 2M aqueous solution of potassium carbonate (0.5 ml) at room temperature, and the mixture was stirred at 105° C. for 2 hours. This reaction mixture was cooled to room temperature and after removing an aqueous layer, an organic layer was filtered through silica gel (5 g), and subjected to elution with ethyl acetate. The filtrate was concentrated under reduced pressure, and the resulting residue was purified by silica gel thin-layer chromatography (eluent: n-hexane/ethyl acetate=3/2) to give the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08846746B2 |
|---|
| Source dataset | uspto-grants-2014_09 |
|---|
| ORD ID | ord-90a2fe479b5943d98e512e16de6e4e0a |
|---|
| Source note | uspto-grants-2014_09 |
|---|