HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733131Generated: October 31, 2026
Sodium Carbonate → 1-[4'-Fluoro-2'-(trifluoromethyl)-1,1'-biphenyl-3-yl]-5-methyl-1h-pyrazole-3-carboxamide
https://huagongshe.com/reaction/733131
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | 2-Bromo-5-fluorobenzotrifluoride | HCID 520983 | — |
| Reactant | ethyl 1-(3-bromophenyl)-5-methyl-1H-pyrazole-3-carboxamide | HCID 69062233 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-[4'-Fluoro-2'-(trifluoromethyl)-1,1'-biphenyl-3-yl]-5-methyl-1h-pyrazole-3-carboxamide | HCID 11417163 | 41% |
Reaction Steps
To a solution of ethyl 1-(3-bromophenyl)-5-methyl-1H-pyrazole-3-carboxamide (from step 2 of EXAMPLE 1) (0.069 g, 0.24 mmol) in DMSO (1.14 mL), bis(pinacoloato)diboron (0.075 g, 0.3 mmol) was added followed by potassium acetate (0.072 g, 0.74 mmol) and PdCl2(dppf)2 (0.005 g, 3 mol %). The solution was heated in a Smith Creator™ microwave reactor (commercially available from Personal Chemistry, Inc.) at 140° C. for 1200 seconds. The reaction mixture was cooled to room temperature, and 2-bromo-5-fluorobenzotrifluoride (0.12 g, 0.5 mmol), PdCl2(dppf)2 (0.005 g, 3 mol %) and 2M sodium carbonate (0.61 mL, 1.2 mmol) were added to the reaction mixture. The reaction was then subjected to microwave radiation at 140° C. for 2800 seconds. After cooling to room temperature, the reaction mixture was partitioned between EtOAc and water. The organic layer was washed with saturated sodium bicarbonate and brine, then dried over sodium sulfate, filtered and concentrated. Purification of the crude product by reverse phase HPLC (acetonitrile/water system) (gradient: 45% to 100% acetonitrile over 10 minutes) yielded 0.036 mg of the product (41% yield, retention time 5.1 minutes).
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-337a3bc5ca0a46a6a8bace89eaf0c5be |
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| Source note | uspto-grants-2009_09 |
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