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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733125Generated: November 1, 2026

Sodium Carbonate → 5-Methyl-1-[2'-(trifluoromethoxy)-1,1'-biphenyl-3-yl]-1H-pyrazole-3-carboxamide

https://huagongshe.com/reaction/733125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-(Trifluoromethoxy)phenylboronic Acid (contains varying amounts of Anhydride)HCID 2777204—
Reactantethyl 1-(3-bromophenyl)-5-methyl-1H-pyrazole-3-carboxamideHCID 69062233—
CatalystHCID 178418397HCID 178418397—
SolventHCID 22495535HCID 22495535—
Product5-Methyl-1-[2'-(trifluoromethoxy)-1,1'-biphenyl-3-yl]-1H-pyrazole-3-carboxamideHCID 995080493.4%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of ethyl 1-(3-bromophenyl)-5-methyl-1H-pyrazole-3-carboxamide (0.237 g, 0.8 mmol) and 2-trifluoromethoxyphenyl boronic acid (0.262 g, 1.2 mmol) in n-propanol/toluene (1.27 ml:0.42 ml) mixture were added tetrakis(triphenylphosphine)palladium (0.019 g, 0.01 mmol) and 2M sodium carbonate (0.84 ml). The reaction mixture was heated at 90° C. for 16 hours, and then cooled and partitioned between ethyl acetate and water. The organic phase was washed with saturated sodium bicarbonate and brine, then dried over sodium sulfate and concentrated. The crude product was purified by silica-gel column chromatography (3.5:1.5 hexanes/acetone) to give the product (0.270 g, 88%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07589116B2
Source datasetuspto-grants-2009_09
ORD IDord-81c0a498528944c4a627c9d2b4bdaf35
Source noteuspto-grants-2009_09