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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624971Generated: October 31, 2026

Potassium Carbonate → 1h-Pyrazole-3-carboxamide,4-[3-(hydroxymethyl)phenyl]-1-[(4-methoxyphenyl)methyl]-n-phenyl-

https://huagongshe.com/reaction/1624971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant[3-(Hydroxymethyl)phenyl]boronic acidHCID 2734662—
Reactant1h-Pyrazole-3-carboxamide,4-iodo-1-[(4-methoxyphenyl)methyl]-n-phenyl-HCID 66857314—
CatalystHCID 178418851HCID 178418851—
SolventEthanol toluene waterHCID 86587398—
Product1h-Pyrazole-3-carboxamide,4-[3-(hydroxymethyl)phenyl]-1-[(4-methoxyphenyl)methyl]-n-phenyl-HCID 66855422131.9%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 4-iodo-1-(4-methoxy-benzyl)-1H-pyrazole-3-carboxylic acid phenylamide (50 mg; 0.11 mmol), bis(tri-tert-butylphosphine)palladium (12 mg), potassium carbonate (100 mg; 0.66 mmol) and 3-(hydroxymethyl)benzene boronic acid (21 mg; 0.14 mmol) in ethanol/toluene/water (4 ml:1 ml:1 ml) was heated at 120° C. (50 W) for 15 minutes in a CEM Discover microwave synthesiser. The reaction was evaporated and the residue partitioned between ethyl acetate and brine. The ethyl acetate layer was separated, dried (MgSO4), filtered and evaporated and the crude material purified by flash column chromatography eluting with 1:2 then 2:1 ethyl acetate/hexane. Product containing fractions were combined and evaporated to give 60 mg of 4-(3-hydroxymethyl-phenyl)-1-(4-methoxy-benzyl)-1H-pyrazole-3-carboxylic acid phenylamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08779147B2
Source datasetuspto-grants-2014_07
ORD IDord-f6251ceffdad495685d59fdb9c44ca13
Source noteuspto-grants-2014_07