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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524346Generated: October 30, 2026

Potassium Carbonate → 1-Cyclobutyl-6-methyl-4-oxo-5-(3-trifluoromethyl-phenyl)-1,4-dihydro-pyridine-3-carboxylic acid (5-methyl-[1,3,4]oxadiazol-2-ylmethyl)-amide

https://huagongshe.com/reaction/524346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-(Trifluoromethyl)phenylboronic acidHCID 2734388—
Reactant5-Bromo-1-cyclobutyl-6-methyl-4-oxo-1,4-dihydro-pyridine-3-carboxylic acid (5-methyl-[1,3,4]oxadiazol-2-ylmethyl)-amideHCID 86711592—
SolventAcetonitrileHCID 6342—
Product1-Cyclobutyl-6-methyl-4-oxo-5-(3-trifluoromethyl-phenyl)-1,4-dihydro-pyridine-3-carboxylic acid (5-methyl-[1,3,4]oxadiazol-2-ylmethyl)-amideHCID 86711599—

Reaction Conditions

Temperature75 °C

Reaction Steps

To a solution of 5-bromo-1-cyclobutyl-6-methyl-4-oxo-1,4-dihydro-pyridine-3-carboxylic acid (5-methyl-[1,3,4]oxadiazol-2-ylmethyl)-amide (preparation 24, 44 mg, 0.115 mmol), 3-(trifluoromethyl)phenyl-boronic acid (26 mg, 0.137 mmol), 1,1′-[bis(diphenylphosphino)ferrocene]dichloropalladium(II) (13 mg, 0.018 mmol) in acetonitrile (0.5 mL) is added 2 M aqueous K2CO3 solution (0.10 mL, 0.20 mmol). After stirring for 18 h at 75° C., the reaction mixture is filtered and purified by preparative reversed-phase HPLC (XBridge, gradient of methanol in water, 0.3% NH4OH, 60° C.). Yield: 40 mg (78% of theory); ESI mass spectrum: [M+H]+=447; Retention time HPLC: 1.09 min (Z003_001).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340507B2
Source datasetuspto-grants-2016_05
ORD IDord-ee1ac6f8f1384a259a350ca5ca36cdf2
Source noteuspto-grants-2016_05