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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927020Generated: November 2, 2026

Dichloromethane → US9290457, Example 17

https://huagongshe.com/reaction/927020

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Methyl-2-oxo-1,2-dihydropyridine-4-boronic acidHCID 67814299—
Reactant4-[5-Acetyl-3,6-dimethyl-2-oxo-1-(3-trifluoromethyl-phenyl)-1,2,3,4-tetrahydro-pyrimidin-4-yl]-3-bromo-benzonitrileHCID 118691686—
SolventAcetonitrileHCID 6342—
ProductUS9290457, Example 17HCID 118691698—

Reaction Conditions

Temperature75 °C

Reaction Steps

4-[5-Acetyl-3,6-dimethyl-2-oxo-1-(3-trifluoromethyl-phenyl)-1,2,3,4-tetrahydro-pyrimidin-4-yl]-3-bromo-benzonitrile (intermediate 4)(300 mg, 0.61 mmol) and (1-methyl-2-oxo-4-pyridyl)boronic acid (121 mg, 0.79 mmol) are suspended in acetonitrile (9 mL) and are degassed with a stream of argon. Potassium carbonate solution (2 mol/L, 914 μL, 1.83 mmol) and 1.1-bis(diphenylphosphino)-ferrocendichloropalladium(II), complex with dichloromethane (1:1) (9.95 mg, 0.012 mmol) are added and the reaction is shaken at 75° C. overnight. The reaction mixture is filtrated over a layer of silica gel and basic aluminum oxide 1:1 and purified by reversed phase HPLC. Yield: 142 mg; ESI mass spectrum [M+H]+=521; Retention time HPLC: 0.99 min (HPLC method Z018_S04).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290457B2
Source datasetuspto-grants-2016_03
ORD IDord-4e8ae0ba6d324dc9a0b6185c5ca5473a
Source noteuspto-grants-2016_03