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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 630484Generated: October 30, 2026

Potassium Carbonate → (1-(5-(1-Methyl-1H-pyrazol-4-yl)pyrimidin-2-yl)-3-(methylthio)-1H-indol-6-yl)(morpholino)methanone

https://huagongshe.com/reaction/630484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTri-tert-butylphosphine tetrafluoroborateHCID 2734635—
Reactant1-Methyl-1H-pyrazole-4-boronic acidHCID 11263501—
Reactant(1-(5-Bromopyrimidin-2-yl)-3-(methylthio)-1H-indol-6-yl)(morpholino)methanoneHCID 118666053—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventEthyl AcetateHCID 8857—
SolventOxolane--water (1/1)HCID 21881883—
Product(1-(5-(1-Methyl-1H-pyrazol-4-yl)pyrimidin-2-yl)-3-(methylthio)-1H-indol-6-yl)(morpholino)methanoneHCID 118676819—

Reaction Conditions

Temperature30 °C

Reaction Steps

Potassium carbonate (254 mg, 1.846 mmol, 2.0 eq), Pd2(dba)3 (84 mg, 0.0923 mmol, 0.1 eq) and tri-tert-butylphosphonium tetrafluoroborate (13 mg, 0.046 mmol, 0.05 eq) were added to a solution of (1-(5-bromopyrimidin-2-yl)-3-(methylthio)-1H-indol-6-yl)(morpholino)methanone (400 mg, 0.923 mmol, 1.0 eq) and (1-methyl-1H-pyrazol-4-yl)boronic acid (140 mg, 1.108 mmol, 1.2 eq) in THF/water (20 mL, 4:1) stirred under an argon atmosphere at 30° C. The reaction mixture was stirred at the same temperature for 2 h and the cooled to ambient temperature and diluted with ethyl acetate (10 mL). The mixture was filtered through a pad of celite, washed with water, dried over sodium sulfate and evaporated. The residue was purified by column chromatography [100-200 mesh, 2% methanol in dichloromethane]. White solid. Yield: 380 mg (95% of theory)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315490B2
Source datasetuspto-grants-2016_04
ORD IDord-0e3424909e1f4df08fb0053a5ea42797
Source noteuspto-grants-2016_04