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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478598Generated: November 2, 2026

Potassium Carbonate → HCID 118364750, compound

https://huagongshe.com/reaction/1478598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 73507292HCID 73507292—
ReactantHCID 131330026HCID 131330026—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 118364750HCID 11836475078%

Reaction Conditions

Temperature80 °C

Reaction Steps

1-((1-(5-bromopyrimidin-2-yl)piperidin-3-yl)methyl)-6-(1-methyl-1H-pyrazol-4-yl)-1H-[1,2,3]triazolo[4,5-b]pyrazine (30 mg, 0.066 mmol), 1-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolane-2-yl)-1H-pyrazole (32 mg, 0.099 mmol), Pd(dppf)2Cl2(2.7 mg, 0.003 mmol), and K2CO3(28 mg, 0.20 mmol) were dissolved in dioxane (1.2 ml)+H2O (0.3 ml), and the mixture was degassed with N2(gas), followed by stirring at 80° C. for 2 hours. After the completion of the reaction, the reaction mixture was extracted with H2O, EA, and brine, followed by drying (Na2SO4), filtration, and concentration under reduced pressure, and the residue was purified by column chromatography (MeOH:MC=1:20), to give 6-(1-methyl-1H-pyrazol-4-yl)-1-((1-(5-(1-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)-1H-pyrazol-3-yl)pyrimidin-2-yl)piperidin-3-yl)methyl)-1H-[1,2,3]triazolo[4,5-b]pyrazine (28 mg, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403831B2
Source datasetuspto-grants-2016_08
ORD IDord-48caa82b87904da5923c79dc73dbb2b3
Source noteuspto-grants-2016_08