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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930586Generated: November 1, 2026

Potassium Carbonate → HCID 178480074, compound

https://huagongshe.com/reaction/1930586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2773987—
ReactantHCID 178451653HCID 178451653—
CatalystDichloro[1,1'-bis(di-tert-butylphosphino)ferrocene]palladium(II)HCID 53384307—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178480074HCID 178480074—

Reaction Conditions

Temperature110 °C

Reaction Steps

tert-Butyl 2-(4-bromophenylamino)-4-hydroxy-7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylate (1.4 g, 3.32 mmol), 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H pyrazole (0.691 g, 3.32 mmol), dichloro[1,1′-bis(di-tert-butylphosphino)ferrocene]palladium (II), Pd-118 (0.108 g, 0.17 mmol) and potassium carbonate (1.837 g, 13.29 mmol) in DMF (5 mL), water (2.5 mL) and ethanol (0.833 mL) were charged in a thick wall glass, which was sealed and heated at 110° C. for 20 minutes. The raction mixture was allowed to cool down, the crude was filtered through celite and the filtercake washed with ethanol. The solvent was evaporated under reduced pressure. The crude was used in the next step without further purification. MS (ESI) (M+1) m/z 423

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188101B2
Source datasetuspto-grants-2012_05
ORD IDord-475ac817a732471586a262ced4452c7c
Source noteuspto-grants-2012_05