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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278850Generated: November 2, 2026

Potassium Carbonate → HCID 71621533, compound

https://huagongshe.com/reaction/2278850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTricyclohexylphosphineHCID 75806—
Reactant3-Pyridinylboronic acidHCID 2734378—
ReactantHCID 89690930HCID 89690930—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 71621533HCID 7162153375.5%

Reaction Steps

Under an argon atmosphere, 140 mg (purity 65%, 0.256 mmol) of 6-chloro-3-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-1,2,4-triazine-5-amine were suspended in 5 ml of absolute dioxane. 94 mg (0.767 mmol) of pyridin-3-ylboronic acid, 1.023 ml (1.023 mmol) of 1N aqueous potassium carbonate solution and 14 mg (0.051 mmol) of tricyclohexylphosphine were added and argon was passed through the suspension for 10 min with stirring. Then, 28 mg (0.038 mmol) of 1,1′-bis(diphenylphosphino)ferrocenepalladium(II) chloride were added and the reaction mixture was stirred for 30 min in the microwave at 140° C. After cooling, the mixture was filtered over an Extrelut cartridge and after-washed with a mixture of dichloromethane/methanol (v/v=20:1). The filtrate was concentrated and the residue was purified by preparative HPLC (mobile phase: acetonitrile/water, gradient 20:80→100:0). 77 mg of the target compound were obtained (65% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133191B2
Source datasetuspto-grants-2015_09
ORD IDord-0a61455aeccb42c9b8ea4637e39a0bd5
Source noteuspto-grants-2015_09