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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466213Generated: November 2, 2026

Potassium Phosphate, Tribasic → HCID 86271598, compound

https://huagongshe.com/reaction/1466213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTricyclohexylphosphineHCID 75806—
ReactantCyclopropylboronic acidHCID 2760897—
ReactantHCID 89480386HCID 89480386—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 86271598HCID 86271598—

Reaction Conditions

Temperature100 °C

Reaction Steps

5-(((3,5-bis(trifluoromethyl)benzyl)(5-bromopyridin-2-yl)amino)methyl)-1-(tert-butyl)-N,N-bis(cyclopropylmethyl)-3-methyl-1H-pyrazolo[3,4-b]pyridin-6-amine (0.05 g, 0.069 mmol) as prepared above, cyclopropyl boronic acid (0.007 g, 0.083 mmol) were dissolved in toluene (10 ml). To this tricyclohexylphosphine (0.002 g, 0.0069 mmol), Pd(OAc)2 (0.0007 g, 0.0034 mmol), K3PO4 (0.051 g, 0.241 mmol) were added. The mixture was stirred at 100° C. for 16 hr. The reaction mixture was diluted with water, extracted with EtOAc. The combined organic layer was washed with brine, dried over Na2SO4, and concentrated under reduced pressure. The crude product thus obtained, was purified by column chromatography using silica gel 60-120 mesh, 10% EtOAc in petroleum ether as the eluent to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000007B2
Source datasetuspto-grants-2015_04
ORD IDord-6382162085684776ad46e81118b21146
Source noteuspto-grants-2015_04