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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709955Generated: November 1, 2026

Water → HCID 54673226, compound

https://huagongshe.com/reaction/709955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CyanideHCID 8929—
ReactantHCID 66608836HCID 66608836—
CatalystCopper iodideHCID 83717—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventAcetonitrileHCID 6342—
ProductHCID 54673226HCID 5467322630.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of (S)-3-(1-((2-amino-5-iodopyrimidin-4-yl)amino)ethyl)-8-(1-methyl-1H-pyrazol-4-yl)-2-phenylisoquinolin-1(2H)-one (65) (240 mg, 0.43 mmol) in anhydrous acetonitrile (12 mL) in a sealed tube, sodium cyanide (209 mg, 4.26 mmol), tetrakis(triphenylphosphine) palladium(0) (246 mg, 0.21 mmol), and copper iodide (57 mg, 0.30 mmol) were added and the resulting mixture was stirred at 80° C. for 16 h. The mixture was allowed to cool to RT, quenced with water and extracted with ethyl acetate (50 mL×2). The combined organic layer was washed with brine, dried over Na2SO4 and filtered. The filtrate was concentrated in vacuo and the residue was purified by ISCO (silica gel cartridge, 0-10% MeOH-DCM) to afford the product, (S)-2-amino-4-((1-(8-(1-methyl-1H-pyrazol-4-yl)-1-oxo-2-phenyl-1,2-dihydroiso-quinolin-3-yl)ethyl)amino)pyrimidine-5-carbonitrile (69) (60 mg, 30% yield). ESI-MS m/z: 463.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181221B2
Source datasetuspto-grants-2015_11
ORD IDord-1e4dd23facc844fa8675d3c4505e566c
Source noteuspto-grants-2015_11