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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522814Generated: November 1, 2026

Water → HCID 178461595, compound

https://huagongshe.com/reaction/522814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium fluorideHCID 25953—
Reactant(4-(1H-Imidazol-2-yl)phenyl)boronic acidHCID 66575043—
ReactantHCID 178461594HCID 178461594—
CatalystHCID 178418397HCID 178418397—
SolventIsopropanolHCID 3776—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 178461595HCID 17846159550.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

8-Bromo-2,6-bis-((R)-3-methyl-morpholin-4-yl)-9H-purine (99 mg, 250 μmol) was dissolved in 2 mL of acetonitrile and 0.2 mL of water under argon. 4-(1H-imidazol-2-yl)phenyl boronic acid (58.7 mg, 313 μmol), CsF (57 mg, 375 μmol), and Pd(PPh3)4 (28.9 mg, 25 μmol) were added. The suspension was stirred at 50° C. for 10 minutes in a closed microwave vial. Then it was irradiated for 40 minutes in a microwave apparatus at 150° C. The vial was cooled and uncapped, and the reaction mixture was diluted with 50 mL of CH2Cl2 and 10 mL of isopropanol. The organic solvents were washed with brine and aqueous NaHCO3, dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by column chromatography (40 g SiO2, CH2Cl2/EtOH/aqueous NH3 in a gradient from 100/0/0.1 to 90/10/0.1) to give the product as a solid (58 mg, 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334271B2
Source datasetuspto-grants-2016_05
ORD IDord-6a5c567c6cf84e85a83f7265ee75d0bc
Source noteuspto-grants-2016_05