Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586896Generated: November 3, 2026

Potassium Carbonate → HCID 22329144, compound

https://huagongshe.com/reaction/586896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 22329057HCID 22329057—
Reactant4-(2-Ethoxyethoxy)-3-fluorophenyl borateHCID 86756793—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
SolventEthanol toluene waterHCID 86587398—
ProductHCID 22329144HCID 2232914476.3%

Reaction Steps

In a mixture of water:ethanol:toluene (1:1:10, v/v, 18.0 ml) were dissolved 4-[(2-ethoxy)ethoxy]-3-fluorophenyl borate (355 mg) and 7-bromo-1-formyl-N-(4-[[N-methyl-N-(tetrahydro-2H-pyran-4-yl)amino]methyl]phenyl]-2,3-dihydro-1H-1-benzazepine-4-carboxamide (517 mg). To the solution was added potassium carbonate (344 mg), and the mixture was stirred under argon atmosphere at room temperature for 30 minutes. To the mixture was added tetrakistriphenylphosphinepalladium (48 mg), and the mixture was heated to reflux under argon atmosphere for 10 hours. The mixture was diluted with ethyl acetate, and washed with water and saturated brine, and the organic layer was dried with anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified with silica gel column chromatography (30 g, ethyl acetate→ethyl acetate:ethanol=10:1→ethyl acetate:ethanol:triethylamine=100:10 :1) and recrystallized from ethanol to give 7-[4-(2-ethoxy)ethoxy-3-fluorophenyl]-1-formyl-N-[4-[[N-methyl-N-(tetrahydro-2H-pyran-4-yl)amino]methyl]phenyl]-2,3-dihydro-1H-1-benzazepine-4-carboxamide (Compound 20) (476 mg, 76%) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936602B1
Source datasetuspto-grants-2005_08
ORD IDord-132e596cc6604389935ce20f24067382
Source noteuspto-grants-2005_08