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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340782Generated: October 31, 2026

Potassium Carbonate → HCID 71073942, compound

https://huagongshe.com/reaction/340782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(2-Hydroxyphenyl)boronic acidHCID 2773454—
ReactantHCID 71073922HCID 71073922—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
ProductHCID 71073942HCID 71073942—

Reaction Conditions

Temperature120 °C

Reaction Steps

A 50 mL flask was charged with ethyl 3-{[5-(4-bromophenyl)-6-chloro-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-benzimidazol-2-yl]oxy}cyclobutanecarboxylate (150 mg, 0.259 mmol), 2-hydroxybenzeneboronic acid, pinacol ester (60 mg, 0.273 mmol), Pd(PPh3)4 (20 mg, 0.017 mmol), DMF (5 mL), and 1 M aqueous K2CO3 (0.78 ml, 0.780 mmol). The reaction was degassed with N2 and then heated at 120° C. for 1 hour. Then the volatiles were removed in vacuo and the residue partitioned between EtOAc and H2O. The aqueous phase was extracted with EtOAc. The combined organic layers were washed with brine, dried over (MgSO4), filtered, and concentrated. Chromatography of the resulting residue over silica (preparative TLC) eluting with 45% EtOAc/hexanes afforded the desired product. LC-MS: calculated for C32H37ClN2O5Si 592.22, observed m/e: 593.05 (M+H)+ (Rt 2.67/4 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895596B2
Source datasetuspto-grants-2014_11
ORD IDord-96bd535de1d04754b3f22206a9e48ad9
Source noteuspto-grants-2014_11