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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17599Generated: October 27, 2026

Cesium carbonate → 4-Amino-3'-chloro-6-fluoro-5-hydroxy-3-methylbiphenyl-3-carbonitrile

https://huagongshe.com/reaction/17599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant(3-Chlorophenyl)boronic acidHCID 2734323—
Reactant2-Amino-5-bromo-4-fluoro-3-hydroxy-6-methylbenzonitrileHCID 86097514—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product4-Amino-3'-chloro-6-fluoro-5-hydroxy-3-methylbiphenyl-3-carbonitrileHCID 6858543378%

Reaction Conditions

Temperature100 °C

Reaction Steps

2-Amino-5-bromo-4-fluoro-3-hydroxy-6-methylbenzonitrile (I-75) (2.0 g, 8.16 mmol), 3-chlorophenylboronic acid (2.63 g, 16.3 mmol) and cesium carbonate (5.32 g, 16.3 mmol) were dissolved in 1,4-dioxane (90 ml)/water (10 ml), and at room temperature, (tetrakistriphenylphosphine)palladium(0) (943 mg, 0.82 mmol) was added. The solution was stirred in a nitrogen steam at 100° C. for 12 hours. After cooling to room temperature, the insoluble matter was separated by filtration with washing with ethyl acetate. The filtrate was concentrated under reduced pressure, and the residue was fractionated with ethyl acetate and saturated brine. The aqueous layer was separated, this was further extracted twice with ethyl acetate. The organic layers were combined, washed with saturated brine, and dried over anhydrous sodium sulfate. The insoluble matter was separated by filtration, the solvent was evaporated away, and the resulting residue was purified by middle-pressure liquid chromatography (eluent, chloroform:ethyl acetate=95:5, v/v) to obtain the entitled compound (1.76 g, 78%) as a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737166B2
Source datasetuspto-grants-2010_06
ORD IDord-aa631540665a49e59cd3384132a16db5
Source noteuspto-grants-2010_06