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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17303Generated: October 30, 2026

Potassium Phosphate, Tribasic → 4-Amino-3-cyano-6-fluoro-5-methoxy-2-methylbiphenyl

https://huagongshe.com/reaction/17303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantPhenylboronic AcidHCID 66827—
Reactant2-Amino-5-bromo-4-fluoro-3-methoxy-6-methylbenzonitrileHCID 86097453—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product4-Amino-3-cyano-6-fluoro-5-methoxy-2-methylbiphenylHCID 86097441—

Reaction Conditions

Temperature110 °C

Reaction Steps

Under nitrogen atmosphere, 2-amino-5-bromo-4-fluoro-3-methoxy-6-methylbenzonitrile (I-45) (20.0 g, 77.20 mmol), phenylboronic acid (11.3 g, 92.64 mmol), potassium phosphate (34.4 g, 162.11 mmol) were dissolved in a mixed liquid of 1,4-dioxane (400 ml) and water (20 ml), tetrakis(triphenylphosphine)palladium (2.6 g, 2.32 mmol) was added, followed by stirring at 110° C. for 15 hours. After cooling, the insoluble matter was separated by filtration through Celite, the reaction solvent was evaporated away under reduced pressure. The resulting residue was dissolved in ethyl acetate, washed with water and saturated brine, the organic layer was dried over anhydrous sodium sulfate, then the solvent was evaporated away under reduced pressure. The resulting residue was subjected to silica gel column chromatography, eluted wrath a mixed solvent of n-hexane/ethyl acetate (3:1, v/v) to obtain the entitled compound (20.12 g, quant) as a yellow white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737166B2
Source datasetuspto-grants-2010_06
ORD IDord-712fca5e5a9043b1b1ed8c4e58a18591
Source noteuspto-grants-2010_06