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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909131Generated: October 25, 2026

Diisopropylamine → 2-(2,4-Difluorophenyl)-6-(2-methylpyrimidin-5-yl)isonicotinic acid

https://huagongshe.com/reaction/1909131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantTrisodium 3,3',3''-phosphinetriyltris(benzene-1-sulphonate)HCID 6099338—
Reactant2-Methylpyrimidine-5-boronic acidHCID 45787274—
Reactant2-Chloro-6-(2,4-difluorophenyl)isonicotinic acidHCID 82305710—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-(2,4-Difluorophenyl)-6-(2-methylpyrimidin-5-yl)isonicotinic acidHCID 67339022—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 2-chloro-6-(2,4-difluorophenyl)isonicotinic acid (0.10 g, 0.37 mmol) in DMF (1.9 mL) and water (0.6 mL) were added (2-methylpyrimidin-5-yl)boronic acid (0.31 g, 2.23 mmol), palladium(II)acetate (12.5 mg, 0.06 mmol), 3,3′,3″-phosphinidynetris(benzenesulfonic acid) trisodium salt (95.0 mg, 0.17 mmol) and diisopropylamine (0.19 mL, 1.30 mmol). The mixture was heated to 80° C. After 2 h, the mixture was filtered and the filtrate was purified by reverse phase chromatography (C-18, 95% water/acetonitrile→25% water/acetonitrile with 0.1% trifluoroacetic acid). To the product fractions was added HCl (2.0 M in ether) and the mixture was concentrated to give the hydrochloride salt of the title compound. MS 328.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598209B2
Source datasetuspto-grants-2013_12
ORD IDord-a6351b7a675d4686931e681a64c80b55
Source noteuspto-grants-2013_12