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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909130Generated: October 26, 2026

Hydrochloric Acid → 2-Chloro-6-(2,4-difluorophenyl)isonicotinic acid

https://huagongshe.com/reaction/1909130

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropylamineHCID 7912—
Reactant2,6-Dichloroisonicotinic acidHCID 94830—
Reactant2,4-Difluorophenylboronic acidHCID 2734334—
ReactantTri(m-sulfophenyl)phosphine sodium saltHCID 86657030—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-Chloro-6-(2,4-difluorophenyl)isonicotinic acidHCID 8230571036.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 2,6-dichloroisonicotinic acid (2.43 g, 12.67 mmol) in DMF (38 mL) and water (12.7 mL) were added (2,4-difluorophenyl)boronic acid (2.0 g, 12.67 mmol), tri(m-sulfophenyl)phosphine sodium salt (0.54 g, 0.95 mmol), palladium(II) acetate (71.0 mg, 0.32 mmol) and diisopropylamine (6.3 mL, 44.3 mmol). The mixture was heated 50° C. After 2.5 h, the mixture was cooled to ambient temperature and stirred for 18 h. HCl (1.0 M in water) was added and the mixture was was extracted with ethyl acetate (3×). The combined organic extracts were washed with brine, dried over magnesium sulfate, filtered and concentrated. Purification by reverse phase chromatography (C-18, 85% water/acetonitrile→5% water/acetonitrile with 0.1% trifluoroacetic acid) gave the title compound (1.24 g). MS 270.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598209B2
Source datasetuspto-grants-2013_12
ORD IDord-d14bf500784748c383ab7a142485f4c2
Source noteuspto-grants-2013_12