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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201013Generated: October 28, 2026

Triphenylphosphine → HCID 86663078, compound

https://huagongshe.com/reaction/2201013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Methoxyphenylboronic acidHCID 2733958—
Reactant2-Chloro-5-iodopyridin-4-amineHCID 45480366—
Catalystpalladium(II) acetateHCID 167845—
ProductHCID 86663078HCID 8666307880.5%

Reaction Conditions

Temperature75 °C

Reaction Steps

Potassiumphosphate (18.28 g, 79 mmol), triphenyl phosphine (1.04 g, 3.97 mmol), 2-chloro-5-iodo-4-aminopyridine (10.1 g, 39. mmol), 2-methoxybenzeneboronic acid (8.44 g, 55.57 mmol) and palladium acetate (0.45 g, 1.98 mmol) were sequentially added to degassed acetonitrile (300 mL) and water (100 mL) under nitrogen. The reaction mixture was heated at 75° C. for overnight, then cooled to room temperature. The organic layer was separated and aqueous layer and was extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate, concentrated and performed column chromatography using hexanes and ethyl acetate as eluent. 7.5 g of title compound was isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359549B2
Source datasetuspto-grants-2016_06
ORD IDord-5f08475a938642769fb31de21fbb3332
Source noteuspto-grants-2016_06