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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201016Generated: October 29, 2026

Triphenylphosphine → HCID 86663080, compound

https://huagongshe.com/reaction/2201016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Methoxyphenylboronic acidHCID 2733958—
Reactant6-Chloro-5-iodopyridin-2-amineHCID 70700961—
Catalystpalladium(II) acetateHCID 167845—
ProductHCID 86663080HCID 8666308071.9%

Reaction Conditions

Temperature75 °C

Reaction Steps

Potassium phosphate (12.72 g, 60 mmol), triphenyl phosphine (0.682 g, 2.40 mmol), 6-chloro-5-iodo-2-aminopyridine (6.1 g, 24 mmol), 2-methoxybenzeneboronic acid (5.10 g, 33.5 mmol) and palladium acetate (0.27 g, 1.20 mmol) were sequentially added to degassed acetonitrile (200 mL) and water (60 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 purified by silica column using hexanes and ethyl acetate as eluent furnishing 4.05 g of title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359549B2
Source datasetuspto-grants-2016_06
ORD IDord-afb4646395c1452f832fe7ea2fb73afd
Source noteuspto-grants-2016_06