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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787027Generated: October 31, 2026

Triphenylphosphine → 4-Phenoxy-6-prop-1-yn-1-ylpyrimidin-5-amine

https://huagongshe.com/reaction/1787027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantSodium BicarbonateHCID 516892—
ReactantPotassium FluorideHCID 522689—
Reactant4-Iodo-6-phenoxy-5-pyrimidinamineHCID 86084785—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Solvent1-(Trimethylsilyl)prop-1-yneHCID 80363—
Product4-Phenoxy-6-prop-1-yn-1-ylpyrimidin-5-amineHCID 56851054730%

Reaction Conditions

Temperature60 °C

Reaction Steps

4-Iodo-6-phenoxypyrimidin-5-amine (5.00 g) was dissolved in a mixed solvent of N,N-dimethylformamide (100 mL)/triethylamine (50 mL), and 1-(trimethylsilyl)-1-propyne (3.3 mL), trans-dichlorobis(triphenylphosphine)palladium(II) (557.7 mg), triphenylphosphine (421.1 mg), copper(I) iodide (303.0 mg) and potassium fluoride (1.29 g) were sequentially added. The mixture was stirred at 60° C. under an argon stream for 16 hrs. The reaction mixture was treated with saturated aqueous sodium hydrogen carbonate solution and extracted with diethyl ether. The organic layer washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was separated and purified by silica gel column chromatography (eluent, hexane:ethyl acetate=80:20→50:50) to give the title compound (2.64 g) as a orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507740B2
Source datasetuspto-grants-2009_03
ORD IDord-dac612e5b1094d8cb4d10e4b5dcb4f11
Source noteuspto-grants-2009_03