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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 4-Iodo-6-phenoxy-5-pyrimidinamine | HCID 86084785 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | 1-(Trimethylsilyl)prop-1-yne | HCID 80363 | — |
| Product | 4-Phenoxy-6-prop-1-yn-1-ylpyrimidin-5-amine | HCID 56851054 | 730% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07507740B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-dac612e5b1094d8cb4d10e4b5dcb4f11 |
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| Source note | uspto-grants-2009_03 |
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