HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160004Generated: October 28, 2026
2,4-Dichloropyrimidine → N-[5-[(2-Chloro-4-pyrimidinyl)ethynyl]-2-(methyloxy)phenyl]-2,2,2-trifluoroacetamide
https://huagongshe.com/reaction/1160004
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4-Dichloropyrimidine | HCID 77531 | — |
| Reactant | N-[5-ethynyl-2-(methyloxy)phenyl]-2,2,2-trifluoroacetamide | HCID 59511434 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[5-[(2-Chloro-4-pyrimidinyl)ethynyl]-2-(methyloxy)phenyl]-2,2,2-trifluoroacetamide | HCID 59511410 | 83.1% |
Reaction Steps
To an oven-dried flask under N2 was added 2,4-dichloropyrimidine (860 mg, 5.76 mmol), anhydrous degassed THF (100 mL), dichlorobis(triphenylphosphine)palladium(II) (81 mg, 0.12 mmol), copper(I) iodide (13 mg, 0.07 mmol), and TEA (1.26 g, 0.013 mol). After heating the reaction at 60° C. for 30 min, N-[5-ethynyl-2-(methyloxy)phenyl]-2,2,2-trifluoroacetamide (560 mg, 2.30 mmol, obtained from composite batches) was added dropwise as a solution in THF (10 mL) and the resulting mixture was allowed to heat overnight at 60° C. The crude reaction mixture was adsorbed to silica gel and purified by column chromatography (0-10% EtOAc in hexanes) to afford the desired product (0.68 g, 42%) as an off white solid. ESIMS (M+H)+=356.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07812022B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-6f3e4ed9bfd9484cbbe15b1382513896 |
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| Source note | uspto-grants-2010_10 |
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