HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530428Generated: October 31, 2026
Triethylamine → 1-{2-[(3-Aminophenyl)ethynyl]phenyl}urea
https://huagongshe.com/reaction/530428
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Benzenamine, 3-ethynyl- | HCID 104682 | — |
| Reactant | Urea, (2-iodophenyl)- | HCID 139387 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-{2-[(3-Aminophenyl)ethynyl]phenyl}urea | HCID 121254629 | — |
Reaction Steps
To the nitrogen degassed solution of 1-(2-iodophenyl)urea (1.31 g, 5 mmol, 1 eq), 3-ethynylaniline (0.8 mL, 1.5 eq), triphenylphosphine (32.8 mg, 0.025 eq), and triethylamine (2.1 mL, 3 eq) in anhydrous DMF (12.5 mL) was added copper(I) iodide (190.4 mg, 0.2 eq) and bis(triphenylphosphine)palladium(II) dichloride (351 mg, 0.1 eq). After the reaction mixture was stirred at room temperature for 10 minutes, it was diluted with ethyl acetate, washed sequentially with aqueous ammonium chloride, saturated aqueous sodium bicarbonate, brine, and lastly dried with anhydrous sodium sulfate. The upper solution was decanted, concentrated, and the solid mixture was subject to a gradient column chromatography (EtOAc-Hex 1:2 to MeOH-EtOAc 1:9) to give 1-{2-[(3-aminophenyl)ethynyl]phenyl}urea as a brown solid in amount of 1.26 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09353093B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-04637a0d363e4c53acfb0a02963fd6b2 |
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| Source note | uspto-grants-2016_05 |
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