HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 230367Erstellt: 24. Oktober 2026
2-(4-Iodophenoxy)pyrimidine → 2-(2,6-Dichlorobenzamido)-5-[4-(pyrimidin-2-yloxy)phenyl]pent-4-ynoic acid methyl ester
https://huagongshe.com/de/reaction/230367
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-(4-Iodophenoxy)pyrimidine | HCID 1484617 | — |
| Edukt | 2-(2,6-Dichlorobenzamido)pent-4-ynoic acid methyl ester | HCID 20610296 | — |
| Katalysator | Copper iodide | HCID 83717 | — |
| Katalysator | HCID 178418476 | HCID 178418476 | — |
| Lösungsmittel | THF diisopropylamine | HCID 18968793 | — |
| Produkt | 2-(2,6-Dichlorobenzamido)-5-[4-(pyrimidin-2-yloxy)phenyl]pent-4-ynoic acid methyl ester | HCID 57762477 | 86,2% |
Reaktionsschritte
Under an argon atmosphere, copper iodide (2.8 mg) and dichlorobis(triphenylphosphine)palladium (5.2 mg) were added to a solution of 2-(2,6-dichlorobenzamido)pent-4-ynoic acid methyl ester (74 mg), 2-(4-iodophenoxy)pyrimidine (81 mg) in THF/diisopropylamine (3/1) mixture (5 ml), and the resulting mixture was stirred at room temperature for 2 hours. The reaction solution was concentrated and ethyl acetate was added to the residue. The insoluble matter was removed by filtration, and the filtrate was washed once with water and once with saturated brine and dried over anhydrous sodium sulfate. After removing anhydrous sodium sulfate by filtration, the filtrate was concentrated. The residue was purified by column chromatography (silica gel, eluent: cyclohexane/chloroform 10=2/1-cyclohexane/chloroform=1/3) to obtain 2-(2,6-dichlorobenzamido)-5-[4-(pyrimidin-2-yloxy)phenyl]pent-4-ynoic acid methyl ester (100 mg).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07566724B2 |
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| Quelldatensatz | uspto-grants-2009_07 |
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| ORD ID | ord-1356b306c5a748a58c42535df6be0692 |
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| Quellennotiz | uspto-grants-2009_07 |
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