HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 650797Erstellt: 25. Oktober 2026
Phosphorus pentachloride → 4,6-Dichloro-5-(2-methoxyphenoxy)-2,2'-bipyrimidine
https://huagongshe.com/reaction/650797
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phosphorus pentachloride | HCID 24819 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 2-Cyanopyrimidine | HCID 2757979 | — |
| Edukt | Sodium Methoxide | HCID 10942334 | — |
| Edukt | Diethyl (2-methoxyphenoxy)propanedioate | HCID 11140560 | — |
| Edukt | 5-(2-Methoxyphenoxy)-2-(pyrimidin-2-yl)-tetrahydropyrimidin-4,6-dione | HCID 21979567 | — |
| Edukt | 2-Amidinopyrimidine hydrochloride | HCID 21983731 | — |
| Edukt | Sodium methanolate methanol | HCID 23694274 | — |
| Edukt | Ammonia ammonium chloride | HCID 86743336 | — |
| Produkt | 4,6-Dichloro-5-(2-methoxyphenoxy)-2,2'-bipyrimidine | HCID 10545706 | — |
Reaktionsschritte
The process of the present invention is especially useful for the preparation of 4-tert.butyl-N-6-(2-hydroxy-ethoxy)-5-(2-methoxy-phenoxy)-2-(pyrimidine-2-yl)-pyrimidine-4-yl-benzenesulphonamide (bosentan). For the preparation of this compound 2-cyanopyrimidine is prepared as described above and converted into pyrimidin-2-carboxamidine hydrochloride by means of NH3/NH4Cl in a sodium methanolate/methanol solution. This compound is converted in the presence of sodium methanolate with diethyl (o-methoxy-phenoxy-malonate) into rac-5-(2-methoxy-phenoxy)-2-pyrimidin-2-yl-tetrahydro-pyrimidin-4,6-dione. The obtained product is reacted with N,N-diisopropyl-N-ethylamine and phosphorus pentachloride to give 4,6-dichloro-5-(2-methoxy-phenoxy)-2,2′-bipyrimidine. This substance is then reacted with p-tert.butylbenzenesulphonamide to give 4-tert.butyl-N-6-chloro-5-[2-(2-methoxy-phenoxy)-2-(pyrimidin-2-yl)-pyrimidin-4-yl]-benzenesulphonamide and further reacted with sodium ethylene glycolate to give 4-tert.butyl-N-6-(2-hydroxy-ethoxy)-5-(2-methoxy-phenoxy)-2-(pyrimidin-2-yl)-pyrimidin-4-yl-benzenesulphonamide (bosentan).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06274734B1 |
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| Quelldatensatz | uspto-grants-2001_08 |
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| ORD ID | ord-241e0788f69d4e2f8b251b0f174be803 |
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| Quellennotiz | uspto-grants-2001_08 |
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