HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 326712Erstellt: 25. Oktober 2026
Ethylene Glycol → N-[6-(2-hydroxyethoxy)-5-(o-methoxybenzyl)-4-pyrimidinyl]-p-methoxybenzenesulfonamide
https://huagongshe.com/reaction/326712
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethylene Glycol | HCID 174 | — |
| Edukt | Sodium Glycolate | HCID 517347 | — |
| Edukt | Sodium | HCID 5360545 | — |
| Edukt | HCID 12396954 | HCID 12396954 | — |
| Produkt | N-[6-(2-hydroxyethoxy)-5-(o-methoxybenzyl)-4-pyrimidinyl]-p-methoxybenzenesulfonamide | HCID 19735392 | — |
Reaktionsschritte
300 mg of N-[6-chloro-5-(p-methoxybenzyl)-4-pyrimidinyl]-p-methoxybenzenesulfonamide were added to a sodium glycolate solution from 1 ml of dry ethylene glycol and 46 mg of sodium. The reaction mixture was heated at 125° C. for 4 hours under an argon atmosphere. Thereafter, the ethylene glycol was distilled under reduced pressure. The residue was partitioned between ethyl acetate and 1N hydrochloric acid. The organic phase was washed neutral, dried and evaporated. The residue was chromatographed on silica gel with methylene chloride/ethyl acetate (1:1 v/v). There were obtained 250 mg of N-[6-(2-hydroxyethoxy)-5-(o-methoxybenzyl)-4-pyrimidinyl]-p-methoxybenzenesulfonamide, melting point 161°-162° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05270313 |
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| Quelldatensatz | uspto-grants-1993_12 |
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| ORD ID | ord-e0b87538e9714a53aab5aecb6702ad63 |
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| Quellennotiz | uspto-grants-1993_12 |
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