HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 848727Erstellt: 25. Oktober 2026
Sodium Iodide → 2-(2-carbamoyl-5-chlorophenylamino)-N-(3,4-dimethoxyphenethyl)acetamide
https://huagongshe.com/reaction/848727
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Iodide | HCID 5238 | — |
| Edukt | 2-Chloro-N-(2-(3,4-dimethoxy-phenyl)-ethyl)-acetamide | HCID 26622 | — |
| Edukt | Magnesium monoxide | HCID 6850729 | — |
| Edukt | 2-Amino-4-chlorobenzamide | HCID 12374837 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 2-(2-carbamoyl-5-chlorophenylamino)-N-(3,4-dimethoxyphenethyl)acetamide | HCID 10091881 | 68,2% |
Reaktionsschritte
To a mixture of 7.73 g of 2-chloro-N-(3,4-dimetoxyphenethyl)acetamide, 5.12 g of 2-amino-4-chlorobenzamide, 13.5 g of sodium iodide and 3.63 g of magnesium oxide was added 30 ml of dimethylformamide and the resulting mixture was stirred at 90° to 100° C. for 4.5 hours. The reaction solution was concentrated under reduced pressure and the residue was extracted with 500 ml of chloroform. The chloroform extract was washed successively with 10% hydrochloric acid, water, a 5% aqueous sodium carbonate solution, a 5% aqueous sodium sulfite solution and water, dried and then concentrated to dryness under reduced pressure. The residue was recrystallized from methanol to obtain 8.01 g of 2-(2-carbamoyl-5-chlorophenylamino)-N-(3,4-dimethoxyphenethyl)acetamide having a melting point of 167.5°-168.5° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04297357 |
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| Quelldatensatz | uspto-grants-1981_10 |
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| ORD ID | ord-1b4f0eca18164eb1a151fd9e5085d218 |
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| Quellennotiz | uspto-grants-1981_10 |
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