HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Dimethylformamide → 2-Cyano-N-cyclopropyl-N-[[(2-fluoro-4-iodophenyl)amino]carbonyl]acetamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Cyanoacetic acid | HCID 9740 | — |
| Edukt | Methanesulfonyl chloride | HCID 31297 | — |
| Edukt | N-Cyclopropyl-N'-(2-fluoro-4-iodophenyl)urea | HCID 59717054 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Propan-2-ol--water (1/1) | HCID 21889133 | — |
| Produkt | 2-Cyano-N-cyclopropyl-N-[[(2-fluoro-4-iodophenyl)amino]carbonyl]acetamide | HCID 59717036 | 95,1% |
Reaktionsschritte
Under a nitrogen atmosphere, to 1-cyclopropyl-3-(2-fluoro-4-iodo-phenyl)-urea 48 (167 g) and cyanoacetic acid 73 (80.0 g), was added N,N-dimethylformamide (836 ml), and methanesulfonyl chloride (72.8 ml) was added dropwise with stirring at room temperature. The mixture was stirred at room temperature for 4 hrs. The reaction mixture was cooled with water, and water-isopropanol [2:1 (volume ratio), 1670 ml] was added dropwise. The mixture was stirred under water-cooling for 1 hr, and the precipitated crystals were collected by filtration and dried to give 1-(2-cyano-acetyl)-1-cyclopropyl-3-(2-fluoro-4-iodo-phenyl)-urea 74 (192 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08835443B2 |
| Quelldatensatz | uspto-grants-2014_09 |
| ORD ID | ord-49db73fa634d49f2ad82112751b7b222 |
| Quellennotiz | uspto-grants-2014_09 |