HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Methylethanimidothioate hydroiodide → HCID 178465574, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Methylethanimidothioate hydroiodide | HCID 11680130 | — |
| Edukt | N-(4-[2-(4-aminophenyl)ethyl]-5-[4-(methylsulfonyl)benzyl]-1,3-thiazol-2-yl)acetamide | HCID 21914845 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | HCID 178465574 | HCID 178465574 | 46,7% |
Reaktionsschritte
N-{4-[2-(4-Aminophenyl)ethyl]-5-[4-(methylsulfonyl)benzyl]-1,3-thiazol-2-yl}acetamide (200 mg), methyl ethanimidothioate hydroiodide (202 mg) and MeOH (4 ml) were combined under N2 atmosphere. The reaction mixture was refluxed for 3 hours. After cooled to room temperature, the mixture was concentrated in vacuo. The residue was purified by preparative NH silica gel chromatography with CHCl3/MeOH (10:1) as an eluent. The amorphous substance was solidified with ethyl ether to give N-{4-{2-[4-(ethanimidoylamino)phenyl]ethyl}-5-[4-(methylsulfonyl)benzyl]-1,3-thiazol-2-yl}acetamide (102.4 mg) as a pale yellow amorphous solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07442715B2 |
| Quelldatensatz | uspto-grants-2008_10 |
| ORD ID | ord-e2a5a29b4dc94a7e926b643fd4c34ffc |
| Quellennotiz | uspto-grants-2008_10 |