HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Dichloromethane → N-(4-acetylamino-5-chloro-2-methoxyphenyl)-4-benzylpiperazine-1-carboxamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Dichloromethane | HCID 6344 | — |
| Edukt | 1-Benzylpiperazine | HCID 75994 | — |
| Edukt | Isocyanate | HCID 105034 | — |
| Edukt | 4-Acetylamino-5-chloro-2-methoxy-benzoyl azide | HCID 20538742 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | N-(4-acetylamino-5-chloro-2-methoxyphenyl)-4-benzylpiperazine-1-carboxamide | HCID 20538750 | — |
Reaktionsschritte
A solution of the 4-acetylamino-5-chloro-2-methoxy-benzoyl azide (e7) (1.35 g) in dry toluene (30 ml) was heated to 90° for 30 minutes with stirring under dry nitrogen until the evolution of nitrogen ceased. A dichloromethane solution of 1-benzylpiperazine (0.9 g) was then added to the cooled suspension of the isocyanate (e8) and the resulting solution stirred at room temperature for 1 hour. The reaction mixture was then poured into petrol (200 ml) and the precipitated solid filtered off. Recrystallisation from toluene give the N-(4-acetylamino-5-chloro-2-methoxyphenyl)-4-benzylpiperazine-1-carboxamide (e9) (1.4 g) m.p. 174°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04223034 |
| Quelldatensatz | uspto-grants-1980_09 |
| ORD ID | ord-cb73b9cea51b451aadaa1b85f473c6f0 |
| Quellennotiz | uspto-grants-1980_09 |