HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Acetic Anhydride → 4-(1-Acetyl-4-piperidinyl)-2-aminoquinazoline
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Acetic Anhydride | HCID 7918 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 2-Amino-4-(4-piperidinyl)quinazoline | HCID 15428775 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-(1-Acetyl-4-piperidinyl)-2-aminoquinazoline | HCID 15428776 | 76,3% |
Reaktionsschritte
To an ice-cold solution of 2-amino-4-(4-piperidyl)quinazoline (500 mg, 2.19 mmol) and triethylamine (233 mg, 2.3 mmol) in N,N-dimethylformamide (10 ml) was added dropwise acetic anhydride (0.22 ml, 2.30 mmol) under a nitrogen atmosphere. The reaction mixture was stirred for about 3 hours and was evaporated. The residue was partitioned between dichloromethane and saturated sodium hydrogencarbonate aqueous solution. The organic layer was washed with water and then dried over sodium sulfate and evaporated in vacuo. The residue was crystallized from ethanol. Recrystallization from methanol gave the titled compound(452 mg).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05948786 |
| Quelldatensatz | uspto-grants-1999_09 |
| ORD ID | ord-260fcdb2392148ba881ea8ed6c2255f6 |
| Quellennotiz | uspto-grants-1999_09 |