HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 19608059, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Chloroacetamide | HCID 6580 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 19607777 | HCID 19607777 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 19608059 | HCID 19608059 | 95.4% |
Reaction Steps
To a solution of 5-oxo-1-[4-(2-hydroxybenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine (400 mg) in acetone (20 ml) are added potassium carbonate (210 mg), potassium iodide (250 mg) and 2-chloroacetamide (120 mg), and the mixture is refluxed for 2 hours. The insoluble materials are removed by filtration, and the filtrate is distilled off. Dichloromethane is added to the resulting residue, and the mixture is washed with saturated saline solution, and dried over magnesium sulfate. The solvent is distilled off and the resulting residue is recrystallized from ethyl acetate/n-hexane to give 5-oxo-1-[4-(2-carbamoylmethoxybenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine (436 mg) as white powder, m.p. 226°-228° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05559230 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-526bb22f9c23455b900c7641cee6da9b |
| Source note | uspto-grants-1996_09 |