Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(4-Bromobutyl)phthalimide | HCID 93575 | — |
| Reactant | 5-Methoxy-3,4-dihydro-2H-1-benzopyran-3-amine | HCID 13928948 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10429859 | HCID 10429859 | 67% |
Reaction Steps
In a round bottomed flask, 2.2 mmol of 3-amino -5-methoxychroman (described in Patent EP 279,150) are dissolved in 6 ml of dimethylformamide in the presence of 2.4 mmol of N-(4-bromobutyl)phthalimide, 6.6 mmol of potassium carbonate and a catalytic amount of potassium iodide. The mixture is left stirring at 60° C. for 6 hours. After cooling, the solvent is evaporated off and, after aqueous hydrolysis, the crude reaction mixture is extracted with dichloromethane. After washing, drying and evaporation of-the organic phase, the expected product is obtained after purification by chromatography on a silica column (elution solvent: ether/petroleum ether, 5:95).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05314907 |
|---|
| Source dataset | uspto-grants-1994_05 |
|---|
| ORD ID | ord-7aab8da8aff34ec39a5b2301bfc633a9 |
|---|
| Source note | uspto-grants-1994_05 |
|---|