Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1H-Isoindole-1,3(2H)-dione, hexahydro- | HCID 73559 | — |
| Reactant | HCID 14576385 | HCID 14576385 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14576386 | HCID 14576386 | 49.1% |
Reaction Steps
To a mixture of 60% sodium hydride (0.12 g) and dimethylformamide (5 ml), cyclohexane-1,2-dicarboximide (0.5 g) was portionwise added. A solution of 1-(3,4-epoxybutyl)-4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidine (0.8 g) in dimethylformamide (10 ml) was dropwise added thereto at room temperature, and the resultant mixture was kept at an inner temperature of 90 to 100° C. for 16.5 hours. Insoluble materials were removed by filtration, and the residue was combined with water and extracted with ethyl acetate. The organic layer was washed with a saturated sodium chloride solution, dried over magnesium sulfate and concentrated under reduced pressure. The resulting crude crystals were recrystallized from a mixture of isopropyl ether and isopropanol to give the objective compound (0.6 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04937249 |
|---|
| Source dataset | uspto-grants-1990_06 |
|---|
| ORD ID | ord-74929d15930e409c9f5e16930ccbd9d0 |
|---|
| Source note | uspto-grants-1990_06 |
|---|