HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → HCID 14202062, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(benzyloxycarbonyl)-4-(mesyloxy)butylamine | HCID 11141145 | — |
| Reactant | Dimethylamine tetrahydrofuran | HCID 22320367 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14202062 | HCID 14202062 | 76% |
Reaction Steps
To a solution of N-(benzyloxycarbonyl)-4-(mesyloxy)butylamine (2.51 g) in anhydrous dimethylformamide (28 ml) are added 2.0 M dimethylamine THF solution 12.5 ml. anhydrous potassium carbonate (1.72 g) and sodium iodide (3.74 g), and the mixture is stirred at room temperature overnight. Water is added to the reaction mixture, and the whole is extracted with ether. The organic layer is washed with water and saturated brine successively, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue is purified by silica gel column chromatography to give 1.59 g (76%) of N-(benzyloxycarbonyl)-4-(dimethylamino)butylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06492370B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-c0e7d30ceb06427d9861a42c7a286e85 |
| Source note | uspto-grants-2002_12 |