HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → HCID 11857527, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 2-Methylpyrrolidine | HCID 13003 | — |
| Reactant | HCID 59457512 | HCID 59457512 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 11857527 | HCID 11857527 | 50% |
Reaction Steps
To a solution of 2-[4-(3-chloropropoxy)phenyl]-4-(2-oxo-2-pyrrolidin-1-ylethyl)-1,3-oxazole ax64 (0.51 g, 1.46 mmol, 1 eq) in acetonitrile (10 ml) is added sodium iodide (0.022 g, 0.15 mmol, 0.1 eq) and 2-methylpyrrolidine (0.25 ml, 2.92 mmol, 2 eq). The mixture is stirred at reflux overnight. The mixture is poured into dichloromethane and washed with water. The organic layer is dried over magnesium sulfate and the solvent is removed under vacuum. The crude product is purified by chromatography over silica gel (eluent: dichloromethane/methanol/ammonia 95:4.5:0.5) to give 0.29 g of 2-{4-[3-(2-methylpyrrolidin-1-yl)propoxy]phenyl}-4-(2-oxo-2-pyrrolidin-1-ylethyl)-1,3-oxazole 52 as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07790720B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-5243c1bb543d4bba8d53bd92b5bcf508 |
| Source note | uspto-grants-2010_09 |