HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 2-(1-Benzhydryl-2-oxo-pyrrolodin-3-yl-amino)-N,N-diphenyl acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Bromo-n,n-diphenylacetamide | HCID 232041 | — |
| Reactant | 3-Amino-1-benzhydryl-pyrrolidin-2-one | HCID 57597562 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(1-Benzhydryl-2-oxo-pyrrolodin-3-yl-amino)-N,N-diphenyl acetamide | HCID 57597568 | 73% |
Reaction Steps
To a solution of 3-amino-1-benzhydryl-pyrrolidin-2-one (42) (0.2 g, 0.75 mmol in dry DMF (15 ml) was added 2-bromo-N,N-diphenyl acetamide (0.24 g, 0.82 mmol) and NaH (50 mg) under nitrogen. The reaction mixture was heated at 100 degrees overnight. After cooling, the solvent was evaporated and residue was taken up with ethyl acetate (50 ml) and washed with water (2×10 ml). The organic was dried over MgSO4 and evaporated to dryness. The resulting residue was purified by column chromatography using hexane:ethyl acetate (2:1) to give desired product in 73% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07507760B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-f49a2e9c3a4b49999eae65a12fbe610b |
| Source note | uspto-grants-2009_03 |