HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → (R)-2-[(1-Benzyl-pyrrolidin-3-yl)methyl-amino]-N,N-diphenyl-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 2-Bromo-n,n-diphenylacetamide | HCID 232041 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (R)-(1-benzoyl-pyrrolidin-3-yl)-methyl-amine | HCID 70216545 | — |
| Product | (R)-2-[(1-Benzyl-pyrrolidin-3-yl)methyl-amino]-N,N-diphenyl-acetamide | HCID 69053726 | — |
Reaction Steps
To a solution of (R)-(1-benzoyl-pyrrolidin-3-yl)-methyl-amine(0.32 g, 1.68 mmol) in dry CH3CN (10 ml) was added 2-bromo-N,N-diphenyl acetamide(0.49 g, 1.68 mmol) and NaHCO3 (0.28 g, 3.36 mmol) under nitrogen. The reaction mixture was refluxed overnight. After cooling, the solvent was evaporated. The residue was taken up with water (5 ml) and extracted with CHCl3 (3×25 ml). The organic was dried over MgSO4 and evaporated to dryness. The resulting residue was purified by column chromatography using CH2Cl2:CH3OH (15:1) to give 680 mg of desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07507760B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-b9d361fa95a640f9a04b086442faf109 |
| Source note | uspto-grants-2009_03 |