Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Methylpyrrolidine | HCID 13003 | — |
| Reactant | HCID 59457504 | HCID 59457504 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 11858317 | HCID 11858317 | 41% |
Reaction Steps
1-({2-[4-(3-chloropropoxy)phenyl]-1,3-oxazol-4-yl}methyl)piperidin-2-one i55 (0.564 g, 1.62 mmol, 1 eq) is reacted with 2-methylpyrrolidine (0.19 ml, 1.94 mmol, 1.2 eq) in the presence of potassium carbonate (0.45 g, 3.24 mmol, 2 eq) and a catalytic quantity of sodium iodide in refluxing acetonitrile (20 ml). After 45 h, the solvent is evaporated. The residue is then taken up in ethyl acetate and washed two times with an aqueous solution of sodium hydrogenocarbonate. The organic layer is dried over magnesium sulfate, filtered and concentrated under vacuum. Purification by chromatography over silicagel (eluent: dichloromethane/methanol/ammonia 95:4.5:0.5) affords 0.27 g of 1-[(2-{4-[3-(2-methylpyrrolidin-1-yl)propoxy]phenyl}-1,3-oxazol-4-yl)methyl]piperidin-2-one 122.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07790720B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-f3917507cbfc428e8905402495f862c3 |
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| Source note | uspto-grants-2010_09 |
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