Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | HCID 59457505 | HCID 59457505 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11858316 | HCID 11858316 | 23% |
Reaction Steps
A solution of 1-[(2-{4-[2-(2-methylpyrrolidin-1-yl)ethoxy]phenyl}-1,3-oxazol-4-yl)acetyl]piperidine i54 (0.13 g, 0.33 mmol, 1 eq) in tetrahydrofuran (5 ml) is treated with borane-tetrahydrofuran complex (1.0 M in tetrahydrofuran, 1.3 ml, 1.3 mmol, 4 eq) and the resulting mixture is refluxed overnight. A 2 N sodium hydroxide solution is added to reach pH 10 and the mixture is refluxed for 6 h. A saturated solution of aqueous ammonium chloride is added and the solution is extracted two times with ethyl acetate. The organic layers are dried over magnesium sulfate, filtered and concentrated under vacuum. Purification by chromatography over silicagel (eluent: dichloromethane/methanol/ammonia 96/3.6/0.4) gives 0.115 g of 1-[2-(2-{4-[2-(2-methylpyrrolidin-1-yl)ethoxy]phenyl}-1,3-oxazol-4-yl)ethyl]piperidine 121.
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-c465326610784bfdb10cc6954154787a |
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| Source note | uspto-grants-2010_09 |
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