Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 2-(2-Oxo-2-phenyl-ethylcarbamoyl)-piperidine-1-carboxylic acid benzyl ester | HCID 23570718 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 178420113 | HCID 178420113 | — |
| Product | HCID 178525127 | HCID 178525127 | — |
Reaction Steps
2-(2-Oxo-2-phenyl-ethylcarbamoyl)-piperidine-1-carboxylic acid benzyl ester (22.83 g, 60 mmol), NH4OAc (ammonium acetate) (63.5 g, 824 mmol), AcOH (acetic acid) (30 mL), and xylene (350 mL) were mixed at room temperature, and with stirring the reaction mixture was warmed in an oil bath at 165° C. for about 6 hours. The reaction mixture was then cooled to room temperature and poured into brine. The organic phase was dried over MgSO4, filtered, and concentrated under reduced pressure to yield 31.24 g of off white powder. This sample was triturated in ethyl ether (100 mL), filtered, and rinsed liberally with ethyl ether to yield 15.12 g (70% over two steps) of the desired product 2-(4-phenyl-1H-imidazol-2-yl)-piperidine-1-carboxylic acid benzyl ester as a white solid. HPLC analysis showed the compound to be 100% pure at 254 nm and 98.1% pure at 214 nm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07041681B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-7701b4cde6e04fc8a45e1e95d6e1c0ac |
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| Source note | uspto-grants-2006_05 |
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