Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | (2S,3S)-2-phenylpiperidin-3-amine | HCID 9812908 | — |
| Reactant | HCID 22049660 | HCID 22049660 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86592317 | HCID 86592317 | — |
Reaction Steps
In 10 ml of methylene chloride were suspended 176 mg of (±)-cis-2-phenylpiperidin-3-ylamine, 280 mg of 2-methoxy-5-(2-trifluoromethylphenyl)benzaldehyde, 424 mg of sodium triacetoxyborohydride and 0.2 ml of acetic acid. This reaction mixture was stirred at room temperature for 16 hours, a saturated aqueous sodium hydrogen carbonate solution was added to the mixture and the resulting mixture was extracted with chloroform. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated. The concentrated residue was purified by silica gel column chromatography (chloroform/methanol=10/1) to give a colorless oily product. This product was dissolved in ethyl acetate, and treated with an ethyl acetate solution of 4N hydrochloric acid. The precipitated white crystals were collected by filtration and washed with ethanol, and dried under reduced pressure to give 243 mg of [(±)-cis-2-phenylpiperidin-3-yl][2-methoxy-5-(2-trifluoromethylphenyl)benzyl]amine dihydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07067535B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-304619208ebe47349928d79aba424114 |
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| Source note | uspto-grants-2006_06 |
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