Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | 3-Pyridinecarboxaldehyde | HCID 10371 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 68765446 | HCID 68765446 | — |
| Reactant | HCID 69040547 | HCID 69040547 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Catalyst | zinc(II)iodide | HCID 9883512 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59553540 | HCID 59553540 | — |
Reaction Steps
To a solution of rac 1-(3,4-dimethoxy-phenyl)-3-(4-trifluoromethyl-phenyl)-propylamine (accessed according to the procedure described for example 126 and 127, step 2 from 2-methyl-propane-2-sulfinic acid [1-(3,4-dimethoxy-phenyl)-3-(4-trifluoromethyl-phenyl)-propyl]-amide, 213 mg, 0.63 mmol) in THF (2 mL) was added 3-pyridinecarboxaldehyde (71 μl, 0.75 mmol), trimethylsilyl cyanide (118 μl, 0.94 mmol) and a catalytic amount of zinc iodide. The solution was stirred for 3 h at ambient temperature before it was diluted with DMSO (0.5 mL) and potassium carbonate (35 mg, 0.25 mmol) and hydrogen peroxide (35% in water, 82 μl, 0.94 mmol) were added. After stirring for 18 h at ambient temperature further hydrogen peroxide (35% in water, 41 μl, 0.47 mmol) was added and stirring continued for 3 h. It was diluted with methanol (0.5 mL) and palladium on charcoal 10% (5 mg) and acetic acid (50 μl) were added. Under an hydrogen atmosphere of hydrogen the reaction mixture was stirred for 3 h at ambient temperature. Sodium borohydride (50 mg) was added and the stirring was continued for 1 h. Purification by chromatography (SiO2, heptane:(ethyl acetate:triethylamine=95:5)=50:50 to 0:100) afforded the title compound as a racemic mixture (1:1) of diastereomers (127 mg, 43%) as a white solid. MS m/e: 472.5 [M−H]−
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07829563B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-1e816d11c31f4cfa9df8c09e8f60911c |
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| Source note | uspto-grants-2010_11 |
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