Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 1-Phenethylamine, (+)- | HCID 643189 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 1-(1-(4-fluorobenzyl)-1H-indole-2-carbonyl)piperidine-4-carbaldehyde | HCID 86671899 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66571570 | HCID 66571570 | — |
Reaction Steps
1-(1-(4-fluorobenzyl)-1H-indole-2-carbonyl)piperidine-4-carbaldehyde (91 mg, 0.250 mmol) was dissolved in THF (4 mL) and (R)-α-methylbenzylamine (0.048 mL, 0.375 mmol) was added. The solution was stirred at rt for 10 h, at which time the THF was removed in vacuo and the residue dissolved in EtOH (5 mL), and sodium cyanoborohydride (47 mg, 0.749 mmol) and a catalytic drop of glacial acetic acid were added. Stirring was permitted for 15 h, at which time the solvent was removed in vacuo, the residue was taken up in EtOAc. The organic phase was washed with 10% aq. sodium carbonate, dried over magnesium sulfate, and concentrated. Purification was accomplished via silica gel flash chromatography (30 g silica gel, 5:95 7M methanolic ammonia:ethyl acetate.) The title compound was obtained as a yellow oil. (Yield: 52 mg, 0.111 mmol, 44%) 1H NMR (400 MHz, CDCl3) 7.62, 7.39-7.22, 7.14, 7.07-6.99, 6.89-6.80, 6.57, 5.41, 4.56, 4.02, 3.76, 2.73, 2.36-2.18, 1.60, 1.39, 0.97, 0.52
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846684B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-3334ec0d372f4223ace19fa732351d5f |
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| Source note | uspto-grants-2014_09 |
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