Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butanal | HCID 261 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 10845131 | HCID 10845131 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59717705 | HCID 59717705 | — |
Reaction Steps
Triethylamine (1.9 mL, 13.72 mmol) and butanal (1.3 mL, 14.41 mmol) were added to a solution of (S)-1-(trifluoroacetyl)pyrrolidin-3-yl amine (3.0 g, 13.72 mmol) (J. Med. Chem., 1996, 39(14), pg. 2771, No. 6) in ethanol (60 mL). The reaction mixture was treated with 10% Pd/C (300 mg) and placed under about 415 kPa (about 60 psi) of hydrogen at room temperature for 18 hours. The reaction mixture was filtered through Arbocel®, washing through with ethyl acetate. The filtrate was washed with saturated sodium hydrogencarbonate solution, dried over magnesium sulphate and concentrated in vacuo. The crude product was purified by column chromatography on silica gel eluting with ethyl acetate:pentane:triethylamine 25:75:0 to 100:0:0 to 99:0:1 to yield the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07378436B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-437f5ae62c5e41758c89b630bdb9868e |
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| Source note | uspto-grants-2008_05 |
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