Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 66930031 | HCID 66930031 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 66929718 | HCID 66929718 | — |
Reaction Steps
To tert-butyl 4-((1S)-1-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-2-hydroxyethyl)piperdine-1-carboxylate (0.95 g, 2.03 mmol) was added 20% piperidine in dimethylformamide (20 mL) all at once. The reaction was stirred overnight at 25° C. The dimethylformamide was evaporated off and the crude residue was subjected to flash chromatography using methylene chloride-methanol-ammonium hydroxide, 95-5-0.1% as eluent. This yielded the amine product as an oil that crystallized upon standing (0.392 g, 80%). MS (+ESI) 245.2 ([M+M]+); 189.2; 150.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06878742B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-3e190c9e800c4e888c89d19119d94ab7 |
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| Source note | uspto-grants-2005_04 |
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