Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 86600473 | HCID 86600473 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 66929778 | HCID 66929778 | 225.2% |
Reaction Steps
20% Piperidine in DMF (15 mL) was added to a solution of 9H-fluoren-9-ylmethyl-(1S)-1-(2,3-dihydro-1H-inden-2-yl)-2-hydroxyethylcarbamate (1.05 g, 2.63 mmol) in DMF (5 mL). The reaction was stirred at 25° C. for 19 h. After solvent evaporation, the crude product was dissolved in ethyl acetate (50 mL) and dried over MgSO4, filtered and concentrated to obtain a crude yellow oil (1.05 g). Mass Spectrum (+ESI): 179 (M+H)+.
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-84e42102b8ad421eb357f8057541b54f |
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| Source note | uspto-grants-2005_04 |
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