HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Nitrogen → (S)-tert-butyl 1-amino-3-cyclohexylpropan-2-ylcarbamate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Nitrogen | HCID 947 | — |
| Edukt | (S)-tert-butyl 1-azido-3-cyclohexylpropan-2-ylcarbamate | HCID 59382971 | — |
| Katalysator | Palladium | HCID 23938 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | (S)-tert-butyl 1-amino-3-cyclohexylpropan-2-ylcarbamate | HCID 10988904 | 90,2% |
Reaktionsschritte
A solution of (S)-tert-butyl 1-azido-3-cyclohexylpropan-2-ylcarbamate (7.2 g, 25.5 mmol) in methanol (250 mL) was added to wetted Pd/C (1.0 g) in a N2-filled Parr bottle. After 3 vac/purge cycles with H2, the vessel was charged to 50 psi and shaken on a Parr apparatus overnight. Theoretical equivalents (36 psi) of H2 were consumed. The reaction mixture was filtered through a pad of Celite and the solvent was removed to give (S)-tert-butyl 1-amino-3-cyclohexylpropan-2-ylcarbamate (5.9 g, 90%) as a white solid. 1H NMR (D6-DMSO) δ 0.70-1.30 (m 10H), 1.38 (s, 9H), 1.58 (d, 2H), 1.80 (d, 1H), 2.66 (m, 1H), 2.78 (d, 1H), 3.74 (m, 1H), 6.77 (d, 1H), 8.0 (bs, 2H). MS ESI +ve m/z 157 (M(−BOC)+1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08455521B2 |
| Quelldatensatz | uspto-grants-2013_06 |
| ORD ID | ord-128650d90ecc4ef9b5616a591a67c812 |
| Quellennotiz | uspto-grants-2013_06 |