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HRID 1254217Erstellt: 25. Oktober 2026

Nitrogen → (S)-tert-butyl 1-amino-3-cyclohexylpropan-2-ylcarbamate

https://huagongshe.com/reaction/1254217

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitrogenHCID 947—
Edukt(S)-tert-butyl 1-azido-3-cyclohexylpropan-2-ylcarbamateHCID 59382971—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
Produkt(S)-tert-butyl 1-amino-3-cyclohexylpropan-2-ylcarbamateHCID 1098890490,2%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08455521B2
Quelldatensatzuspto-grants-2013_06
ORD IDord-128650d90ecc4ef9b5616a591a67c812
Quellennotizuspto-grants-2013_06