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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448231Generated: October 27, 2026

tert-Butyl [(3S,5S,6R)-6-methyl-1-(2-methylpropyl)-2-oxo-5-phenylpiperidin-3-yl]carbamate → (3S,5S,6R)-3-amino-6-methyl-1-(2-methylpropyl)-5-phenylpiperidin-2-one

https://huagongshe.com/reaction/448231

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl [(3S,5S,6R)-6-methyl-1-(2-methylpropyl)-2-oxo-5-phenylpiperidin-3-yl]carbamateHCID 86665202—
SolventEthyl AcetateHCID 8857—
Product(3S,5S,6R)-3-amino-6-methyl-1-(2-methylpropyl)-5-phenylpiperidin-2-oneHCID 68750701—

Reaction Conditions

Temperature23 °C

Reaction Steps

A solution of tert-butyl[(3S,5S,6R)-6-methyl-1-(2-methylpropyl)-2-oxo-5-phenylpiperidin-3-yl]carbamate (140 mg, 0.39 mmol) in ethyl acetate (10 mL), pre-cooled to 0° C. was sparged with HCl gas for ˜1 min. The ice-bath was removed and the acidic solution was allowed to warm to 23° C. as stirring was continued for 2 h. The mixture was then concentrated to dryness to afford the title compound as a hydrochloride salt. MS: m/z=261.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481556B2
Source datasetuspto-grants-2013_07
ORD IDord-551614d04cc741a3b62e54f94c382b82
Source noteuspto-grants-2013_07