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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225064Generated: October 31, 2026

HCID 66998378, compound → tert-butyl (3R,4R)-4-amino-3-methylpiperidine-1-carboxylate

https://huagongshe.com/reaction/2225064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66998378HCID 66998378—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
Producttert-butyl (3R,4R)-4-amino-3-methylpiperidine-1-carboxylateHCID 66998328—

Reaction Steps

(3R, 4R)-3-Methyl-4-(1-(S)-phenyl-ethylamino)-piperidine-1-carboxylic acid tert-butyl ester (810 mg, 2.55 mmol) was dissolved in methanol (15 mL). Palladium hydroxide (20%, 100 mg) was added and the mixture was shaken under a hydrogen atmosphere overnight at 55 psi. The reaction was filtered and concentrated in vacuo to give the title compound as a clear oil. Wt.: 500 mg (92%). NMR (300 MHz, CDCl3) δ4.06 (m, 1H), 3.96 (m, 1H), 2.73 (m, 1H), 2.34 (m, 2H), 1.77 (m, 1H), 1.43 (s, 9H), 1.27 (m, 2H), 0.94 (d, 3H); LC/MS m/z 215 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378525B2
Source datasetuspto-grants-2008_05
ORD IDord-35011ec1762c41a4af1677fe33abecc6
Source noteuspto-grants-2008_05