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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882795Generated: November 1, 2026

(1R,3S,4S)-3-(benzylamino-methyl)-2-aza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl ester → tert-butyl (1R,3S,4S)-3-(aminomethyl)-2-azabicyclo[2.2.1]heptane-2-carboxylate

https://huagongshe.com/reaction/882795

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1R,3S,4S)-3-(benzylamino-methyl)-2-aza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl esterHCID 66865917—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Producttert-butyl (1R,3S,4S)-3-(aminomethyl)-2-azabicyclo[2.2.1]heptane-2-carboxylateHCID 66866957—

Reaction Steps

A solution of (1R,3S,4S)-3-(benzylamino-methyl)-2-aza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl ester (39.8 mmol) in EtOH (120 mL) is treated with Pd/C (10%, 4.0 g) and stirred under a hydrogen atmosphere (7 bar) for 1 d. An additional amount of Pd/C (1.0 g) is added and the mixture is stirred for further 6 h under a hydrogen atmosphere (7 bar). After filtration through celite and removal of the solvents in vacuo the desired amine is obtained which is used without further purification. LC-MS (basic): tR=0.85 min; [M+H]+=227.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236801B2
Source datasetuspto-grants-2012_08
ORD IDord-11205cd6a04f4a65b28cc3f5567ee946
Source noteuspto-grants-2012_08