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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371171Generated: October 31, 2026

Benzyl (S)-4-((1-(tert-butoxycarbonyl)piperidin-3-yl)methyl)piperazine-1-carboxylate → tert-butyl (3S)-3-(piperazin-1-ylmethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/2371171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl (S)-4-((1-(tert-butoxycarbonyl)piperidin-3-yl)methyl)piperazine-1-carboxylateHCID 59846076—
SolventMethanolHCID 887—
Producttert-butyl (3S)-3-(piperazin-1-ylmethyl)piperidine-1-carboxylateHCID 2488666099.6%

Reaction Steps

Benzyl 4-{[(3S)-1-(tert-butoxycarbonyl)piperidin-3-yl]methyl}piperazine-1-carboxylate (5.0 g, 12.4 mmol) was dissolved in methanol (50 ml) in a three-necked flask. The air was removed under reduced pressure and replaced with argon before the addition of 10% Pd/C (1.24 g). A balloon of hydrogen was then added and the reaction stirred at room temperature for 18 h. The hydrogen was evacuated and replaced with argon. The catalyst was then filtered and the solvent removed under reduced pressure to afford the desired product as a white foam (3.5 g). The compound was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710224B2
Source datasetuspto-grants-2014_04
ORD IDord-0d8b8af7ab294dd59c4c4abb29ec5f39
Source noteuspto-grants-2014_04