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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1402762Generated: November 1, 2026

Benzyl 3-[(4-cyclobutylpiperazin-1-yl)carbonyl]azetidine-1-carboxylate → 1-(Azetidin-3-ylcarbonyl)-4-cyclobutylpiperazine

https://huagongshe.com/reaction/1402762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 3-[(4-cyclobutylpiperazin-1-yl)carbonyl]azetidine-1-carboxylateHCID 66739735—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-(Azetidin-3-ylcarbonyl)-4-cyclobutylpiperazineHCID 6673931574.6%

Reaction Steps

To a stirred solution of benzyl 3-[(4-cyclobutylpiperazin-1-yl)carbonyl]azetidine-1-carboxylate (130 mg, 0.36 mmol) in EtOH (10 mL) was added 10% Pd/C (13 mg, 10% wt/wt). The flask was evacuated and the vacuum purged with N2 gas. The flask was evacuated again and the vacuum purged with H2 gas. After 16 hours the reaction mixture was filtered through Celite® and charged with 10% Pd/C (13 mg, 10% wt/wt). The flask was evacuated and the vacuum purged with N2 gas. The flask was evacuated again and the vacuum purged with H2 gas. After 23 hours, the reaction mixture was filtered through Celite® and the filtrate concentrated at reduced pressure to give the final compound (60 mg, 74%) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912176B2
Source datasetuspto-grants-2014_12
ORD IDord-006811dfd83144d2a5bc891c8af923eb
Source noteuspto-grants-2014_12