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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873559Generated: October 30, 2026

Tert-butyl 4-(4-(1-(benzyloxycarbonyl)azetidine-3-carboxamido)phenoxy)piperidine-1-carboxylate → Tert-butyl 4-(4-(azetidine-3-carboxamido)phenoxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/873559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(4-(1-(benzyloxycarbonyl)azetidine-3-carboxamido)phenoxy)piperidine-1-carboxylateHCID 86702035—
CatalystPalladium hydroxideHCID 9942167—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(4-(azetidine-3-carboxamido)phenoxy)piperidine-1-carboxylateHCID 86702036—

Reaction Steps

tert-Butyl 4-(4-(1-(benzyloxycarbonyl)azetidine-3-carboxamido)phenoxy)piperidine-1-carboxylate (50 mg, 0.098 mmol) and tetrahydrofuran (5 ml) were added to 20% wet palladium hydroxide on carbon (10 mg, 0.071 mmol) in a 50 ml pressure bottle and the mixture was stirred for 16 hours at 30 psi and room temperature. The mixture was filtered through a nylon membrane and the filtrate was concentrated to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975398B2
Source datasetuspto-grants-2015_03
ORD IDord-2afe1bd1c8c94c4bbf7a5f785740ec48
Source noteuspto-grants-2015_03