Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406354Generated: November 2, 2026

5-(1-Methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-1''-tert-butoxycarbonyl-dispiro[2,3-dihydrofuro[2,3-c]pyridine-2,1'-cyclobutane-3',4''-piperidine] → 5-(1-Methanesulfonyl-piperidin-4-yl)-1''-tert-butoxycarbonyl-dispiro[2,3-dihydrofuro[2,3-c]pyridine-2,1'-cyclobutane-3',4''-piperidine]

https://huagongshe.com/reaction/2406354

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(1-Methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-1''-tert-butoxycarbonyl-dispiro[2,3-dihydrofuro[2,3-c]pyridine-2,1'-cyclobutane-3',4''-piperidine]HCID 72194850—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product5-(1-Methanesulfonyl-piperidin-4-yl)-1''-tert-butoxycarbonyl-dispiro[2,3-dihydrofuro[2,3-c]pyridine-2,1'-cyclobutane-3',4''-piperidine]HCID 86701213—

Reaction Steps

A flask charged with 5-(1-methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-1″-tert-butoxycarbonyl-dispiro[2,3-dihydrofuro[2,3-c]pyridine-2,1′-cyclobutane-3′,4″-piperidine] (50 mg), 10% palladium on carbon (5 mg), and methanol (5 mL) is shaken under H2 atmosphere (1 bar) at room temperature for 2 h. The catalyst is separated by filtration and the filtrate is concentrated to give the title compound. LC (method 3): tR=0.93 min; Mass spectrum (ESI+): m/z=492 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809361B2
Source datasetuspto-grants-2014_08
ORD IDord-e4853f5b31ef49ae8ff773455b15a51b
Source noteuspto-grants-2014_08